性激素与男性和绝经后女性痴呆发生的风险。

IF 2.4 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Yanqing Zhao, Qi Wang, Chunying Fu, Meiling Li, Wenting Hao, Xiaoyi Wang, Qixiang Song, Dongshan Zhu
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引用次数: 0

摘要

背景:痴呆症是一项重大的全球公共卫生挑战,其风险因性别而异。女性患阿尔茨海默氏症和其他形式的痴呆症的可能性几乎是男性的两倍。尽管睾酮水平被认为会影响老年人的认知功能,但现有的研究报告的结果并不一致,这使得性激素与痴呆症之间的关系尚不清楚。方法:我们使用来自UK Biobank的数据。免疫分析法测定血清总睾酮和性激素结合球蛋白(SHBG)水平。血清游离睾酮用维马伦法计算。从医院住院患者数据中记录痴呆和阿尔茨海默病(AD)事件。采用Cox比例风险回归来评估性激素与痴呆之间的关系,并对年龄和其他变量进行了调整。限制三次样条模型用于量化剂量-反应关系。结果:共纳入186296名男性(平均年龄56.68岁,SD: 8.18)和126109名绝经后女性(平均年龄59.73岁,SD: 5.78)。经过12.0年(IQR: 11.0-13.0)年的随访,3874名(2.08%)男性参与者和2523名(2.00%)女性参与者出现痴呆。游离睾酮水平最高的五分之一的男性患全因痴呆(HR: 0.63, 95%CI: 0.56-0.71)和AD(0.49, 0.60-0.72)的风险低于最低五分之一的男性。相反,与最低五分位数的男性相比,SHBG水平最高的五分位数的男性患全因痴呆(1.47,1.32-1.64)和AD(1.32, 1.11-1.58)的风险更高。在绝经后妇女中,游离睾酮水平处于第四个五分位数的妇女患全因痴呆(0.84,0.78-0.95)和AD(0.76, 0.63-0.91)的风险较低。较高的SHBG与绝经妇女全因痴呆(1.35,1.28-1.55)和AD(1.52, 1.25-1.85)发生率增加有关。结论:我们的研究结果显示,较高的SHBG和较低的游离睾酮浓度似乎与较高的全因痴呆和AD发病率有关,必须进行进一步的研究以确定因果关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex Hormones and Risk of Incident Dementia in Men and Postmenopausal Women

Background

Dementia poses a major global public health challenge, with its risk varying by sex. Women were nearly twice as likely to have Alzheimer's and other forms of dementia compared to men. Although testosterone levels are believed to influence cognitive function in older adults, existing studies have reported inconsistent findings, leaving the relationship between sex hormones and dementia unclear.

Methods

We used data from UK Biobank. Serum total testosterone and sex hormone binding globulin (SHBG) were measured by immunoassay. Serum free testosterone was calculated using vermeulen method. The incident dementia and Alzheimer's disease (AD) was recorded from hospital inpatient data. Cox proportional hazards regression was conducted to assess the association between sex hormones and dementia, adjusted for age and other variables. Restricted cubic spline models were employed to quantify dose–response relationships.

Result

A total of 186,296 men (mean age: 56.68 years, SD: 8.18) and 126,109 postmenopausal women (mean age: 59.73 years, SD: 5.78) were included. After 12.0 (IQR: 11.0−13.0)-year follow-up, 3874 (2.08%) male participants and 2523 (2.00%) female participants developed dementia. Men in the highest quintile of free testosterone levels had a reduced risk of all-cause dementia (HR: 0.63, 95%CI: 0.56−0.71) and AD (0.49, 0.60−0.72) compared to those in the lowest quintile. Conversely, men in the highest quintile of SHBG levels had an increased risk of all-cause dementia (1.47, 1.32−1.64) and AD (1.32, 1.11−1.58) compared to those in the lowest quintile. Among postmenopausal women, those in the fourth quintile of free testosterone levels exhibited a lower risk of all-cause dementia (0.84, 0.78−0.95) and AD (0.76, 0.63−0.91). Higher SHBG was linked to an increased incidence of all-cause dementia (1.35, 1.28−1.55) and AD (1.52, 1.25−1.85) in menopausal women.

Conclusion

Our findings revealed that higher SHBG and lower free testosterone concentrations seem to be associated with higher incidence of all-cause dementia and AD and further studies must be done to determine causality.

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来源期刊
Clinical Endocrinology
Clinical Endocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
3.10%
发文量
192
审稿时长
1 months
期刊介绍: Clinical Endocrinology publishes papers and reviews which focus on the clinical aspects of endocrinology, including the clinical application of molecular endocrinology. It does not publish papers relating directly to diabetes care and clinical management. It features reviews, original papers, commentaries, correspondence and Clinical Questions. Clinical Endocrinology is essential reading not only for those engaged in endocrinological research but also for those involved primarily in clinical practice.
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