THE ROLE OF INTERLEUKIN 1β GENE POLYMORPHISM IN DEVELOPMENT OF PREDOMINANTY SENSORY CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY
https://doi.org/10.15789/1563-0625-2019-1-141-148
Abstract
The aim of the present study was a search for associations between the polymorphic allelic variants 3954 C>T (rs1143644) and -511C>T (rs16944) of IL1B gene in the patients with sensory predominant chronic inflammatory demyelinating polyneuropathies (SP-CIDP) from Krasnoyarsk Region and the Sakha (Yakutia) Republic. A total of 95 people were examined, having been divided into 2 groups according to their residence. The first group consisted of 42 patients living in the Sakha (Yakutia) Republic. The second group included 53 patients living in the Krasnoyarsk Region. It was revealed that the carriers of homozygous CC genotype in the 3954C>T locus were more often detected in patients from the Sakha (Yakutia) Republic, and the carriage of TT genotype is found exclusively in the patients from Krasnoyarsk Region. When comparing the different genotype frequencies in the -511CT locus, we did not reveal any statistically significant differences between the two groups of patients. Presence of the CC genotype of the 3954C>T locus was associated with a significantly increased risk of disease in the patients from Sakha (Yakutia) Republic, while carrying CT and TT genotypes at the locus 3954C>T and the TT genotype at the locus -511C>T, is associated with increased risk disorder among patients of the Krasnoyarsk Region. The frequency of carriage of various genotypes in the 3954C>T and -511C>T loci of the IL1B gene was prevalent among the patients from the Sakha (Yakutia) Republic, the association of genotypes of CC/CT prevailed in patients from the Krasnoyarsk Region (p = 0.005), as well as prevalence of CC/CC and CC/CT (p = 0.023). However, there was no statistically significant difference in occurrence of individual genotypes between the two study groups. When analyzing the carrier frequency of high-producing alleles of 3954C and -511C in patients with SP-CIDP, it was shown that they were significantly more common among patients from the Sakha (Yakutia) Republic and patients from the Krasnoyarsk Region than the low-producing 3954T and -511T alleles. Moreover, the 3954C allele was more often found in the Yakut group (p = 0.001), and in the -511C allele for the Krasnoyarsk group of patients (p = 0.05). The presence of 3954C and -511C alleles increases the risk of SP-CIDP development in patients from the Sakha (Yakutia) Republic, as well as carriage of 3954T allele in patients from the Krasnoyarsk Region.
About the Authors
T. E. PopovaRussian Federation
PhD, MD (Medicine), Associate Professor, Professor, Department of Neurology and Psychiatry, Medical Institute
677013, Yakutsk, Oyunsky str., 27.
Phone: 7 (4112) 36-30-46. Fax: 7 (4112) 49-68-26.
N. A. Shnayder
Russian Federation
PhD, MD (Medicine), Professor, Head, Department of Medical Genetics and Clinical Neurophysiology
Krasnoyarsk
M. M. Petrova
Russian Federation
PhD, MD (Medicine), Professor, Vice-Rector for Research
Krasnoyarsk
A. A. Tappakhov
Russian Federation
Postgraduate Student, Department of Neurology and Psychiatry, Medical Institute
Yakutsk
References
1. Азнабаева Л.Ф., Шарипова Э.Р., Арефьева Н.А., Зайнуллина А.Г., Симбирцев А.С. Иммуногенетические особенности продукции интерлейкина-1β при затяжной и хронической (рецидивирующей) форме бактериального воспаления верхних дыхательных путей (гнойного риносинусита) // Медицинская иммунология, 2007. Т. 9, № 4-5. С. 535-540. [Azanbaeva L.F., Sharipova E.R., Arepheva N.A., Zaynullina A.G., Simbirtsev A.S. Immunogenetic features of production of interleukin-1βwith prolonged and chronic (recurrent) form of bacterial inflammation of the upper respiratory tract (purulent rhinosinusitis). Meditsinskaya immunologiya = Medical Immunology (Russia), 2007, Vol. 9, no. 4-5, pp. 535-540.(In Russ.)] doi: 10.15789/1563-0625-2007-4-5-535-540.
2. Кантимирова Е.А., Шнайдер Н.А. Хроническая воспалительная демиелинизирующая полинейропатия: дефиниция, эпидемиология, классификация, диагностика // Вестник клинической больницы № 51, 2009. № 7. С. 22-25. [Kantimirova E.A., Schnayder N.A. Chronic inflammatory demyelinating polyneuropathy: definition, epidemiology, classification, diagnosis. Vestnik klinicheskoy bolnitsy no. 51 = Bulletin of the Clinical Hospital no. 51, 2009, no. 7, pp. 22-25. (In Russ.)]
