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Association of polymorphic markers of genes FTO, KCNJ11, CDKAL1, SLC30A8, and CDKN2B with type 2 diabetes mellitus in the Russian population
Author(s) -
Aleksey Nikitin,
Viktor Y. Potapov,
Olga Brovkina,
Ekaterina Koksharova,
Dmitry Khodyrev,
Yury I. Philippov,
Marina Michurova,
Минара Шамхаловна Шамхалова,
Olga Konstantinovna Vikulova,
С. А. Сметанина,
Л. А. Суплотова,
Ирина Владимировна Кононенко,
V. Y. Kalashnikov,
О. М. Смирнова,
Alexander Yur'evich Mayorov,
В. В. Носиков,
Alexander Averyanov,
М. В. Шестакова
Publication year - 2017
Publication title -
peerj
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.927
H-Index - 70
ISSN - 2167-8359
DOI - 10.7717/peerj.3414
Subject(s) - genetics , population , gene , biology , type 2 diabetes mellitus , diabetes mellitus , medicine , endocrinology , environmental health
Background The association of type 2 diabetes mellitus (T2DM) with the KCNJ11, CDKAL1, SLC30A8, CDKN2B, and FTO genes in the Russian population has not been well studied. In this study, we analysed the population frequencies of polymorphic markers of these genes. Methods The study included 862 patients with T2DM and 443 control subjects of Russian origin. All subjects were genotyped for 10 single nucleotide polymorphisms (SNPs) of the genes using real-time PCR (TaqMan assays). HOMA-IR and HOMA- β were used to measure insulin resistance and β -cell secretory function, respectively. Results The analysis of the frequency distribution of polymorphic markers for genes KCNJ11, CDKAL1, SLC30A8 and CDKN2B showed statistically significant associations with T2DM in the Russian population. The association between the FTO gene and T2DM was not statistically significant. The polymorphic markers rs5219 of the KCNJ11 gene, rs13266634 of the SLC30A8 gene, rs10811661 of the CDKN2B gene and rs9465871 , rs7756992 and rs10946398 of the CDKAL1 gene showed a significant association with impaired glucose metabolism or impaired β -cell function. Conclusion In the Russian population, genes, which affect insulin synthesis and secretion in the β -cells of the pancreas, play a central role in the development of T2DM.

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