A distribution of two SNPs in exon 10 of the FSHR gene among the women with a diminished ovarian reserve in Ukraine

J Assist Reprod Genet. 2009 Jan;26(1):29-34. doi: 10.1007/s10815-008-9279-1. Epub 2008 Nov 25.

Abstract

Purpose: To evaluate the association between phenotype and follicle stimulating hormone receptor (FSHR) genotype in women with ovarian dysfunction and patients with "poor response" to gonadotropin stimulation of ovulation.

Methods: FSHR gene SNPs were analyzed by PCR and RFLP. "Poor responders" (ovarian dysfunction) group and "good responders" group constituted the study group. Normo-ovulatory women who gave birth to naturally conceived children formed control groups: under 35 years of age (control I) and over 35 years of age (control II).

Results: The frequency of Ala307-Ser680/Ala307-Ser680 genotype was significantly more prevalent in the ovarian dysfunction group (26%) compared to the control I (7.7%) (P < 0.001) and a "good responders" group (12.5%) (P < 0.05); and in a "poor responders" group (33.3%) compared to a "good responders" group (P < 0.05), control I (P < 0.001) and control II (17.5%) (P < 0.05).

Conclusions: Our data shows the prevalence of the Ala307-Ser680/ Ala307-Ser680 genotype in the both groups of patients. The finding should have impact on the delineation of stimulation protocols.

MeSH terms

  • Adult
  • Amino Acid Substitution
  • Exons
  • Female
  • Follicle Stimulating Hormone, Human / therapeutic use
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Infertility, Female / drug therapy
  • Infertility, Female / genetics*
  • Infertility, Female / physiopathology
  • Ovarian Follicle / drug effects
  • Ovarian Follicle / physiopathology*
  • Ovulation Induction
  • Polymorphism, Single Nucleotide*
  • Pregnancy
  • Receptors, FSH / genetics*
  • Receptors, FSH / metabolism
  • Ukraine

Substances

  • Follicle Stimulating Hormone, Human
  • Receptors, FSH