Roles of Heart Rate Variability in Assessing Autonomic Nervous System in Functional Gastrointestinal Disorders: A Systematic Review
Abstract
:1. Introduction
1.1. Gut-Brain Communication
1.2. Assessment of the Autonomic Function
1.3. Heart Rate Variability-Based Assessment of the Autonomic Function
2. Methods
2.1. Gastroesophageal Reflux
2.2. Functional Dyspepsia and Gastroparesis
2.3. Irritable Bowel Syndrome
2.4. Constipation
3. Results
3.1. Gastroesophageal Reflux and Autonomic Nervous System
3.2. Functional Dyspepsia, Gastroparesis and Autonomic Nervous System
3.3. Irritable Bowel Syndrome and Autonomic Nervous System
3.4. Constipation and Autonomic Nervous System
4. Discussions
Funding
Conflicts of Interest
References
- Winston, J.H.; Sarna, S.K. Enhanced sympathetic nerve activity induced by neonatal colon inflammation induces gastric hypersensitivity and anxiety-like behavior in adult rats. Am. J. Physiol.-Gastrointest. Liver Physiol. 2016, 311, G32–G39. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Browning, K.N.; Travagli, R.A. Central control of gastrointestinal motility . Curr. Opin. Endocrinol. Diabetes Obes. 2019, 26, 11–16. [Google Scholar] [CrossRef] [PubMed]
- Browning, K.N.; Travagli, R.A. Central Nervous System Control of Gastrointestinal Motility and Secretion and Modulation of Gastrointestinal Functions. In Comprehensive Physiology; Terjung, R., Ed.; Wiley: New York, NY, USA, 2014; pp. 1339–1368. ISBN 978-0-470-65071-4. [Google Scholar]
- Drossman, D.; Li, Z.; Andruzzi, E.; Temple, R.; Talley, N.; Thompson, W.; Whitehead, W.; Janssens, J.; Funch-Jensen, P.; Corazziari, E.U.S. Householder survey of functional gastrointestinal disorders. Prevalence, sociodemography, and health impact. Dig. Dis. Sci. 1993, 38, 1569–1580. [Google Scholar] [CrossRef] [PubMed]
- Fikree, A.; Byrne, P. Management of functional gastrointestinal disorders. Clin. Med. 2021, 21, 44–52. [Google Scholar] [CrossRef]
- Sperber, A.D.; Bangdiwala, S.I.; Drossman, D.A.; Ghoshal, U.C.; Simren, M.; Tack, J.; Whitehead, W.E.; Dumitrascu, D.L.; Fang, X.; Fukudo, S.; et al. Worldwide Prevalence and Burden of Functional Gastrointestinal Disorders, Results of Rome Foundation Global Study. Gastroenterology 2021, 160, 99–114.e3. [Google Scholar] [CrossRef]
- World Gastroenterology Organisation (WGO). Available online: https://www.worldgastroenterology.org (accessed on 12 October 2022).
- Corazziari, E. Definition and epidemiology of functional gastrointestinal disorders. Best Pract. Res. Clin. Gastroenterol. 2004, 18, 613–631. [Google Scholar] [CrossRef]
- Djeddi, D.-D.; Kongolo, G.; Stéphan-Blanchard, E.; Ammari, M.; Léké, A.; Delanaud, S.; Bach, V.; Telliez, F. Involvement of Autonomic Nervous Activity Changes in Gastroesophageal Reflux in Neonates during Sleep and Wakefulness. PLoS ONE 2013, 8, e83464. [Google Scholar] [CrossRef]
- Milovanovic, B.; Filipovic, B.; Mutavdzin, S.; Zdravkovic, M.; Gligorijevic, T.; Paunovic, J.; Arsic, M. Cardiac autonomic dysfunction in patients with gastroesophageal reflux disease. WJG 2015, 21, 6982–6989. [Google Scholar] [CrossRef]
- Yu, Y.; Wei, R.; Liu, Z.; Xu, J.; Xu, C.; Chen, J.D.Z. Ameliorating Effects of Transcutaneous Electrical Acustimulation Combined With Deep Breathing Training on Refractory Gastroesophageal Reflux Disease Mediated via the Autonomic Pathway. Neuromodul. Technol. Neural Interface 2019, 22, 751–757. [Google Scholar] [CrossRef] [Green Version]
- Parkman, H.P.; Camilleri, M.; Farrugia, G.; McCallum, R.W.; Bharucha, A.E.; Mayer, E.A.; Tack, J.F.; Spiller, R.; Horowitz, M.; Vinik, A.I.; et al. Gastroparesis and Functional Dyspepsia: Excerpts from the AGA/ANMS Meeting. Neurogastroenterol. Motil. 2010, 22, 113–133. [Google Scholar] [CrossRef]
- Tominaga, K.; Fujikawa, Y.; Tsumoto, C.; Kadouchi, K.; Tanaka, F.; Kamata, N.; Yamagami, H.; Tanigawa, T.; Watanabe, T.; Fujiwara, Y.; et al. Disorder of autonomic nervous system and its vulnerability to external stimulation in functional dyspepsia. J. Clin. Biochem. Nutr. 2016, 58, 161–165. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Tu, L.; Gharibani, P.; Yang, Y.; Zhang, B.; Ji, F.; Yin, J.; Chen, J.D.Z. A Novel Approach in Spinal Cord Stimulation for Enhancing Gastric Motility: A Preliminary Study on Canines. J. Neurogastroenterol. Motil. 2020, 26, 147–159. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Jang, A.; Hwang, S.-K.; Padhye, N.S.; Meininger, J.C. Effects of Cognitive Behavior Therapy on Heart Rate Variability in Young Females with Constipation-predominant Irritable Bowel Syndrome: A Parallel-group Trial. J. Neurogastroenterol. Motil. 2017, 23, 435–445. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Kano, M.; Yoshizawa, M.; Kono, K.; Muratsubaki, T.; Morishita, J.; Van Oudenhove, L.; Yagihashi, M.; Mugikura, S.; Dupont, P.; Takase, K.; et al. Parasympathetic activity correlates with subjective and brain responses to rectal distension in healthy subjects but not in non-constipated patients with irritable bowel syndrome. Sci. Rep. 2019, 9, 7358. [Google Scholar] [CrossRef] [Green Version]
- Tanaka, Y.; Kanazawa, M.; Palsson, O.S.; Tilburg, M.A.V.; Gangarosa, L.M.; Fukudo, S.; Drossman, D.A.; Whitehead, W.E. Increased Postprandial Colonic Motility and Autonomic Nervous System Activity in Patients With Irritable Bowel Syndrome: A Prospective Study. J. Neurogastroenterol. Motil. 2018, 24, 87–95. [Google Scholar] [CrossRef] [Green Version]
- Duan, H.; Cai, X.; Luan, Y.; Yang, S.; Yang, J.; Dong, H.; Zeng, H.; Shao, L. Regulation of the Autonomic Nervous System on Intestine. Front. Physiol. 2021, 12, 700129. [Google Scholar] [CrossRef]
- Phillips, R.J.; Powley, T.L. Innervation of the gastrointestinal tract: Patterns of aging. Auton. Neurosci. 2007, 136, 1–19. [Google Scholar] [CrossRef] [Green Version]
- Agustí, A.; García-Pardo, M.P.; López-Almela, I.; Campillo, I.; Maes, M.; Romaní-Pérez, M.; Sanz, Y. Interplay Between the Gut-Brain Axis, Obesity and Cognitive Function. Front. Neurosci. 2018, 12, 155. [Google Scholar] [CrossRef] [Green Version]
- Callaghan, B.; Furness, J.B.; Pustovit, R.V. Neural pathways for colorectal control, relevance to spinal cord injury and treatment: A narrative review. Spinal Cord 2018, 56, 199–205. [Google Scholar] [CrossRef] [Green Version]
- Rao, M.; Gershon, M.D. The bowel and beyond: The enteric nervous system in neurological disorders. Nat. Rev. Gastroenterol. Hepatol. 2016, 13, 517–528. [Google Scholar] [CrossRef]
- Carabotti, M.; Scirocco, A.; Maselli, M.A.; Severi, C. The gut-brain axis: Interactions between enteric microbiota, central and enteric nervous systems. Ann. Gastroenterol. 2015, 28, 203–209. [Google Scholar]
- Ali, M.K.; Saha, S.; Milkova, N.; Liu, L.; Sharma, K.; Huizinga, J.D.; Chen, J.-H. Modulation of the autonomic nervous system by one session of spinal low-level laser therapy in patients with chronic colonic motility dysfunction. Front. Neurosci. 2022, 16, 882602. [Google Scholar] [CrossRef] [PubMed]
- Yuan, Y.; Ali, M.K.; Mathewson, K.J.; Sharma, K.; Faiyaz, M.; Tan, W.; Parsons, S.P.; Zhang, K.K.; Milkova, N.; Liu, L.; et al. Associations Between Colonic Motor Patterns and Autonomic Nervous System Activity Assessed by High-Resolution Manometry and Concurrent Heart Rate Variability. Front. Neurosci. 2020, 13, 1447. [Google Scholar] [CrossRef] [PubMed]
- Ali, M.K.; Liu, L.; Chen, J.-H.; Huizinga, J.D. Optimizing Autonomic Function Analysis via Heart Rate Variability Associated With Motor Activity of the Human Colon. Front. Physiol. 2021, 12, 619722. [Google Scholar] [CrossRef]
- Ali, M.K. Development of Methodologies to Assess Autonomic Nervous System Functioning and Neuromodulation for the Diagnosis and Treatment of Colonic Motility Disorders. 2022. Available online: https://macsphere.mcmaster.ca/handle/11375/27757 (accessed on 13 October 2022).
