Exploring the Link Between Allergies and Neurological Diseases: Unveiling the Hidden Connections
Abstract
1. Introduction
2. Multiple Sclerosis
3. Neurodegenerative Diseases
4. Epilepsy
5. Migraine
6. Neurodevelopmental Disorders
7. Discussion
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Bosnjak, B.; Stelzmueller, B.; Erb, K.J.; Epstein, M.M. Treatment of allergic asthma: Modulation of Th2 cells and their responses. Respir. Res. 2011, 12, 114. [Google Scholar] [CrossRef] [PubMed]
- de Morales, J.M.G.R.; Puig, L.; Daudén, E.; Cañete, J.D.; Pablos, J.L.; Martín, A.O.; Juanatey, C.G.; Adán, A.; Montalbán, X.; Borruel, N. Critical role of interleukin (IL)-17 in inflammatory and immune disorders: An updated review of the evidence focusing in controversies. Autoimmun. Rev. 2020, 19, 102429. [Google Scholar] [CrossRef] [PubMed]
- Wang, Y.-H.; Liu, Y.-J. The IL-17 cytokine family and their role in allergic inflammation. Curr. Opin. Immunol. 2008, 20, 697–702. [Google Scholar] [CrossRef]
- Pracucci, E.; Pillai, V.; Lamers, D.; Parra, R.; Landi, S. Neuroinflammation: A signature or a cause of epilepsy? Int. J. Mol. Sci. 2021, 22, 6981. [Google Scholar] [CrossRef] [PubMed]
- Sun, J.; Zhang, S.; Zhang, X.; Zhang, X.; Dong, H.; Qian, Y. IL-17A is implicated in lipopolysaccharide-induced neuroinflammation and cognitive impairment in aged rats via microglial activation. J. Neuroinflamm. 2015, 12, 165. [Google Scholar] [CrossRef]
- Liu, Z.; Qiu, A.-W.; Huang, Y.; Yang, Y.; Chen, J.-N.; Gu, T.-T.; Cao, B.-B.; Qiu, Y.-H.; Peng, Y.-P. IL-17A exacerbates neuroinflammation and neurodegeneration by activating microglia in rodent models of Parkinson’s disease. Brain Behav. Immun. 2019, 81, 630–645. [Google Scholar] [CrossRef]
- Kostic, M.; Zivkovic, N.; Cvetanovic, A.; Stojanovic, I.; Colic, M. IL-17 signalling in astrocytes promotes glutamate excitotoxicity: Indications for the link between inflammatory and neurodegenerative events in multiple sclerosis. Mult. Scler. Relat. Disord. 2017, 11, 12–17. [Google Scholar] [CrossRef]
- Nakhal, M.M.; Yassin, L.K.; Alyaqoubi, R.; Saeed, S.; Alderei, A.; Alhammadi, A.; Alshehhi, M.; Almehairbi, A.; Al Houqani, S.; BaniYas, S. The microbiota–gut–brain axis and neurological disorders: A comprehensive review. Life 2024, 14, 1234. [Google Scholar] [CrossRef]
- Houghton, V.; Eiwegger, T.; Florsheim, E.B.; Knibb, R.C.; Thuret, S.; Santos, A.F. From bite to brain: Neuro-immune interactions in food allergy. Allergy 2024, 79, 3326–3340. [Google Scholar] [CrossRef]
- Kim, J.-H.; Yamamoto, T.; Lee, J.; Yashiro, T.; Hamada, T.; Hayashi, S.; Kadowaki, M. CGRP, a neurotransmitter of enteric sensory neurons, contributes to the development of food allergy due to the augmentation of microtubule reorganization in mucosal mast cells. Biomed. Res. 2014, 35, 285–293. [Google Scholar] [CrossRef]
- Yamamoto, T.; Kodama, T.; Lee, J.; Utsunomiya, N.; Hayashi, S.; Sakamoto, H.; Kuramoto, H.; Kadowaki, M. Anti-allergic role of cholinergic neuronal pathway via α7 nicotinic ACh receptors on mucosal mast cells in a murine food allergy model. PLoS ONE 2014, 9, e85888. [Google Scholar] [CrossRef] [PubMed]
- Lee, J.; Yamamoto, T.; Hayashi, S.; Kuramoto, H.; Kadowaki, M. Enhancement of CGRP sensory afferent innervation in the gut during the development of food allergy in an experimental murine model. Biochem. Biophys. Res. Commun. 2013, 430, 895–900. [Google Scholar] [CrossRef] [PubMed]
- Yashiro, T.; Ogata, H.; Zaidi, S.F.; Lee, J.; Hayashi, S.; Yamamoto, T.; Kadowaki, M. Pathophysiological roles of neuro-immune interactions between enteric neurons and mucosal mast cells in the gut of food allergy mice. Cells 2021, 10, 1586. [Google Scholar] [CrossRef]
- Sindher, S.B.; Sampath, V.; Chin, A.R.; Nadeau, K.; Chinthrajah, R.S. Neuroimmunology and Allergic Disease. Allergies 2022, 2, 80–86. [Google Scholar] [CrossRef]
- Dunalska, A.; Saramak, K.; Szejko, N. The role of gut microbiome in the pathogenesis of multiple sclerosis and related disorders. Cells 2023, 12, 1760. [Google Scholar] [CrossRef]
- Tremlett, H.; Evans, J.; Wiles, C.; Luscombe, D. Asthma and multiple sclerosis: An inverse association in a case-control general practice population. QJM Int. J. Med. 2002, 95, 753–756. [Google Scholar] [CrossRef]
- Bergamaschi, R.; Villani, S.; Crabbio, M.; Ponzio, M.; Romani, A.; Verri, A.; Bargiggia, V.; Cosi, V. Inverse relationship between multiple sclerosis and allergic respiratory diseases. Neurol. Sci. 2009, 30, 115–118. [Google Scholar] [CrossRef]
- Van Langelaar, J.; van der Vuurst de Vries, R.M.; Janssen, M.; Wierenga-Wolf, A.F.; Spilt, I.M.; Siepman, T.A.; Dankers, W.; Verjans, G.M.; De Vries, H.E.; Lubberts, E. T helper 17.1 cells associate with multiple sclerosis disease activity: Perspectives for early intervention. Brain 2018, 141, 1334–1349. [Google Scholar] [CrossRef] [PubMed]
- Pedotti, R.; DeVoss, J.J.; Youssef, S.; Mitchell, D.; Wedemeyer, J.; Madanat, R.; Garren, H.; Fontoura, P.; Tsai, M.; Galli, S. Multiple elements of the allergic arm of the immune response modulate autoimmune demyelination. Proc. Natl. Acad. Sci. USA 2003, 100, 1867–1872. [Google Scholar] [CrossRef]
- Lock, C.; Hermans, G.; Pedotti, R.; Brendolan, A.; Schadt, E.; Garren, H.; Langer-Gould, A.; Strober, S.; Cannella, B.; Allard, J. Gene-microarray analysis of multiple sclerosis lesions yields new targets validated in autoimmune encephalomyelitis. Nat. Med. 2002, 8, 500–508. [Google Scholar] [CrossRef]
