Association of polymorphisms of genes TCF7L2, FABP2, KCNQ1, ADIPOQ with the prognosis of the development of type 2 diabetes mellitus
- Authors: Mel’nikova E.S.1, Rymar O.D.1, Ivanova A.A.1, Mustafina S.V.1, Shapkina M.J.1, Bobak M.2, Maljutina S.K.1, Voevoda M.I.1, Maksimov V.N.1
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Affiliations:
- Research Institute of Internal and Preventive Medicine
- Department of Epidemiology & Public Health, University College London
- Issue: Vol 92, No 10 (2020)
- Pages: 40-47
- Section: Original articles
- URL: https://journals.rcsi.science/0040-3660/article/view/50975
- DOI: https://doi.org/10.26442/00403660.2020.10.000393
- ID: 50975
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Abstract
Aim. To study the possibility of using polymorphisms of genes TCF7L2, FABP2, KCNQ1, ADIPOQ as markers for predicting the development of type 2 diabetes mellitus (T2D) in the population of Novosibirsk.
Materials and methods. On the basis of prospective observation of a representative population sample of residents of Novosibirsk (HAPIEE), 2 groups were formed according to the “case-control” principle (case – people who had diabetes mellitus 2 over 10 years of observation, and control – people who did not developed disorders of carbohydrate metabolism). T2D group (n=443, mean age 56.2±6.7 years, men – 29.6%, women – 70.4%), control group (n=532, mean age 56.1±7.1 years, men – 32.7%, women – 67.3%). DNA was isolated by phenol-chloroform extraction. Genotyping was performed by the method of polymerase chain reaction with subsequent analysis of restriction fragment length polymorphism, polymerase chain reaction in real time. Statistical processing was carried out using the SPSS 16.0 software package.
Results and discussion. No significant effect of rs1799883 of the FABP2 gene, rs2237892 of the KCNQ1 gene, and rs6773957 of the ADIPOQ gene on the risk of developing T2D was found. Genotypes TT and TC rs7903146 of the TCF7L2 gene are genotypes for the risk of developing T2D (relative risk – RR 3.90, 95% confidence interval – CI 2.31–6.61, p<0.001; RR 1.86, 95% CI 1.42–2.43, p<0.001, respectively). The CC genotype rs7903146 of the TCF7L2 gene is associated with a protective effect against T2D (RR 0.37, 95% CI 0.29–0.49, p<0.001). When the TCF7L2 gene is included in the model for assessing the risk of developing T2D rs7903146, it retains its significance in both men and women.
Conclusion. The rs7903146 polymorphism of the TCF7L2 gene confirmed its association with the prognosis of the development of T2D, which indicates the possibility of considering it as a candidate for inclusion in a diabetes risk meter. Variants of risk meters have been developed to assess the prognosis of the development of diabetes mellitus 2 in men and women aged 45–69 years during 10 years of follow-up. The association with the prognosis of the development of T2D polymorphisms rs1799883 of the FABP2 gene, rs2237892 of the KCNQ1 gene and rs6773957 of the ADIPOQ gene was not found.
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##article.viewOnOriginalSite##About the authors
E. S. Mel’nikova
Research Institute of Internal and Preventive Medicine
Author for correspondence.
Email: jarinaleksi@list.ru
ORCID iD: 0000-0002-9033-1588
ординатор НИИТПМ – филиала ФГБНУ ИЦиГ
Russian Federation, NovosibirskO. D. Rymar
Research Institute of Internal and Preventive Medicine
Email: jarinaleksi@list.ru
ORCID iD: 0000-0003-4095-0169
д.м.н., зав. лаб. клинико-популяционных и профилактических исследований терапевтических и эндокринных заболеваний НИИТПМ – филиала ФГБНУ ИЦиГ
Russian Federation, NovosibirskA. A. Ivanova
Research Institute of Internal and Preventive Medicine
Email: jarinaleksi@list.ru
ORCID iD: 0000-0002-9460-6294
к.м.н., мл. науч. сотр. лаб. молекулярно-генетических исследований терапевтических заболеваний НИИТПМ – филиала ФГБНУ ИЦиГ
Russian Federation, NovosibirskS. V. Mustafina
Research Institute of Internal and Preventive Medicine
Email: jarinaleksi@list.ru
ORCID iD: 0000-0003-4716-876X
д.м.н., ст. науч. сотр. лаб. клинико-популяционных и профилактических исследований терапевтических и эндокринных заболеваний НИИТПМ – филиала ФГБНУ ИЦиГ
Russian Federation, NovosibirskM. Ju. Shapkina
Research Institute of Internal and Preventive Medicine
Email: jarinaleksi@list.ru
ORCID iD: 0000-0002-8577-8801
мл. науч. сотр. лаб. этиопатогенеза и клиники внутренних заболеваний НИИТПМ – филиала ФГБНУ ИЦиГ
Russian Federation, NovosibirskMartin Bobak
Department of Epidemiology & Public Health, University College London
Email: jarinaleksi@list.ru
ORCID iD: 0000-0003-2357-5918
проф. эпидемиологии, зам. рук. отд. эпидемиологии и общественного здоровья Университетского колледжа
Anguilla, LondonS. K. Maljutina
Research Institute of Internal and Preventive Medicine
Email: jarinaleksi@list.ru
ORCID iD: 0000-0001-6539-0466
д.м.н., проф., зав. лаб. этиопатогенеза и клиники внутренних заболеваний НИИТПМ – филиала ФГБНУ ИЦиГ
Russian Federation, NovosibirskM. I. Voevoda
Research Institute of Internal and Preventive Medicine
Email: jarinaleksi@list.ru
ORCID iD: 0000-0001-9425-413X
акад. РАН, д.м.н., проф., НИИТПМ – филиал ФГБНУ ИЦиГ
Russian Federation, NovosibirskV. N. Maksimov
Research Institute of Internal and Preventive Medicine
Email: jarinaleksi@list.ru
ORCID iD: 0000-0002-7165-4496
д.м.н., проф., зав. лаб. молекулярно-генетических исследований терапевтических заболеваний НИИТПМ – филиала ФГБНУ ИЦиГ
Russian Federation, NovosibirskReferences
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