低总睾酮浓度与不良血脂和增加的血脂异常事件的前瞻性关联。

Robin Haring, Sebastian E Baumeister, Henry Völzke, Marcus Dörr, Stephan B Felix, Heyo K Kroemer, Matthias Nauck, Henri Wallaschofski
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引用次数: 78

摘要

背景:早期的研究表明,总睾酮浓度影响脂质代谢。这些浓度是否与不良的脂质特征和增加的突发血脂异常的风险有前瞻性的联系,目前还没有研究。方法和结果:我们的研究人群包括1468名年龄在20-79岁之间的男性,作为波美拉尼亚基于人群的健康研究的一部分,他们被反复检查。化学发光酶免疫分析法测定的血清总睾酮浓度被分为年龄特异性四分位数。我们使用广义估计方程模型来评估总睾酮浓度与血脂成分(包括总胆固醇(TC)、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇和甘油三酯(TG)浓度)以及5年随访后血脂异常发生率之间的前瞻性关联。多变量模型显示,最低四分位数的总睾酮浓度与两个横截面较高的TC和TG浓度相关[TC: 0.23 mmol/l(95%置信区间,CI, 0.02-0.42);TG: 0.73 mmol/l (95% CI, 0.53-0.94)和纵向分析[TC: 0.20 mmol/l (95% CI, 0.03-0.27);TG: 0.62 mmol/l (95% CI, 0.43-0.80)],但与高密度脂蛋白胆固醇或低密度脂蛋白胆固醇浓度无关。血脂异常的基线患病率为57.1%,粗发病率为每1000人年46.6例。最低四分位数的总睾酮浓度预测血脂异常;与四分位数4(最高,参考)相比,四分位数1、2和3中男性的年龄调整相对危险度(RR)分别为1.28 (95% CI, 1.06-1.54)、1.10 (95% CI, 0.91-1.33)和1.05 (95% CI, 0.86-1.29)。这种影响在20-39岁的男性中尤为明显(相对风险,1.51;95% ci, 1.08-2.10)。结论:低总睾酮浓度可能与不良的脂质特征和增加的血脂异常风险相关。这些发现特别有趣,可能有助于解释总睾酮浓度较低的男性患心血管疾病的风险较高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prospective association of low total testosterone concentrations with an adverse lipid profile and increased incident dyslipidemia.

Background: Earlier studies have suggested that total testosterone concentrations influence the lipid metabolism. Whether these concentrations are prospectively associated with an adverse lipid profile and an increased risk of incident dyslipidemia has not yet been investigated.

Methods and results: Our study population consisted of 1468 men, aged 20–79 years, who were repeatedly examined as part of the population-based Study of Health in Pomerania. Serum total testosterone concentrations measured by the chemiluminescent enzyme immunoassays were categorized into age-specific quartiles. We used generalized estimating equations models to assess the prospective association between total testosterone concentrations and lipid profile components including total cholesterol (TC), low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and triglyceride (TG) concentrations, as well as incident dyslipidemia after 5 years of follow-up. Multivariate models revealed that total testosterone concentrations in the lowest quartile were associated with higher TC and TG concentrations in both cross-sectional [TC: 0.23 mmol/l (95% confidence interval, CI, 0.02–0.42); TG: 0.73 mmol/l (95% CI, 0.53–0.94)] and longitudinal analyses [TC: 0.20 mmol/l (95% CI, 0.03–0.27); TG: 0.62 mmol/l (95% CI, 0.43–0.80)], but not with high-density lipoprotein cholesterol or low-density lipoprotein cholesterol concentrations. Baseline prevalence of dyslipidemia was 57.1% with a crude incidence rate of 46.6 per 1000 person-years. Total testosterone concentrations in the lowest quartile predicted dyslipidemia; age-adjusted relative risks (RR) for men in quartiles 1, 2, and 3 as compared to quartile 4 (highest, reference) were 1.28 (95% CI, 1.06–1.54), 1.10 (95% CI, 0.91–1.33), and 1.05 (95% CI, 0.86–1.29), respectively. This effect was particularly strong among men aged 20–39 years (relative risk, 1.51; 95% CI, 1.08–2.10).

Conclusion: Low total testosterone concentrations are prospectively associated with an adverse lipid profile and increased risk of incident dyslipidemia. These findings are particularly interesting and may contribute to an explanation for the higher cardiovascular disease risk in men with lower total testosterone concentrations.

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