- Gregory, G.D.; Robbie-Ryan, M.; Secor, V.H.; Sabatino Jr, J.J.; Brown, M.A. Mast cells are required for optimal autoreactive T cell responses in a murine model of multiple sclerosis. Eur. J. Immunol. 2005, 35, 3478–3486. [Google Scholar] [CrossRef]
- Musio, S.; Gallo, B.; Scabeni, S.; Lapilla, M.; Poliani, P.L.; Matarese, G.; Ohtsu, H.; Galli, S.J.; Mantegazza, R.; Steinman, L. A key regulatory role for histamine in experimental autoimmune encephalomyelitis: Disease exacerbation in histidine decarboxylase-deficient mice. J. Immunol. 2006, 176, 17–26. [Google Scholar] [CrossRef]
- Lapilla, M.; Gallo, B.; Martinello, M.; Procaccini, C.; Costanza, M.; Musio, S.; Rossi, B.; Angiari, S.; Farina, C.; Steinman, L. Histamine regulates autoreactive T cell activation and adhesiveness in inflamed brain microcirculation. J. Leukoc. Biol. 2011, 89, 259–267. [Google Scholar] [CrossRef]
- Thangam, E.B.; Jemima, E.A.; Singh, H.; Baig, M.S.; Khan, M.; Mathias, C.B.; Church, M.K.; Saluja, R. The role of histamine and histamine receptors in mast cell-mediated allergy and inflammation: The hunt for new therapeutic targets. Front. Immunol. 2018, 9, 1873. [Google Scholar] [CrossRef]
- Aielli, L.; Serra, F.; Costantini, E. Multiple sclerosis and allergic diseases: Is there a relationship? AIMS Allergy Immunol. 2022, 6, 126–152. [Google Scholar] [CrossRef]
- Ponsonby, A.; Dwyer, T.; Van Der Mei, I.; Kemp, A.; Blizzard, L.; Taylor, B.; Kilpatrick, T.; Simmons, R. Asthma onset prior to multiple sclerosis and the contribution of sibling exposure in early life. Clin. Exp. Immunol. 2006, 146, 463–470. [Google Scholar] [CrossRef]
- Alonso, A.; Hernan, M.; Ascherio, A. Allergy, family history of autoimmune diseases, and the risk of multiple sclerosis. Acta Neurol. Scand. 2008, 117, 15–20. [Google Scholar] [CrossRef]
- Alonso, A.; Jick, S.S.; Hernán, M.A. Allergy, histamine 1 receptor blockers, and the risk of multiple sclerosis. Neurology 2006, 66, 572–575. [Google Scholar] [CrossRef]
- Pedotti, R.; Farinotti, M.; Falcone, C.; Borgonovo, L.; Confalonieri, P.; Campanella, A.; Mantegazza, R.; Pastorello, E.; Filippini, G. Allergy and multiple sclerosis: A population-based case-control study. Mult. Scler. J. 2009, 15, 899–906. [Google Scholar] [CrossRef]
- Ramagopalan, S.V.; Dyment, D.A.; Guimond, C.; Orton, S.-M.; Yee, I.M.; Ebers, G.C.; Sadovnick, A.D. Childhood cow’s milk allergy and the risk of multiple sclerosis: A population based study. J. Neurol. Sci. 2010, 291, 86–88. [Google Scholar] [CrossRef]
- Karimi, P.; Modarresi, S.Z.; Sahraian, M.A.; Shoormasti, R.S.; Mahlooji, M.; Kazemnejad, A.; Pourpak, Z. The relation of multiple sclerosis with allergy and atopy: A case control study. Iran. J. Allergy Asthma Immunol. 2013, 12, 182–189. [Google Scholar]
- Sahraian, M.A.; Jafarian, S.; Sheikhbahaei, S.; Safavi, F. Respiratory tract rather than cutaneous atopic allergy inversely associate with multiple sclerosis: A case–control study. Clin. Neurol. Neurosurg. 2013, 115, 2099–2102. [Google Scholar] [CrossRef]
- Hughes, A.; Lucas, R.; McMichael, A.; Dwyer, T.; Pender, M.; Van Der Mei, I.; Taylor, B.; Valery, P.; Chapman, C.; Coulthard, A. Early-life hygiene-related factors affect risk of central nervous system demyelination and asthma differentially. Clin. Exp. Immunol. 2013, 172, 466–474. [Google Scholar] [CrossRef]
- Ashtari, F.; Jamshidi, F.; Shoormasti, R.S.; Pourpak, Z.; Akbari, M. Cow’s milk allergy in multiple sclerosis patients. J. Res. Med. Sci. 2013, 18, S62. [Google Scholar]
- Mansouri, B.; Asadollahi, S.; Heidari, K.; Fakhri, M.; Assarzadegan, F.; Nazari, M.; Divani, A. Risk factors for increased multiple sclerosis susceptibility in the Iranian population. J. Clin. Neurosci. 2014, 21, 2207–2211. [Google Scholar] [CrossRef]
- Skaaby, T.; Husemoen, L.L.N.; Thuesen, B.H.; Fenger, R.V.; Linneberg, A. Specific IgE positivity against inhalant allergens and development of autoimmune disease. Autoimmunity 2015, 48, 282–288. [Google Scholar] [CrossRef]
- Manouchehrinia, A.; Edwards, L.J.; Roshanisefat, H.; Tench, C.R.; Constantinescu, C.S. Multiple sclerosis course and clinical outcomes in patients with comorbid asthma: A survey study. BMJ Open 2015, 5, e007806. [Google Scholar] [CrossRef]
- Ren, J.; Ni, H.; Kim, M.; Cooley, K.L.; Valenzuela, R.M.; Asche, C.V. Allergies, antibiotics use, and multiple sclerosis. Curr. Med. Res. Opin. 2017, 33, 1451–1456. [Google Scholar] [CrossRef]
- Bourne, T.; Waltz, M.; Casper, T.; Kavak, K.; Aaen, G.; Belman, A.; Benson, L.; Candee, M.; Chitnis, T.; Graves, J. Evaluating the association of allergies with multiple sclerosis susceptibility risk and disease activity in a pediatric population. J. Neurol. Sci. 2017, 375, 371–375. [Google Scholar] [CrossRef]
- Fakih, R.; Diaz-Cruz, C.; Chua, A.S.; Gonzalez, C.; Healy, B.C.; Sattarnezhad, N.; Glanz, B.I.; Weiner, H.L.; Chitnis, T. Food allergies are associated with increased disease activity in multiple sclerosis. J. Neurol. Neurosurg. Psychiatry 2019, 90, 629–635. [Google Scholar] [CrossRef]
- Krishna, M.T.; Subramanian, A.; Adderley, N.J.; Zemedikun, D.T.; Gkoutos, G.V.; Nirantharakumar, K. Allergic diseases and long-term risk of autoimmune disorders: Longitudinal cohort study and cluster analysis. Eur. Respir. J. 2019, 54, 190047. [Google Scholar] [CrossRef]
