Department of Obstetrics & Gynaecology, Saarland University, Homburg/Saar, Germany.
Department of Basic Medical Sciences, Faculty of Medicine, Yarmouk University, Irbid, Jordan.
Andrologia. 2021 Sep;53(8):e14139. doi: 10.1111/and.14139. Epub 2021 Jun 12.
Male infertility is a multifactorial condition associated with different genetic abnormalities in at least 15%-30% of cases. The purpose of this study was to identify suspected correlations between infertility and polymorphisms in mitochondrial NADH dehydrogenase subunits 3 and 4L (MT-ND3 and MT-ND4L) in subfertile male spermatozoa. Sanger sequencing of the mitochondrial DNA target genes was performed on 68 subfertile and 44 fertile males. Eight single nucleotide polymorphisms (SNPs) in MT-ND3 (rs2853826, rs28435660, rs193302927, rs28358278, rs41467651, rs3899188, rs28358277 and rs28673954) and seven SNPs in MT-ND4L (rs28358280, rs28358281, rs28358279, rs2853487, rs2853488, rs193302933 and rs28532881) were detected and genotyped. The genotypes and allele frequencies of the study population have shown a lack of statistically significant association between MT-ND3 and MT-ND4L SNPs and male infertility. However, no statistically significant association was found between the asthenozoospermia, oligozoospermia, teratozoospermia, asthenoteratozoospermia, oligoasthenoteratozoospermia and oligoteratozoospermia subgroups of subfertile males. However, rs28358278 genotype of the MT-ND3 gene was reported in the subfertile group but not in the fertile group, which implies a possible role of this SNP in male infertility. In conclusion, the investigated polymorphic variants in the MT-ND3 and MT-ND4L genes did not show any significant association with the occurrence of male infertility. Further studies are required to evaluate these findings. Moreover, the subfertile individuals who exhibit a polymorphism at rs28358278 require further monitoring and evaluation.
男性不育是一种多因素疾病,至少有 15%-30%的病例与不同的遗传异常有关。本研究的目的是确定亚生育男性精子中线粒体 NADH 脱氢酶亚单位 3 和 4L(MT-ND3 和 MT-ND4L)的多态性与不育之间的可疑相关性。对 68 名亚生育男性和 44 名生育男性的线粒体 DNA 靶基因进行了 Sanger 测序。在 MT-ND3 中发现了 8 个单核苷酸多态性(SNP)(rs2853826、rs28435660、rs193302927、rs28358278、rs41467651、rs3899188、rs28358277 和 rs28673954)和 MT-ND4L 中的 7 个 SNP(rs28358280、rs28358281、rs28358279、rs2853487、rs2853488、rs193302933 和 rs28532881),并对其进行了基因分型。研究人群的基因型和等位基因频率显示,MT-ND3 和 MT-ND4L SNP 与男性不育之间不存在统计学显著关联。然而,在亚生育男性的弱精子症、少精子症、畸形精子症、弱精畸形精子症、少弱畸形精子症亚组中,没有发现统计学显著关联。然而,MT-ND3 基因的 rs28358278 基因型在亚生育组中报告,但在生育组中没有报告,这表明该 SNP 可能在男性不育中起作用。总之,在所研究的 MT-ND3 和 MT-ND4L 基因的多态性变异与男性不育的发生没有显示出任何显著关联。需要进一步的研究来评估这些发现。此外,表现出 rs28358278 多态性的亚生育个体需要进一步的监测和评估。