Next Article in Journal
Effect of Ulinastatin on Syndecan-2-Mediated Vascular Damage in IDH2-Deficient Endothelial Cells
Next Article in Special Issue
Arsenic Trioxide Triggers Apoptosis of Metastatic Oral Squamous Cells Carcinoma with Concomitant Downregulation of GLI1 in Hedgehog Signaling
Previous Article in Journal
Ribosome Biogenesis Serves as a Therapeutic Target for Treating Endometriosis and the Associated Complications
Previous Article in Special Issue
Disorders of Dental Hard Tissues Induced by Radioiodine-131 (I-131) Therapy Used in Differentiated Thyroid Cancer: An In Vitro Study
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

Oral Microbiome, Oral Health and Systemic Health: A Multidirectional Link

by
Elena Maria Varoni
1,* and
Lia Rimondini
2
1
Department of Biomedical, Surgical and Dental Sciences, University of Milan, Via Beldiletto 1, 20142 Milan, Italy
2
Department of Health Sciences, University of Piemonte Orientale, Via Solaroli 17, 28100 Novara, Italy
*
Author to whom correspondence should be addressed.
Biomedicines 2022, 10(1), 186; https://doi.org/10.3390/biomedicines10010186
Submission received: 4 January 2022 / Accepted: 10 January 2022 / Published: 17 January 2022
The oral cavity can be regarded as the mirror of systemic health, since many systemic diseases may have manifestations in the oral cavity, as in the case, among oral, potentially malignant disorders, of lupus erythematosus oral lichenoid lesions, and, vice-versa, oral diseases may affect systemic health, impairing patient’s nutrition and wellbeing, reducing the quality of life and increasing stress and anxiety.
Worldwide, oral diseases affect 3.5 billion individuals, and oral and lip cancers rank among the 15 most common oral diseases, with potential repercussions on the systemic health of patients [1]. In this perspective, the World Health Organization recognizes oral health as a “key indicator of overall health, well-being and quality of life” and it shares “modifiable risk factors with the leading noncommunicable diseases (cardiovascular diseases, cancer, chronic respiratory diseases and diabetes)” [1]. An emblematic example is the bi-directional link between diabetes and periodontitis [2]. Strategies to prevent and treat periodontitis should consider a multi-factorial and multi-disciplinary approach, in the perspective of a personalized medicine and of a holistic view; for example, physical exercise, along with nutritional counselling, is a cornerstone in the treatment and prevention of type 2 diabetes, but it can also reduce the prevalence of cardiovascular risk and of periodontal disease [3,4].
One of the most important discoveries of the last decades is the role of the microbiome in the pathogenesis of several systemic and oral diseases, and it may represent a putative component at the base of the bond between oral and systemic health. In 2017, the World Workshop in Oral Medicine designated the “oral microbiome” as a focus area to encourage and promote research related to the development of oral mucosal diseases, including potentially malignant disorders and oral cancer [5,6]. Recently, differences in oral microbial community composition and the functions of patients with oral cancer, with and without lymph node metastases, were also found, showing a potential in patient prognosis [7]. The pre-operative accurate cancer staging of the patient is, indeed, pivotal to identify sentinel lymph node and/or distant metastases, even in the most complicated cases, such as head and neck cutaneous melanoma, which does not always follow standard lymphatic drainage and may benefit from lymphoscintigraphy [8].
Nowadays, a growing body of literature supports the finding that oral dysbiosis is implicated in periodontitis, resulting in a personalized pathogenesis, where each individual may experience different microbiome impairments and host risk factors [9,10]. Periodontitis-related oral dysbiosis results in chronic inflammation, which correlates with peculiar inflammatory and vascular patterns, according to the presence of an individual’s risk factors, e.g., smoking habit, gender and age [11], and diabetes [12], as well as specific genetic conditions, as in the case of the hereditary form of gingival fibromatosis [13,14]. In the long term, periodontitis can imbalance pro-inflammatory and anti-inflammatory gene responses, including IL-10 gene polymorphisms and polymorphisms of tumor necrosis factor alpha (TNFα), interleukin 1α-β-RN (IL-1α-β-RN), collagen type-l alpha (COLIA1), and vitamin D receptor (VDRs) genes [15].