- Hill, E.; Abboud, H.; Briggs, F.B. Prevalence of asthma in multiple sclerosis: A United States population-based study. Mult. Scler. Relat. Disord. 2019, 28, 69–74. [Google Scholar] [CrossRef]
- Albatineh, A.N.; Alroughani, R.; Al-Temaimi, R. Predictors of multiple sclerosis severity score in patients with multiple sclerosis. Int. J. MS Care 2020, 22, 233–238. [Google Scholar] [CrossRef]
- Chen, J.; Taylor, B.; Winzenberg, T.; Palmer, A.J.; Kirk-Brown, A.; van Dijk, P.; Simpson Jr, S.; Blizzard, L.; van der Mei, I. Comorbidities are prevalent and detrimental for employment outcomes in people of working age with multiple sclerosis. Mult. Scler. J. 2020, 26, 1550–1559. [Google Scholar] [CrossRef]
- Kang, L.-L.; Chen, P.-E.; Tung, T.-H.; Chien, C.-W. Association between asthma and migraine: A systematic review and meta-analysis of observational studies. Front. Allergy 2021, 2, 741135. [Google Scholar] [CrossRef]
- Lo, L.M.P.; Taylor, B.V.; Winzenberg, T.; Palmer, A.J.; Blizzard, L.; Hussain, M.A.; van der Mei, I. Comorbidity patterns in people with multiple sclerosis: A latent class analysis of the Australian multiple sclerosis longitudinal study. Eur. J. Neurol. 2021, 28, 2269–2279. [Google Scholar] [CrossRef]
- Jankovic, J. Parkinson’s disease: Clinical features and diagnosis. J. Neurol. Neurosurg. Psychiatry 2008, 79, 368–376. [Google Scholar] [CrossRef]
- Xu, K.; Li, Y.; Zhou, Y.; Zhang, Y.; Shi, Y.; Zhang, C.; Bai, Y.; Wang, S. Neuroinflammation in Parkinson’s disease: Focus on the relationship between miRNAs and microglia. Front. Cell. Neurosci. 2024, 18, 1429977. [Google Scholar] [CrossRef]
- Tansey, M.G.; Wallings, R.L.; Houser, M.C.; Herrick, M.K.; Keating, C.E.; Joers, V. Inflammation and immune dysfunction in Parkinson disease. Nat. Rev. Immunol. 2022, 22, 657–673. [Google Scholar] [CrossRef]
- Cai, Y.; Liu, J.; Wang, B.; Sun, M.; Yang, H. Microglia in the neuroinflammatory pathogenesis of Alzheimer’s disease and related therapeutic targets. Front. Immunol. 2022, 13, 856376. [Google Scholar] [CrossRef]
- Bożek, A.; Bednarski, P.; Jarzab, J. Allergic rhinitis, bronchial asthma and other allergies in patients with Alzheimer’s disease: Unnoticed issue. Adv. Dermatol. 2016, 33, 353–358. [Google Scholar] [CrossRef]
- Perry, V.H. The influence of systemic inflammation on inflammation in the brain: Implications for chronic neurodegenerative disease. Brain Behav. Immun. 2004, 18, 407–413. [Google Scholar] [CrossRef]
- Perry, V.H.; Cunningham, C.; Holmes, C. Systemic infections and inflammation affect chronic neurodegeneration. Nat. Rev. Immunol. 2007, 7, 161–167. [Google Scholar] [CrossRef]
- Sarlus, H.; Höglund, C.O.; Karshikoff, B.; Wang, X.; Lekander, M.; Schultzberg, M.; Oprica, M. Allergy influences the inflammatory status of the brain and enhances tau-phosphorylation. J. Cell. Mol. Med. 2012, 16, 2401–2412. [Google Scholar] [CrossRef]
- Chen, M.-H.; Li, C.-T.; Tsai, C.-F.; Lin, W.-C.; Chang, W.-H.; Chen, T.-J.; Pan, T.-L.; Su, T.-P.; Bai, Y.-M. Risk of dementia among patients with asthma: A nationwide longitudinal study. J. Am. Med. Dir. Assoc. 2014, 15, 763–767. [Google Scholar] [CrossRef]
- Woo, Y.R.; Minah, C.; Do Han, K.; Cho, S.H.; Lee, J.H. Increased risk of dementia in patients with atopic dermatitis: A Nationwide Population-Based Cohort Study. Acta Derm. Venereol. 2023, 103, adv4557. [Google Scholar] [CrossRef]
- Hu, J.; Ma, H.; Ning, Z.; Xu, Q.; Luo, J.; Jiang, X.; Zhang, B.; Liu, Y. Asthma and cognitive dysfunction in older adults: The mediating role of systemic immune-inflammation index. Sci. Rep. 2024, 14, 27194. [Google Scholar] [CrossRef]
- Joh, H.K.; Kwon, H.; Son, K.Y.; Yun, J.M.; Cho, S.H.; Han, K.; Park, J.H.; Cho, B. Allergic diseases and risk of incident dementia and Alzheimer’s disease. Ann. Neurol. 2023, 93, 384–397. [Google Scholar] [CrossRef]
- Wang, Y.; Wang, S.; Wu, J.; Liu, X.; Zhang, L. Causal Association Between Allergic Diseases and Dementia: Evidence from Multivariate Mendelian Randomization Study. J. Alzheimer’s Dis. 2024, 98, 505–517. [Google Scholar] [CrossRef]
- Bower, J.; Maraganore, D.; Peterson, B.; Ahlskog, J.; Rocca, W. Immunologic diseases, anti-inflammatory drugs, and Parkinson disease: A case-control study. Neurology 2006, 67, 494–496. [Google Scholar] [CrossRef]
- Cheng, C.M.; Wu, Y.H.; Tsai, S.J.; Bai, Y.M.; Hsu, J.W.; Huang, K.L.; Su, T.P.; Li, C.T.; Tsai, C.F.; Yang, A. Risk of developing P arkinson’s disease among patients with asthma: A nationwide longitudinal study. Allergy 2015, 70, 1605–1612. [Google Scholar] [CrossRef]
- Nam, J.Y.; Park, S.J.; Song, J.; Jeong, S.; Choi, S.; Park, S.M. Association of allergic disease with Parkinson’s disease: A nationally representative retrospective cohort study. Allergol. Int. 2024, 73, 107–114. [Google Scholar] [CrossRef]
- He, C.H.; Zhao, J.; Zhu, T.T. Association between allergic diseases and epilepsy: A systematic review and meta-analysis. Epilepsy Behav. 2021, 116, 107770. [Google Scholar] [CrossRef]
- Frediani, T.; Lucarelli, S.; Pelliccia, A.; Vagnucci, B.; Cerminara, C.; Barbato, M.; Cardi, E. Allergy and childhood epilepsy: A close relationship? Acta Neurol. Scand. 2001, 104, 349–352. [Google Scholar] [CrossRef]