- La Rovere, M.T.; Pinna, G.D.; Raczak, G. Baroreflex Sensitivity: Measurement and Clinical Implications. Ann. Noninv. Electrocard. 2008, 13, 191–207. [Google Scholar] [CrossRef]
- Bisogni, V.; Pengo, M.F.; Maiolino, G.; Rossi, G.P. The sympathetic nervous system and catecholamines metabolism in obstructive sleep apnoea. J. Thorac. Dis. 2016, 8, 243–254. [Google Scholar]
- Goldstein, D.S.; Cheshire, W.P. Roles of cardiac sympathetic neuroimaging in autonomic medicine. Clin. Auton. Res. 2018, 28, 397–410. [Google Scholar] [CrossRef]
- Ghiasi, S.; Greco, A.; Barbieri, R.; Scilingo, E.P.; Valenza, G. Assessing Autonomic Function from Electrodermal Activity and Heart Rate Variability During Cold-Pressor Test and Emotional Challenge. Sci. Rep. 2020, 10, 5406. [Google Scholar] [CrossRef] [Green Version]
- Taralov, Z.Z.; Terziyski, K.V.; Kostianev, S.S. Heart Rate Variability as a Method for Assessment of the Autonomic Nervous System and the Adaptations to Different Physiological and Pathological Conditions. Folia Med. 2016, 57, 173–180. [Google Scholar] [CrossRef] [Green Version]
- Bernardi, L.; Spallone, V.; Stevens, M.; Hilsted, J.; Frontoni, S.; Pop-Busui, R.; Ziegler, D.; Kempler, P.; Freeman, R.; Low, P.; et al. Methods of investigation for cardiac autonomic dysfunction in human research studies: Investigation Methods for Cardiac Autonomic Function. Diabetes Metab. Res. Rev. 2011, 27, 654–664. [Google Scholar] [CrossRef] [Green Version]
- Shaffer, F.; McCraty, R.; Zerr, C.L. A healthy heart is not a metronome: An integrative review of the heart’s anatomy and heart rate variability. Front. Psychol. 2014, 5, 1040. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Shaffer, F.; Ginsberg, J.P. An Overview of Heart Rate Variability Metrics and Norms. Front. Public Health 2017, 5, 258. [Google Scholar] [CrossRef] [PubMed]
- Yilmaz, M.; Kayancicek, H.; Cekici, Y. Heart rate variability: Highlights from hidden signals. J. Integr. Cardiol. 2018, 4, 1–8. [Google Scholar] [CrossRef]
- Baevsky, R.M.; Chernikova, A.G. Heart rate variability analysis: Physiological foundations and main methods. Cardiometry 2017, 10, 66–76. [Google Scholar] [CrossRef] [Green Version]
- Liu, L.; Milkova, N.; Nirmalathasan, S.; Ali, M.K.; Sharma, K.; Huizinga, J.D.; Chen, J.-H. Diagnosis of colonic dysmotility associated with autonomic dysfunction in patients with chronic refractory constipation. Sci. Rep. 2022, 12, 12051. [Google Scholar] [CrossRef]
- Colombo, J.; Arora, R.; DePace, N.L.; Vinik, A.I. Clinical Autonomic Dysfunction; Springer International Publishing: Cham, Switzerland, 2015; ISBN 978-3-319-07370-5. [Google Scholar]
- Murakami, H.; Li, S.; Foreman, R.; Yin, J.; Hirai, T.; Chen, J.D.Z. Ameliorating Effects of Electroacupuncture on Dysmotility, Inflammation, and Pain Mediated via the Autonomic Mechanism in a Rat Model of Postoperative Ileus. J. Neurogastroenterol. Motil. 2019, 25, 286–299. [Google Scholar] [CrossRef] [Green Version]
- Rowan, W.H.; Campen, M.J.; Wichers, L.B.; Watkinson, W.P. Heart rate variability in rodents: Uses and caveats in toxicological studies. Cardiovasc. Toxicol. 2007, 7, 28–51. [Google Scholar] [CrossRef]
- Johnston, B.W.; Barrett-Jolley, R.; Krige, A.; Welters, I.D. Heart rate variability: Measurement and emerging use in critical care medicine. J. Intensive Care Soc. 2020, 21, 148–157. [Google Scholar] [CrossRef]
- Finsterer, J.; Scorza, F.A.; Scorza, C.A.; Fiorini, A.C. Consider differentials before diagnosing COVID-19 associated polyradiculitis. Eur. J. Transl. Myol. 2022, 32. [Google Scholar] [CrossRef]
- Lee, Y.-C.; Wang, H.-P.; Lin, L.-Y.; Lee, B.-C.; Chiu, H.-M.; Wu, M.-S.; Chen, M.-F.; Lin, J.-T. Heart rate variability in patients with different manifestations of gastroesophageal reflux disease. Auton. Neurosci. 2004, 116, 39–45. [Google Scholar] [CrossRef]
- Huang, W.-J.; Shu, C.-H.; Chou, K.-T.; Wang, Y.-F.; Hsu, Y.-B.; Ho, C.-Y.; Lan, M.-Y. Evaluating the Autonomic Nervous System in Patients with Laryngopharyngeal Reflux. Otolaryngol. Head Neck Surg. 2013, 148, 997–1002. [Google Scholar] [CrossRef] [PubMed]
- Chen, C.-L.; Orr, W.C. Autonomic responses to heartburn induced by esophageal acid infusion. J. Gastroenterol. Hepatol. 2004, 19, 922–926. [Google Scholar] [CrossRef] [PubMed]
- Lee, Y.-C.; Wang, H.-P.; Lin, L.-Y.; Chuang, K.-J.; Chiu, H.-M.; Wu, M.-S.; Chen, M.-F.; Lin, J.-T. Circadian change of cardiac autonomic function in correlation with intra-esophageal pH. J. Gastroenterol. Hepatol. 2006, 21, 1302–1308. [Google Scholar] [CrossRef]
- Hollerbach, S.; Bulat, R.; May, A.; Kamath, M.V.; Upton, A.R.M.; Fallen, E.L.; Tougas, G. Abnormal cerebral processing of oesophageal stimuli in patients with noncardiac chest pain (NCCP). Neurogastroenterol. Motil. 2000, 12, 555–565. [Google Scholar] [CrossRef] [PubMed]
- Jones, E.L.; Perring, S.; Khattab, A.; Allenby-Smith, O. The effects of proton pump inhibitors on autonomic tone in patients with erosive and non-erosive esophagitis. Neurogastroenterol. Motil. 2016, 28, 659–664. [Google Scholar] [CrossRef] [PubMed]
- Tirosh, E.; Ariov-Antebi, N.; Cohen, A. Autonomic function, gastroesophageal reflux in apparent life threatening event. Clin. Auton. Res. 2010, 20, 161–166. [Google Scholar] [CrossRef]
- Swiatkowski, M.; Budzyński, J.; Kłopocka, M.; Ziółkowski, M.; Bujak, R.; Sinkiewicz, W. Parameters of the functional and morphological status of the upper digestive tract in alcohol-dependent male patients with depression and alexithymia in the context of autonomic nervous system activity and nitric oxide plasma level. Med. Sci. Monit. 2004, 10, CR68–CR74. [Google Scholar]
- Hu, Y.; Zhang, B.; Shi, X.; Ning, B.; Shi, J.; Zeng, X.; Liu, F.; Chen, J.D.; Xie, W.-F. Ameliorating Effects and Autonomic Mechanisms of Transcutaneous Electrical Acustimulation in Patients With Gastroesophageal Reflux Disease. Neuromodul. Technol. Neural Interface 2020, 23, 1207–1214. [Google Scholar] [CrossRef]
- Nowak, J.K.; Łaźniak, A.; Lisowska, A.; Kycler, Z.; Bobkowski, W.; Walkowiak, J. Gastroesophageal reflux is not associated with short-term variability of parasympathetic activity in children. Adv. Med. Sci. 2017, 62, 103–109. [Google Scholar] [CrossRef]
- Floria, M.; Bărboi, O.; Grecu, M.; Cijevschi Prelipcean, C.; Balan, G. Atrial fibrillation and sympathovagal balance in patients with gastroesophageal reflux disease. Turk. J. Gastroenterol. 2017, 28, 88–93. [Google Scholar] [CrossRef] [PubMed]
- Campo, S.M.A.; Capria, A.; Antonucci, F.; Martino, G.; Ciamei, A.; Rossini, P.M.; Bologna, E.; Cannata, D. Decreased sympathetic inhibition in gastroesophageal reflux disease. Clin. Auton. Res. 2001, 11, 45–51. [Google Scholar] [CrossRef] [PubMed]
- Guo, W.-J.; Yao, S.-K.; Zhang, Y.-L.; Du, S.-Y.; Wang, H.-F.; Yin, L.-J.; Li, H.-L. Impaired vagal activity to meal in patients with functional dyspepsia and delayed gastric emptying. J. Int. Med. Res. 2018, 46, 792–801. [Google Scholar] [CrossRef] [Green Version]
- Lee, I.-S.; Preissl, H.; Giel, K.; Schag, K.; Enck, P. Attentional and physiological processing of food images in functional dyspepsia patients: A pilot study. Sci. Rep. 2018, 8, 1388. [Google Scholar] [CrossRef] [PubMed]
- Ye, F.; Liu, Y.; Li, S.; Zhang, S.; Foreman, R.D.; Chen, J.D. Sacral nerve stimulation increases gastric accommodation in rats: A spinal afferent and vagal efferent pathway. Am. J. Physiol.-Gastrointest. Liver Physiol. 2020, 318, G574–G581. [Google Scholar] [CrossRef] [PubMed]
- Zhu, Y.; Xu, F.; Lu, D.; Rong, P.; Cheng, J.; Li, M.; Gong, Y.; Sun, C.; Wei, W.; Lin, L.; et al. Transcutaneous auricular vagal nerve stimulation improves functional dyspepsia by enhancing vagal efferent activity. Am. J. Physiol.-Gastrointest. Liver Physiol. 2021, 320, G700–G711. [Google Scholar] [CrossRef]
- Zhang, S.; Liu, Y.; Li, S.; Ye, F.; Foreman, R.D.; Chen, J.D.Z. Effects of electroacupuncture on stress-induced gastric dysrhythmia and mechanisms involving autonomic and central nervous systems in functional dyspepsia. Am. J. Physiol.-Regul. Integr. Comp. Physiol. 2020, 319, R106–R113. [Google Scholar] [CrossRef]
- Zhou, J.; Li, S.; Wang, Y.; Lei, Y.; Foreman, R.D.; Yin, J.; Chen, J.D.Z. Effects and mechanisms of auricular electroacupuncture on gastric hypersensitivity in a rodent model of functional dyspepsia. PLoS ONE 2017, 12, e0174568. [Google Scholar] [CrossRef]
- Okamoto, H.; Nomura, M.; Nakaya, Y.; Uehara, K.; Saito, K.; Kimura, M.; Chikamori, K.; Ito, S. Effects of epalrestat, an aldose reductase inhibitor, on diabetic neuropathy and gastroparesis. Intern. Med. 2003, 42, 655–664. [Google Scholar] [CrossRef] [Green Version]
- Yin, J.; Chen, J.; Chen, J.D.Z. Ameliorating effects and mechanisms of electroacupuncture on gastric dysrhythmia, delayed emptying, and impaired accommodation in diabetic rats. Am. J. Physiol.-Gastrointest. Liver Physiol. 2010, 298, G563–G570. [Google Scholar] [CrossRef] [Green Version]
- Ouyang, H.; Yin, J.; Wang, Z.; Pasricha, P.J.; Chen, J.D.Z. Electroacupuncture accelerates gastric emptying in association with changes in vagal activity. Am. J. Physiol.-Gastrointest. Liver Physiol. 2002, 282, G390–G396. [Google Scholar] [CrossRef] [Green Version]
- Cai, F.Z.; Lester, S.; Lu, T.; Keen, H.; Boundy, K.; Proudman, S.M.; Tonkin, A.; Rischmueller, M. Mild autonomic dysfunction in primary Sjögren’s syndrome: A controlled study. Arthritis Res. Ther. 2008, 10, R31. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Nguyen, L.; Wilson, L.A.; Miriel, L.; Pasricha, P.J.; Kuo, B.; Hasler, W.L.; McCallum, R.W.; Sarosiek, I.; Koch, K.L.; Snape, W.J.; et al. Autonomic function in gastroparesis and chronic unexplained nausea and vomiting: Relationship with etiology, gastric emptying, and symptom severity. Neurogastroenterol. Motil. 2020, 32, e13810. [Google Scholar] [CrossRef] [PubMed]
- Stocker, A.; Abell, T.L.; Rashed, H.; Kedar, A.; Boatright, B.; Chen, J. Autonomic Evaluation of Patients With Gastroparesis and Neurostimulation: Comparisons of Direct/Systemic and Indirect/Cardiac Measures. Gastroenterol. Res. 2016, 9, 10–16. [Google Scholar] [CrossRef] [PubMed]
- Kumar, M.S.; Vinod, K.V.; Pandit, N.; Sharma, V.K.; Dhanapathi, H.; Parameswaran, S. Delayed Gastric Emptying among Indian Patients with Non-Diabetic Chronic Kidney Disease. Indian J. Nephrol. 2021, 31, 135–141. [Google Scholar]
- Søfteland, E.; Brock, C.; Frøkjær, J.B.; Simrén, M.; Drewes, A.M.; Dimcevski, G. Rectal Sensitivity in Diabetes Patients with Symptoms of Gastroparesis. J. Diabetes Res. 2014, 2014, 784841. [Google Scholar] [CrossRef] [Green Version]
- Vargas-Luna, F.M.; Huerta-Franco, M.R.; Schurman, J.V.; Deacy, A.D.; Bagherian, A.; Harvey, L.; Friesen, C.A. Heart Rate Variability and Gastric Electrical Response to a Cold Pressor Task in Youth with Functional Dyspepsia. Dig. Dis. Sci. 2020, 65, 1074–1081. [Google Scholar] [CrossRef]
