酒精对精子染色质结构影响的回顾性分析

IF 2.4 3区 医学 Q2 ANDROLOGY
Ariadne Trautman, Aarabhi Gurumoorthy, Keith A Hansen
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引用次数: 0

摘要

背景:对不育夫妇的评价往往是复杂的,因为男性和女性都有多种因素,包括社会历史。先前的研究表明,男性酒精摄入会扰乱精子活力、核成熟和脱氧核糖核酸(DNA)的完整性。本研究的主要目的是评估男性饮酒对精子染色质结构分析(SCSA®)的影响。本研究是对209对夫妇的回顾性图表回顾,这些夫妇在中西部一家中型不育诊所就诊,并进行了精液分析和SCSA®。从电子病历中提取的数据包括人口统计、烟草使用、酒精使用、职业暴露、精液分析结果和SCSA®结果(DNA片段化指数(DFI)和高DNA染色度(HDS))。对该数据集进行统计分析,以p水平0.05确定显著性,主要输入为酒精使用水平,主要结局为SCSA®参数。结果:总体而言,11%的队列患者重度饮酒(> 10次/周),27%中度饮酒(3-10次/周),34%罕见饮酒(0.5- 10%(未成熟精子染色质的标志)。酒精使用水平与HDS > 10%或DFI无显著相关性。重度饮酒与精子数量降低显著相关(p = 0.042)。随着年龄的增加,DNA断裂指数增加(p = 0.006),精子数量增加(p = 0.002),精液体积减少(p = 0.022)。工作时受热与精液量减少显著相关(p = 0.042)。吸烟与精子活力降低有关(p)。结论:饮酒水平与精子的高DNA染色性或DNA断裂指数之间无显著关联。正如预期的那样,年龄增加与精液参数有关,热暴露与精液量减少有关,吸烟与精子活力和密度降低有关。进一步的研究可能会调查酒精的使用和精子中的活性氧化物种。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effects of alcohol use on sperm chromatin structure, a retrospective analysis.

Effects of alcohol use on sperm chromatin structure, a retrospective analysis.

Effects of alcohol use on sperm chromatin structure, a retrospective analysis.

Effects of alcohol use on sperm chromatin structure, a retrospective analysis.

Background: The evaluation of the infertile couple is often complex as multiple factors in both the male and female can contribute, including social history. Previous studies have displayed that male ethanol consumption can disturb sperm motility, nuclear maturity, and deoxyribonucleic acid (DNA) integrity. The main purpose of this study is to evaluate the effects of male alcohol use on sperm chromatin structure analysis (SCSA®). This study was a retrospective chart review of 209 couples that presented to a midsize infertility clinic in the Midwest and had a semen analysis and SCSA® performed. Data extracted from the electronic medical record included demographics, tobacco use, alcohol use, occupational exposures, semen analysis results, and SCSA® results (DNA Fragmentation index (DFI) and High DNA stainability (HDS)). Statistical analysis was performed on this data set to determine significance with a p-level of 0.05, with the primary input being level of alcohol use and primary outcome being the SCSA® parameters.

Results: Overall, 11% of the cohort had heavy alcohol use (> 10 drinks/week), 27% moderate (3-10/week), 34% rare (0.5- < 3/week), and 28% none. 36% of the cohort had HDS > 10% (a marker of immature sperm chromatin). Level of alcohol use was not significantly associated with HDS > 10% or DFI. Heavier alcohol use was significantly associated with lower sperm count (p = 0.042). Increasing age was significantly associated with increasing DNA Fragmentation Index (p = 0.006), increased sperm count (p = 0.002), and lower semen volume (p = 0.022). Exposure to heat at work was significantly associated with lower semen volume (p = 0.042). Tobacco use was associated with lower sperm motility (p < 0.0001) and lower sperm count (p = 0.002).

Conclusions: There was not a significant association between the level of alcohol use and the High DNA Stainability or DNA Fragmentation Index of sperm. Increasing age was associated with semen parameters as expected, heat exposure was associated with lower semen volume, and tobacco use was associated with lower sperm motility and density. Further studies could investigate alcohol use and reactive oxidative species in sperm.

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来源期刊
Basic and Clinical Andrology
Basic and Clinical Andrology Medicine-Urology
CiteScore
3.50
自引率
0.00%
发文量
21
审稿时长
22 weeks
期刊介绍: Basic and Clinical Andrology is an open access journal in the domain of andrology covering all aspects of male reproductive and sexual health in both human and animal models. The journal aims to bring to light the various clinical advancements and research developments in andrology from the international community.
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