- Kobau, R.; DiIorio, C.A.; Price, P.H.; Thurman, D.J.; Martin, L.M.; Ridings, D.L.; Henry, T.R. Prevalence of epilepsy and health status of adults with epilepsy in Georgia and Tennessee: Behavioral Risk Factor Surveillance System, 2002. Epilepsy Behav. 2004, 5, 358–366. [Google Scholar] [CrossRef]
- Strine, T.W.; Kobau, R.; Chapman, D.P.; Thurman, D.J.; Price, P.; Balluz, L. Psychological distress, comorbidities, and health behaviors among US adults with seizures: Results from the 2002 National Health Interview Survey. Epilepsia 2005, 46, 1133–1139. [Google Scholar] [CrossRef]
- Elliott, J.O.; Moore, J.L.; Lu, B. Health status and behavioral risk factors among persons with epilepsy in Ohio based on the 2006 Behavioral Risk Factor Surveillance System. Epilepsy Behav. 2008, 12, 434–444. [Google Scholar] [CrossRef]
- Babu, C.S.; Satishchandra, P.; Sinha, S.; Subbakrishna, D. Co-morbidities in people living with epilepsy: Hospital based case–control study from a resource-poor setting. Epilepsy Res. 2009, 86, 146–152. [Google Scholar] [CrossRef]
- Karlstad, Ø.; Nafstad, P.; Tverdal, A.; Skurtveit, S.; Furu, K. Comorbidities in an asthma population 8–29 years old: A study from the Norwegian Prescription Database. Pharmacoepidemiol. Drug Saf. 2012, 21, 1045–1052. [Google Scholar] [CrossRef]
- Silverberg, J.; Joks, R.; Durkin, H. Allergic disease is associated with epilepsy in childhood: A US population-based study. Allergy 2014, 69, 95–103. [Google Scholar] [CrossRef]
- Chen, M.H.; Wu, Y.H.; Su, T.P.; Chen, Y.S.; Hsu, J.W.; Huang, K.L.; Li, C.T.; Lin, W.C.; Chang, W.H.; Chen, T.J. Risk of epilepsy among patients with atopic dermatitis: A nationwide longitudinal study. Epilepsia 2014, 55, 1307–1312. [Google Scholar] [CrossRef]
- Lin, W.-Y.; Muo, C.-H.; Ku, Y.-C.; Sung, F.-C.; Kao, C.-H. Risk of subsequent asthma in children with febrile seizures: A nationwide population-based retrospective cohort study. Pediatr. Neurol. 2014, 51, 795–799. [Google Scholar] [CrossRef]
- Kauppi, P.; Linna, M.; Jantunen, J.; Martikainen, J.E.; Haahtela, T.; Pelkonen, A.; Mäkelä, M. Chronic comorbidities contribute to the burden and costs of persistent asthma. Mediat. Inflamm. 2015, 2015, 819194. [Google Scholar] [CrossRef]
- Strom, M.A.; Silverberg, J.I. Allergic disease is associated with childhood seizures: An analysis of the 1997-2013 National Health Interview Survey. J. Allergy Clin. Immunol. 2016, 137, 951–953.e2. [Google Scholar] [CrossRef]
- Chiang, K.-L.; Kuo, F.-C.; Lee, J.-Y.; Huang, C.-Y. Association of epilepsy and asthma: A population-based retrospective cohort study. PeerJ 2018, 6, e4792. [Google Scholar] [CrossRef]
- Machluf, Y.; Farkash, R.; Rotkopf, R.; Fink, D.; Chaiter, Y. Asthma phenotypes and associated comorbidities in a large cohort of adolescents in Israel. J. Asthma 2020, 57, 722–735. [Google Scholar] [CrossRef]
- Ferretti, A.; Gatto, M.; Velardi, M.; Di Nardo, G.; Foiadelli, T.; Terrin, G.; Cecili, M.; Raucci, U.; Valeriani, M.; Parisi, P. Migraine, allergy, and histamine: Is there a link? J. Clin. Med. 2023, 12, 3566. [Google Scholar] [CrossRef]
- Alstadhaug, K.B. Histamine in migraine and brain. Headache J. Head Face Pain 2014, 54, 246–259. [Google Scholar] [CrossRef]
- Wang, L.; Deng, Z.-R.; Zu, M.-D.; Zhang, J.; Wang, Y. The comorbid relationship between migraine and asthma: A systematic review and meta-analysis of population-based studies. Front. Med. 2021, 7, 609528. [Google Scholar] [CrossRef]
- Davey, G.; Sedgwick, P.; Maier, W.; Visick, G.; Strachan, D.P.; Anderson, H.R. Association between migraine and asthma: Matched case-control study. Br. J. Gen. Pract. 2002, 52, 723–727. [Google Scholar]
- Aamodt, A.H.; Stovner, L.J.; Langhammer, A.; Hagen, K.; Zwart, J.A. Is headache related to asthma, hay fever, and chronic bronchitis? The Head-HUNT Study. Headache J. Head Face Pain 2007, 47, 204–212. [Google Scholar] [CrossRef]
- Becker, C.; Brobert, G.P.; Almqvist, P.M.; Johansson, S.; Jick, S.S.; Meier, C.R. The risk of newly diagnosed asthma in migraineurs with or without previous triptan prescriptions. Headache J. Head Face Pain 2008, 48, 606–610. [Google Scholar] [CrossRef]
- Le, H.; Tfelt-Hansen, P.; Russell, M.B.; Skytthe, A.; Kyvik, K.O.; Olesen, J. Co-morbidity of migraine with somatic disease in a large population-based study. Cephalalgia 2011, 31, 43–64. [Google Scholar] [CrossRef]
- Chen, Y.-C.; Tang, C.-H.; Ng, K.; Wang, S.-J. Comorbidity profiles of chronic migraine sufferers in a national database in Taiwan. J. Headache Pain 2012, 13, 311–319. [Google Scholar] [CrossRef]
- Czerwinski, S.; Gollero, J.; Qiu, C.; Sorensen, T.K.; Williams, M.A. Migraine-asthma comorbidity and risk of hypertensive disorders of pregnancy. J. Pregnancy 2012, 2012, 858097. [Google Scholar] [CrossRef]
- Lateef, T.M.; Cui, L.; Nelson, K.B.; Nakamura, E.F.; Merikangas, K.R. Physical comorbidity of migraine and other headaches in US adolescents. J. Pediatr. 2012, 161, 308–313.e1. [Google Scholar] [CrossRef]
- Peng, Y.-H.; Chen, K.-F.; Kao, C.-H.; Chen, H.-J.; Hsia, T.-C.; Chen, C.-H.; Liao, W.-C. Risk of migraine in patients with asthma: A nationwide cohort study. Medicine 2016, 95, e2911. [Google Scholar] [CrossRef]
- Tsiakiris, G.; Neely, G.; Lind, N.; Nordin, S. Comorbidity in allergic asthma and allergic rhinitis: Functional somatic syndromes. Psychol. Health Med. 2017, 22, 1163–1168. [Google Scholar] [CrossRef]