- Friesen, C.A.; Lin, Z.; Schurman, J.V.; Andre, L.; McCallum, R.W. The Effect of a Meal and Water Loading on Heart Rate Variability in Children with Functional Dyspepsia. Dig. Dis. Sci. 2010, 55, 2283–2287. [Google Scholar] [CrossRef]
- Silva Lorena, S.L.; de Oliveira Figueiredo, M.J.; Souza Almeida, J.R.; Mesquita, M.A. Autonomic Function in Patients with Functional Dyspepsia Assessed by 24-Hour Heart Rate Variability. Dig. Dis. Sci. 2002, 47, 27–31. [Google Scholar] [CrossRef]
- Pellissier, S.; Dantzer, C.; Canini, F.; Mathieu, N.; Bonaz, B. Psychological adjustment and autonomic disturbances in inflammatory bowel diseases and irritable bowel syndrome. Psychoneuroendocrinology 2010, 35, 653–662. [Google Scholar] [CrossRef] [Green Version]
- Tillisch, K. Sex specific alterations in autonomic function among patients with irritable bowel syndrome. Gut 2005, 54, 1396–1401. [Google Scholar] [CrossRef] [Green Version]
- Robert, J.J.T.; Orr, W.C.; Elsenbruch, S. Modulation of Sleep Quality and Autonomic Functioning by Symptoms of Depression in Women with Irritable Bowel Syndrome. Dig. Dis. Sci. 2004, 49, 1250–1258. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Jarrett, M.E.; Cain, K.C.; Barney, P.G.; Burr, R.L.; Naliboff, B.D.; Shulman, R.; Zia, J.; Heitkemper, M.M. Balance of Autonomic Nervous System Predicts Who Benefits from a Self-management Intervention Program for Irritable Bowel Syndrome. J. Neurogastroenterol. Motil. 2015, 22, 102–111. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Cheng, P.; Shih, W.; Alberto, M.; Presson, A.P.; Licudine, A.; Mayer, E.A.; Naliboff, B.D.; Chang, L. Autonomic response to a visceral stressor is dysregulated in irritable bowel syndrome and correlates with duration of disease. Neurogastroenterol. Motil. 2013, 25, e650–e659. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Jarrett, M.; Heitkemper, M.; Czyzewski, D.; Zeltzer, L.; Shulman, R.J. Autonomic Nervous System Function in Young Children With Functional Abdominal Pain or Irritable Bowel Syndrome. J. Pain 2012, 13, 477–484. [Google Scholar] [CrossRef] [PubMed]
- Davydov, D.M.; Naliboff, B.; Shahabi, L.; Shapiro, D. Baroreflex mechanisms in Irritable Bowel Syndrome: Part I. Traditional indices. Physiol. Behav. 2016, 157, 102–108. [Google Scholar] [CrossRef] [Green Version]
- Jarrett, M.E.; Han, C.J.; Cain, K.C.; Burr, R.L.; Shulman, R.J.; Barney, P.G.; Naliboff, B.D.; Zia, J.; Heitkemper, M.M. Relationships of abdominal pain, reports to visceral and temperature pain sensitivity, conditioned pain modulation, and heart rate variability in irritable bowel syndrome. Neurogastroenterol. Motil. 2016, 28, 1094–1103. [Google Scholar] [CrossRef] [Green Version]
- Walker, L.S.; Stone, A.L.; Smith, C.A.; Bruehl, S.; Garber, J.; Puzanovova, M.; Diedrich, A. Interacting influences of gender and chronic pain status on parasympathetically mediated heart rate variability in adolescents and young adults. Pain 2017, 158, 1509–1516. [Google Scholar] [CrossRef]
- Pellissier, S.; Dantzer, C.; Mondillon, L.; Trocme, C.; Gauchez, A.-S.; Ducros, V.; Mathieu, N.; Toussaint, B.; Fournier, A.; Canini, F.; et al. Relationship between Vagal Tone, Cortisol, TNF-Alpha, Epinephrine and Negative Affects in Crohn’s Disease and Irritable Bowel Syndrome. PLoS ONE 2014, 9, e105328. [Google Scholar] [CrossRef] [Green Version]
- Tanaka, Y.; Kanazawa, M.; Kano, M.; Tashiro, M.; Fukudo, S. Relationship between sympathoadrenal and pituitary-adrenal response during colorectal distention in the presence of corticotropin-releasing hormone in patients with irritable bowel syndrome and healthy controls. PLoS ONE 2018, 13, e0199698. [Google Scholar] [CrossRef] [Green Version]
- Karling, P.; Nyhlin, H.; Wiklund, U. Nyhlin, U. Wiklund, Spectral Analysis of Heart Rate Variability in Patients with Irritable Bowel Syndrome. Scand. J. Gastroenterol. 1998, 33, 572–576. [Google Scholar] [CrossRef]
- Cain, K.C.; Jarrett, M.E.; Burr, R.L.; Hertig, V.L.; Heitkemper, M.M. Heart rate variability is related to pain severity and predominant bowel pattern in women with irritable bowel syndrome. Neurogastroenterol. Motil. 2007, 19, 110–118. [Google Scholar] [CrossRef] [PubMed]
- Polster, A.; Friberg, P.; Gunterberg, V.; Öhman, L.; Le Nevé, B.; Törnblom, H.; Cvijovic, M.; Simren, M. Heart rate variability characteristics of patients with irritable bowel syndrome and associations with symptoms. Neurogastroenterol. Motil. 2018, 30, e13320. [Google Scholar] [CrossRef] [PubMed]
- Orr, W.C.; Elsenbruch, S.; Harnish, M.J. Autonomic Regulation of Cardiac Function During Sleep in Patients With Irritable Bowel Syndrome. Am. J. Gastroenterol. 2000, 95, 2865–2871. [Google Scholar] [CrossRef]
- Adeyemi, E.O.A.; Desai, K.D.; Towsey, M.; Ghista, D. Characterization of autonomic dysfunction in patients with irritable bowel syndrome by means of heart rate variability studies. Am. J. Gastroenterol. 1999, 94, 816–823. [Google Scholar] [CrossRef]
- Wang, X.; Yang, B.; Yin, J.; Wei, W.; Chen, J.D.Z. Electroacupuncture via chronically implanted electrodes improves gastrointestinal motility by balancing sympathovagal activities in a rat model of constipation. Am. J. Physiol.-Gastrointest. Liver Physiol. 2019, 316, G797–G805. [Google Scholar] [CrossRef] [PubMed]
- Miyagi, T.; Yamazato, M.; Nakamura, T.; Tokashiki, T.; Namihira, Y.; Kokuba, K.; Ishihara, S.; Sakima, H.; Ohya, Y. Power spectral analysis of heart rate variability is useful as a screening tool for detecting sympathetic and parasympathetic nervous dysfunctions in Parkinson’s disease. BMC Neurol. 2022, 22, 339. [Google Scholar] [CrossRef]
- Huang, Z.; Li, S.; Foreman, R.D.; Yin, J.; Dai, N.; Chen, J.D.Z. Sacral nerve stimulation with appropriate parameters improves constipation in rats by enhancing colon motility mediated via the autonomic-cholinergic mechanisms. Am. J. Physiol.-Gastrointest. Liver Physiol. 2019, 317, G609–G617. [Google Scholar] [CrossRef]
- Liu, Z.; Ge, Y.; Xu, F.; Xu, Y.; Liu, Y.; Xia, F.; Lin, L.; Chen, J.D.Z. Preventive effects of transcutaneous electrical acustimulation on ischemic stroke-induced constipation mediated via the autonomic pathway. Am. J. Physiol.-Gastrointest. Liver Physiol. 2018, 315, G293–G301. [Google Scholar] [CrossRef]
- Jin, H.; Liu, J.; Foreman, R.D.; Chen, J.D.Z.; Yin, J. Electrical neuromodulation at acupoint ST36 normalizes impaired colonic motility induced by rectal distension in dogs. Am. J. Physiol.-Gastrointest. Liver Physiol. 2015, 309, G368–G376. [Google Scholar] [CrossRef] [Green Version]
- Gondim, R.; Gorjão, J.; Nacif, A.; Franco, I.; Barroso, U., Jr. Evaluation of autonomic function in children and adolescents with overactive bladder. Int. Braz. J. Urol. 2021, 47, 1178–1188. [Google Scholar] [CrossRef]
- Liu, J.; Chen, H.; Wu, D.; Wei, R.; Lv, C.; Dong, J.; Wu, D.; Yu, Y. Ameliorating Effects of Transcutaneous Electrical Acustimulation at Neiguan (PC6) and Zusanli (ST36) Acupoints Combined with Adaptive Biofeedback Training on Functional Outlet Obstruction Constipation. Evid.-Based Complement. Altern. Med. 2020, 2020, 8798974. [Google Scholar] [CrossRef] [PubMed]
- Enevoldsen, J.; Vistisen, S.T.; Krogh, K.; Nielsen, J.F.; Knudsen, K.; Borghammer, P.; Andersen, H. Gastrointestinal transit time and heart rate variability in patients with mild acquired brain injury. PeerJ 2018, 6, e4912. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Liu, J.; Wang, W.; Tian, J.; Lv, C.; Fu, Y.; Fass, R.; Song, G.; Yu, Y. Sleep Deficiency Is Associated With Exacerbation of Symptoms and Impairment of Anorectal and Autonomic Functions in Patients With Functional Constipation. Front. Neurosci. 2022, 16, 912442. [Google Scholar] [CrossRef]
- Zhang, N.; Huang, Z.; Xu, F.; Xu, Y.; Chen, J.; Yin, J.; Lin, L.; Chen, J.D.Z. Transcutaneous Neuromodulation at Posterior Tibial Nerve and ST36 for Chronic Constipation. Evid.-Based Complement. Altern. Med. 2014, 2014, 560802. [Google Scholar] [CrossRef]
- Ding, M.; Lin, Z.; Lin, L.; Zhang, H.; Wang, M. The Effect of Biofeedback Training on Patients With Functional Constipation. Gastroenterol. Nurs. 2012, 35, 85–92. [Google Scholar] [CrossRef]
- Wu, G.; Xu, F.; Sun, X.; Chen, J.D.Z. Transcutaneous Neuromodulation at ST36 (Zusanli) is More Effective than Transcutaneous Tibial Nerve Stimulation in Treating Constipation. J. Clin. Gastroenterol. 2020, 54, 536–544. [Google Scholar] [CrossRef] [PubMed]
- Chen, C.-Y.; Chen, J.-R.; Ke, M.-D.; Huang, C.-H.; Hsueh, Y.-H.; Kuo, C.-D. Treatment effect of acupuncture and electric stimulation on chronic constipation patients. In Proceedings of the 2010 IEEE Asia Pacific Conference on Circuits and Systems, Kuala Lumpur, Malaysia, 6–9 December 2010; pp. 450–452. [Google Scholar]
- De Palma, G.; Collins, S.M.; Bercik, P. The microbiota-gut-brain axis in functional gastrointestinal disorders. Gut Microbes 2014, 5, 419–429. [Google Scholar] [CrossRef] [Green Version]
- Chen, J. Neuromodulation and Neurostimulation for the Treatment of Functional Gastrointestinal Disorders. Gastroenterol. Hepatol. 2022, 18, 47–49. [Google Scholar]
- Hayano, J.; Yuda, E. Pitfalls of assessment of autonomic function by heart rate variability. J. Physiol. Anthropol. 2019, 38, 3. [Google Scholar] [CrossRef] [Green Version]
- Colombo, J.; Arora, R.; DePace, N.L.; Vinik, A.I. Drawbacks of Heart Rate Variability Analysis and Application of Parasympathetic and Sympathetic Monitoring. In Clinical Autonomic Dysfunction: Measurement, Indications, Therapies, and Outcomes; Colombo, J., Arora, R., DePace, N.L., Vinik, A.I., Eds.; Springer International Publishing: Cham, Switzerland, 2015; pp. 27–52. ISBN 978-3-319-07371-2. [Google Scholar]
- Lu, C.-L.; Zou, X.; Orr, W.C.; Chen, J.D.Z. Postprandial Changes of Sympathovagal Balance Measured by Heart Rate Variability. Dig. Dis. Sci. 1999, 44, 857–861. [Google Scholar] [CrossRef]
HRV Parameter (Unit) | Description | Represents |
---|---|---|
RMSSD (ms) | Root mean square (rms) of the successive differences between the RR intervals where n is the total number of RR intervals, RRi is the current RR interval, and RRi+1 is the next RR interval | Parasympathetic activity |
pNN50 (%) | Percentage of successive RR intervals which differ by more than 50 ms | Parasympathetic activity |
SDRR (ms) | Standard deviation of RR intervals | Parasympathetic activities |
SDNN (ms) | Standard deviation of NN (RR intervals after removing artifacts from the recorded ECG signal) | Parasympathetic activities |
SDANN (ms) | Standard deviation of averages of NN intervals in all of the 5 min segments of a 24-h recording | Influenced by both sympathetic and parasympathetic activities |
SDNN index (ms) | Average of the standard deviations of all the NN intervals of each 5 min segment of a 24-h recording | Influenced by both sympathetic and parasympathetic activities |