The oral microbiome has gained more and more interest, also in association with the pathogenesis of several chronic systemic diseases and their treatments. Oral microorganisms can spread to distant body tissues via the blood vessels of the oral cavity or via the gastrointestinal tract, reaching different organs and producing distant local dysbiosis. Recent studies, for instance, have reported a correlation between oral microbiome impairments and an increased risk of pancreatic and liver diseases, with the presence of oral pathogens, predominantly P. gingivalis, in the diseased organ [16]. Furthermore, cancer therapies, including chemotherapy, head and neck radiation therapy, or thyroid cancer radioiodine therapy, can damage dental tissues and alter the oral microbiome [17,18,19,20]. In this perspective, innovative strategies for fine tuning the oral microbiome, counteracting dysbiosis, may help in preventing the disease and the complications of therapies. Different approaches may include oral hygiene procedures, prebiotics, probiotics, host response modulators, and the use of nano-sized drug delivery systems to modulate the microbiota [21]. Novel glutathione-stabilized silver nanoparticles (GSH-AgNPs) were demonstrated to possess antibacterial activity against Porphyromonas gingivalis, Fusobacterium nucleatum, and Streptococcus mutans, with negligible cytotoxic effects when used at low concentrations [22]. Essential oils can also be regarded as promising [23,24,25,26].
In the last decades, literature has also supported the role of the brain–gut–microbiome axis in the etiology of depression and other psychiatric disorders [27], and, similarly, a recent study suggests that the oral microbiome could be implicated in the depression of young adults [28]. Although the impact of the oral microbiota on the psychological health of patients still needs to be better elucidated, oral health is recognized to play a fundamental role in wellbeing and the quality of life [29]. Oral disorders can significantly affect the functional, social and psychological sphere of individuals. Several studies report a reduced quality of life in patients suffering from the most common dental diseases, i.e., periodontitis and caries [30,31], and in patients with oral, potentially malignant disorders or oral cancer [32,33]. Nonetheless, quality of life appears to also be deteriorated in the case of specific systemic conditions, which can affect oral hygiene, such as in hemophilia [34], or in patients experiencing oral complications of particular drugs, including medication-related osteonecrosis of the jaw (MRONJ) [35]. The latter mainly occurs in individuals who receive anti-resorptive drugs (bisphosphonates or denosumab) for the treatment of bone cancer or severe osteoporosis and who need tooth extractions, so a preventive approaches are pivotal [36,37]. The relation between oral disease and psychological or psychiatric disturbances is even closer in the case of burning mouth syndrome (BMS), a neuropathic pain that has psychogenic components [38], for which the management mainly includes the use of psychotropic drugs and psychological support; alternative medicine approaches, based on phytomedicine and acupuncture, are possible, albeit less supported [39,40].
The past and future findings about the oral microbiome open new avenues in terms of pathogenesis and treatment, showing an impact on both oral and systemic health, and improving the way we manage patients, contributing towards creating a personalized, multidisciplinary and holistic medicine.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. World Health Organization. Available online: https://Www.Who.Int/Health-Topics/Oral-Health/#tab=tab_1 (accessed on 4 January 2022).
