在参加生育诊所的男性中,MTHFR c.677C>T变异和勃起功能障碍之间的关联
Shun Bai1, Ming-Zhen Li2, Yang-Yang Wan1
1Department of Gynecology and Obstetrics, Reproductive and Genetic Hospital, The First Affiliated Hospital of University of Science and Technology of China, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei 230001, China.
Asian journal of andrology
|September 22, 2023
概括
MTHFR 677TT基因变异与严重勃起功能障碍 (ED) 的更高风险有关. 这一发现可能有助于临床诊断ED男性.
科学领域:
- 遗传学 是一个遗传学.
- 泌尿器科 泌尿器科 泌尿器科 泌尿器科
- 分子生物学分子生物学
背景情况:
- 遗传因素导致性功能障碍.
- 在勃起功能障碍 (ED) 风险中,甲基基酸减少酶 (MTHFR) 基因变异的特定作用尚不清楚.
研究的目的:
- 调查MTHFR基因变异,特别是c.677C>T多态,与勃起功能障碍风险之间的关联.
主要方法:
- 招募了1254名男性参与者.
- 用国际勃起功能指数-5.5来评估勃起功能障碍.
- 使用光聚合酶链反应 (PCR) 进行了MTHFR c.677C>T变异的基因定型.
主要成果:
- 总体而言,ED和非ED组之间没有发现MTHFR C677T基因型频率的显著差异.
- 在患有严重和中度勃起障碍的男性中,MTHFR 677TT基因型的发生率明显高 (P=0.02).
- 后勤回归证实了MTHFR 677TT多态和严重ED风险 (OR=2.46,P=0.02) 之间的正相关性.
结论:
- MTHFR 677TT多态性与严重勃起功能障碍的风险增加有关.
- 识别MTHFR基因多态可能为ED患者提供补充诊断信息.
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