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高龄男性不育患者精子 DNA 损伤的高发生率。

High prevalence of isolated sperm DNA damage in infertile men with advanced paternal age.

机构信息

Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, McGill University, Montreal, Quebec, Canada.

出版信息

J Assist Reprod Genet. 2013 Jun;30(6):843-8. doi: 10.1007/s10815-013-0015-0. Epub 2013 Jun 1.

Abstract

BACKGROUND

Sperm DNA damage is associated with male infertility, lower pregnancy rates and pregnancy loss.

OBJECTIVE

The primary aim of our study was to evaluate the prevalence of sperm DNA damage in younger and older men with normozoospermia.

DESIGN, SETTING AND PARTICIPANTS: We obtained semen from 277 consecutive non-azoospermic men presenting for sperm DNA testing.

OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS

The main outcome measures included sperm % DNA fragmentation index (%DFI, using sperm chromatin structure assay), sperm concentration, motility and morphology, and, paternal age.

RESULTS AND LIMITATIONS

Sperm % DFI was positively correlated with paternal age (r = 0.20, P < 0.001) and inversely correlated % progressive motility (r = -0.16, P = 0.01). Sperm %DFI was significantly higher in older (≥40 years) compared to younger (<40 years) normozoospermic men (17 ± 13 vs. 12 ± 8, respectively P = 0.008), whereas, sperm concentration, progressive motility and morphology were not significantly different in these two groups. Moreover, the prevalence of high levels of sperm DNA damage (>30 % DFI) was significantly higher in older compared to younger normozoospermic men (17 % vs. 3 %, respectively, P < 0.001).

CONCLUSION

The data indicate that a conventional semen analysis can often fail to detect a defect in spermatogenesis (high %DFI) in older men and suggest that infertile couples with advanced paternal age, including those with normal semen parameters, should consider sperm DNA testing as part of the couple evaluation.

摘要

背景

精子 DNA 损伤与男性不育、较低的妊娠率和妊娠丢失有关。

目的

我们研究的主要目的是评估具有正常精子浓度的年轻和年老男性精子 DNA 损伤的发生率。

设计、地点和参与者:我们从 277 名前来进行精子 DNA 检测的非无精子症男性中获得了精液。

主要结局测量和统计分析

主要结局指标包括精子 DNA 碎片化指数(使用精子染色质结构分析)、精子浓度、活力和形态以及父亲年龄。

结果和局限性

精子 DNA 碎片化指数与父亲年龄呈正相关(r=0.20,P<0.001),与精子前向运动活力呈负相关(r=-0.16,P=0.01)。与年轻(<40 岁)正常精子浓度男性相比,年龄较大(≥40 岁)的男性精子 DNA 碎片化指数明显更高(分别为 17±13%和 12±8%,P=0.008),而两组间精子浓度、前向运动活力和形态无显著差异。此外,与年轻正常精子浓度男性相比,年龄较大的男性精子 DNA 损伤水平较高(>30%DFI)的发生率明显更高(分别为 17%和 3%,P<0.001)。

结论

数据表明,传统的精液分析通常无法检测到年龄较大男性的生精缺陷(高 DNA 碎片化指数),并提示高龄不孕夫妇,包括那些具有正常精液参数的夫妇,应考虑将精子 DNA 检测作为夫妇评估的一部分。

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