  2. Stöhr, J.; Barbaresko, J.; Neuenschwander, M.; Schlesinger, S. Bidirectional Association between Periodontal Disease and Diabetes Mellitus: A Systematic Review and Meta-Analysis of Cohort Studies. Sci. Rep. 2021, 11, 13686. [Google Scholar] [CrossRef] [PubMed]
  3. Codella, R.; Della Guardia, L.; Terruzzi, I.; Solini, A.; Folli, F.; Varoni, E.M.; Carrassi, A.; Luzi, L. Physical Activity as a Proxy to Ameliorate Inflammation in Patients with Type 2 Diabetes and Periodontal Disease at High Cardiovascular Risk. Nutr. Metab. Cardiovasc. Dis. 2021, 31, 2199–2209. [Google Scholar] [CrossRef]
  4. De Ferreira, R.O.; Corrêa, M.G.; Magno, M.B.; Almeida, A.P.C.P.S.C.; Fagundes, N.C.F.; Rosing, C.K.; Maia, L.C.; Lima, R.R. Physical Activity Reduces the Prevalence of Periodontal Disease: Systematic Review and Meta-Analysis. Front. Physiol. 2019, 10, 234. [Google Scholar] [CrossRef]
  5. Varoni, E.M.; Bavarian, R.; Robledo-Sierra, J.; Ben-Amy, D.P.; Wade, W.G.; Paster, B.; Kerr, R.; Peterson, D.E.; Lau, E.F. World Workshop on Oral Medicine VII: Targeting the Microbiome for Oral Medicine Specialists-Part 1. A Methodological Guide. Oral Dis. 2019, 25 (Suppl. 1), 12–27. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Robledo-Sierra, J.; Ben-Amy, D.P.; Varoni, E.; Bavarian, R.; Simonsen, J.L.; Paster, B.J.; Wade, W.G.; Kerr, R.; Peterson, D.E.; Lau, E.F. World Workshop on Oral Medicine VII: Targeting the Oral Microbiome Part 2: Current Knowledge on Malignant and Potentially Malignant Oral Disorders. Oral Dis. 2019, 25 (Suppl. 1), 28–48. [Google Scholar] [CrossRef]
  7. Eun, Y.-G.; Lee, J.-W.; Kim, S.W.; Hyun, D.-W.; Bae, J.-W.; Lee, Y.C. Oral Microbiome Associated with Lymph Node Metastasis in Oral Squamous Cell Carcinoma. Sci. Rep. 2021, 11, 23176. [Google Scholar] [CrossRef] [PubMed]
  8. Lavelli, V.; Ferrari, C.; Santo, G.; Altini, C.; Ballini, A.; Sardaro, A.; Fanelli, M.; Pisani, A.R.; Nappi, A.G.; Giudice, G.; et al. The Lymphoscintigraphic Study of Unpredictable Head and Neck Cutaneous Melanoma Lymphatic Drainage. Biomedicines 2020, 8, 70. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Lau, E.F.; Peterson, D.E.; Leite, F.R.M.; Nascimento, G.G.; Robledo-Sierra, J.; Amy, D.P.B.; Kerr, R.; Lopez, R.; Baelum, V.; Lodi, G.; et al. Embracing Multi-Causation of Periodontitis: Why Aren’t We There Yet? Oral Dis. 2021. [Google Scholar] [CrossRef]
  10. Scannapieco, F.A.; Dongari-Bagtzoglou, A. Dysbiosis Revisited: Understanding the Role of the Oral Microbiome in the Pathogenesis of Gingivitis and Periodontitis: A Critical Assessment. J. Periodontol. 2021, 92, 1071–1078. [Google Scholar] [CrossRef]
  11. Buffoli, B.; Garzetti, G.; Calza, S.; Scotti, E.; Borsani, E.; Cappa, V.; Rimondini, L.; Mensi, M. Periodontitis Stage III–IV, Grade C and Correlated Factors: A Histomorphometric Study. Biomedicines 2019, 7, 43. [Google Scholar] [CrossRef] [Green Version]
  12. Preshaw, P.M.; Bissett, S.M. Periodontitis and Diabetes. Br. Dent. J. 2019, 227, 577–584. [Google Scholar] [CrossRef]
  13. Casavecchia, P.; Uzel, M.I.; Kantarci, A.; Hasturk, H.; Dibart, S.; Hart, T.C.; Trackman, P.C.; Van Dyke, T.E. Hereditary Gingival Fibromatosis Associated with Generalized Aggressive Periodontitis: A Case Report. J. Periodontol. 2004, 75, 770–778. [Google Scholar] [CrossRef] [PubMed]
  14. Guglielmi, F.; Staderini, E.; Iavarone, F.; Di Tonno, L.; Gallenzi, P. Zimmermann-Laband-1 Syndrome: Clinical, Histological, and Proteomic Findings of a 3-Year-Old Patient with Hereditary Gingival Fibromatosis. Biomedicines 2019, 7, 48. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Inchingolo, F.; Martelli, F.S.; Isacco, C.G.; Borsani, E.; Cantore, S.; Corcioli, F.; Boddi, A.; Nguyễn, K.C.D.; De Vito, D.; Aityan, S.K.; et al. Chronic Periodontitis and Immunity, Towards the Implementation of a Personalized Medicine: A Translational Research on Gene Single Nucleotide Polymorphisms (SNPs) Linked to Chronic Oral Dysbiosis in 96 Caucasian Patients. Biomedicines 2020, 8, 115. [Google Scholar] [CrossRef]
