期刊
HUMAN REPRODUCTION
卷 23, 期 12, 页码 2858-2866出版社
OXFORD UNIV PRESS
DOI: 10.1093/humrep/den277
关键词
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资金
- Institut National de la Sante et de la Recherche Medicale
- Ministere de l'Enseignement Superieur et de la Recherche, France
- Organon France through a FARO (Fond d'Aide a la Recherche Organon) fellowship
One of the most well-documented cytokines suspected as a hazard to male fertility is tumor necrosis factor-alpha (TNF alpha). Genetic factors such as single-nucleotide polymorphisms (SNPs) in the TNF gene cluster impact TNF alpha levels. Our objective was to establish the potential involvement of -308 TNF SNP in male infertility risk. In 684 infertile male patients undergoing an intracytoplasmic sperm injection procedure, we used allele-specific polymerase chain reaction (PCR) and PCR-RFLP to investigate the distribution of the guanine (G)-to-adenosine (A) substitution at position -308 in the promoter region of the TNF alpha gene. An increased frequency of the -308 TNF alpha A allele was found in patients with low sperm count of testicular origin [P = 0.002; odds ratio (OR) = 2.93] or with normal production count but altered sperm motility (P = 0.003; OR = 2.32), compared with a patient group with normal sperm count and quality (morphology and motility). In patients with low sperm count exhibiting TNF alpha A allele, compared with those with G allele, an alteration in hormonal balance was observed with increased inhibin B levels and subsequent reduced FSH plasma levels, leading to an FSH/inhibin B ratio roughly half as high (from 0.07 +/- 0.01 in TNFA versus 0.13 +/- 0.02 in TNFG allele groups, P < 0.0001). As the -308 TNF alpha A allele has been associated with an increased expression/production of TNF alpha, the potential use of therapies based on inhibition of TNF alpha activities could represent possible therapeutic opportunities for patients with low sperm count (i.e. primary testicular dysfunction) or with altered sperm motility.
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