- Peng, Y.H.; Chen, K.F.; Liao, W.C.; Hsia, T.C.; Chen, H.J.; Yin, M.C.; Ho, W.C. Association of migraine with asthma risk: A retrospective population-based cohort study. Clin. Respir. J. 2018, 12, 1030–1037. [Google Scholar] [CrossRef]
- Graif, Y.; Shohat, T.; Machluf, Y.; Farkash, R.; Chaiter, Y. Association between asthma and migraine: A cross-sectional study of over 110,000 adolescents. Clin. Respir. J. 2018, 12, 2491–2496. [Google Scholar] [CrossRef]
- Zhao, P.; Ignacio, S.; Beattie, E.C.; Abood, M.E. Altered presymptomatic AMPA and cannabinoid receptor trafficking in motor neurons of ALS model mice: Implications for excitotoxicity. Eur. J. Neurosci. 2008, 27, 572–579. [Google Scholar] [CrossRef] [PubMed]
- Kim, S.Y.; Min, C.; Oh, D.J.; Lim, J.-S.; Choi, H.G. Bidirectional association between asthma and migraines in adults: Two longitudinal follow-up studies. Sci. Rep. 2019, 9, 18343. [Google Scholar] [CrossRef] [PubMed]
- Buse, D.C.; Reed, M.L.; Fanning, K.M.; Bostic, R.; Dodick, D.W.; Schwedt, T.J.; Munjal, S.; Singh, P.; Lipton, R.B. Comorbid and co-occurring conditions in migraine and associated risk of increasing headache pain intensity and headache frequency: Results of the migraine in America symptoms and treatment (MAST) study. J. Headache Pain 2020, 21, 23. [Google Scholar] [CrossRef] [PubMed]
- Saunes, M.; Smidesang, I.; Holmen, T.; Johnsen, R. Atopic dermatitis in adolescent boys is associated with greater psychological morbidity compared with girls of the same age: The Young-HUNT study. Br. J. Dermatol. 2007, 156, 283–288. [Google Scholar] [CrossRef]
- Wei, C.-C.; Lin, C.-L.; Shen, T.-C.; Chen, A.-C. Children with allergic diseases have an increased subsequent risk of migraine upon reaching school age. J. Investig. Med. 2018, 66, 1064–1068. [Google Scholar] [CrossRef]
- Chua, R.X.Y.; Tay, M.J.Y.; Ooi, D.S.Q.; Siah, K.T.H.; Tham, E.H.; Shek, L.P.-C.; Meaney, M.J.; Broekman, B.F.; Loo, E.X.L. Understanding the link between allergy and neurodevelopmental disorders: A current review of factors and mechanisms. Front. Neurol. 2021, 11, 603571. [Google Scholar] [CrossRef]
- Casella, R.; Miniello, A.; Buta, F.; Yacoub, M.-R.; Nettis, E.; Pioggia, G.; Gangemi, S. Atopic Dermatitis and Autism Spectrum Disorders: Common Role of Environmental and Clinical Co-Factors in the Onset and Severity of Their Clinical Course. Int. J. Mol. Sci. 2024, 25, 8936. [Google Scholar] [CrossRef]
- Kovacheva, E.; Gevezova, M.; Maes, M.; Sarafian, V. The mast cells-Cytokines axis in Autism Spectrum Disorder. Neuropharmacology 2024, 249, 109890. [Google Scholar] [CrossRef]
- Rossi, C.C.; Van de Water, J.; Rogers, S.J.; Amaral, D.G. Detection of plasma autoantibodies to brain tissue in young children with and without autism spectrum disorders. Brain Behav. Immun. 2011, 25, 1123–1135. [Google Scholar] [CrossRef]
- Mostafa, G.A.; Al-Ayadhi, L.Y. The possible relationship between allergic manifestations and elevated serum levels of brain specific auto-antibodies in autistic children. J. Neuroimmunol. 2013, 261, 77–81. [Google Scholar] [CrossRef]
- Theoharides, T.C.; Asadi, S.; Patel, A.B. Focal brain inflammation and autism. J. Neuroinflamm. 2013, 10, 46. [Google Scholar] [CrossRef] [PubMed]
- Theoharides, T.; Tsilioni, I.; Patel, A.; Doyle, R. Atopic diseases and inflammation of the brain in the pathogenesis of autism spectrum disorders. Transl. Psychiatry 2016, 6, e844. [Google Scholar] [CrossRef] [PubMed]
- Moaaz, M.; Youssry, S.; Elfatatry, A.; Abd El Rahman, M. Th17/Treg cells imbalance and their related cytokines (IL-17, IL-10 and TGF-β) in children with autism spectrum disorder. J. Neuroimmunol. 2019, 337, 577071. [Google Scholar] [CrossRef] [PubMed]
- Akintunde, M.E.; Rose, M.; Krakowiak, P.; Heuer, L.; Ashwood, P.; Hansen, R.; Hertz-Picciotto, I.; Van de Water, J. Increased production of IL-17 in children with autism spectrum disorders and co-morbid asthma. J. Neuroimmunol. 2015, 286, 33–41. [Google Scholar] [CrossRef]
- Skaper, S.D.; Facci, L.; Giusti, P. Neuroinflammation, microglia and mast cells in the pathophysiology of neurocognitive disorders: A review. CNS Neurol. Disord. Drug Targets 2014, 13, 1654–1666. [Google Scholar] [CrossRef]
- Dong, H.; Zhang, X.; Wang, Y.; Zhou, X.; Qian, Y.; Zhang, S. Suppression of brain mast cells degranulation inhibits microglial activation and central nervous system inflammation. Mol. Neurobiol. 2017, 54, 997–1007. [Google Scholar] [CrossRef]
- Kovacheva, E.; Gevezova, M.; Maes, M.; Sarafian, V. Mast Cells in Autism Spectrum Disorder—The Enigma to Be Solved? Int. J. Mol. Sci. 2024, 25, 2651. [Google Scholar] [CrossRef] [PubMed]
- Estes, M.L.; McAllister, A.K. Maternal immune activation: Implications for neuropsychiatric disorders. Science 2016, 353, 772–777. [Google Scholar] [CrossRef]
- Careaga, M.; Murai, T.; Bauman, M.D. Maternal immune activation and autism spectrum disorder: From rodents to nonhuman and human primates. Biol. Psychiatry 2017, 81, 391–401. [Google Scholar] [CrossRef]
- Braunschweig, D.; Ashwood, P.; Krakowiak, P.; Hertz-Picciotto, I.; Hansen, R.; Croen, L.A.; Pessah, I.N.; Van de Water, J. Autism: Maternally derived antibodies specific for fetal brain proteins. Neurotoxicology 2008, 29, 226–231. [Google Scholar] [CrossRef]
- Braunschweig, D.; Duncanson, P.; Boyce, R.; Hansen, R.; Ashwood, P.; Pessah, I.N.; Hertz-Picciotto, I.; Van de Water, J. Behavioral correlates of maternal antibody status among children with autism. J. Autism Dev. Disord. 2012, 42, 1435–1445. [Google Scholar] [CrossRef]
