INIBIC-Complexo Hospitalario Universitario A Coruña (CHUAC), Spain.
Laboratory of Molecular Genetics and Radiobiology, Centro Oncológico de Galicia, Doctor Camilo Veiras, Spain.
Andrology. 2024 May;12(4):870-880. doi: 10.1111/andr.13539. Epub 2023 Oct 2.
While it is common to clinically evaluate sperm nuclear DNA fragmentation, less attention has been given to sperm mitochondrial DNA. Recently, a digital PCR assay has allowed accurate estimation of the proportion of fragmented mtDNA molecules and relative copy number.
To determine the correlation of classical sperm parameters, average mtDNA copies per spermatozoon and the level of mtDNA fragmentation (SDF-mtDNA) to that of nuclear DNA fragmentation (SDF-nDNA), measured as the proportion of global, single-strand DNA (SDF-SSBs) and double-strand DNA breaks (SDF-DSBs). To determine whether the level of nuclear and mitochondrial DNA fragmentation and/or copy number can differentiate normozoospermic from non-normozoospermic samples.
Ejaculates from 29 normozoospermic and 43 non-normozoospermic were evaluated. SDF was determined using the sperm chromatin dispersion assay. mtDNA copy number and SDF-mtDNA were analyzed using digital PCR assays.
Relative mtDNA copy increased as sperm concentration or motility decreased, or abnormal morphology increased. Unlike SDF-mtDNA, mtDNA copy number was not correlated with SDF-nDNA. SDF-mtDNA increased as the concentration or proportion of non-vital sperm increased; the higher the mtDNA copy number, the lower the level of fragmentation. Non-normozoospermic samples showed double the level of SDF-nDNA compared to normozoospermic (median 25.00 vs. 13.67). mtDNA copy number per spermatozoon was 3× higher in non-normozoospermic ejaculates (median 16.06 vs. 4.99). Although logistic regression revealed SDF-Global and mtDNA copy number as independent risk factors for non-normozoospermia, when SDF-Global and mtDNA copy number were combined, ROC curve analysis resulted in an even stronger discriminatory ability for predicting the probability of non-normozoospermia (AUC = 0.85, 95% CI 0.76-0.94, p < 0.001).
High-quality ejaculates show lower nuclear SDF and retain less mtDNA copies, with approximately half of them fragmented, so that the absolute number of non-fragmented mtDNA molecules per spermatozoon is extremely low.
虽然临床上常评估精子核 DNA 碎片化,但对精子线粒体 DNA 的关注较少。最近,一种数字 PCR 检测方法可准确估计碎片化 mtDNA 分子的比例和相对拷贝数。
确定经典精子参数、每个精子的平均 mtDNA 拷贝数以及线粒体 DNA 碎片化(SDF-mtDNA)与核 DNA 碎片化(SDF-nDNA)的相关性,后者通过测量总 DNA 单链(SDF-SSBs)和双链 DNA 断裂(SDF-DSBs)的比例来衡量。确定核和线粒体 DNA 碎片化和/或拷贝数是否可以区分正常精子和非正常精子样本。
评估了 29 例正常精子和 43 例非正常精子的精子样本。使用精子染色质扩散试验测定 SDF。采用数字 PCR 检测分析 mtDNA 拷贝数和 SDF-mtDNA。
相对 mtDNA 拷贝数随着精子浓度或活力降低或畸形率增加而增加。与 SDF-mtDNA 不同,mtDNA 拷贝数与 SDF-nDNA 不相关。SDF-mtDNA 随着非活力精子的浓度或比例增加而增加;mtDNA 拷贝数越高,碎片化程度越低。非正常精子样本的 SDF-nDNA 水平是正常精子样本的两倍(中位数分别为 25.00 和 13.67)。非正常精子样本中的每个精子的 mtDNA 拷贝数高出 3 倍(中位数分别为 16.06 和 4.99)。尽管逻辑回归显示 SDF-Global 和 mtDNA 拷贝数是非正常精子症的独立危险因素,但当 SDF-Global 和 mtDNA 拷贝数结合时,ROC 曲线分析对预测非正常精子症的概率具有更强的鉴别能力(AUC=0.85,95%CI 0.76-0.94,p<0.001)。
高质量的精子样本显示较低的核 SDF 并保留较少的 mtDNA 拷贝数,其中约一半发生碎片化,因此每个精子的非碎片化 mtDNA 分子的绝对数量极低。