印度人口中 MTHFR C677T 多态性与男性不育症的相关性:病例对照研究。

IF 0.7 Q4 PHARMACOLOGY & PHARMACY Journal of pharmacy & bioallied sciences Pub Date : 2024-07-01 Epub Date: 2024-07-18 DOI:10.4103/jpbs.jpbs_207_24
Akash More, Namrata Anjankar, Jarul Shrivastava, Nancy Nair, Ritesh Jadhav
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引用次数: 0

摘要

这项病例对照研究调查了印度男性不育症与亚甲基四氢叶酸还原酶(MTHFR)C677T 变异之间的相关性。研究将不育男性作为病例组,将育有男性作为对照组。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析法对 C677T 多态性进行基因分型。在统计分析方法中,采用了卡方检验和几率计算,以评估 C677T 突变与不孕症之间的相关性。研究结果显示,病例组(9.4%)的C677T变异发生率大大高于对照组(1.6%)。通过卡方检验(P值:0.006),C677T变异与男性不育有明显相关性。根据这些结果,MTHFR 基因的 C677T 变异可能会增加印度人群中男性不育症的发病率。此外,还进行了其他评估,以调查 C677T 变异与特定不育指标之间的关联。结果表明,C677T 变异与精子数量低或缺失有显著相关性(P 0.05)。这些发现凸显了 MTHFR 基因在生殖健康中的潜在功能,并推进了我们对男性不育遗传基础的了解。我们鼓励对其潜在机制进行研究,并对潜在机制进行更多的调查,以支持建立诊断和管理男性不育症的个体化方法。
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Correlation of MTHFR C677T Polymorphism with Male Infertility among Indian Population: Case-Control Study.

This case-control study investigated the correlation between male infertility in India and the methylenetetrahydrofolate reductase (MTHFR) C677T variant. Infertile males were utilized as the case group in the study, whereas fertile individuals served as the control group. The C677T polymorphism was genotyped using PCR-RFLP analysis (polymerase chain reaction-restriction fragment length polymorphism). The Chi-square test and odds ratio calculation were implemented in the statistical analysis method for assessing the correlation between the C677T mutation and infertility. The results of this study revealed that the case group (9.4%) had a substantially greater prevalence of the C677T variation than the control group (1.6%). The C677T variation is significantly associated with male infertility by the Chi-square test (P value: 0.006). According to these results, the MTHFR gene›s C677T variation may increase the incidence of male infertility in the Indian population. Additional evaluations were also conducted to investigate the association between the C677T variation and particular infertility indicators. The C677T variation has been demonstrated to have been significantly correlated with a low or missing sperm count (p 0.05). These findings highlight the potential function of the MTHFR gene in reproductive health and advance our understanding of the genetic underpinnings of male infertility. It is encouraged to investigate the underlying mechanisms and additional investigation of the underlying mechanisms and to support the creation of individualized approaches to diagnosing and managing male infertility.

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