Schederecker Florian, Cecil Alexander, Prehn Cornelia, Nano Jana, Koenig Wolfgang, Adamski Jerzy, Zeller Tanja, Peters Annette, Thorand Barbara
Institute of Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health (GmbH), Neuherberg, Germany.
Molecular Endocrinology and Metabolism, Genome Analysis Center, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany.
Endocr Connect. 2020 Apr;9(4):326-336. doi: 10.1530/EC-20-0080.
Sex hormone-binding globulin (SHBG) and androgens have been associated with mortality in women and men, but controversy still exists. Our objective was to investigate associations of SHBG and androgens with all-cause and cause-specific mortality in men and women.
1006 men and 709 peri- and postmenopausal women (age range: 45-82 years) from the German population-based KORA F4 cohort study were followed-up for a median of 8.7 years.
SHBG was measured with an immunoassay, total testosterone (TT) and dihydrotestosterone (DHT) with mass-spectrometry in serum samples and we calculated free testosterone (cFT). To assess associations between SHBG and androgen levels and mortality, we calculated hazard ratios (HRs) with 95% CIs using Cox proportional-hazards models.
In the cohort, 128 men (12.7%) and 70 women (9.9%) died. In women, we observed positive associations of SHBG with all-cause (HR: 1.54, 95% CI: 1.16-2.04) and with other disease-related mortality (HR: 1.86, 95% CI: 1.08-3.20) and for DHT with all-cause mortality (HR: 1.32, 95% CI: 1.00-1.73). In men, we found a positive association of SHBG (HR: 1.24 95% CI: 1.00-1.54) and inverse associations of TT (HR: 0.87, 95% CI: 0.77-0.97) and cFT (HR: 0.84, 95% CI: 0.73-0.97) with all-cause mortality. No other associations were found for cause-specific mortality.
Higher SHBG levels were associated with increased risk of all-cause mortality in men and women. Lower TT and cFT levels in men and higher DHT levels in women were associated with increased risk of all-cause mortality. Future, well-powered population-based studies should further investigate cause-specific mortality risk.
性激素结合球蛋白(SHBG)和雄激素与男性及女性的死亡率相关,但仍存在争议。我们的目的是研究SHBG和雄激素与男性及女性全因死亡率和特定病因死亡率之间的关联。
对来自德国基于人群的KORA F4队列研究的1006名男性和709名围绝经期及绝经后女性(年龄范围:45 - 82岁)进行了中位时间为8.7年的随访。
采用免疫分析法测定血清样本中的SHBG,用质谱法测定总睾酮(TT)和双氢睾酮(DHT),并计算游离睾酮(cFT)。为评估SHBG和雄激素水平与死亡率之间的关联,我们使用Cox比例风险模型计算了95%置信区间的风险比(HRs)。
在该队列中,128名男性(12.7%)和70名女性(9.9%)死亡。在女性中,我们观察到SHBG与全因死亡率(HR:1.54,95%置信区间:1.16 - 2.04)以及与其他疾病相关死亡率(HR:1.86,95%置信区间:1.08 - 3.20)呈正相关,DHT与全因死亡率呈正相关(HR:1.32,95%置信区间:1.00 - 1.73)。在男性中,我们发现SHBG与全因死亡率呈正相关(HR: 1.24,95%置信区间:1.00 - 1.54),TT(HR:0.87,95%置信区间:0.77 - 0.97)和cFT(HR:0.84,95%置信区间:0.73 - 0.97)与全因死亡率呈负相关。未发现特定病因死亡率的其他关联。
较高的SHBG水平与男性和女性全因死亡率风险增加相关。男性较低的TT和cFT水平以及女性较高的DHT水平与全因死亡率风险增加相关。未来,有充分样本量的基于人群的研究应进一步调查特定病因的死亡风险。