Khademi Bami Maryam, Dehghan Tezerjani Masoud, Montazeri Fateme, Ashrafzadeh Mehrjardi Hamid Reza, Ghasemi-Esmailabad Saeed, Sheikhha Mohammad Hasan, Kalantar Seyed Mehdi
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.
Int J Fertil Steril. 2017 Jul-Sep;11(2):112-116. doi: 10.22074/ijfs.2017.4830. Epub 2017 Feb 16.
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.
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.
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).
Our data suggest that this single nucleotide polymorphism (SNP) maybe associated with the risk of sperm abnormality in infertile men of Iranian origin.
细胞因子等信号分子在生殖细胞成熟和精子凋亡过程中调节精子发生。肿瘤坏死因子α(TNFα)是参与精子发生的记录最为详尽的细胞因子之一。我们研究了伊朗男性中TNFα -308 G/A单核苷酸多态性与精子异常的关联。
这项病例对照研究纳入了180名前往亚兹德不孕研究与临床中心就诊的不育男性以及100名健康的正常精子对照者。不育男性被分为无精子症组(n = 91)、少精子症组(n = 26)、畸形精子症组(n = 30)和弱畸精子症组(n = 33)。精子分析后,从血液中提取DNA,并进行聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)以对TNFα -308 G/A进行基因分型。
在我们的研究人群中,A等位基因与精子异常显著相关[(P < 0.001,比值比(OR)95%置信区间(CI)= 2.31]。此外,A等位基因还与无精子症(P < 0.001,OR(95% CI)= 2.484)、少精子症(P = 0.005,OR(95% CI)= 2.51)和畸形精子症(P < 0.001,OR(95% CI)= 3.385)相关,但与弱畸精子症无关(P = 0.623)。
我们的数据表明,这种单核苷酸多态性(SNP)可能与伊朗裔不育男性的精子异常风险相关。