Pre-ejection period PEP (ms) | Time interval between the electrical activity (Q point on ECG signal) and mechanical activity (B point on the impedance signal) of the heart. PEP is inversely proportional to the sympathetic activity | Sympathetic activity |
Sympathetic index SI (s−2) | Calculated from the histogram of the RR intervals using 50 ms bin size: where AMo = amplitude of mode, Mo = mode of RR intervals, MxDMn = range of RR intervals | Sympathetic activity |
SD1 (ms) | The length of the minor axis of the fitted eclipse on the Poincare Plot of RR intervals RRi and RRi+1 represent the current and next RR intervals. | Parasympathetic activity |
SD2 (ms) | The length of the major axis of the fitted eclipse on the Poincare Plot of RR intervals RRi and RRi+1 represent the current and next RR interval, and is the mean value of RR intervals used | Influenced by both sympathetic and parasympathetic activities |
SD2/SD1 | The ratio of the lengths of major and minor axes of the Poincare plot of RR intervals | Autonomic balance |
SI/RSA (s−2/ln(ms2)) | Ratio of sympathetic index to respiratory sinus arrythmia | Autonomic balance |
SI/RMSSD (s−3) | Ratio of sympathetic index to RMSSD | Autonomic balance |
Sr. | Study | Population (n) | Study Design | HRV Parameters | Results | Conclusion |
---|---|---|---|---|---|---|
1 | Lee et al., 2004 [44] | 164 participants, including 57 controls, 34 with non-erosive reflux disease (NERD), 40 with symptomatic esophagitis (SE) and 33 with asymptomatic esophagitis (AE) | 5-min resting autonomic activity was recorded via heart rate variability and compared between all of the patient and control groups. | SDNN, RMSSD, LF power, HF power, LF/HF power ratio. | HF power was significantly higher in patients with NERD in comparison with both SE and AE patient groups. All of the HRV parameters for autonomic tones were significantly lower in erosive as compared to non-erosive group. No difference was observed in time domain parameters. | The patients with endoscopically confirmed esophagitis (with or without symptoms) had low autonomic tone as compared to those with NERD. |
2 | J. Huang et al., 2013 [45] | 17 patients with laryngopharyngeal reflux (LPR) and 19 healthy controls (age between 19 and 50) | 5-min recording in supine position using blood volume pulse (BVP) sensor to record the heartbeat from the fingertip. 10 min adaption time before the actual recording. | RR interval, LF power, HF power, LF%, HF%, LF/HF | HF% was significantly lower (p = 0.003) and LF/HF ratio (p = 0.12) was significantly higher in patients with LPR, compared to healthy controls, indicating poor autonomic modulation and high sympathetic activity in patients. No significant difference in LF power and HF power in two groups. | Autonomic dysfunction seemed to be involved in the pathogenesis of LPR. |
3 | Djeddi et al., 2013 [9] | 19 newborns with suspected gastroesophageal reflux (GER) | All participants underwent simultaneous 12-h polysomnography and esophageal pH monitoring. HRV parameters were recorded and compared during three types of periods (control, prior to and during the reflux) | RR, SDSD, RMSSD, pNN50, LF, HF, lFnu, hFnu, LF/HF | A significant increase in sympathovagal ratio (+32%, p = 0.013) was observed in the period prior to reflux which is caused by the 15% reduction in PNS activity (p = 0.017) relative to control period. | Gastroesophageal reflux events were preceded by a decrease in parasympathetic tone. |
4 | Milovanovic et al., 2015 [10] | 29 patients (14 males and 15 females) aged (51.14 ± 18.34 years) with diagnosed GERD and 116 healthy controls | The study protocol included the evaluation of autonomic function and hemodynamic status, short-term heart rate variability (HRV) analysis, 24 h ambulatory ECG monitoring with long-term HRV analysis and 24 h ambulatory blood pressure monitoring. | Short-term HRV Average dRR, SD dRR, MD drr, pNN50%, RMSSD, VLF, LF, HF, LF/HF Long-term HRV Mean RR, SDNN, SDANN index, SDNN index, RMSSD, pNN50%, total power, VLF, LF, HF | Short-term HRV analysis All of the spectral and time domain HRV parameters were significantly lower in patients with GERD compared to controls, except for the LF/HF ratio. Long-term HRV analysis All of the HRV parameters had significantly lower values in patients with GERD compared to controls except for the mean RR. | GERD patients exhibited distortions of both the sympathetic and parasympathetic nervous systems with parasympathetic function appeared more congruent to GERD |
5 | Chen & Orr et al., 2004 [46] | 12 GERD patients (6 males, 6 females; mean age = 37.2 ± 2.7 yrs) and 12 healthy controls (5 males, 7 females; mean age = 32.8 ± 2.2 yrs) | All the participants had 20-min water infusion (6 mL/min) and 20-min acid infusion (0.1 N HCL, 6 mL/min). ECG was recorded during each infusion period and HRV parameters were compared between the patients with GERD and control groups. | HF power, LF power, and LF/HF ratio (LF was considered as a measure of sympathetic activity) | Comparison of patient and control groups indicated that there was no significant change in LF band power in any period. The HF band power was significantly lower in GERD patients during all infusion periods. The LF/HF ratio was significantly larger in GERD patients. | Enhanced sympathetic dominance to esophageal acid infusion in patients with GERD. |
6 | Lee et al., 2006 [47] | 30 GERD patients (21 males, 9 females; age range 28–83 years) with at least three episodes per week of heartburn and acid regurgitation. The patients were divided into two groups: pathological reflux group (n = 15) and functional heartburn group (n = 15) | All the participants referred for 48 h ambulatory pH monitoring underwent simultaneous 24 h cardiac monitoring for HRV to study the relationship between esophageal acid exposure and HRV. | LF power, HF power, LF/HF ratio | Patients with pathological reflux had lower average LF and HF powers than patients with functional heartburn. A significantly higher HF power and lower LF/HF ratio was found during sleep time, regardless of the diagnosis. The esophageal pH was positively associated with change in both LF and HF powers during waking and only HF power during sleeping. This association decreases with time. | Esophageal reflux was found to be associated with a decreased autonomic tone. A predominant parasympathetic fluctuation during sleeping and a superimposed sympathetic interaction during waking dictate during the daytime. |
7 | Yu et al., 2019 [11] | 21 patients with refectory gastroesophageal reflux (rGERD) were divided into three groups with n = 7 in each group. | Group A received esomeprazole (ESO, 20 mg bid); group B received transcutaneous electrical acustimulation (TEA)+ deep breathing training (DBT) + ESO; group C received sham-TEA +DBT + ESO in a four-week study. ECG was recorded and HRV was evaluated at baseline and at the end of each treatment. Acetylcholine (Ach) and nitric oxide (NO) were measured from blood samples. Esophageal manometry and 24 h pH monitoring was performed before and after the treatment. | LF/(LF + HF) HF/(LF + HF) | Low frequency band (LF)/(LF + HF) ratio in groups B and C was decreased, compared with group A (p = 0.010, p = 0.042, respectively); high frequency band (HF)/(LF + HF) ratio in B and C groups was significantly increased, compared with group A (p = 0.010, p = 0.042, respectively). The serum Ach in groups B and C was significantly higher than group A (p = 0.022, p = 0.046, respectively); the serum NO in groups B and C was significantly lower than group A (p = 0.010, p = 0.027, respectively). | TEA combined with DBT significantly increased lower esophageal sphincter pressure (LESP), reduced acid reflux, and improved clinical indices of GERD. Both TEA and DBT significantly enhanced vagal activity and suppressed sympathetic activity assessed by the spectral analysis of HRV. |
8 | Hollerbach et al., 2000 [48] | 12 healthy volunteers (1 female, 11 males aged 32 ± 8 yrs); 8 patients with non-cardiac chest pain (NCCP) (3 females, 5 males, aged = 40.5 ± 10 yrs) | Electrical oesophageal stimulation (EOS; 200 ls, 0.2 Hz, 25 stimuli) was applied to the oesophageal wall 5 cm above the lower oesophageal sphincter (LOS), and perception thresholds (measured in mA) were determined. EP responses were recorded using 22 standard electroencephalograms scalp electrodes. Heart Rate variability was used to assess the autonomic activity before, during, and after the oesophageal stimulation. | HF power, LF power, and LF/HF ratio (LF was considered as a measure of sympathetic activity) | Electrical stimulation decreased the sympathetic outflow and increased the vagal activity as represented by significantly higher values of LF area and HF area in patients compared to the healthy controls. LF/HF ratio decreased significantly during the stimulations in patients. The HR decreased in patients during EOS and not in controls. | NCCP patients in comparison with healthy controls modulated their autonomic nervous system in response to the oesophageal stimulations. |
9 | Jones et al., 2016 [49] | Control group included 71 participants (18M, age = 48.6 ± 11.9 yrs) 14 patients (8M, age = 49.1 ± 13.6 yrs) with non-erosive reflux disease (NERD) and 10 patients (6M, age = 51.6 ± 11.3 yrs) with erosive reflux disease (ERD) | HRV was assessed for all of the participants before starting a course of proton pump inhibitor (PPI) therapy and 8 weeks from the start of PPI therapy. The values were compared between patients and control groups. | I/E Diff (bpm) HR difference between maximum and minimum heart rate at 5 breaths/min Valsalva ratio Hand grip ratio Ratio of HR during maximal handgrip to heart rate during resting Lying/Standing ratio Ratio of maximum to minimum HR following standing Deep Breathing Analysis of HRV during 2 min of metronome-guided breathing at 6 breaths per minute. | ERD group had low HRV which improved significantly after PPI therapy as measured by I/E ratio on forced breathing, Valsalva ratio, and breathing at 6 breaths per minute. NERD group also shown increase in HRV after PPI but did not reach statistical significance. | The cardiac autonomic neuropathy, as measured by HRV, was associated with gastroesophageal reflux disease and th successful treatment of the inflammation could lead to reversal of the deterioration of autonomic tone. |