3. Кетлинский С.А., Симбирцев А.С., Воробьев А.А. Эндогенные иммуномодуляторы. СПб.: Гиппократ, 1992. 256 с. [Ketlinksky S.A., Simbirtsev A.S., Vorobyev A.A. Endogenic immunomodulators. St. Petersburg, 1992. 256 p. (In Russ.)
4. Маев И.В., Кучерявый Ю.А., Оганесян Т.С. Аллельный полиморфизм интерлейкина 1β при гелибактериозе // Российский журнал гастроэнтерологии, гепатологии, колопроктологии,2008. Т. 18, № 5. С. 4-11. [Mayev I.V., Kucheryavyy Yu.A., Oganesyan T.C. Interleukin-1βallelic polymorphism at H. pyloriinfection. Rossijskij zhurnal gastroehnterologii, gepatologii, koloproktologii = Russian Journal of Gastroenterology, Hepatology, Coloproctology, 2008, Vol. 18, no. 5, pp. 4-11.(In Russ.)]
5. Супонева Н.А., Никитин С.С., Пирадов М.А., Меркулова Д.М. Хроническая воспалительная демиелинизирующая полиневропатия с острым началом и дыхательной недостаточностью // Нервные болезни, 2007. № 1. C. 40-44. [Suponeva N.A., Nikitin S.S., Piradov M.A., Merkulova D.M. Chronic inflammatory demyelinating polyneuropathy with acute onset and respiratory failure. Nervnye bolezni = Neurological Diseases, 2007, no. 1, pp. 40-44.(In Russ.)]
6. Супонева Н.А. Клиническая и диагностическая роль аутоантител к ганглиозидам периферических нервов: обзор литературы и собственные данные // Нервно-мышечные болезни, 2013. № 1. C. 26-33. [Suponeva N.A. Clinical and diagnostic role of autoantibodies to gangliosides of peripheral nerves: literature review and own expirience. Nervno-myshechnye bolezni = Neuromuscular Diseases, 2013, no. 1, pp. 26-34. (In Russ.)]
7. Терскова Н.В., Шнайдер Н.А., Вахрушев С.Г., Иконникова Е.В., Пилюгина М.С. Роль полиморфизма гена интерлейкина-1β в развитии воспаления глоточной миндалины // Российская оториноларингология, 2010. Т. 49, № 6. С. 87-93. [Terskova N.V., Shnayder N.A., Vakhrushev S.G., Ikonnikova E.V., Pilyugina M.S. Тhe role of interleukin-1β gene polymorphism in pathogenesis of tornwaldt disease. Rossiyskaya otorinolaringologiya = Russian Otorhinolaryngology, 2010, Vol. 49, no. 6, pp. 87-93.(In Russ.)]
8. Шнайдер Н.А., Кантимирова Е.А. Эпидемиологическая и клиническая характеристика отдельных форм полиневропатий (на примере ЗАТО Железногорск Красноярского края) // Нервно-мышечные болезни, 2011. № 1. C. 34-40. [Schnayder N.A., Kantimirova E.A. Epidemiological and clinical characteristics of individual forms of polyneuropathies (in Zheleznogorsk, Krasnoyarsk Region). Nervno-myshechnye bolezni = Neuromuscular Diseases, 2011, no. 1, pp. 34-40. (In Russ.)]
9. Abuzarova E.R. Polymorphism of Helicobacter pylorigenotypes and cytokines (IL1 и IL10) in patients with gastric and duodenal ulcer. Helicobacter, 2007, Vol. 12, no. 4, p. 401.
10. Dalakas M.C. Advances in the diagnosis, pathogenesis and treatment of CIDP. Nat. Rev. Neurol., 2011, Vol. 7, pp. 507-517.
11. Lünemann J., Tackenberg B., Stein A., Wandinger K., Oertel W., Wagner H., Münz C., Meisel H., Sommer N., Zipp F. Dysregulated Epstein–Barr virus infection in patients with CIDP. J. Neuroimmunol., 2010, Vol. 218, no. 1-2, pp. 107-111.
12. Stübgen J.-P. A review on the use biological agents for chronic inflammatory demyelinating polyradiculoneuropathy. J. Neuro. Sci., 2013, Vol. 326, pp. 1-9.
13. Vanasse M., Rossignol E., Hadad E. Chronic inflammatory demyelinating polyneuropathy. Handb. Clin. Neurol., 2013, Vol. 112, pp. 1163-1169.
Review
For citations:
Popova T.E., Shnayder N.A., Petrova M.M., Tappakhov A.A. THE ROLE OF INTERLEUKIN 1β GENE POLYMORPHISM IN DEVELOPMENT OF PREDOMINANTY SENSORY CHRONIC INFLAMMATORY DEMYELINATING POLYNEUROPATHY. Medical Immunology (Russia). 2019;21(1):141-148. (In Russ.) https://doi.org/10.15789/1563-0625-2019-1-141-148