- Genuneit, J.; Braig, S.; Brandt, S.; Wabitsch, M.; Florath, I.; Brenner, H.; Rothenbacher, D. Infant atopic eczema and subsequent attention-deficit/hyperactivity disorder–a prospective birth cohort study. Pediatr. Allergy Immunol. 2014, 25, 51–56. [Google Scholar] [CrossRef] [PubMed]
- Mogensen, N.; Larsson, H.; Lundholm, C.; Almqvist, C. Association between childhood asthma and ADHD symptoms in adolescence–a prospective population-based twin study. Allergy 2011, 66, 1224–1230. [Google Scholar] [CrossRef] [PubMed]
- Lee, C.-Y.; Chen, M.-H.; Jeng, M.-J.; Hsu, J.-W.; Tsai, S.-J.; Bai, Y.-M.; Hung, G.-Y.; Yen, H.-J.; Chen, T.-J.; Su, T.-P. Longitudinal association between early atopic dermatitis and subsequent attention-deficit or autistic disorder: A population-based case–control study. Medicine 2016, 95, e5005. [Google Scholar] [CrossRef] [PubMed]
- Strom, M.; Fishbein, A.; Paller, A.; Silverberg, J. Association between atopic dermatitis and attention deficit hyperactivity disorder in US children and adults. Br. J. Dermatol. 2016, 175, 920–929. [Google Scholar] [CrossRef]
- Yang, C.-F.; Yang, C.-C.; Wang, I.-J. Association between allergic diseases, allergic sensitization and attention-deficit/hyperactivity disorder in children: A large-scale, population-based study. J. Chin. Med. Assoc. 2018, 81, 277–283. [Google Scholar] [CrossRef]
- Tsai, J.-D.; Chang, S.-N.; Mou, C.-H.; Sung, F.-C.; Lue, K.-H. Association between atopic diseases and attention-deficit/hyperactivity disorder in childhood: A population-based case-control study. Ann. Epidemiol. 2013, 23, 185–188. [Google Scholar] [CrossRef]
- Kwon, H.J.; Lee, M.Y.; Ha, M.; Yoo, S.J.; Paik, K.C.; Lim, J.-H.; Sakong, J.; Lee, C.-G.; Kang, D.-M.; Hong, S.J.; et al. The associations between ADHD and asthma in Korean children. BMC Psychiatry 2014, 14, 70. [Google Scholar] [CrossRef]
- Jiang, X.; Shen, C.; Dai, Y.; Jiang, F.; Li, S.; Shen, X.; Hu, Y.; Li, F. Early food allergy and respiratory allergy symptoms and attention-deficit/hyperactivity disorder in Chinese children: A cross-sectional study. Pediatr. Allergy Immunol. 2018, 29, 402–409. [Google Scholar] [CrossRef]
- Chen, M.-H.; Su, T.-P.; Chen, Y.-S.; Hsu, J.-W.; Huang, K.-L.; Chang, W.-H.; Chen, T.-J.; Pan, T.-L.; Bai, Y.-M. Is atopy in early childhood a risk factor for ADHD and ASD? A longitudinal study. J. Psychosom. Res. 2014, 77, 316–321. [Google Scholar] [CrossRef]
- Liao, T.-C.; Lien, Y.-T.; Wang, S.; Huang, S.-L.; Chen, C.-Y. Comorbidity of atopic disorders with autism spectrum disorder and attention deficit/hyperactivity disorder. J. Pediatr. 2016, 171, 248–255. [Google Scholar] [CrossRef] [PubMed]
- Tsai, P.-H.; Chen, M.-H.; Su, T.-P.; Chen, Y.-S.; Hsu, J.-W.; Huang, K.-L.; Chang, W.-H.; Chen, T.-J.; Bai, Y.-M. Increased risk of autism spectrum disorder among early life asthma patients: An 8-year nationwide population-based prospective study. Res. Autism Spectr. Disord. 2014, 8, 381–386. [Google Scholar] [CrossRef]
- Xu, G.; Snetselaar, L.G.; Jing, J.; Liu, B.; Strathearn, L.; Bao, W. Association of food allergy and other allergic conditions with autism spectrum disorder in children. JAMA Netw. Open 2018, 1, e180279. [Google Scholar] [CrossRef]
- Lyall, K.; Van de Water, J.; Ashwood, P.; Hertz-Picciotto, I. Asthma and allergies in children with autism spectrum disorders: Results from the CHARGE study. Autism Res. 2015, 8, 567–574. [Google Scholar] [CrossRef] [PubMed]
- Kotey, S.; Ertel, K.; Whitcomb, B. Co-occurrence of autism and asthma in a nationally-representative sample of children in the United States. J. Autism Dev. Disord. 2014, 44, 3083–3088. [Google Scholar] [CrossRef]
- Amirian, E.S.; Zhou, R.; Wrensch, M.R.; Olson, S.H.; Scheurer, M.E.; Il’Yasova, D.; Lachance, D.; Armstrong, G.N.; McCoy, L.S.; Lau, C.C. Approaching a scientific consensus on the association between allergies and glioma risk: A report from the glioma international case-control study. Cancer Epidemiol. Biomark. Prev. 2016, 25, 282–290. [Google Scholar] [CrossRef] [PubMed]
- Wiemels, J.L.; Wiencke, J.K.; Sison, J.D.; Miike, R.; McMillan, A.; Wrensch, M. History of allergies among adults with glioma and controls. Int. J. Cancer 2002, 98, 609–615. [Google Scholar] [CrossRef] [PubMed]
- Wigertz, A.; Lönn, S.; Schwartzbaum, J.; Hall, P.; Auvinen, A.; Christensen, H.C.; Johansen, C.; Klæboe, L.; Salminen, T.; Schoemaker, M.J. Allergic conditions and brain tumor risk. Am. J. Epidemiol. 2007, 166, 941–950. [Google Scholar] [CrossRef]
- Schlehofer, B.; Blettner, M.; Moissonnier, M.; Deltour, I.; Giles, G.G.; Armstrong, B.; Siemiatycki, J.; Parent, M.-E.; Krewski, D.; Johansen, C. Association of allergic diseases and epilepsy with risk of glioma, meningioma and acoustic neuroma: Results from the INTERPHONE international case–control study. Eur. J. Epidemiol. 2022, 37, 503–512. [Google Scholar] [CrossRef]
- Krishnamachari, B.; Il’yasova, D.; Scheurer, M.E.; Bondy, M.; Zhou, R.; Wrensch, M.; Davis, F. A pooled multisite analysis of the effects of atopic medical conditions in glioma risk in different ethnic groups. Ann. Epidemiol. 2015, 25, 270–274. [Google Scholar] [CrossRef]
- Yamasaki, R.; Fujii, T.; Wang, B.; Masaki, K.; Kido, M.A.; Yoshida, M.; Matsushita, T.; Kira, J.-I. Allergic inflammation leads to neuropathic pain via glial cell activation. J. Neurosci. 2016, 36, 11929–11945. [Google Scholar] [CrossRef] [PubMed]