10 | Tirosh et al., 2010 [50] | 17 infants diagnosed with idiopathic apparent life-threatening event (IALTE) and gastroesophageal reflux (GER) and 17 infants with only IALTE without GER were selected for this study. The age of all of the infants ranged from 3–28 weeks. | All of the participants Underwent a polysomnography, including esophageal pH measurements. Obstructive apneas with and without associated GER were identified. HRV was assessed using time domain analysis for short and long-term variability. Forty R-R intervals for each epoch before, during, and after the episodes, as well as 10 segments of 40 R-R intervals unrelated to apneic episodes were analyzed. | SDNN, SDNNi, RMSSD, pNN50% | Infants with IALTE and GER had low baseline short-term variability compared to the comparison group. All the HRV parameters (both short and long term) increased before, as well after the obstructive apnea as compared to baseline values. This was not observed in infants with both IALTE and GER. | Infants suffering from GER and IALTE had significant abnormalities in their autonomic control, as marked in coupled events of apnea and GER. |
11 | Swiatkowski et al., 2004 [51] | 52 alcohol dependent males with chest pain Subgroups: with (n = 37, age = 40.9 ± 7.8 yrs) and without (n = 15, age = 41.9 ± 8.9 yrs) depression and alexithymia | Gastroduodenoscopy, esophageal and gastric pH, 24-h esophageal manometry, treadmill stress test, Holter monitoring, and blood sampling and HRV were recorded and compared between the two groups. | Mean HR, HR range, mean RR, SDNN, SDNNi, SDANNi, RMSSD, PNN50%, total power of HRV spectrum (TPS), LF, HF, VLF, LF/HF ratio. | No significant difference was observed in any HRV parameter in two groups. | Alcoholic patients with depression and alexithymia were more prone to functional disturbances in the upper GI tract. The differences between groups were not related to changes in ANS activity. |
12 | Hu et al., 2020 [52] | 30 Patients with GERD | All the patients underwent two randomized sessions of TEA and sham-TEA at PC6 and ST36 acupoints with simultaneous esophageal high-resolution manometry (HRM), gastric accommodation, and ECG recordings and postprandial dyspeptic symptoms | HF power | HF power increased significantly during TEA in postprandial state. HF power was positively correlated with the percentage of normal slow waves and negatively correlated with regurgitation score. | TEA increased gastric accommodation and slow waves while decreasing postprandial fullness via mediating the vagal activity. |
13 | Nowak et al., 2017 [53] | 16 children (aged 6–18 years), including 8 with asthma, 2 with GERD | 24-h esophageal multichannel intraluminal impedance-pH and ECG were monitored simultaneously. Parasympathetic activity was calculated before, during and after the gastroesophageal reflux (GER) episodes | HF power, RMSSD | No change in HF power as well as RMSSD was observed before, during, and after the GER episodes | GER episodes were not associated with short term HRV or parasympathetic activity in children. |
14 | Floria et al., 2017 [54] | 135 GI patients were divided into two groups: group I (n = 61 with GERD; age = 61.5 ± 9 yrs, 41% male, BMI = 28.8 ± 4 kg/m2) and group II (n = 74 without GERD; age = 58 ± 9 yrs, 46% male, BMI = 29 ± 4 kg/m2) | All patients underwent gastrointestinal endoscopy and 24-h ECG Holter monitoring. | SDNN, LF/HF ratio | SDNN was significantly lower in GERD group. LF/HF ratio was lower in GERD group without statistical significance. | Sympathovagal balance was disrupted in patients with GERD with PNS, contributing more to this disruption. |
15 | Campo et al., 2001 [55] | C group (12 healthy subjects); 28 patients with GERD (age = 41 yrs, range = 20–62 yrs) Subgroups: R group (GERD patients with dyspepsia; n = 21) NR group (n = 7; with normal pH results) | All participants underwent esophageal manometry, ambulatory 24-h pH study, and ECG recording. | LF/HF ratio | No difference in LF/HF ratio was observed in supine and upright position in both R and NR groups compared to the C group. | The sympathetic nervous system was lowered in patients with GERD based on the Blood pressure change during hand grip test. However, HRV did not differ from controls. |
Sr. | Study | Population (n) | Study Design | HRV Parameters | Results | Conclusion |
---|---|---|---|---|---|---|
1 | Guo et al., 2018 [56] | 85 patients with functional dyspepsia (FD) with (age = 39.4 ± 12.82 years) and without (age = 36.5 ± 11.61 years) delayed gastric emptying. | HRV was recorded for 30 min before and after a meal. HRV parameters were compared for patients with and without delayed overall and proximal gastric emptying. | LF power, HF power, LF/HF | HF power was significantly lower and LF/HF ratio was significantly higher in patients with delayed proximal gastric emptying compared to those with normal proximal gastric emptying (GE) after the meal | Delayed GE was associated with disrupted sympathovagal balance due to decreased vagal activity after the meal. |
2 | I.-S Lee et al., 2018 [57] | 15 patients (41 ± 4.72 years) with FD and 17 healthy controls (37.65 ± 4.02 years) | The physiological (including autonomic), emotional, and attentional response of FD patients and controls to high fat food, low fat food, and non-food images after taking an ad-libitum breakfast were compared. | SDNN, HF power, LF/HF ratio | FD patients showed higher SDNN value and lower LF/HF ratio (p < 0.05) compared to HC group. HF power showed no difference. | FD was associated with lower LF/HF ratio |
3 | Winston & Sarna, 2016 [1] | Animal Study: 12 rats with gastric hypersensitivity (GHS) and 12 control rats | The HRV of the rats was recorded for 30 min using BIOPAC system via a pair of electrodes placed under the skin overlaying the chest and behind the nape of neck. | LF/HF ratio | The GHS group had a significantly higher value of LF/HF ratio compared to the control group. | Neonatal programming triggered by colon inflammation increased the ratio of sympathetic to vagal tone (LF/HF) |
4 | Ye et al., 2020 [58] | Animal Study: 8 male Sprague-Dawley rats (450–500 g) with a chronically implanted gastric cannula and ECG electrodes | Beside testing the sham and sacral nerve stimulation (SNS) parameters and involvement of spinal efferent pathways via detecting c-fos immunoreactive cells in nucleus tractus solitarius (NTS), the involvement of vagal efferent activity was studied using spectral analysis of HRV signal. | HF power, LF/HF ratio | SNS at 5 Hz. increased the HF power and decreased sympathovagal balance (LF/HF ratio) compared to sham stimulations. | SNS with certain parameters improved gastric accommodation mediated via a spinal afferent and vagal efferent pathway. |
5 | Zhu et al., 2021 [59] | 36 patients with FD (21F) and 39 healthy controls (23F; mean age = 43.8 yrs) | Patients were randomized into 2 groups (n = 18 each) to receive 2-wk taVNS or sham-ES. The dyspeptic symptom scales, anxiety and depression scores, and the same physiological measurements were assessed at the beginning and the end of the 2-wk treatment. | HF power, LF Power | Acute taVNS, significantly increased vagal activity (HF power) and decreased LF power during the 30-min postprandial period as compared to the sham-ES group. The HF was significantly increased (0.29 ±0.03 during taVNS vs. 0.24 ± 0.02 during sham-ES, p = 0.026) and the LF was significantly reduced (0.71 ± 0.03 during taVNS vs. 0.76 ± 0.02, p = 0.026) after acute taVNS in the 30-min postprandial period. | Compared with the HC, the patients showed decreased vagal activity. The non-invasive taVNS improved FD symptoms by improving gastric accommodation and gastric pace-making activity, as well as increasing vagal activity. |
6 | Zhang et al., 2020 [60] | Animal Study: 8 control rats and 8 FD Sprague-Dawley male rats. Stress was induced by placing the rats in cylindrical tube for 30 min. | 8 weeks after treating the neonatal staged rats with intragastric iodoacetamide, the electrodes were implanted in these rats for the measuring gastric slow waves (GSW) and electrodes into acupoints ST36 for electroacupuncture (EA). The involvement of central afferent pathways was studied via detecting c-fos immunoreactive cells in nucleus tractus solitarius (NTS). Autonomic functions were assessed by spectral analysis of heart rate variability. | HF (0.8 -4.0 Hz.) power, LF (0.3–0.8 Hz.)//HF ratio | Electroacupuncture (EA) significantly increased HF power and decreased LF/HF ratio in FD rats under stress compared to the sham group. | EA at ST36 improved GSW under stress in FD rats mediated via the central and autonomic pathways. |
7 | Tominaga et al., 2016 [13] | 45 FD patients [epigastric pain syndrome: EPS type, n = 24, 53.1 ± 2.1 years of age; 10 male and postprandial syndrome: PDS type, n = 21; 52.1 ± 3.3 years of age; 10 males]. 9 healthy volunteers with no GI symptoms (33.5 ± 4.3 yrs; 6 male) | 24-h HRV was examined: the basal level, responses after lunch, cold presser and mental arithmetic tests, and the efficacy of the autonomic drug (tofisopam) were included in analysis. | HF power, LF/HF ratio. | The HF power was higher and LF/HF ratio was decreased in patients. GI symptoms were more severe in patients with ANS disorder (p = 0.085). The abnormal HF response after lunch occurred in 38.2% of patients who had greater tendency of indigestion (p = 0.061). Delay in recovery to the baseline ANS level after the cold pressor and the mental arithmetic tests occurred in a few patients. Tofisopam partly improved autonomic nervous system dysfunction and abdominal pain/indigestion. | Imbalanced ANS function and susceptibility in recovery from external stimuli were observed in functional dyspepsia patients, which was associated with dyspeptic symptoms. |
8 | Zhou et al., 2017 [61] | Animal Study: 10 rodents gavaged with 0.2 mL of 0.1% iodoacetamide in 2% sucrose. Control group had 8 rodents who were given only 0.2 mL of 2% sucrose. Age at experiment time = 8 weeks | Auricular electro-acupuncture (AEA) at the stomach point with different parameters or sham-EA was performed on 8-week-old rats. The sensitivity to gastric distention was recorded under different conditions. Autonomic functions were assessed from the spectral analysis of HRV | HF power, LF/HF ratio | FD rats had lower HF power and higher LF/HF ratio. The HF was increased, and LF/HF ratio was decreased by AEA | AEA reduced gastric hypersensitivity in FD rats by improving sympathovagal balance. |
9 | Okamoto et al, 2003 [62] | 15 diabetic patients (7M, mean age = 59.1 ± 7.8 yrs.) 15 healthy controls (8M, mean age = 56.3 ± 6.5 yrs.) | ECG was recorded before and after the administration of epalrestat (DM group). ANS was evaluated by spectral analysis of HRV. | HF power, LF power, LF/HF ratio | The values of HF power, LF power, and LF/HF ratio were significantly lower in the DM group before administering eparestat as compared to HC which improved after administering eparestat. | Both vagal and sympathetic tones were reduced in patients with DM. |
