探讨原发性和继发性男性不育症的单核苷酸多态性。

IF 4.4 Q1 Medicine
Fatina W Dahadhah, Mohanad Odeh, Heba A Ali, Jihad A M Alzyoud, Manal Issam Abu Alarjah
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引用次数: 0

摘要

背景/目的:不孕症的定义是在一年无保护的定期性交后仍未怀孕,这是一项重大的全球健康挑战,其中男性因素约占50%。在这种流行病学背景下,原发性男性不育症(无法怀孕第一个孩子)和继发性男性不育症(当已经生育一个孩子的男性面临再次怀孕困难时发生)在遗传水平上仍然知之甚少。本研究探讨了线粒体基因(MT-ND3、MT-ND4L和MT-ND4)的单核苷酸多态性(snp)在原发性和继发性男性不育症中的作用。方法:采用Sanger测序方法分析68例不育男性(原发不育49例,继发不育19例)的snp基因型分布。结果:主要发现所研究的snp与不孕症类型显著相关。其中,ND4基因rs2857285 (T>C,G)与TT基因型相关性显著(p = 0.023),在原发性不孕症中表现突出。ND4L基因中的另一个SNP rs28358279 (T>A,C)也与TT基因型有显著相关性(p = 0.046),在原发性不孕症中更为常见。此外,ND4基因中的rs869096886 (A>G)存在临界相关(p = 0.051),表明该SNP与生殖持续时间可能存在关联。结论:本研究强调了线粒体功能障碍与男性不育的潜在相关性,特别是所研究的snp对精子存活和功能的影响。这些发现表明,某些线粒体snp可能是不育风险的潜在生物标志物。需要更大规模的研究来证实这些关联,并检查这些snp的功能影响。将遗传分析与环境和生活方式因素结合起来,可以提高我们对男性不育症的认识,改进诊断和治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring Single-Nucleotide Polymorphisms in Primary and Secondary Male Infertility.

Background/objectives: Infertility, defined as the failure to achieve pregnancy after one year of regular unprotected intercourse, represents a significant global health challenge, with male factors contributing to approximately 50% of cases. In this epidemiological context, both primary male infertility (the inability to conceive a first child) and secondary male infertility (which occurs when a man who has already fathered a child faces difficulty conceiving again) remain poorly understood at the genetic level. This study explored the role of single-nucleotide polymorphisms (SNPs) in mitochondrial genes (MT-ND3, MT-ND4L, and MT-ND4) in primary and secondary male infertility.

Methods: This study analyzed the genotype distributions of SNPs in 68 infertile males (49 with primary infertility and 19 with secondary infertility) using Sanger sequencing.

Results: Key findings revealed that studied SNPs were significantly associated with infertility type. Specifically, rs2857285 (T>C,G) in the ND4 gene showed a significant correlation (p = 0.023) with the TT genotype, which is prominent in primary infertility. Another SNP, rs28358279 (T>A,C) in the ND4L gene, also demonstrated a significant correlation (p = 0.046) with the TT genotype, being more common in primary infertility. In addition, rs869096886 (A>G) in the ND4 gene had a borderline correlation (p = 0.051), indicating a possible association between this SNP and reproductive duration.

Conclusions: This study emphasizes the potential relevance of mitochondrial malfunction in male infertility, specifically the effects of studied SNPs on sperm survival and function over time. These findings suggest that certain mitochondrial SNPs might be potential biomarkers for infertility risk. Larger studies are needed to confirm these associations and examine the functional effects of these SNPs. Combining genetic analysis with environmental and lifestyle factors could enhance our understanding of male infertility and improve diagnostic and therapeutic strategies.

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来源期刊
CiteScore
9.00
自引率
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