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内源性性激素、性激素结合球蛋白与全因及特定病因死亡率风险:前瞻性队列研究的系统评价与剂量反应荟萃分析

Endogenous Sex Steroid Hormones, Sex Hormone-Binding Globulin, and Risk of All-Cause and Cause-Specific Mortality: A Systematic Review and Dose-Response Meta-Analysis of Prospective Cohort Studies.

作者信息

Raeisi-Dehkordi Hamidreza, Amiri Mojgan, Beigrezaei Sara, Quezada-Pinedo Hugo G, Khatami Farnaz, Alijla Fadi, Steur Marinka, Minder Beatrice, Chatelan Angeline, Voortman Trudy, van der Schouw Yvonne T, Franco Oscar H, Muka Taulant

机构信息

Department of Global Public Health and Bioethics, Julius Center for Health Sciences and Primary Care, University Medical Center (UMC) Utrecht, Utrecht University, 3584 CG Utrecht, The Netherlands.

Institute of Social and Preventive Medicine (ISPM), University of Bern, 3012 Bern, Switzerland.

出版信息

J Clin Endocrinol Metab. 2025 Aug 7;110(9):e3131-e3149. doi: 10.1210/clinem/dgaf262.

Abstract

BACKGROUND

While abundant research suggests a sex-specific role of endogenous sex steroid hormones in chronic diseases, research on mortality remains inconclusive. We quantified the sex-specific associations of endogenous sex steroid hormones, including total testosterone (TT), free testosterone, bioavailable testosterone, estradiol, dehydroepiandrosterone (DHEA), and DHEA sulfate (DHEAS), and sex hormone-binding globulin (SHBG) with risk of all-cause and cause-specific mortality in the general population.

METHODS

Embase, Medline, Web of Science, and Cochrane Central were searched and population-based cohort studies investigating the association of interest were included. The risk of bias was assessed using the ROBINS-E tool. The certainty of evidence was evaluated using the GRADE framework. Pooled hazard ratios (HRs) and 95% CI were calculated using a random effects model for the top vs bottom tertile of sex hormones and risk of mortality.

RESULTS

The systematic review included 53 publications with 359 047 participants. A significant association was observed between higher level of TT and risk of all-cause mortality (HR [95% CI]: 0.89 [0.83-0.97], n = 19 studies) in men, while no association was found in women. Dose-response analysis suggested a significant U-shaped association between TT and all-cause mortality in men and a J-shaped association in women. Higher SHBG level was significantly associated with higher risk of all-cause mortality in women (1.25 [1.13-1.39], n = 3) and no association was observed in men. Additionally, higher DHEAS levels were associated with lower risk of all-cause mortality in men (0.72 [0.57-0.91], n = 6) and no association was observed in women.

CONCLUSION

This meta-analysis reveals a dose-response link between endogenous sex steroid hormones and mortality, highlighting the need for sex-specific studies on hormone modulation's impact on mortality and longevity.

摘要

背景

尽管大量研究表明内源性性类固醇激素在慢性疾病中具有性别特异性作用,但关于死亡率的研究尚无定论。我们对一般人群中内源性性类固醇激素(包括总睾酮(TT)、游离睾酮、生物可利用睾酮、雌二醇、脱氢表雄酮(DHEA)和硫酸脱氢表雄酮(DHEAS))以及性激素结合球蛋白(SHBG)与全因死亡率和特定病因死亡率风险之间的性别特异性关联进行了量化。

方法

检索了Embase、Medline、Web of Science和Cochrane Central,并纳入了基于人群的队列研究,这些研究调查了感兴趣的关联。使用ROBINS-E工具评估偏倚风险。使用GRADE框架评估证据的确定性。对于性激素水平最高三分位数与最低三分位数以及死亡率风险,采用随机效应模型计算合并风险比(HRs)和95%置信区间。

结果

该系统评价纳入了53篇文献,共359047名参与者。在男性中,观察到TT水平升高与全因死亡率风险之间存在显著关联(HR [95%置信区间]:0.89 [0.83 - 0.97],n = 19项研究),而在女性中未发现关联。剂量反应分析表明,男性中TT与全因死亡率之间存在显著的U型关联,女性中存在J型关联。较高的SHBG水平与女性全因死亡率风险显著升高相关(1.25 [1.13 - 1.39],n = 3),在男性中未观察到关联。此外,较高的DHEAS水平与男性全因死亡率风险较低相关(0.72 [0.57 - 0.91],n = 6),在女性中未发现关联。

结论

这项荟萃分析揭示了内源性性类固醇激素与死亡率之间的剂量反应联系,强调了针对激素调节对死亡率和寿命影响进行性别特异性研究的必要性。

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