Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, LMU München, Germany; Clinical Cooperation Group Diabetes, Ludwig-Maximilians-Universität München and Helmholtz Zentrum München, Munich, Germany.
Freie Waldorfschule Augsburg, Germany.
Atherosclerosis. 2020 Mar;297:1-7. doi: 10.1016/j.atherosclerosis.2020.01.030. Epub 2020 Feb 4.
Serum uromodulin, a novel biomarker of kidney function and tubular integrity, has been linked to cardiovascular events and total mortality in patients at high cardiovascular risk. Here, we analyze the association of serum uromodulin with cardiovascular morbidity and cardiovascular as well as total mortality in the population-based KORA F4 study stratified by sex.
Baseline serum uromodulin was measured in 1079 participants of the KORA F4 study (age 62-81 years). Using multivariable adjusted Cox proportional hazards models, the associations of serum uromodulin with total mortality and cardiovascular mortality were analyzed after a median follow-up period of 8.6 years, and with non-fatal and fatal stroke and myocardial infarction/coronary death after a median follow-up time of 8.4 years.
Serum uromodulin was significantly inversely associated with total mortality (HR 0.65; 95% CI 0.53-0.79 per standard deviation of logarithmized serum uromodulin; p < 0.001) and cardiovascular mortality (HR 0.70; 95% CI 0.52-0.93) in men, but not in women (HR for all-cause mortality in women 0.98; 95% CI 0.77-1.25, HR for cardiovascular mortality 0.78; 95% CI 0.56-1.11) after adjustment for age, BMI, diabetes and eGFR. In addition, serum uromodulin was significantly inversely associated with incident stroke in men (HR 0.68; 95% CI 0.50-0.92), but not in women (HR 0.96; 95% CI 0.68-1.38) after multivariable adjustment. The association of serum uromodulin with incident myocardial infarction was attenuated and lost significance after multivariable adjustment in both sexes.
Serum uromodulin is an independent biomarker for total and cardiovascular mortality in men from the general community aged 62 years or older.
血清尿调蛋白是一种新型的肾功能和肾小管完整性的生物标志物,与心血管疾病风险较高的患者的心血管事件和全因死亡率相关。在这里,我们分析了血清尿调蛋白与基于人群的 KORA F4 研究中按性别分层的心血管发病率和心血管及全因死亡率的相关性。
在 KORA F4 研究的 1079 名参与者中测量了基线血清尿调蛋白(年龄 62-81 岁)。使用多变量调整的 Cox 比例风险模型,在中位随访 8.6 年后分析血清尿调蛋白与全因死亡率和心血管死亡率的相关性,在中位随访 8.4 年后分析与非致命性和致命性卒中以及心肌梗死/冠心病死亡的相关性。
血清尿调蛋白与男性全因死亡率(HR 0.65;95%CI 每对数血清尿调蛋白标准差 0.53-0.79;p<0.001)和心血管死亡率(HR 0.70;95%CI 0.52-0.93)显著负相关,但在女性中则没有(女性全因死亡率的 HR 0.98;95%CI 0.77-1.25,心血管死亡率的 HR 0.78;95%CI 0.56-1.11),调整年龄、BMI、糖尿病和 eGFR 后。此外,血清尿调蛋白与男性卒中事件显著负相关(HR 0.68;95%CI 0.50-0.92),但在女性中则没有(HR 0.96;95%CI 0.68-1.38),多变量调整后。血清尿调蛋白与女性心肌梗死的相关性减弱且失去统计学意义在多变量调整后在两性中均如此。
血清尿调蛋白是年龄在 62 岁或以上的普通社区男性全因和心血管死亡的独立生物标志物。