Molecular analysis of mutations and polymorphisms in the CFTR gene in male infertility

Reprod Biomed Online. 2008 Jul;17(1):27-35. doi: 10.1016/s1472-6483(10)60289-1.

Abstract

Mutations of the cystic fibrosis transmembrane regulator (CFTR) gene and polymorphisms, such as the (TG)m and Tn polymorphic loci in intron 8 at the splice acceptor site of exon 9, can cause male infertility. The aim of this study was to investigate the frequency of the most prevalent cystic-fibrosis-causing mutations, the IVS8-Tn alleles and IVS8-TG12 variant in the presence of IVS8-5T in patients with altered semen parameters (group I with obstructive azoospermia, group II with secretory azoospermia and group III with severe oligozoospermia) compared with a control group with normozoospermia. CFTR mutations were found in 26.5% and 14.3% of chromosomes of patients of group I and II respectively (P < 0.001, P < 0.05). The frequency of the 5T allele was 23.5% in patients in group I (P < 0.01), and was linked exclusively with TG12 allele. The present study reports for the first time a high proportion of the 5T allele in patients in group III (9.2%, P < 0.05). These results underline the importance of performing molecular analysis of mutations and IVS8-Tn polymorphism in the CFTR gene and appropriate genetic counselling to all couples undergoing assisted reproductive technologies when the partner has azoospermia or severe oligozoospermia.

MeSH terms

  • Alleles
  • Azoospermia / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • DNA Mutational Analysis
  • Exons
  • Genetic Counseling
  • Genotype
  • Humans
  • Infertility, Male / therapy*
  • Introns
  • Male
  • Mutation*
  • Oligospermia / genetics
  • Polymorphism, Genetic*
  • Sperm Count

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator