父亲时钟:揭示晚年父亲年龄对精子DNA碎片化的后果
Eva Kadoch1, Jonas Benguigui2, Mélanie Chow-Shi-Yée1
1Clinique ovo, Montreal, Canada.
Reproductive biology
|August 24, 2024
概括
先进的父亲年龄与精子DNA碎片化 (SDF) 的增加有关,特别是在35岁之后. 这一发现对于35岁以上男性不孕症评估至关重要.
科学领域:
- 生殖科学 生殖科学
- 安德罗学与人类学
- 遗传学 是一个遗传学.
背景情况:
- 晚年父亲的年龄在生殖健康方面越来越令人担忧.
- 精子DNA碎片化 (SDF) 是精子质量和男性生育能力的关键指标.
- 增加SDF的特定年龄门需要进一步调查.
研究的目的:
- 为了研究晚年父亲年龄和精子DNA碎片化 (SDF) 水平之间的关系.
- 确定SDF显著增加的特定年龄.
- 分析不同父亲年龄组中正常,中等和高SDF的流行情况.
主要方法:
- 对4250个精液样本进行了回顾性队列研究.
- 患者分为七个年龄组,从<26岁到>50岁.
- 跨年龄组平均SDF水平和SDF流行率的比较.
主要成果:
- 在父亲年龄和SDF之间发现了显著的正相关性 (r=0.17,p<0.001).
- 在35岁之前,SDF水平保持稳定,然后从那以后显著增加.
- 较老年人群 (≥36岁) 与年轻人群相比,SDF平均水平显著高,SDF高的患病率更高.
结论:
- 父亲年龄超过35岁与精子DNA碎片化显著增加有关.
- 在35岁以上的男性中,SDF评估对于不孕症评估至关重要.
- 在生育评估中考虑男性年龄可以提高诊断准确性和治疗策略.
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