Gerontology and Geriatrics, KU Leuven, Leuven, Belgium; Department of Psychiatry, University of Oxford, UK.
Clinical & Cognitive Neurosciences, Institute of Brain, Behaviour and Mental Health, The University of Manchester, UK.
Physiol Behav. 2022 Aug 1;252:113825. doi: 10.1016/j.physbeh.2022.113825. Epub 2022 Apr 26.
It has been proposed that endogenous sex hormone levels may present a modifiable risk factor for cognitive decline. However, the evidence for effects of sex steroids on cognitive ageing is conflicting. We therefore investigated associations between endogenous hormone levels, androgen receptor CAG repeat length, and cognitive domains including visuoconstructional abilities, visual memory, and processing speed in a large-scale longitudinal study of middle-aged and older men.
Men aged 40-79 years from the European Male Ageing Study (EMAS) underwent cognitive assessments and measurements of hormone levels at baseline and follow-up (mean = 4.4 years, SD ± 0.3 years). Hormone levels measured included total and calculated free testosterone and estradiol, dihydrotestosterone, luteinizing hormone, follicle-stimulating hormone, dehydroepiandrosterone sulphate and sex hormone-binding globulin. Cognitive function was assessed using the Rey-Osterrieth Complex Figure Copy and Recall, the Camden Topographical Recognition Memory and the Digit Symbol Substitution Test. Multivariate linear regressions were used to examine associations between baseline and change hormone levels, androgen receptor CAG repeat length, and cognitive decline.
Statistical analyses included 1,827 and 1,423 participants for models investigating relationships of cognition with hormone levels and CAG repeat length, respectively. In age-adjusted models, we found a significant association of higher baseline free testosterone (β=-0.001, p=0.005) and dihydrotestosterone levels (β=-0.065, p=0.003) with greater decline on Rey-Osterrieth Complex Figure Recall over time. However, these effects were no longer significant following adjustment for centre, health, and lifestyle factors. No relationships were observed between any other baseline hormone levels, change in hormone levels, or androgen receptor CAG repeat length with cognitive decline in the measured domains.
In this large-scale prospective study there was no evidence for an association between endogenous sex hormone levels or CAG repeat length and cognitive ageing in men. These data suggest that sex steroid levels do not affect visuospatial function, visual memory, or processing speed in middle-aged and older men.
内源性性激素水平可能是认知能力下降的可改变的危险因素。然而,关于性激素对认知老化的影响的证据是相互矛盾的。因此,我们在一项对中年和老年男性的大型纵向研究中,研究了内源性激素水平、雄激素受体 CAG 重复长度与认知领域(包括视觉建构能力、视觉记忆和处理速度)之间的关系。
来自欧洲男性衰老研究(EMAS)的 40-79 岁男性在基线和随访时(平均=4.4 年,标准差±0.3 年)进行了认知评估和激素水平测量。测量的激素水平包括总睾酮和计算的游离睾酮和雌二醇、二氢睾酮、黄体生成素、卵泡刺激素、硫酸脱氢表雄酮和性激素结合球蛋白。认知功能使用 Rey-Osterrieth 复杂图形复制和回忆、Camden 拓扑识别记忆和数字符号替代测试进行评估。使用多元线性回归分析来研究基线和变化激素水平、雄激素受体 CAG 重复长度与认知能力下降之间的关系。
在纳入了 1827 名和 1423 名参与者的统计分析中,分别对认知与激素水平和 CAG 重复长度的关系进行了研究。在年龄调整模型中,我们发现基线游离睾酮(β=-0.001,p=0.005)和二氢睾酮水平(β=-0.065,p=0.003)较高与 Rey-Osterrieth 复杂图形回忆的随时间下降有显著关联。然而,在调整中心、健康和生活方式因素后,这些效应不再显著。在测量的认知领域中,没有观察到任何其他基线激素水平、激素水平变化或雄激素受体 CAG 重复长度与认知能力下降之间的关系。
在这项大规模前瞻性研究中,没有证据表明内源性性激素水平或 CAG 重复长度与男性的认知老化有关。这些数据表明,性激素水平不会影响中年和老年男性的空间视觉功能、视觉记忆或处理速度。