  16. Mohammed, H.; Varoni, E.M.; Cochis, A.; Cordaro, M.; Gallenzi, P.; Patini, R.; Staderini, E.; Lajolo, C.; Rimondini, L.; Rocchetti, V. Oral Dysbiosis in Pancreatic Cancer and Liver Cirrhosis: A Review of the Literature. Biomedicines 2018, 6, 115. [Google Scholar] [CrossRef] [Green Version]
  17. de Miranda, R.R.; Ribeiro, T.E.; da Silva, E.L.C.; Júnior, P.C.S.; Soares, C.J.; Novais, V.R. Effects of Fractionation and Ionizing Radiation Dose on the Chemical Composition and Microhardness of Enamel. Arch. Oral Biol. 2021, 121, 104959. [Google Scholar] [CrossRef]
  18. Hou, J.; Zheng, H.; Li, P.; Liu, H.; Zhou, H.; Yang, X. Distinct Shifts in the Oral Microbiota Are Associated with the Progression and Aggravation of Mucositis during Radiotherapy. Radiother. Oncol. 2018, 129, 44–51. [Google Scholar] [CrossRef]
  19. Villafuerte, K.R.V.; de Jesus Hernandez Martinez, C.; Dantas, F.T.; Carrara, H.H.A.; Dos Reis, F.J.C.; Palioto, D.B. The Impact of Chemotherapeutic Treatment on the Oral Microbiota of Patients with Cancer: A Systematic Review. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 2018, 125, 552–566. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Mester, A.; Piciu, A.; Piciu, D.; Petean, I.; Lucaciu, P.O.; Apostu, D.; Moisescu-Goia, C.; Voina-Tonea, A.; Moldovan, M. Disorders of Dental Hard Tissues Induced by Radioiodine-131 (I-131) Therapy Used in Differentiated Thyroid Cancer: An In Vitro Study. Biomedicines 2020, 8, 475. [Google Scholar] [CrossRef] [PubMed]
  21. Radaic, A.; Kapila, Y.L. The Oralome and Its Dysbiosis: New Insights into Oral Microbiome-Host Interactions. Comput. Struct. Biotechnol. J. 2021, 19, 1335–1360. [Google Scholar] [CrossRef] [PubMed]
  22. Zorraquín-Peña, I.; Cueva, C.; de Llano, D.G.; Bartolomé, B.; Moreno-Arribas, M.V. Glutathione-Stabilized Silver Nanoparticles: Antibacterial Activity against Periodontal Bacteria, and Cytotoxicity and Inflammatory Response in Oral Cells. Biomedicines 2020, 8, 375. [Google Scholar] [CrossRef] [PubMed]
  23. Azzimonti, B.; Cochis, A.; Beyrouthy, M.E.; Iriti, M.; Uberti, F.; Sorrentino, R.; Landini, M.M.; Rimondini, L.; Varoni, E.M. Essential Oil from Berries of Lebanese Juniperus Excelsa M. Bieb Displays Similar Antibacterial Activity to Chlorhexidine but Higher Cytocompatibility with Human Oral Primary Cells. Molecules 2015, 20, 9344–9357. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Sharifi-Rad, J.; Soufi, L.; Ayatollahi, S.A.M.; Iriti, M.; Sharifi-Rad, M.; Varoni, E.M.; Shahri, F.; Esposito, S.; Kuhestani, K.; Sharifi-Rad, M. Anti-Bacterial Effect of Essential Oil from Xanthium Strumarium against Shiga Toxin-Producing Escherichia Coli. Cell. Mol. Biol. 2016, 62, 69–74. [Google Scholar] [PubMed]
  25. Aires, A.; Barreto, A.S.; Semedo-Lemsaddek, T. Antimicrobial Effects of Essential Oils on Oral Microbiota Biofilms: The Toothbrush In Vitro Model. Antibiotics 2020, 10, 21. [Google Scholar] [CrossRef] [PubMed]
  26. Piekarz, T.; Mertas, A.; Wiatrak, K.; Rój, R.; Kownacki, P.; Śmieszek-Wilczewska, J.; Kopczyńska, E.; Wrzoł, M.; Cisowska, M.; Szliszka, E.; et al. The Influence of Toothpaste Containing Australian Melaleuca Alternifolia Oil and Ethanolic Extract of Polish Propolis on Oral Hygiene and Microbiome in Patients Requiring Conservative Procedures. Molecules 2017, 22, 1957. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Settanni, C.R.; Ianiro, G.; Bibbò, S.; Cammarota, G.; Gasbarrini, A. Gut Microbiota Alteration and Modulation in Psychiatric Disorders: Current Evidence on Fecal Microbiota Transplantation. Prog. Neuropsychopharmacol. Biol. Psychiatry 2021, 109, 110258. [Google Scholar] [CrossRef]
