Three common variants of LEP, NPY1R and GPR54 show no association with age at menarche

Horm Res. 2009;71(6):331-5. doi: 10.1159/000223417. Epub 2009 Jun 6.

Abstract

Context: Twin and family studies indicate a significant heritability of pubertal timing and more specifically of age at menarche (AAM).

Objective: Test the association of AAM with common variants of three candidate genes suspected to have a prominent role in reproductive physiology: leptin (LEP), neuropeptide Y receptor 1 (NPY1R) and GPR54.

Design and methods: We selected the -2459 LEP, the rs7687423 NPY1R and thers350132 GPR54 variants as the more common coding or regulatory variants (minor allelic frequency >0.10) in these gene regions. To avoid stratification problems that can impair association studies, we used the Q-TDT method based on allele transmission to evaluate the relationship of these variants with AAM in 245 healthy women from 107 families of European ancestry.

Results: We found no association of AAM with any of the studied variants.

Conclusions: Keeping in mind that common variants do not recapitulate the whole genetic variation in a given gene region, this study indicates that the studied LEP, NPY1R and GPR54 variants do not have a major influence upon pubertal timing in Caucasian women. Effects of these genetic loci on age at menarche can definitively be excluded only through determination of extended haplotypes in a larger cohort.

MeSH terms

  • Adolescent
  • Child
  • Female
  • Gene Frequency
  • Genetic Variation*
  • Humans
  • Leptin / genetics*
  • Menarche / genetics*
  • Receptors, G-Protein-Coupled / genetics*
  • Receptors, Kisspeptin-1
  • Receptors, Neuropeptide Y / genetics*
  • White People / genetics

Substances

  • KISS1R protein, human
  • Leptin
  • Receptors, G-Protein-Coupled
  • Receptors, Kisspeptin-1
  • Receptors, Neuropeptide Y