Study | Study Group | Allergic Diseases | Results |
---|---|---|---|
Tremlett et al. (2002) [16] | 346 MS patients in Wales | Asthma | Inverse association between MS and asthma compatible with a Th1/Th2 imbalance. |
Alonso et al. (2006) [28] | 163 patients with MS in the UK | Allergic rhinitis, hay fever, urticaria, eczema, atopic dermatitis | 1. No association between allergies and MS 2. H1R activation was associated with decreased MS risk |
Ponsonby et al. (2006) [26] | 136 patients with MS in Australia | Asthma | Asthma rates were significantly higher in individuals with MS prior to symptom onset. |
Alonso et al. (2008) [27] | 298 women with MS in the USA | Allergy to pollens, house dust, animal dander, food, drug | No association between allergies and MS |
Pedotti et al. (2009) [29] | 423 adults with MS in Italy | Asthma, rhinitis, conjunctivitis, contact and atopic dermatitis, food, drug, insect sting allergy | Inverse association between MS and allergic diseases, especially asthma. |
Bergamaschi et al. (2009) [17] | 200 MS patients in Italy | Allergic respiratory diseases | 1. Inverse association between MS and allergic diseases 2. MS tended to be less severe in individuals with allergic respiratory diseases |
Ramagopalan et al. (2010) [30] | 6638 MS patients in Canada | Cow’s milk allergy | Childhood cow’s milk allergy is not associated with MS |
Karimi et al. (2013) [31] | 40 adults with MS in Iran | rhinitis, conjunctivitis, urticaria and eczema, asthma | No significant relationship between allergy history and IgE levels and MS |
Sahraian et al. (2013) [32] | 195 MS patients in Iran | Asthma, allergic rhinitis, urticaria/angioedema, eczema, food, drug and non specific agents allergies | Inverse association between MS and allergic diseases |
Hughes et al. (2013) [33] | 282 adults with first central nervous system demyelination (FCD) in Australia | Asthma, hay fever, eczema | No association between allergies and FCD |
Ashtari et al. (2013) [34] | 40 MS patients in Iran | Cow’s milk allergy | No association between cow’s milk allergy and MS |
Mansouri et al. (2014) [35] | 1403 MS patients in Iran | Conjunctivitis, rhinitis, urticaria, asthma, food, drug, pollens, house dust, animal dander allergies | History of any allergic condition was a risk factor of MS. |
Skaaby et al. (2015) [36] | 35 adult MS patients in Denmark | Atopy with present serum IgE antibodies against common inhalant allergens | No statistically significant associations between atopy and autoimmune disease |
Manouchehrinia et al. (2015) [37] | 680 MS patients in England | Asthma | No difference in the prevalence of asthma between MS cohort and the England general population. |
Ren et al. (2017) [38] | 829 MS patients in the USA | Respiratory tract and other allergies | Inverse association between MS and allergic diseases. |
Bourne et al. (2017) [39] | 271 MS children and adolescents In the USA | Asthma, food, drug and environmental allergies | Allergies and asthma are not associated with pediatric MS. |
Fakih et. al (2019) [40] | 1349 MS patients in the UK | foods, drugs and environmental allergies | MS patients with food allergy had more relapses and more lesions. |
Krishna et. al (2019) [41] | A total of 3,225,758 patients with allergic diseases in the UK | Allergic rhinitis/conjunctivitis, eczema, asthma | No significant association between allergic diseases and MS. |
Hill et al. (2019) [42] | 141,880 MS patients in the USA | Asthma | Asthma is significantly more common in those with MS than in the general population. |
Albatineh et. al (2020) [43] | 128 Kuwaiti MS patients | Food allergy | No significant association between food allergy and MS. |
Chen et al. (2020) [44] | 929 MS patients in Australia | Allergies, not specified | Significant association between allergies and MS. |
Sorensen et al. (2021) [45] | 2012 MS patients in the USA | Asthma | Asthma is common in MS patients. Asthmatic patients were more likely to be female, obese, hypertensive, and living in neighborhood of medium/low income, and less likely to be on interferons or glatiramer acetate. |
Lo et al. (2021) [46] | 1518 MS patients in Australia | Allergies, not specified | No significant association between allergies and MS. |
Study | Study Group | Allergic Diseases | Results |
---|---|---|---|
Frediani et al. (2001) [64] | 72 children in Italy | Food and drug allergies, asthma, eczema, rhinitis | 1. A significantly higher incidence of allergy to cow’s milk and asthma in the epileptic children. 2. Significantly higher rates of eczema in the mothers and rhinitis in the siblings of the epileptic children. |
Kobau et al. (2004) [65] | 161 adults in the USA (Georgia and Tennessee) | Asthma | Significantly higher incidence of asthma among adults with seizures. |
Strine et al. (2005) [66] | 426 adults in the USA | Asthma | Significantly higher incidence of asthma among adults with seizures. |
Elliott et al. (2008) [67] | 97 adults in the USA | Asthma | Asthma rates were significantly higher in individuals with epilepsy. |
Babu et al. (2009) [68] | 250 adolescents and adults (16 to 60 years) in the USA | Asthma | Asthma rates were not significantly higher in individuals with epilepsy. |
