The role of genes and environment in the etiology of PCOS

Endocrine. 2006 Aug;30(1):19-26. doi: 10.1385/ENDO:30:1:19.

Abstract

Both genes and the environment contribute to PCOS. Obesity, exacerbated by poor dietary choices and physical inactivity, worsens PCOS in susceptible individuals. The role of other environmental modifiers such as infectious agents or toxins are speculative. Phenotype confusion has characterized genetic studies of PCOS. Although several loci have been proposed as PCOS genes including CYP11A, the insulin gene, the follistatin gene, and a region near the insulin receptor, the evidence supporting linkage is not overwhelming. The strongest case can be made for the region near the insulin receptor gene (but not involving this gene), as it has been identified in two separate studies, and perhaps most importantly has not yet been refuted by larger studies. However, the responsible gene at chromosome 19p13.3 remains to be identified. To date, no gene has been identified that causes or contributes substantially to the development of a PCOS phenotype.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Cholesterol Side-Chain Cleavage Enzyme / genetics
  • Cholesterol Side-Chain Cleavage Enzyme / physiology
  • Chromosomes, Human, 19-20 / genetics*
  • Environment*
  • Family
  • Female
  • Follistatin / genetics
  • Follistatin / physiology
  • Genetic Predisposition to Disease
  • Humans
  • Insulin / genetics
  • Insulin / physiology
  • Obesity / genetics*
  • Obesity / pathology
  • Polycystic Ovary Syndrome / genetics*
  • Polycystic Ovary Syndrome / pathology
  • Receptor, Insulin / genetics
  • Receptor, Insulin / physiology

Substances

  • Follistatin
  • Insulin
  • Cholesterol Side-Chain Cleavage Enzyme
  • Receptor, Insulin