Fabbri Elisa, An Yang, Gonzalez-Freire Marta, Zoli Marco, Maggio Marcello, Studenski Stephanie A, Egan Josephine M, Chia Chee W, Ferrucci Luigi
Translational Gerontology Branch, Longitudinal Study Section, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland. Department of Medical and Surgical Sciences, University of Bologna, Italy.
Laboratory of Behavioral Neuroscience, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, Maryland.
J Gerontol A Biol Sci Med Sci. 2016 Sep;71(9):1202-9. doi: 10.1093/gerona/glw021. Epub 2016 Feb 27.
Age-related changes in testosterone levels in older persons and especially in women have not been fully explored. The objective of this study was to describe age-related trajectories of total testosterone (TT), ammonium sulfate precipitation-measured bioavailable testosterone (mBT), and sex hormone-binding glycoprotein (SHBG) in men and women from the Baltimore Longitudinal Study of Aging, with special focus on the oldest adults.
Participants included 788 White men and women aged 30-96 years with excellent representation of old and oldest old, who reported not taking medications known to interfere with testosterone. Longitudinal data were included when available. TT, mBT, and SHBG were assayed. Age-related trajectories of mBT were compared with those obtained using calculated bioavailable testosterone (cBT). Generalized least square models were performed to describe age-related trajectories of TT, mBT, and SHBG in men and women.
mBT linearly declines over the life span and even at older ages in both sexes. In men, TT remains quite stable until the age of 70 years and then declines at older ages, whereas in women TT progressively declines in premenopausal years and slightly increases at older ages. Differences in age-related trajectories between total and bioavailable testosterone are only partially explained by age changes in SHBG, whose levels increases at accelerated rates in old persons. Noteworthy, although mBT and cBT highly correlated with one another, mBT is a much stronger correlate of chronological age than cBT.
In both men and women, mBT linearly declines over the life span and even at old ages. Its relationship with age-related phenotypes should be further investigated.
老年人尤其是女性体内睾酮水平随年龄的变化尚未得到充分研究。本研究的目的是描述巴尔的摩老年纵向研究中男性和女性总睾酮(TT)、硫酸铵沉淀法测定的生物可利用睾酮(mBT)和性激素结合球蛋白(SHBG)随年龄的变化轨迹,特别关注年龄最大的成年人。
参与者包括788名年龄在30 - 96岁的白人男性和女性,很好地代表了老年人和高龄老人,他们报告未服用已知会干扰睾酮的药物。如有可用的纵向数据则纳入分析。检测TT、mBT和SHBG。将mBT随年龄的变化轨迹与使用计算生物可利用睾酮(cBT)获得的轨迹进行比较。采用广义最小二乘法模型描述男性和女性TT、mBT和SHBG随年龄的变化轨迹。
mBT在两性的整个生命过程中甚至在老年时都呈线性下降。在男性中,TT在70岁之前保持相当稳定,之后在老年时下降,而在女性中,TT在绝经前逐渐下降,在老年时略有上升。总睾酮和生物可利用睾酮随年龄变化轨迹的差异仅部分由SHBG的年龄变化解释,SHBG水平在老年人中加速上升。值得注意的是,尽管mBT和cBT彼此高度相关,但mBT与实际年龄的相关性比cBT强得多。
在男性和女性中,mBT在整个生命过程中甚至在老年时都呈线性下降。其与年龄相关表型的关系应进一步研究。