The relationship between sperm nuclear DNA fragmentation, mitochondrial DNA fragmentation, and copy number in normal and abnormal human ejaculates

被引:2
|
作者
Timermans, Ana [1 ,6 ]
Otero, Fatima [1 ,6 ]
Garrido, Manuel [2 ]
Gosalvez, Jaime [3 ]
Johnston, Stephen [4 ,5 ]
Fernandez, Jose Luis [1 ,6 ,7 ]
机构
[1] Complexo Hosp Univ A Coruna CHUAC, INIBIC, La Coruna, Spain
[2] Complexo Hosp Univ A Coruna CHUAC, Clin Anal Serv, La Coruna, Spain
[3] Univ Autonoma Madrid, Fac Biol, Genet Unit, Madrid, Spain
[4] Univ Queensland, Sch Environm, Gatton, Australia
[5] Univ Queensland, Sch Vet Sci, Gatton, Australia
[6] Ctr Oncol Galicia, Lab Mol Genet & Radiobiol, Doctor Camilo Veiras, Spain
[7] Complexo Hosp Univ A Coruna CHUAC, Genet Unit, Xubias 84, La Coruna 15006, Spain
关键词
mitochondrial DNA copy number; sperm chromatin dispersion test; sperm DNA fragmentation; sperm mtDNA damage; TRANSCRIPTION; SPERMATOZOA; PREGNANCY; DAMAGE;
D O I
10.1111/andr.13539
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Background: 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.Objectives: 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.Materials and methodsEjaculates 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.Results: 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 3x 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).Conclusion: 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.
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收藏
页码:870 / 880
页数:11
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