KCNJ11 and KCNQ1 Gene Polymorphisms and Placental Expression in Women with Gestational Diabetes Mellitus

Genes (Basel). 2022 Jul 23;13(8):1315. doi: 10.3390/genes13081315.

Abstract

Gestational diabetes mellitus (GDM) represents carbohydrate intolerance in pregnant women. The pathogenesis of GDM is very complex, but abnormalities in insulin production and secretion underlie the disease. Potassium channels play an important role in insulin production and secretion. The family of potassium channels includes (among others) the potassium inwardly rectifying channel, subfamily J, member 11 (KCNJ11) and voltage-gated K+ channel (KCNQ1). The aim of the study was to examine the distribution of the KCNJ11 rs5219 and KCNQ1 rs151290 and rs2237892 gene polymorphisms in women with GDM and pregnant women with normal carbohydrate tolerance, to verify whether these polymorphisms are risk factors for GDM. This study included 204 Caucasian pregnant women with GDM and 207 pregnant women with normal glucose tolerance (NGT) from the West Pomeranian region of Poland. The diagnosis of GDM was based on a 75 g oral glucose tolerance test (OGTT) at 24-28 weeks gestation. There were no statistically significant differences in distribution of the KCNJ11 rs5219 and KCNQ1 rs151290 and rs2237892 gene polymorphisms between women with GDM and pregnant women with normal carbohydrate tolerance. Moreover, there were no statistically significant associations between the studied genotypes and the selected clinical parameters in women with GDM. The results of our study suggest that the KCNJ11 rs5219 and KCNQ1 rs2237892 and rs151290 gene polymorphisms are not significant risk factors associated with the development of GDM in our population. There were also no differences in the expression of KCNJ11 and KCNQ1 genes in the placenta of women with GDM and normal carbohydrate tolerance. However, an association between KCNJ11 gene expression in placenta and APGAR score in newborns was found.

Keywords: GDM; KCNJ11; KCNQ1; polymorphism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrates
  • Diabetes, Gestational* / genetics
  • Female
  • Humans
  • Infant, Newborn
  • Insulin
  • KCNQ1 Potassium Channel* / genetics
  • Placenta
  • Polymorphism, Genetic
  • Potassium Channels, Inwardly Rectifying* / genetics
  • Pregnancy

Substances

  • Carbohydrates
  • Insulin
  • KCNQ1 Potassium Channel
  • KCNQ1 protein, human
  • Kir6.2 channel
  • Potassium Channels, Inwardly Rectifying

Grants and funding

The project is financed from the program of the Minister of Science and Higher Education under the name “Regional Initiative of Excellence” in 2019–2022 project number 002/RID/2018-19.