Karlstad et al. (2012) [69] | 37,060 children and adults (8–29 years) with asthma in Norway | Asthma | Significantly higher incidence of epilepsy and migraine among patients with asthma. |
Silverberg et al. (2014) [70] | 944 children with asthma in the USA | Asthma, eczema, hay fever, food allergies | The US prevalence of epilepsy is associated with allergic diseases in children. |
Chen et al. (2014) [71] | 35,312 children and adults with atopic dermatitis in Taiwan | Atopic dermatitis | Subjects with atopic dermatitis were associated with an increased risk of developing epilepsy in later life. |
Lin et al. (2014) [72] | 991 children (1 month–2 years) in Taiwan | Asthma | Significantly higher cumulative incidence of asthma occurrence in children with more febrile seizure-related medical visits. |
Kauppi et al. (2015) [73] | 251,540 adults and children with asthma in Finland | Asthma | The most common other reimbursed chronic conditions in addition to asthma in the youngest age groups were epilepsy or other comparable convulsive disorders. |
Strom et al. (2016) [74] | 63,064 children with one or more allergic diseases in the USA | Asthma, hay fever, eczema, and food allergies | 1. Children with hay fever, eczema, and food allergies had higher odds of experiencing seizures. 2. No significant association between asthma and seizures. |
Chiang et al. (2018) [75] | 150,827 children and adults with asthma in Taiwan | Asthma | The asthma group exhibited a higher epilepsy incidence than did the control group |
Machluf et al. (2020) [76] | 113,671 Israeli adolescents with asthma | Asthma | Asthma was associated with epilepsy and migraine. |
Study | Study Group | Results |
---|---|---|
Davey et al. (2002) [80] | 64,678 adults in the UK | Significant association between migraine and asthma. |
Aamodt et al. (2007) [81] | A total number of 51,383 adult individuals in Norway | Both migraine and nonmigraine headache were 1.5 times more likely among individuals with asthma, asthma related symptoms, hay fever, and chronic bronchitis. |
Becker et al.(2008) [82] | 51,688 adult migraineurs in the UK | The risk of developing asthma was not higher for patients with migraine diagnosis, regardless of triptan use. |
Le et al. (2011) [83] | 46,418 adult twins Denmark | Conditions with a positive association to migraine were asthma, stroke, and epilepsy. The concomitant diseases were more frequent in female patients with aura. |
Chen et al. (2012) [84] | 681 adult patients with chronic migraine in Taiwan | Individuals with chronic migraine had significantly increased risks of cardiovascular disease, sinusitis, asthma, gastrointestinal ulcers, vertigo and psychiatric disorders by 1.6–3.9-fold. |
Czerwinski et al. (2012) [85] | 3731 pregnant women with migraine in the USA | Migraineurs had 1.38-fold increased odds of asthma as compared with non migraineurs). The odds of hypertensive disorders of pregnancy were highest among women with comorbid migraine-asthma. |
Lateef et al. (2012) [86] | 6843 adolescents with headache in the USA | Adolescents with migraine more often reported asthma (or seasonal allergies compared to those with non-specific headache. |
Peng et al. (2016) [87] | 25,560 patients more than 12 years old with asthma in Taiwan | The risk of migraine in the asthmatic group was 1.45-fold higher. |
Tsiakiris et al. (2017) [88] | 462 individuals with asthma and allergic rhinitis in Sweden | Allergic asthma and rhinitis are associated with migraine, fibromyalgia, and irritable bowel syndrome. |
Peng et al. (2018) [89] | 6647 adult patients with migraine in Taiwan | Adult patients with migraine have significantly higher risk of asthma. |
Graif et al. (2018) [90] | A total of 113,671 adolescents in Israel | A significant association between migraine and both asthma and allergic rhinitis. |
Wei et. al. (2018) [91] | 16,130 children with migraine in Taiwan | Children with preexisting atopic dermatitis, allergic conjunctivitis, allergic rhinitis, and asthma had a significantly higher risk of devel-oping migraines, with a cumulative effect |
Kim et al., 2019 [92] | 113,059 adult asthma participants 36,044 migraine participants | Asthma and migraines in adults are reciprocally associated. |
Buse et al., 2020 [93] | 15,133 adult individuals with migraine in the USA | 1. The migraine group was at least twice as likely to experience allergies/hay fever and asthma. 2. Severe headache pain intensity was associated with an increased risk of allergy but not with asthma. 3. Increasing migraine frequency was associated with increasing risk for allergy/hay fever and asthma. |
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Saramak, K. Exploring the Link Between Allergies and Neurological Diseases: Unveiling the Hidden Connections. Allergies 2025, 5, 18. https://doi.org/10.3390/allergies5020018
Saramak K. Exploring the Link Between Allergies and Neurological Diseases: Unveiling the Hidden Connections. Allergies. 2025; 5(2):18. https://doi.org/10.3390/allergies5020018
Chicago/Turabian StyleSaramak, Kamila. 2025. "Exploring the Link Between Allergies and Neurological Diseases: Unveiling the Hidden Connections" Allergies 5, no. 2: 18. https://doi.org/10.3390/allergies5020018
APA StyleSaramak, K. (2025). Exploring the Link Between Allergies and Neurological Diseases: Unveiling the Hidden Connections. Allergies, 5(2), 18. https://doi.org/10.3390/allergies5020018