人类射精中的双链 DNA 断裂与精子总 DNA 断裂之间存在密切联系。

Jaime Gosálvez, Stephen D Johnston, Ahinoa Prado, Carmen López-Fernández, Pablo Contreras, Javier Bartolomé-Nebreda, Mercedes González-Martínez, José Luis Fernández, Carlos García de la Vega, Alfredo Góngora
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引用次数: 0

摘要

背景:精子中的双链和单链DNA断裂(DSBs和SSBs)分别来自内在和外在的退化过程,可能与潜在的男性病理学有关。目的:确定人类射精中DSBs的发生率是否是整个精子DNA碎片(W-SDF = SSBs + DSBs)的一致预测指标:显示全W-SDF的精子比例与DNA中仅显示DSB的精子比例之间存在相关性。建立了两个患者群:结果:W-SDF ≤30%(低 SDF;n = 153)和 W-SDF ≥30%(高 SDF;n = 222):结果:W-SDF水平的增加与射精中DSB发生率的增加有关。将低 W-SDF 组和高 W-SDF 组的数据合并后,观察到一种线性关系,W-SDF 每增加一个单位,DSB 就增加 0.799 个单位。然而,如果对这两组数据分别进行分析,其关系则有所不同。在低 SDF 组,W-SDF 每增加一个单位,DSB 线性增加 0.559 个单位。而在高 SDF 组中,W-SDF 每增加一个单位,DSB 就以 0.602 个单位的指数形式增加。此外,两个变量之间的数据离散度在不同组别之间存在显著差异,高 SDF 组的变异性是低 SDF 组的 0.8 倍:结论:虽然精子中DSB的存在与原始精液样本中的W-SDF相关,但在DNA损伤水平较高的射精中,造成DSB的生物机制的表达比例和/或水平不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strong correlation between double-strand DNA Breaks and total sperm DNA fragmentation in the human ejaculate.

Background: Double- and single-strand DNA breaks (DSBs and SSBs, respectively) in spermatozoa, which emerge from intrinsic and extrinsic degenerative processes, are likely related to the underlying male pathology.

Aim: To determine whether the incidence of DSBs in the human ejaculate is a consistent predictor of whole sperm DNA fragmentation (W-SDF = SSBs + DSBs).

Methods: A correlation between the proportion of spermatozoa that showed whole W-SDF and those displaying only DSBs in DNA. Two patient cohorts were established: W-SDF ≤30% (low SDF; n = 153) and W-SDF ≥30% (high SDF; n = 222).

Results: An increasing level of W-SDF is associated with an increased incidence of DSBs in the ejaculate. When data from both the low and high W-SDF groups were combined, a linear relationship was observed, with DSBs increasing by 0.799 units for each unit increase in W-SDF. However, when the cohorts were analyzed separately, the relationships differed. In the low SDF group, DSBs increased linearly by 0.559 units for each unit increase in W-SDF. In the high SDF group, DSBs increased exponentially by 0.602 units per unit of W-SDF. Furthermore, the data dispersion between the two variables was significantly different between the cohorts, with the high SDF group showing 0.8 times greater variability than the low SDF group.

Conclusions: While the presence of DSBs in sperm is correlated with the W-SDF present in raw semen samples, the biological mechanisms responsible for DSBs are expressed in different proportions and/or at different levels in ejaculates with higher levels of DNA damage.

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