Lahimer Marwa, Montjean Debbie, Cabry Rosalie, Capelle Severine, Lefranc Elodie, Bach Véronique, Ajina Mounir, Ben Ali Habib, Khorsi-Cauet Hafida, Benkhalifa Moncef
Reproductive Medicine, Reproductive Biology & Genetics, University Hospital and School of Medicine, Picardie University Jules Verne, CHU Sud, 80054 Amiens, France.
PERITOX-Périnatalité et Risques Toxiques-UMR-I1, Picardie University Jules Verne, CHU Sud, 80025 Amiens, France.
J Clin Med. 2023 Jul 27;12(15):4928. doi: 10.3390/jcm12154928.
Advanced age has been reported to negatively affect sperm parameters and spermatozoa DNA integrity. A decline in sperm criteria was also associated with altered epigenetic marks such as DNA methylation with a potential downstream impact on in vitro fertilization success and clinical outcomes. The aim of the present retrospective study was to clarify the association between advanced paternal age (APA) and sperm parameters, DNA integrity and DNA methylation profile. A total of 671 patients consulting for infertility underwent sperm analysis, sperm DNA integrity assessment and methylation level measurement. The principal finding was that individuals over 40 years of age exhibit a significant increase in DNA fragmentation levels compared to the younger group (15% versus 9%, respectively, = 0.04). However, there was no significant difference in DNA decondensation and sperm parameters in association with APA. In addition, a drop in the global methylation level was also found in men over 40 years (6% in the young group versus 2% in the old group, = 0.03). As a conclusion, men over 40 years are at higher risk of elevated sperm DNA fragmentation and lower methylation level. Based on these observations, it is recommended that the assessment of sperm DNA fragmentation should be taken into consideration particularly after the age of 40. Our findings support the idea that paternal age is a crucial factor that should not be neglected during fertility evaluation and treatment since it is associated with epigenetics changes in sperm. Although the underlying mechanism remains to be clarified, we believe that environmental and professional exposure factors are likely involved in the process.
据报道,高龄会对精子参数和精子DNA完整性产生负面影响。精子标准的下降还与表观遗传标记的改变有关,如DNA甲基化,这可能对体外受精成功率和临床结果产生潜在的下游影响。本回顾性研究的目的是阐明父亲高龄(APA)与精子参数、DNA完整性和DNA甲基化谱之间的关联。共有671名因不孕前来咨询的患者接受了精子分析、精子DNA完整性评估和甲基化水平测量。主要发现是,与年轻组相比,40岁以上的个体DNA片段化水平显著增加(分别为15%和9%,P = 0.04)。然而,与APA相关的DNA解聚和精子参数没有显著差异。此外,40岁以上男性的整体甲基化水平也有所下降(年轻组为6%,老年组为2%,P = 0.03)。结论是,40岁以上男性精子DNA片段化升高和甲基化水平降低的风险更高。基于这些观察结果,建议尤其在40岁以后应考虑评估精子DNA片段化。我们的研究结果支持这样一种观点,即父亲年龄是生育评估和治疗过程中不应忽视的关键因素,因为它与精子的表观遗传学变化有关。尽管潜在机制仍有待阐明,但我们认为环境和职业暴露因素可能参与了这一过程。