Benny Paula, Yuan Xi, Yang Qian, Chavarro Jorge, Kennedy Brian, Huang Zhongwei
NUS Bia-Echo Asia Centre for Reproductive Longevity and Equality, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Department of Obstetrics and Gynaecology, National University Hospital, National University Health System, 1E Kent Ridge Rd, Singapore, 119228, Singapore.
Geroscience. 2025 Sep 10. doi: 10.1007/s11357-025-01876-3.
In the past century, the human Lifespan has doubled. However, this is not equivalent to Healthspan which refers to the number of years spent healthy and free from disease. Women have an additional level of complexity on the path to optimal healthspan where health resilience dramatically decreases following menopause and this is due to their ovaries aging by midlife. It still remains elusive on why and how the ovaries in women, albeit their distinct and vital reproductive functions, start to age before any other organs. Following menopause, women are at increased risks of age-associated chronic diseases such as cardiometabolic disease, osteoporosis, sarcopenia, frailty, and neurocognitive decline. By preserving reproductive longevity through targeting the ovary as the organ to rejuvenate in women, optimal healthspan could be obtained in women. Interestingly, population studies have shown that women who conceive naturally and give birth at advanced reproductive ages are demonstrated to have superior postmenopausal longevity. Correspondingly, men Lived longer with a sister reproducing after 45 years of age in natural fertility conditions, suggesting that late female fertility and slow somatic aging may be promoted by the same genetic variants. Causal inference analysis showed a link between increased reproductive lifespan (prolonged ovarian lifespan or later age at natural menopause) and a reduction of diseases such as diabetes and osteoporosis. Essentially, fewer ovarian follicles and shorter ovarian lifespan were associated with poorer health later in life. Therefore, innovative ways to understand and target the ovaries in women for gero-protection have the potential to avert aging diseases triggered by the female menopause. Our narrative review aims to integrate existing information from systemic and reproductive aging from preclinical and human studies to devise novel methodologies to avert ovarian aging which could potentially improve the health trajectory in aging women. Similar strategies can be applied to men to achieve healthy longevity in the population. While there are certain things one has little control over, such as genetics and the inevitable reduction of reproductive hormone levels over time, there are modifiable risk factors which can be targeted to preserve reproductive longevity by uniquely targeting the ovary especially in modifying and improving the ovarian microenvironment to ensure survival of the ovarian follicles which determine true reproductive lifespan and healthspan. This can be achieved by modifying diet, sleep patterns, and exercise and limiting toxin exposure to ensure optimal ovarian health, through healthy and functional ovarian follicles, which could bring us a step closer to enhancing women's healthspan and human longevity.
在过去的一个世纪里,人类的寿命翻了一番。然而,这并不等同于健康寿命,健康寿命是指健康无病的年数。在通往最佳健康寿命的道路上,女性面临着额外的复杂性,因为绝经后健康恢复力会急剧下降,这是由于她们的卵巢在中年时就开始衰老。女性的卵巢尽管具有独特且至关重要的生殖功能,但为何以及如何比其他任何器官都更早开始衰老,这仍然是个谜。绝经后,女性患与年龄相关的慢性疾病的风险增加,如心血管代谢疾病、骨质疏松症、肌肉减少症、身体虚弱和神经认知能力下降。通过将卵巢作为女性恢复活力的器官来维持生殖寿命,可以使女性获得最佳的健康寿命。有趣的是,人口研究表明,自然受孕并在较高生殖年龄生育的女性绝经后的寿命更长。相应地,在自然生育条件下,有姐妹在45岁后生育的男性寿命更长,这表明女性的晚育和缓慢的身体衰老可能受相同的基因变异影响。因果推断分析表明,生殖寿命延长(卵巢寿命延长或自然绝经年龄推迟)与糖尿病和骨质疏松症等疾病的减少之间存在联系。从本质上讲,卵巢卵泡数量减少和卵巢寿命缩短与晚年健康状况较差有关。因此,了解并针对女性卵巢进行老年保护的创新方法有可能避免由女性绝经引发的衰老疾病。我们的叙述性综述旨在整合来自临床前和人体研究的系统衰老和生殖衰老的现有信息,以设计新的方法来避免卵巢衰老,这可能会改善老年女性的健康轨迹。类似的策略也可以应用于男性,以实现人群的健康长寿。虽然有些事情人们几乎无法控制,如遗传因素以及生殖激素水平不可避免地随时间下降,但存在一些可改变的风险因素,可以通过独特地针对卵巢,特别是通过改变和改善卵巢微环境以确保决定真正生殖寿命和健康寿命的卵巢卵泡存活,来维持生殖寿命。这可以通过改变饮食、睡眠模式和运动以及限制毒素暴露来实现,以确保卵巢健康,通过健康且功能正常的卵巢卵泡,这可能会让我们在提高女性健康寿命和人类寿命方面更进一步。