Department of Biology, The University of Alabama at Birmingham.
J Gerontol A Biol Sci Med Sci. 2018 Jan 16;73(2):166-174. doi: 10.1093/gerona/glx105.
Aging is characterized by decreasing physiological integration, reduced function, loss of resilience, and increased risk of death. Paradoxically, although women live longer, they suffer greater morbidity particularly late in life. These sex differences in human lifespan and healthspan are consistently observed in all countries and during every era for which reliable data exist. While these differences are ubiquitous in humans, evidence of sex differences in longevity and health for other species is more equivocal. Among fruit flies, nematodes, and mice, sex differences in lifespan vary depending on strain and treatment. In this review, we focus on sex differences in age-related alterations in DNA damage and mutation rates, telomere attrition, epigenetics, and nuclear architecture. We find that robust sex differences exist, eg, the higher incidence of DNA damage in men compared to women, but sex differences are not often conserved between species. For most mechanisms reviewed here, there are insufficient data to make a clear determination regarding the impact of sex, largely because sex differences have not been analyzed. Overall, our findings reveal an urgent need for well-designed studies that explicitly examine sex differences in molecular drivers of aging.
衰老是指生理整合度下降、功能降低、弹性丧失以及死亡风险增加。矛盾的是,尽管女性的寿命更长,但她们在晚年遭受的发病率更高。在所有有可靠数据的国家和每个时代,人类的寿命和健康跨度都存在这种性别差异。虽然这些差异在人类中普遍存在,但其他物种在寿命和健康方面存在性别差异的证据则更加不确定。在果蝇、线虫和老鼠中,寿命的性别差异取决于菌株和处理方式。在这篇综述中,我们重点关注与年龄相关的 DNA 损伤和突变率、端粒损耗、表观遗传学和核结构变化方面的性别差异。我们发现存在明显的性别差异,例如男性的 DNA 损伤发生率高于女性,但在不同物种之间,性别差异并不总是保守的。对于这里综述的大多数机制,由于没有分析性别差异,因此没有足够的数据来明确确定其对衰老的影响。总的来说,我们的研究结果表明,迫切需要进行精心设计的研究,明确分析衰老的分子驱动因素中的性别差异。