Combined effects of the variants FSHB -211G>T and FSHR 2039A>G on male reproductive parameters

J Clin Endocrinol Metab. 2012 Oct;97(10):3639-47. doi: 10.1210/jc.2012-1761. Epub 2012 Jul 12.

Abstract

Context: A polymorphism in the FSHB promoter (-211G>T, rs10835638) was shown to influence male serum FSH levels, whereas a polymorphism in the FSH receptor gene (FSHR; 2039A>G, rs6166) was previously shown to be associated with FSH levels in women only.

Objective: The objective of the study was to analyze the effects of both FSHB -211G>T and FSHR 2039A>G on male reproductive parameters.

Design and setting: A total of 1213 German men attending an infertility clinic were genotyped by TaqMan assay.

Patients: Patients included male partners in infertile couples without known causes for male infertility.

Main outcome measures: An association analysis of single and combined single-nucleotide polymorphism genotypes with clinical parameters was performed.

Results: The FSHB -211G>T T-allele showed significant dosage effects for FSH (-0.51 U/liter per T-allele), LH (0.28 U/liter), and bitesticular volume (-3.2 ml). Statistical significance was enhanced severalfold after a meta-analysis comprising 3017 men. TT carriers were significantly more prevalent among men with lower sperm counts. The FSHR 2039A>G G-allele exhibited nonsignificant trends for associations with higher FSH and reduced testicular volumes. However, in the combined model, FSHR 2039A>G significantly modulated the more dominant effect of FSHB -211G>T on serum FSH and testicular volume among the T-allele carriers.

Conclusions: By analyzing both single-nucleotide polymorphisms for the first time, we convincingly show that indeed FSHR 2039A>G has an effect also in males. In the proposed model of the combined effects, FSHB -211G>T acts strongly on male reproductive parameters, whereas the FSHR 2039A>G effects were approximately 2-3 times smaller. Clinically this is of importance because oligozoospermic patients carrying unfavorable variants affecting FSH action may benefit from FSH treatment.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Fertility / genetics*
  • Follicle Stimulating Hormone, Human / blood
  • Follicle Stimulating Hormone, Human / genetics*
  • Gene Frequency
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Genetic Variation / genetics
  • Genotype
  • Germany / epidemiology
  • Humans
  • Infertility, Male / epidemiology
  • Infertility, Male / genetics*
  • Male
  • Polymorphism, Single Nucleotide / genetics
  • Receptors, FSH / genetics*
  • Registries / statistics & numerical data
  • Retrospective Studies
  • Risk Factors

Substances

  • Follicle Stimulating Hormone, Human
  • Receptors, FSH