10 | Yin et al., 2010 [63] | Animal Study: Sixty-three Sprague-Dawley rats (male, 300–350 g) were randomly divided into five groups. One of the five groups, group E had 10 rats with cutaneous electrodes for recording the HRV | Five experiments were performed in five groups of streptozotocin (STZ)-induced diabetic rats to study the effects of electroacupuncture (EA) at ST-36 on gastric slow-wave dysrhythmia, delayed GE and intestinal transit, impaired gastric accommodation, and the mechanisms of EA involving the autonomic and opioidergic pathways. Here we discuss the HRV results only. | HF power, LF power, LF/HF ratio | EA increased the vagal activity (HF power) and decreased LF/HF power compared to baseline. | EA at ST-36 increased vagal activity, resulting in improvement in gastric dysrhythmia, delayed GE and intestinal transit, and accommodation in STZ-induced diabetic rats. |
11 | Ouyang et al., 2002 [64] | Animal Study: 7 healthy female hound dogs (13–20 kg) that had undergone preparation with duodenal cannulation and placement of gastric serosal electrodes during a prior laparotomy | Electroacupuncture (EA) was performed from 30 min before until 45 min after the meal. Gastric myoelectrical activity and electrocardiogram were recorded. Vagal activity assessed from the spectral analysis of HRV recorded before during and after the EA. | HF power, LF/HF ratio | EA significantly increased the HF power and accelerated gastric emptying and decreased the LF/HF ratio. | The increased vagal activity due to EA could be involved in accelerating the gastric emptying. |
12 | Cai et al., 2008 [65] | 27 female patients (60 yrs; range = 40–79 yrs) with primary Sjogren’s Syndrome (pSS). 25 female healthy controls (60 yrs; range = 42–79 yrs) | Beat-to-beat heart rate and blood pressure data was recorded in response to five standard cardiovascular reflex tests i.e., supine to standing ΔSBP, supine to standing 30/15 ratio, isometric grip ΔMBP, Valsalva ratio, and breathing E/I ratio. | Mean RR, pNN50%, LF power, HF power, breathing E/I ratio, Valsalva ratio, blood pressure variability (SBP) | The pSS patient group had several mild autonomic disturbances compared to control group i.e., decreased HRV, decreased BP variability, and increased heart rate, especially in response to postural change. The severity of the gastroparesis is corelated with decrease in HRV. | There was mild autonomic dysfunction (low HRV) associated with pSS. |
13 | Nguyen et al., 2020 [66] | 242 patients with chronic gastroparetic symptoms which included 45 diabatic (13M, age = 45 ± 11 yrs) and 179 idiopathic patients (16M, age = 42 ± 13 yrs). | Baseline or resting HRV, sympathetic challenge (Valsalva), parasympathetic challenge (deep breathing), parasympathetic response to Valsalva or standing and sympathetic response to standing were recorded. | Lfa, Rfa, lFa/rFa | 89% of diabatic and 74% of idiopathic patients had low sympathetic response to Valsalva or standing. Patients with delayed gastric emptying are more likely to have paradoxical parasympathetic excessive during Valsalva or standing. Patients having severe symptoms have parasympathetic dysfunction compared to those with mild symptoms. | ANS dysfunction was common in gastroparesis patients. PNS dysfunction was associated with severe upper GI symptoms and delayed gastric emptying and SNS dysfunction was associated with milder symptoms. |
14 | Stocker et al., 2016 [67] | rp A: 39 patients (6M, mean age = 38 years) Grp B: 35 patients (7M, mean age = 37 years) Grp C: 5 patients (0M, mean age = 48.6 yrs) | All of the patients underwent gastric neuromodulation. The autonomic response in Grp A was studied by systemic autonomic testing. Grp B was studied by both systemic autonomic testing and heart rate variability. Grp C suffering from diabatic gastroparesis was included in a pilot study to test their baseline autonomic activity by both systemic and HRV methods. | HF power, LF power | Both methods of autonomic testing predicted the abnormal baseline autonomic activity and improvement after neuromodulation in grp A and B. Pilot study indicated that both methods agree. | Both direct autonomic measurement and indirect measurement (HRV) predicted autonomic dysfunctions during baseline in patients with gastroparesis. |
15 | Kumar et al., 2021 [68] | 89 patients (62M, mean age = 50 yrs ranged 38–57 yrs) with chronic kidney disease (CKD), with or without delayed gastric emptying (GE) | Patients were evaluated for gastroparesis symptoms via questionnaire, nutritional status, autonomic function via HRV and GE. | Mean RR, SDNN, RMSSD, VLF power, LF power, HF power, TP, LF/HF ratio, lFnu, hFnu | 22/89 patients had delayed GE and 8/89 had rapid GE. No association between delayed GE and gastroparesis symptoms and autonomic neuropathy. All the HRV parameters were not statistically different in delayed and non-delayed patients. | No association between delayed GE and autonomic neuropathy in non-diabatic CKD patients. |
16 | Softeland et al., 2014 [69] | 20 patients (5M, age = 44.5 ± 9.6 yrs) with diabetes and symptoms of gastroparesis 16 healthy controls (5M, age = 44.8 ± 9.3 yrs) | All of the patients were evaluated for gastric emptying rate followed by rectal sensory assessment and heart rate variability assessment and compared to that of controls. | Mean RR, SDNN, SDANN, pNN50%, RMSSD | 60% of patients had delayed gastric emptying. The rectal hypersensitivity was also prevalent in patients compared to controls. The HRV parameters were low in patients compared to that of controls. Shortened RR interval correlated with reduced rectal temperature sensitivity. | The patients with signs and symptoms of diabetic gastroparesis, rectal sensitivity had decreased HRV. |
17 | Varges-Luna et al., 2020 [70] | 15 FD patients (age: 8–17 yrs) 12 healthy controls with matching age range | ECG was recorded for 30-min before and 60-min after a cold pressor task (CPT). Gastric ECG and HRV parameters were calculated before and after CPT and in short intervals. | SDNN, RMSSD, pNN50%, LF power, HF power LF/HF | No significant change in RMSSD, pNN50%, HF, LF, and LF/HF ratio was observed in pre and post CPT in both patients and controls. SDNN increased significantly from pre to post CPT in controls but not in FD patients. | CPT did not induce any change in HRV of FD patients in youth. Youth with FD lacked normal flexibility in ANS in response to physical stressor. |
18 | Friesen et al., 2010 [71] | 1st part: Children with FD (n = 9) Healthy children (n = 28) 2nd part: Children with FD (n = 8) Healthy children (n = 26) | In 1st part, the ECG was recorded and HRV parameters were calculated for all the participants for 30-min pre and 60-min post meal. In second part, the ECG was recorded and HRV parameters were calculated for all the participants for 30-min pre and 60-min post rapid water loading. | HF power, LF power, LF/HF ratio | HF power was high and LF power and LF/HF ratio were low in FD patients post meal. Baseline LF/HF was positively correlated with water load volume in controls and negatively correlated in FD patients. | FD was associated with abnormal autonomic response to meal and water loading in children. |
19 | Silva Lorena et al., 2002 [72] | 23 FD patients (7F, mean age = 38 ± 7 yrs) and 12 healthy controls (7F, mean age = 34 ± 4 yrs) | 24 h ECG was recorded and HRV parameters were calculated and compared between FD patients and controls. | LF power, LF%, lnLF, HF power, HF%, lnHF, LF/HF, SDNN, RMSSD, pNN50% | HF power, HF%, lnHF, and RMSSD were significantly lowered in FD patients compared to healthy controls. | FD patients had impaired vagal function. |
Sr. | Study | Population (n) | Study Design | HRV Parameters | Results | Conclusion |
---|---|---|---|---|---|---|
1 | Pellissier et al., 2010 [73] | Patients: IBS = 27 (9M, mean age = 40 ± 14 yrs) Healthy subjects = 21 (8M, mean age = 39 ± 12 yrs) | HRV was recorded after 30 min of relaxation period for 10-min. | HR, lFnu, hFnu, LF/HF, VLFnu | The values of lFnu and LF/HF were significantly higher while those of hFnu was significantly lower in IBS patients in comparison to that of healthy controls. | IBS was associated with a high sympathetic tone and low parasympathetic tone. |
2 | Kano et al., 2019 [16] | Patients with non-constipated IBS = 27 Healthy Controls = 33 | HRV was assessed for 5-min during baseline, 3-min resting with bag in the rectum and 3-min during tonic distension. Brain responses to colorectal distention were measured using fMRI and correlated with individual HRV parameters. | ln(HF power), ln(LF/HF), ln(HR) | ln(LF/HF) was low in the IBS group in response to colorectal distention compared with controls (p = 0.003). The baseline ln(HF) was negatively correlated with toleration threshold to the rectal distention in controls only. | The IBS patients exhibited abnormal interactions between ANS activity and the brain mechanisms underlying visceral perception. |
3 | Tillisch et al., 2005 [74] | 130 IBS patients 55 healthy controls Subgroups for sigmoid balloon distension study: 46 IBS patients 16 healthy controls | For ANS assessment, ECG was recorded for 10 min at the end of the 20-min initial rest period in all subjects. In subgroup analysis, ECG was recorded during last 10 min of a 20-min rest period following sigmoidoscopic balloon placement, and during the 10-min period of phasic sigmoid distensions | Peak power ratio (LF/HF), peak power high frequency (PPHF) | IBS patients had higher PPR and lower PPHF across conditions. Male IBS patients had higher PPR and lower PPHF as compared to female patients. | IBS patients showed increased sympathetic and decreased parasympathetic activity compared to healthy controls. These variances were mainly observed in males. |
4 | Robert et al, 2004 [75] | 70 women with IBS divided into 2 groups, with and without depressive symptoms: IBD-DS (n = 44, age = 33 ± 1.1 yrs) IBS + DS (n = 26, age = 40.1 ± 2.6 yrs) Healthy controls (n = 21, age = 34.7 ± 1.9 yrs) | HRV analysis was carried out for 15-min segments selected from 1-baseline pre-sleep period 2-stage 2 sleep 3-slow-wave sleep 4-rapid-eye movement sleep | LF/HF ratio | No significant difference was observed in LF/HF values for any group compared to HC during any type of sleep. | No difference in LF/HF at baseline or in any sleep stages between IBS patients with/without depressive symptoms and health controls. |
5 | Jarrett et al., 2015 [76] | In a two-armed randomized controlled trial Comprehensive self-management (CSM) group (n = 41, age = 40.5 ± 14.6 yr) was compared to a usual care (n = 44, age = 37.9 ± 15.9 yr) group. | ECG was recorded for each participant 3 and 6 months after randomized controlled trials for (1) CSM and (2) usual care groups to test whether these HRV predicts improvements in primary outcome, including abdominal pain, GI symptom score, and IBS-specific quality of life. | HF power, LF/HF ratio | Participants with lower nighttime HF power and higher LF/HF had less benefit from CSM on abdominal pain. | Patients with higher sympathetic tone were less benefitted from the cognitively focused therapies to reduce the IBS related abdominal pain. |
