Current Issue

Volume 11, Number 2, Jul-Sep 2017 Pages: 112-116

Tumor Necrosis Factor Alpha -308 G/A Single Nucleotide Polymorphism and Risk of Sperm Abnormalities in Iranian Males


Maryam Khademi Bami, M.Sc, 1, Masoud Dehghan Tezerjani, M.Sc, 2, Fateme Montazeri, Ph.D, 2, Hamid Reza Ashrafzadeh Mehrjardi, M.Sc, 2, Saeed Ghasemi-Esmailabad, M.Sc, 2, Mohammad Hasan Sheikhha, M.D., Ph.D, 2, Seyed Mehdi Kalantar, Ph.D, 2, *,
Medical Biotechnology Research Center, Ashkezar Branch, Islamic Azad University, Ashkezar, Yazd, Iran
Genetic Unit, Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
*Corresponding Address: P.O. Box: 89195-999 Genetic Unit Research and Clinical Center for Infertility Shahid Sadoughi University of Medical Sciences Bouali Ave Safaeie Yazd Iran Email:kalantar.yzd@gmail.com

Abstract

Background

Signaling molecules such as cytokines regulate spermatogenesis during the maturation of germ cells and sperm apoptosis. Tumor necrosis factor alpha (TNFα) is one of the most-documented cytokines that is involved in spermatogenesis. We investigated the association of the TNFα -308 G/A single nucleotide polymorphism with sperm abnormalities in Iranian males.

Materials and Methods

This case-control study included 180 infertile men who re- ferred to Yazd Research and Clinical Center for Infertility and 100 healthy normospermic controls. Infertile men were classified into four groups of azoospermia (n=91), oligospermia (n=26), teratospermia (n=30) and asthenoteratospermia (n=33). After sperm analysis, DNA was extracted from blood and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was carried out for the genotyping of TNFα- 308 G/A.

Results

The A allele was significantly associated with sperm abnormality in our population [(P<0.001, odds ratios (OR) 95% confidence interval (CI)=2.31]. In addition, the A allele was also associated with azoospermia (P<0.001, OR (95% CI)=2.484), oligospermia (P=0.005, OR (95% CI)=2.51) and teratospemia (P<0.001, OR (95% CI)=3.385) but not with asthenoteratospermia (P=0.623).

Conclusion

Our data suggest that this single nucleotide polymorphism (SNP) maybe associated with the risk of sperm abnormality in infertile men of Iranian origin.