Droździk Marek, Kaczmarek Maciej, Malinowski Damian, Broś Urszula, Kazienko Anna, Kurzawa Rafał, Kurzawski Mateusz
Department of Experimental and Clinical Pharmacology, Pomeranian Medical University, Szczecin, 70-111, Poland.
Department of Reproductive Medicine and Gynecology, Pomeranian Medical University, Police, 72-010, Poland.
Sci Rep. 2015 Nov 27;5:17151. doi: 10.1038/srep17151.
Factors affecting the blood-testis barrier function may be involved in testicular damage and male infertility. Two cytokines play an important role in the barrier regulation, namely transforming growth factor beta 3 (TGF-β3) and tumor necrosis factor (TNF-α). The aim of this study was to investigate the potential association between TGF-β3 (TGFB3) and TNF-α (TNF) gene polymorphisms and male infertility. A total of 846 subjects, 423 diagnosed with male infertility and 423 fertile men were enrolled. TGFB3 (rs2268626:T > C, rs3917158:C > T, rs2284792:A > G, rs2268625:T > C, rs3917187:C > T) and TNF (rs1800629:-308G > A) gene polymorphisms were genotyped. No association between TNF genotype and infertility was observed. As for TGFB3, the genotypes distribution was similar in infertile and fertile men. However, rs2284792 minor allele frequency was significantly higher among infertile subjects. Heterozygous rs2284792 AG genotype was associated with increased odds for infertility [OR = 1.40 (95% CI 1.05-1.86), p = 0.021] and similar results were observed for G allele carrier status [OR = 1.40 (95% CI 1.06-1.84), p = 0.017]. Heterozygosity in TGFB3 rs3917158 was also associated with the infertility [OR = 1.37 (95% CI 1.01-1.87), p = 0.041]. The TGFB3 variant genotypes were associated with lower spermatozoa motility parameters in fertile men. The results indicate that variants in TGFB3 gene may be associated with male infertility. However, the findings require further replication and validation.
影响血睾屏障功能的因素可能与睾丸损伤和男性不育有关。两种细胞因子在屏障调节中起重要作用,即转化生长因子β3(TGF-β3)和肿瘤坏死因子(TNF-α)。本研究的目的是探讨TGF-β3(TGFB3)和TNF-α(TNF)基因多态性与男性不育之间的潜在关联。共纳入846名受试者,其中423名被诊断为男性不育,423名生育能力正常的男性。对TGFB3(rs2268626:T>C、rs3917158:C>T、rs2284792:A>G、rs2268625:T>C、rs3917187:C>T)和TNF(rs1800629:-308G>A)基因多态性进行基因分型。未观察到TNF基因型与不育之间的关联。至于TGFB3,不育男性和生育能力正常男性的基因型分布相似。然而,rs2284792次要等位基因频率在不育受试者中显著更高。杂合子rs2284792 AG基因型与不育几率增加相关[比值比(OR)=1.40(95%置信区间1.05-1.86),p=0.021],G等位基因携带者状态也观察到类似结果[OR=1.40(95%置信区间1.06-1.84),p=0.017]。TGFB3 rs3917158杂合性也与不育相关[OR=1.37(95%置信区间1.01-1.87),p=0.041]。TGFB3变异基因型与生育能力正常男性较低的精子活力参数相关。结果表明,TGFB3基因变异可能与男性不育有关。然而,这些发现需要进一步重复和验证。