6 | Jang et al., 2017 [15] | 43 participants (age = 21.4 ± 2.1 yr) with IBS-C Subgroups: cognitive behavior therapy (CBT) group (n = 23, age = 21.6 ± 1.8 yr) received cognitive behavior therapy and control group (n = 20, age = 21.2 ± 2.4 yr) | All the participants completed a questionnaire assessing their GI symptoms and their HRV was measured via ECG at baseline and 8, 16, and 24 weeks. | HF power, LF/HF ratio | In CBT group, the HF power was higher and LF/HF ratio was lower than that of control group at 8 weeks. Changes in the HF power were significantly and inversely associated while changes in LF/HF ratio were significantly and positively associated with changes in GI symptoms, anxiety, depression, and stress at 16 and 24 weeks. | ANS measurement via HRV could be a valuable objective parameter for evaluating response to CBT in young IBS-C patients. |
7 | Tanaka, Kanazawa, Palsson et al., 2018 [17] | 156 Rome III positive IBS patients (131F, mean age = 35 ± 11 yr) 31 healthy controls (24F, mean age = 37 ± 13 yr) | All the participants underwent colonic manometry with descending colon bag distention, followed by an 810-kcal meal. HRV was measured during baseline, colonic distention, and after the meal. | HF power (%), LF power (%), LF/HF ratio | %HF was decreased, and the LF/HF ratio was increased by both eating and colonic distension. In IBS patients, the %HF and LF/HF ratios were correlated with psychological symptoms but not bowel symptoms. | In IBS patients, HF and LF/HF were correlated with psychological symptoms but not bowel symptoms. |
8 | Cheng et al., 2013 [77] | Rome III positive IBS patients (n = 35, 53% F, mean age = 37.89 yrs) and healthy controls (n = 31, 58% F, mean age = 37.26 yrs) | All of the participants underwent ECG recording and plasma catecholamines measurement at rest and during flexible sigmoidoscopy (FS). | HF power, LF/HF ratio | At rest, IBS patients had slightly lower HF and LF/HF compared to controls (not statistically significant). During FS, controls showed a transient increase in LF/HF and decrease in HF power. IBS patients had significantly less sympathetic and vagal responsiveness both before and after the stimulus. Those with longer period of disease had less sympathetic and vagal responsiveness than those with shorter period. | Dysregulated ANS responses to a visceral stressor were observed in IBS patients, which might be associated to the duration of the disease. |
9 | Jarrett et al., 2012 [78] | Children with functional abdominal pain (FAP) or IBS (n = 100, 70F, age = 8.9 ± 1.1) Healthy controls (n = 62, 44F, age = 9.3 ± 1.1) | Participants completed a questionnaire, filled a 2-week pain/stool diary, and wore a 24-h Holter monitor to assess vagal activity. HRV was compared for both groups. | HF power, LF/HF ratio | No difference was observed in the vagal HRV parameters among FAP/IBS children and HC. A negative correlation between vagal activity and psychological distress was observed in FAP/IBS girls but not boys. | In girls with FAP/IBS, there was an inverse relationship between vagal activity and psychological distress. |
10 | Davydov et al., 2016 [79] | 78 female IBS patients (age = 35.3 ± 12.8 yrs) 27 healthy females (age = 33.3 ± 11.7 yrs) | All of the participants were assessed for IBS symptoms, blood pressure (BP), HR, HRV, and baroreceptor sensitivity (BRS) at rest. | Ln(HF), ln(LF) | Lower BRS was associated with higher IBS severity if the effect was transferred through the decrease of LF power while it was associated with lower IBS severity if the effect was transferred through diastolic BP increase. Lower BRS was associated with higher abdominal pain severity if the effect was transferred through the decrease of HF power. | The IBS development and its symptoms’ severity were associated to different cardiovascular mechanisms. |
11 | Jarrett et al., 2016 [80] | Patients with IBS (n = 47) Healthy Controls (n = 29) All women with age between 18 and 49 years. Patients subgroup: IBS-diarrhea [IBS-D] (n = 22) IBS-constipation plus mixed [IBS-CM] (n = 25) | All of the Participants kept a four-week symptom diary and had a 12-h Holter placed to assess night-time HRV | HF power, LF power, TP, LF/HF, HR | No HRV parameter differ between the groups or IBS subgroups. | Spectral HRV parameters could not differentiate the IBS-D, IBS-CM, and/or healthy controls. |
12 | Walker et al., 2017 [81] | Pain-remit patients (n = 130, 58.5%F, age = 20.50 ± 3.33 yrs) Pain-persist patients (n = 96, 71.6%F, age = 19.73 ± 3.68 yrs) Healthy controls (n = 123, 53.7%F, age = 18.25 ± 2.72 yrs) | Recorded ECG data at rest and during laboratory stressors. | SDRRI, HF power | Pain-persist females had significantly lowered SDRRI, and HF power compared to males in their group, as well as to that of female controls, and all males regardless of pain category. | Young women with persistent functional abdominal pain showed a low parasympathetic and high sympathetic tone. |
13 | Pellissier et al., 2014 [82] | Healthy controls (n = 26, 18F, age = 36 ± 10 yrs) Patients with IBS (n = 26, 19F, age = 38 ± 10 yrs) Patients with Crohn’s disease (CD) (n = 21, 12F, age = 40 ± 11 yrs) | After 30 min of rest, ECG was recorded for HRV analysis. Blood samples were taken after the ECG recording for plasma cortisol, epinephrine, norepinephrine, TNF-alpha, and IL-6 levels. | hFnu | Control subjects with higher hFnu had significantly lower evening salivary cortisol levels. This was not observed in CD and IBS patients. Negative correlation was observed between the hFnu and TNF-alpha level in CD patients. In IBS patients, vagal tone was inversely correlated with plasma epinephrine. | HF was negatively correlated with TNF-alpha in CD patients and negatively correlated with plasma epinephrine in IBS patients. |
14 | Tanaka, Kanazawa, Kano et al., 2018 [83] | 32 patients with IBS (16F, age = 21.7 ± 1.6 yrs) 32 healthy controls (16F age = 22.0 ± 2.1 yrs) | The patients received no, mild, or strong colorectal distension. The heart rate and HRV were analyzed using ECG. At each distension, plasma noradrenaline, adrenaline, adrenocorticotropic hormone (ACTH), and cortisol levels were taken. | LF power, HF power, LF/HF ratio | In controls a strong correlation was observed between adrenaline and HRV upon corticotropin-releasing hormone (CRH) injection, but not IBS patients. | The relationship between HPA-sympathoadrenal responses and CRH levels during colorectal distention differed between patients with IBS and controls. |
15 | Karling et al., 1998 [84] | 18 IBS patients (4 men, mean age = 20.6 ± 49.2 yrs) 36 healthy controls (mean age = 31.4 yrs) | After 10 min rest, ECG blood pressure and respiration rate were recorded in supine position in normal breathing followed by 12 br/min breathing rate followed by 70° tilt and for 3-min after the tilt. HRV parameters were compared between IBS patients and controls | LF power (called mid frequency in this paper) HF band | LF power in IBS patients was significantly higher compared to the healthy controls during supine and tilt. No significant difference in HF power was observed. | IBS patients had significantly increased sympathetic activity while parasympathetic activity was same as controls. |
16 | Cain et al., 2007 [85] | Healthy controls (n = 50) Women with IBS (n = 165) Subgroups: Constipation predominant (n = 45); diarrhea predominant (n = 64) alternating (n = 56) | 24 h ECG was recorded to assess autonomic activity for all the participants and the HRV parameters’ values were compared among subgroups and against control. The severity of the gut pain was also recorded. | LF power, HF power, LF/HF ratio | No difference in HRV parameters was found upon comparing 165 IBS patients and 50 healthy controls. The women with severe gut pain had lower value HF power and higher value of LF/HF ratio compared to the women with no severe gut pain among all groups. | IBS patients with severe gut pain have lower parasympathetic tone and predominant sympathetic activity compared to those with no severe gut pain. |
17 | Polster et al., 2018 [86] | Healthy controls (n = 39, age = 29 yrs, age range = 19–49, BMI = 22.8 ± 3.3) IBS patients (n = 158, age = 35, age range = 19–64, BMI = 23.4 ± 3.9) | HRV was measured in supine, standing with controlled respiration, and ambulatory 24 h period. Frequency domain parameters (5 min, supine and standing) and time domain parameters (24 h) were calculated and compared between patients and controls. | SDNN, RMSSD, pNN50%, SDNN index, lFnu, hFnu, LF/HF ratio | During the daytime, all the time domain parameters (SDNN, RMSSD, pNN50, SDNN index) were significantly lower in patients compared to controls. No difference was observed during nighttime. HF power, LF power, and LF/HF ratio was significantly different only during standing. No difference was observed during supine. A subgroup of patients with aberrant HRV values had more severe symptoms. | Patients with IBS had altered ANS function compared to controls. |
18 | Orr et al., 2000 [87] | 15 IBS patients (13f, mean age = 34.9 ± 2.1 yrs) 15 healthy controls (13 f, mean age = 36.2 ± 2.3 yrs) | ECG was recorded during 1 h pre-sleep walking and both ECG polysomnography was recorded during 7 h sleep. | HF power, LF power, LF/HF ratio | LF power value was significantly higher during walking and LF/HF ratio was significantly higher during rapid eye movement sleep in IBS patients. No difference in HF power was observed. | IBS patients had higher sympathetic activity during walking and overall sympathetic dominance during rapid eye sleep. |
19 | Adeyemi et al., 1999 [88] | 35 IBS patients (mean age = 39.1 ± 9.5 yrs, M:F ratio 2.9:1) and 18 healthy controls (mean age = 38.2 ± 6.5 yrs, M:F ratio 2:1) | EKG signal was recorded during supine, standing, and deep breathing. | VLF power, LF power, and HF power | IBS patients had significantly high VLF power in supine, high HF power during standing, and low HF power during deep breathing. | IBS patients had reduced sympathetic influence in response to standing and reduced PNS modulation during deep breathing. |
Sr. | Study | Population (n) | Study Design | HRV Parameters | Results | Conclusion |
---|---|---|---|---|---|---|
1 | Liu et al., 2022 [38] | 14 patients with chronic constipation 21 healthy controls | All the participants underwent active standing test and high-resolution colonic manometry (HRCM) with concurrent ECG recording. The autonomic reactivity to the postural change and to the stimuluses during HRCM (meal, balloon distensions, rectal bisacodyl) of the patients were compared to those of healthy controls. | SI, RSA, RMSSD, SI/RSA | In response to standing, SI/RSA was significantly higher in patients compared to healthy controls. 12 of the 14 patients had high (SI) and/or low PNS (RSA, RMSSD) reactivity to either vagal or sacral stimuli. Both patients and controls had similar baseline values of HRV parameters. | High sympathetic tone and reactivity was more responsible for refractory chronic constipation as compared to vagal impairment. |
