School of Population and Global Health, The University of Western Australia, Perth, Western Australia, Australia
School of Population and Global Health, The University of Western Australia, Perth, Western Australia, Australia.
BMJ Open. 2021 Nov 2;11(11):e048013. doi: 10.1136/bmjopen-2020-048013.
The overall study aim is to clarify the relation of endogenous sex hormones with major health outcomes in men. This paper reports a systematic review focusing on published estimates for testosterone associations.
Community-dwelling men.
20 180 adult men participated in the final set of studies identified and selected from a systematic review. Eligible studies included prospective cohort studies with plasma or serum testosterone concentrations measured for adult men using mass spectrometry with at least 5 years of follow-up data and one of the specified outcome measures recorded. Only published or grey literature items written in English were considered.
Planned prospective outcome measures: cardiovascular disease (CVD) events, CVD deaths, all-cause mortality, cancer deaths, cancer diagnoses, cognitive decline, dementia. Meta-analyses were of the most frequently reported outcomes in selected studies: CVD deaths and all-cause mortality. Succinct characterisations of testosterone associations with other outcomes are also presented.
Screening of 1994 deduplicated items identified 9 suitable studies, with an additional 2 identified by colleagues (11 in total). Summary estimates of mean testosterone concentration and age at recruitment for 20 180 adult men were 15.4±0.7 nmol/L and 64.9±3.3 year. Despite considerable variation in mean testosterone, a metaregression estimated no significant dependence on mean age at recruitment among studies (slope=-0.03, 95% CI -0.11 to 0.06). Meta-analyses demonstrated negligible heterogeneity and no significant effect of a 5 nmol/L increase in testosterone on the risk of all-cause mortality (HR=0.96, 95% CI 0.89 to 1.03) or death from CVD (HR=0.95, 95% CI 0.83 to 1.08).
Analyses of published estimates did not demonstrate associations of endogenous testosterone with CVD deaths or with all-cause mortality. Suggested further research includes the planned individual participant data meta-analyses for selected studies, enabling the investigation of non-linear summary effects.
PROSPERO: CRD42019139668.
本研究旨在阐明内源性性激素与男性主要健康结局的关系。本文报告了一项系统综述,重点关注已发表的关于睾酮相关性的研究结果。
社区居住的男性。
最终纳入的研究共纳入了 20180 名成年男性,这些男性均来自一项系统综述,并从其中选取。符合条件的研究包括使用质谱法测量成年男性血浆或血清睾酮浓度的前瞻性队列研究,且这些研究随访时间至少 5 年,并记录了指定的结局指标之一。仅考虑已发表或灰色文献中用英语撰写的项目。
计划前瞻性结局指标:心血管疾病(CVD)事件、CVD 死亡、全因死亡率、癌症死亡、癌症诊断、认知能力下降、痴呆。对选定研究中最常报告的结局进行了荟萃分析:CVD 死亡和全因死亡率。此外,还对与其他结局相关的睾酮关系进行了简明描述。
对 1994 项去重项目进行筛选后,共识别出 9 项合适的研究,另有 2 项由同事识别(共 11 项)。20180 名成年男性的平均睾酮浓度和招募时年龄的汇总估计值分别为 15.4±0.7nmol/L 和 64.9±3.3 岁。尽管平均睾酮浓度存在较大差异,但荟萃回归估计研究之间的平均招募年龄无显著依赖性(斜率=-0.03,95%CI -0.11 至 0.06)。荟萃分析显示,睾酮增加 5nmol/L 与全因死亡率(HR=0.96,95%CI 0.89 至 1.03)或 CVD 死亡(HR=0.95,95%CI 0.83 至 1.08)风险无显著相关性,且异质性较小。
分析已发表的研究结果表明,内源性睾酮与 CVD 死亡或全因死亡率之间无关联。建议进一步研究包括对选定研究进行计划中的个体参与者数据荟萃分析,以便调查非线性汇总效应。
PROSPERO:CRD42019139668。