Polycystic ovary syndrome is not associated with polymorphisms of the TCF7L2, CDKAL1, HHEX, KCNJ11, FTO and SLC30A8 genes

Clin Endocrinol (Oxf). 2012 Sep;77(3):439-45. doi: 10.1111/j.1365-2265.2012.04389.x.

Abstract

Objective: Insulin resistance is a core feature of polycystic ovary syndrome (PCOS). Recently, genome-wide association studies have reported a number of single-nucleotide polymorphisms (SNPs) with reproducible associations and susceptibilities to type 2 diabetes. We examined the potential association between the diabetogenic genes uncovered in the genome-wide association studies and PCOS in Korean women.

Design: Case-control study.

Patients: Women with or without PCOS.

Measurements: DNA samples from 377 patients with PCOS and 386 age-matched controls were genotyped.

Results: None of the 12 SNPs in the six genes (KCNJ11, TCF7L2, SLC30A8, HHEX, FTO and CDKAL1) uncovered in the genome-wide association studies were associated with PCOS. For further analysis, the patients with PCOS were divided into two or three subgroups according to genotype, and the associations between the genotypes and insulin resistance or insulin secretory capacity were assessed. No SNPs were significantly associated with HOMA-IR, HOMA (βcell) (%), or 2-h 75-g oral glucose tolerance test insulin levels in the patients with PCOS; there were no significant associations with other serum hormonal and metabolic markers, such as androgen or glucose levels.

Conclusions: Our results suggest that the six type 2 diabetes-associated genes identified in genome-wide association studies are not associated with PCOS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • Androgens / blood
  • Asian People / genetics
  • Case-Control Studies
  • Cation Transport Proteins / genetics*
  • Cyclin-Dependent Kinase 5 / genetics*
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / metabolism
  • Female
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study
  • Homeodomain Proteins / genetics*
  • Humans
  • Insulin Resistance / genetics
  • Polycystic Ovary Syndrome / genetics*
  • Polycystic Ovary Syndrome / metabolism
  • Polymorphism, Single Nucleotide
  • Potassium Channels, Inwardly Rectifying / genetics*
  • Proteins / genetics*
  • Republic of Korea
  • Risk Factors
  • Transcription Factor 7-Like 2 Protein / genetics*
  • Transcription Factors / genetics*
  • Zinc Transporter 8
  • tRNA Methyltransferases

Substances

  • Androgens
  • Cation Transport Proteins
  • HHEX protein, human
  • Homeodomain Proteins
  • Kir6.2 channel
  • Potassium Channels, Inwardly Rectifying
  • Proteins
  • SLC30A8 protein, human
  • TCF7L2 protein, human
  • Transcription Factor 7-Like 2 Protein
  • Transcription Factors
  • Zinc Transporter 8
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • FTO protein, human
  • tRNA Methyltransferases
  • Cyclin-Dependent Kinase 5
  • CDKAL1 protein, human