2 | Ali et al., 2022 [24] | 41 patients (28F, age = 37 ± 17 yrs). Chronic constipation (n = 28), fecal incontinence (n = 5); both constipation and fecal incontinence (n = 8) | All of the participants had lumbar and sacral neuromodulation via low level laser stimulations (LLLS). ECG was recorded for baseline, LED array stimulations, laser probe stimulations and recovery. | RMSSD, RSA, SI, SI/RMSSD, SI/RSA | Laser probe stimulations increased RSA, RMSSD, and decreased SI, SI/RSA, and SI/RMSSD values compared to baseline | Neuromodulation of lumbar and sacral autonomic nerves of patients with constipation via LLLS increased the PNS and decreased the SNS activity. |
3 | Wang et al., 2019 [89] | Animal Study: 10 adult male Sprague-Dawley (SD) rats, weighting 250–300 g | The rats were given loperamide (Lop) to induce constipation and electroacupuncture (EA) was applied via a pair of electrodes implanted at ST-36. The effects of actual and sham EA on were evaluated via HRV. | LF power, HF power, LF/HF ratio | The HF power was increased and LF power was decreased by EA in both normal rats and rats treated with Lop. The LF/HF ratio was reduced by EA in both normal and Lop-treated rats. | Rats with loperamide-induced constipation exhibited decreased vagal and increased sympathetic activities, which could be reversed by EA at ST36. |
4 | Miyagi et al., 2022 [90] | Patients with Parkinson’s disease (n = 17, mean age = 66 yrs, age range = 60–72, 47%F, 76% constipated) Healthy controls (n = 11, mean age = 63 yrs, age range = 59–64, 55%F, 9% constipated) | Subjects underwent ECG recording during supine and standing. Coefficient of variations of RR intervals (CVRR) was calculated during rest and deep breathing. The values were compared between control group and PD group with constipation as a dominant symptom. | LF power, HF power, LF/HF ratio | During both supine and standing, the patients had low HF and LF power values compared to those in controls. However, the LF/HF ratio was higher during supine and lower during standing in patients. All of the differences were not statistically significant. The resting LF power was associated with constipation | Sympathetic and parasympathetic nerves were concurrently damaged in patients with PD. |
5 | Huang et al., 2019 [91] | Animal Study: Thirty Sprague-Dawley rats (male, 300–350 g). Subgroups: SNS group (n = 10); Sham-SNS (n = 10); control Rats (n = 10) | The effects of SNS with optimized parameters on loperamide induced constipation were studied. SNS was performed at S3 sacral nerve unilaterally (right side of the body), 4 h daily for 7 days in rats and ECG was recorded for autonomic functions assessment. HRV parameters were compared between SNS, Sham-SNS and control groups. | HF power, LF power, LF/HF ratio | Sacral nerve stimulation significantly increased HF power and decreased both the LF power and LF/HF ratio as compared to both the Sham-SNS and control groups. | Sacral nerve stimulation with optimized parameters improved constipation by restoring impaired ANS in rats with loperamide-induced constipation. |
6 | Z. Liu et al., 2018 [92] | Patients with ischemic stroke divided into two groups. Sham-TEA (n = 44, 30M, age = 68.3 ± 12.3 yrs) TEA (n = 42, 27M, age = 70.1 ± 11.2 yrs) | One group received transcutaneous electrical acustimulation (TEA) while another group received Sham-TEA for 2 weeks. ECG was recorded for the assessment of ANS. Constipation and dyspeptic symptom assessment was performed at the end of the 14-day treatment. | HF power, LF power, LF/HF ratio | TEA significantly increased the value of HF power and decreased LF power as well as LF/HF ratio significantly while Sham-TEA did not. | TEA could be used to mediate the autonomic function to treat the stroke-induced constipation |
7 | Jin et al., 2015 [93] | Animal Study: Five adult female hound dogs (3–4 yr, 22–25 kg) | Impaired colonic motility was induced by rectal distension (RD) in dogs. Colon contractions and transit were measured in various sessions with and without electroacupuncture (EA) and ECG was recorded for autonomic assessment. | HF power, LF power, LF/HF ratio | The decrease in HF power and increase in sympathetic activity due to rectal distension was significantly normalized (reversed) by EA. | EA at ST36 reinstated the RD-induced impairment in both colonic contraction and transit by increasing vagal activity |
8 | Gondim et al., 2021 [94] | 41 patients with overactive bladder (19 out of 41 constipated) 20 healthy controls aged between 5 and 17 years | HRV was recorded for 1 min during empty bladder (pre-voiding), the full bladder, and 5 min after the spontaneous voiding (post-voiding) into uroflowmeter. | Mean RR, SDNN, pNN50%, lFnu, LF power, hFnu, HF power, LF/HF ratio | Higher heart rate variability was observed in control group. LF was predominant in the control group only during post-voiding. | Constipation was associated with increased sympathetic tone. |
9 | J. Liu et al., 2020 [95] | 45 patients with functional outlet obstruction constipation (FOOC) Subgroups: Group A (n = 15, 11F, age = 47.20 ± 10.98 yrs) Group B (n = 15, 11F, age = 45.38 ± 12.79 yrs) Group C (n = 15, 12F, age = 43.24 ± 9.22 yrs) | Group A received Macrogol 4000 Powder (MAC) only twice a day, group B received adaptive biofeedback (ABT) +MAC+ Sham-TEA twice a day while group C received TEA + ABT (30-min) + MAC twice a day for 6 weeks study. HRV was calculated at baseline and after each corresponding therapy | HF/(HF + LF), LF/(HF + LF) | LF/(LF + HF) in groups B and C were decreased and HF/(LF + HF) was increased in groups B and C as compared to group A. | Both sham and actual TEA modulated the ANS in patients with FOOC. |
10 | Enevoldsen et al., 2018 [96] | Patients with acquired brain injury (ABI) (n = 25, 18M, age = 61.3 [30.7–74.5] yrs); controls (n = 25, 18M, age = 61.5 [34–70] yrs) | Gastrointestinal transit time (GITT) was measured using radio-opaque markers. HRV was recorded from 24 h and 5-min analysis of ECG recorded using 1-lead wearable device. HRV parameters were correlated with GITT. GITT was also compared between patients and controls. | SDNN, RMSSD, LF power, HF power, LF/HF, total power (TP) | No correlation was observed between GITT and any of the HRV parameters. | Patients with ABI showed prolonged GITT compared to that of controls, which was not related to HRV. |
11 | J. Liu et al., 2022 [97] | Patients with functional constipation (FC): Subgroups: With sleep deficiency (SD) (n = 85, 38M, age = 47.39 ± 9.58 yrs). Without sleep deficiency (n = 193, 76M, age = 46.64 ± 10.09 yrs); | All the participants underwent high-resolution anorectal manometry, they were required to fill in a questionnaire about constipation symptoms. ECG was recorded to generate the HRV parameter for the autonomic function comparison of two groups. | SI, HF/(LF + HF) | SD is associated with higher score of constipation. Constipated patients with SD had significantly low HF/(HF + LF) and significantly higher SI compared to those without SD. | Constipation was associated with sleep deficiency and impaired autonomic function. |
12 | N. Zhang et al., 2014 [98] | 12 patients with chronic functional constipation with at least 1 year history of symptoms | All of the patients underwent 2-weeks of transcutaneous neuromodulation (TN) and 2-weeks of sham-TN with 1 week washout in between. TN and sham-TN were applied at posterior tibial nerve and the acupoint ST36. The ECG was recorded along with symptoms, quality of life score, and anorectal motility. | HF power, LF power, LF/HF ratio | HF power was increased and both LF power and LF/HF ratio decreased during TN compared to the baseline. | TN at posterior tibial and ST36 was effective in chronic constipation; the effect was possibly mediated via autonomic nervous system mechanism. |
13 | Ding et al., 2012 [99] | 21 patients with functional constipation (mean age 44.8 ± 16.2 years) Healthy controls (n = 115; females = 70; average age = 50 yrs) | The psychological status, quality of life and autonomic nervous system activity was recorded using heart rate variability with HANS-1000 autonomic biofeedback apparatus, before and after 10 sessions of biofeedback training. | HF power, LF power, LF/HF ratio | After 10 sessions of biofeedback, the HRV parameters did not change statistically although a slight change in absolute values of HF and LF power was observed. | It was not established that biofeedback training improves the autonomic nervous system in patients with chronic constipation. |
14 | Wu et al., 2020 [100] | 18 patients (M/F: 9/9) with functional constipation | A cross-over study was performed with 2-weeks TN at acupoint ST36 and a 2-week TN at (posterior tibial nerve) PTN. Change in constipation symptoms, QOL anorectal manometry and autonomic function was recorded before and after each case. | HF power, LF power, LF/HF ratio | HF power was increased significantly due to TN at both the points (ST36 and PTN). While the other parameters, such as symptoms, QOL score, number of weekly bowel movements were improved more in case of TN at ST36. | TN at both ST36 and PTN increased the vagal activity of the patients with functional constipation. |
15 | C.-Y Chen et al., 2010 [101] | 36 patients (ave age = 40 ± 12 yrs) with constipation. | The participants were divided into two groups: electro-acupuncture (EA) group and sham (SA) group. The EA group patients were pricked respectively at ST36, ST37, ST25, ST28, CV4, and CV6 for 8 weeks. The HRV parameters were recorded at 1st, 4th, and 8th weeks. | hFnu, lFnu, LF/HF ratio | Both lFnu and LF/HF ratio decreased significantly after 8 weeks in EA group only. hFnu was significantly higher than SA group after 8 weeks; however, it was not different than the same group at week 1. | Electro-acupuncture decreased the sympathetic nervous system with 8 weeks of treatment. |
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Ali, M.K.; Chen, J.D.Z. Roles of Heart Rate Variability in Assessing Autonomic Nervous System in Functional Gastrointestinal Disorders: A Systematic Review. Diagnostics 2023, 13, 293. https://doi.org/10.3390/diagnostics13020293
Ali MK, Chen JDZ. Roles of Heart Rate Variability in Assessing Autonomic Nervous System in Functional Gastrointestinal Disorders: A Systematic Review. Diagnostics. 2023; 13(2):293. https://doi.org/10.3390/diagnostics13020293
Chicago/Turabian StyleAli, M. Khawar, and Jiande D. Z. Chen. 2023. "Roles of Heart Rate Variability in Assessing Autonomic Nervous System in Functional Gastrointestinal Disorders: A Systematic Review" Diagnostics 13, no. 2: 293. https://doi.org/10.3390/diagnostics13020293