  28. Wingfield, B.; Lapsley, C.; McDowell, A.; Miliotis, G.; McLafferty, M.; O’Neill, S.M.; Coleman, S.; McGinnity, T.M.; Bjourson, A.J.; Murray, E.K. Variations in the Oral Microbiome Are Associated with Depression in Young Adults. Sci. Rep. 2021, 11, 15009. [Google Scholar] [CrossRef]
  29. Locker, D.; Slade, G. Oral Health and the Quality of Life among Older Adults: The Oral Health Impact Profile. J. Can. Dent. Assoc. 1993, 59, 830–833, 837–838, 844. [Google Scholar]
  30. Ferreira, M.C.; Dias-Pereira, A.C.; Branco-de-Almeida, L.S.; Martins, C.C.; Paiva, S.M. Impact of Periodontal Disease on Quality of Life: A Systematic Review. J. Periodontal. Res. 2017, 52, 651–665. [Google Scholar] [CrossRef] [PubMed]
  31. Kastenbom, L.; Falsen, A.; Larsson, P.; Sunnegårdh-Grönberg, K.; Davidson, T. Costs and Health-Related Quality of Life in Relation to Caries. BMC Oral Health 2019, 19, 187. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Ang, X.M.; Au, P.C.K.; Kwok, K.; Park, K.Y.; Kujan, O.; Frydrych, A.M.; Farah, C.S. Quality of Life in Patients with Oral Leukoplakia. J. Oral Pathol. Med. 2019, 48, 574–580. [Google Scholar] [CrossRef] [PubMed]
  33. Yuwanati, M.; Gondivkar, S.; Sarode, S.C.; Gadbail, A.; Desai, A.; Mhaske, S.; Pathak, S.K.; N Khatib, M. Oral Health-Related Quality of Life in Oral Cancer Patients: Systematic Review and Meta-Analysis. Future Oncol. 2021, 17, 979–990. [Google Scholar] [CrossRef]
  34. Fiorillo, L.; De Stefano, R.; Cervino, G.; Crimi, S.; Bianchi, A.; Campagna, P.; Herford, A.S.; Laino, L.; Cicciù, M. Oral and Psychological Alterations in Haemophiliac Patients. Biomedicines 2019, 7, 33. [Google Scholar] [CrossRef] [Green Version]
  35. Capocci, M.; Romeo, U.; Guerra, F.; Mannocci, A.; Tenore, G.; Annibali, S.; Ottolenghi, L. Medication-Related Osteonecrosis of the Jaws (MRONJ) and Quality of Life Evaluation: A Pilot Study. Clin. Ther. 2017, 168, e253–e257. [Google Scholar] [CrossRef]
  36. Pispero, A.; Bancora, I.; Khalil, A.; Scarnò, D.; Varoni, E.M. Use of Platelet Rich Fibrin (PRF)-Based Autologous Membranes for Tooth Extraction in Patients under Bisphosphonate Therapy: A Case Report. Biomedicines 2019, 7, 89. [Google Scholar] [CrossRef] [Green Version]
  37. Abed, H.H.; Al-Sahafi, E.N. The Role of Dental Care Providers in the Management of Patients Prescribed Bisphosphonates: Brief Clinical Guidance. Gen. Dent. 2018, 66, 18–24. [Google Scholar] [PubMed]
  38. Orliaguet, M.; Misery, L. Neuropathic and Psychogenic Components of Burning Mouth Syndrome: A Systematic Review. Biomolecules 2021, 11, 1237. [Google Scholar] [CrossRef] [PubMed]
  39. Sardella, A.; Lodi, G.; Tarozzi, M.; Varoni, E.; Franchini, R.; Carrassi, A. Acupuncture and Burning Mouth Syndrome: A Pilot Study. Pain Pract. 2013, 13, 627–632. [Google Scholar] [CrossRef]
  40. Tan, H.L.; Smith, J.G.; Hoffmann, J.; Renton, T. A Systematic Review of Treatment for Patients with Burning Mouth Syndrome. Cephalalgia 2021, 3331024211036152. [Google Scholar] [CrossRef]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Varoni, E.M.; Rimondini, L. Oral Microbiome, Oral Health and Systemic Health: A Multidirectional Link. Biomedicines 2022, 10, 186. https://doi.org/10.3390/biomedicines10010186

AMA Style

Varoni EM, Rimondini L. Oral Microbiome, Oral Health and Systemic Health: A Multidirectional Link. Biomedicines. 2022; 10(1):186. https://doi.org/10.3390/biomedicines10010186

Chicago/Turabian Style

Varoni, Elena Maria, and Lia Rimondini. 2022. "Oral Microbiome, Oral Health and Systemic Health: A Multidirectional Link" Biomedicines 10, no. 1: 186. https://doi.org/10.3390/biomedicines10010186

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop