Abstract

Gestational diabetes mellitus (GDM) is carbohydrate intolerance that occurs during pregnancy. This disease may lead to various maternal and neonatal complications; therefore, early diagnosis is very important. Because of the similarity in pathogenesis of type 2 diabetes and GDM, the genetic variants associated with type 2 diabetes are commonly investigated in GDM. The aim of the present study was to examine the associations between the polymorphisms in the ADCY5 (rs11708067, rs2877716), CAPN10 (rs2975760, rs3792267), and JAZF1 (rs864745) genes and GDM as well as to determine the expression of these genes in the placenta. This study included 272 pregnant women with GDM and 348 pregnant women with normal glucose tolerance. The diagnosis of GDM was based on a 75 g oral glucose tolerance test (OGTT) at 24–28 weeks gestation, according to International Association of Diabetes and Pregnancy Study Groups (IADPSG) criteria. There were no statistically significant differences in the distribution of the ADCY5 gene (rs11708067, rs2877716) and CAPN10 gene (rs2975760, rs3792267) polymorphisms between pregnant women with normal carbohydrate tolerance and pregnant women with GDM. We have shown a lower frequency of JAZF1 gene rs864745 C allele carriers among women with GDM CC + CT vs. TT (OR = 0.60, 95% CI = 0.41–0.87, p = 0.006), and C vs. T (OR = 0.75, 95% CI = 0.60–0.95, p = 0.014). In addition, ADCY5 and JAZF1 gene expression was statistically significantly increased in the placentas of women with GDM compared with that of healthy women. The expression of the CAPN10 gene did not differ significantly between women with and without GDM. Our results indicate increased expression of JAZF1 and ADCY5 genes in the placentas of women with GDM as well as a protective effect of the C allele of the JAZF1 rs864745 gene polymorphism on the development of GDM in pregnant women.

Highlights

  • Gestational diabetes mellitus (GDM) is the metabolic disorder occurring during pregnancy

  • Previous studies have shown that polymorphisms of ADCY5, CAPN10, and Juxtaposed with another zinc finger gene 1 (JAZF1) genes may be associated with an increased risk of type 2 diabetes [7,8,9]

  • We found a lower frequency of the JAZF1 gene rs864745 C allele carriers among women with GDM CC+CT vs. TT (odds ratio (OR) = 0.60, 95% confidence interval (CI) = 0.41–0.87, p = 0.006), and C vs. T (OR = 0.75, 95% CI = 0.60–0.95, p = 0.014)

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Summary

Introduction

Gestational diabetes mellitus (GDM) is the metabolic disorder occurring during pregnancy. The factors predisposing to GDM development are commonly searched. Known risk factors for GDM include maternal age, obesity, impaired carbohydrate tolerance before pregnancy, and history of GDM during previous pregnancies [2,3]. Many genetic and non-genetic factors that may predispose women to GDM have been sought. Various genetic polymorphisms are being studied, as well as the expression of genes in human umbilical vein endothelial cells and in the placenta [4,5]. There are many similarities in the pathogenesis of GDM and type 2 diabetes [6]; genetic polymorphisms associated with type 2 diabetes are taken into account. Previous studies have shown that polymorphisms of ADCY5, CAPN10, and JAZF1 genes may be associated with an increased risk of type 2 diabetes [7,8,9]

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