Nemours/A.I duPont Hospital for children, Division of Allergy, Asthma and Immunology, USA.
Autoimmun Rev. 2012 May;11(6-7):A393-403. doi: 10.1016/j.autrev.2011.12.004. Epub 2011 Dec 11.
For humans and other animals, gender has an influence not only on their physical attributes, but also on life span. In humans, females have a longer life span than males. The reasons for this are not entirely clear. The role of gender in the regulation of longevity may be linked to gender specific genetic differences, including the expression of sex hormone patterns and the changes in these patterns during an individual's lifetime. In addition, the effect of sex hormones on other physiologic responses to environmental influences on cellular stress and oxidative damage may play a role in longevity. Gender can impact many disease states, including autoimmune diseases, and the factors that affect the development of autoimmune diseases and the regulation of longevity may share common mechanistic pathways. Other factors that may play a role include telomere and telomerase related differences, caloric restriction and changes in mitochondrial DNA. Inflammatory and regulatory pathways such as insulin/IGF signaling and Target of Rapamycin (TOR) signaling may also play a role in longevity and aging-related diseases such as Alzheimer's. The role of gender differences in the regulation of these pathways or factors is not entirely clear. The role of X-chromosome inactivation in longevity has also yet to be fully elucidated.
对于人类和其他动物来说,性别不仅对其身体特征有影响,而且对寿命也有影响。在人类中,女性的寿命比男性长。造成这种情况的原因并不完全清楚。性别在调节寿命中的作用可能与性别特异性遗传差异有关,包括性激素模式的表达以及这些模式在个体一生中的变化。此外,性激素对其他生理反应的影响,如对细胞应激和氧化损伤的环境影响,可能在寿命中起作用。性别会影响许多疾病状态,包括自身免疫性疾病,影响自身免疫性疾病发展和调节寿命的因素可能有共同的机制途径。其他可能起作用的因素包括端粒和端粒酶相关差异、热量限制和线粒体 DNA 的变化。炎症和调节途径,如胰岛素/IGF 信号和雷帕霉素靶蛋白 (TOR) 信号,也可能在寿命和与衰老相关的疾病(如阿尔茨海默病)中发挥作用。性别差异在这些途径或因素调节中的作用尚不完全清楚。X 染色体失活在寿命中的作用也尚未完全阐明。