可溶性肿瘤坏死因子受体1型可预测2型糖尿病的心肾结果,并且与先前的肾脏或心血管事件相比,与不同的心血管或肾脏结果更好地相关。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2023-10-29 eCollection Date: 2023-01-01 DOI:10.1177/20420188231207345
Li-Hsin Chang, Chia-Huei Chu, Chin-Chou Huang, Liang-Yu Lin
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引用次数: 0

摘要

背景:炎症是2型糖尿病(T2DM)慢性并发症的关键发病机制。目的:T2DM心血管和肾脏并发症的时间线以及可溶性肿瘤坏死因子受体1型(sTNFR1)水平是否能预测心肾结果尚不清楚。设计:前瞻性观察研究。方法:纳入中国2型糖尿病患者。对心血管复合事件(全因死亡率、急性冠状动脉综合征或非致命性中风)或肾脏复合事件(肾功能下降>30%或蛋白尿恶化)定义的心肾复合事件进行随访。以风险比(HR)和95%置信区间(95%CI)为回归模型,分析sTNFR1水平与心血管、肾脏和心肾复合事件的相关性。结果:在370名受试者中,发生了42起心血管和86起肾脏复合事件。sTNFR1水平越高,心血管复合事件发生的频率和风险越高(HR 1.07,95%CI 1.01-1.13,p = 0.009)和肾脏复合事件(HR 1.05,95%CI 1.02-1.09,p p = 0.03)。所有亚组分析的结果一致。结论:sTNFR1水平与T2DM的心肾并发症相关,TNFR1水平的预测能力优于既往心血管或肾脏事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Soluble tumor necrosis factor receptor type 1 predicts cardiorenal outcomes and better associated with distinct cardiovascular or renal outcomes than precedential renal or cardiovascular events in type 2 diabetes mellitus.

Soluble tumor necrosis factor receptor type 1 predicts cardiorenal outcomes and better associated with distinct cardiovascular or renal outcomes than precedential renal or cardiovascular events in type 2 diabetes mellitus.

Soluble tumor necrosis factor receptor type 1 predicts cardiorenal outcomes and better associated with distinct cardiovascular or renal outcomes than precedential renal or cardiovascular events in type 2 diabetes mellitus.

Soluble tumor necrosis factor receptor type 1 predicts cardiorenal outcomes and better associated with distinct cardiovascular or renal outcomes than precedential renal or cardiovascular events in type 2 diabetes mellitus.

Background: Inflammations are the crucial pathogenesis of chronic complications of type 2 diabetes mellitus (T2DM).

Objectives: The timeline of cardiovascular and renal complications of T2DM and whether soluble tumor necrosis factor receptor type 1 (sTNFR1) levels predict cardiorenal outcomes were still elusive.

Design: Prospectively observational study.

Methods: Chinese patients with T2DM were enrolled. Cardiorenal composite events defined by either cardiovascular composite events (all-cause mortality, acute coronary syndrome, or non-fatal stroke) or renal composite events (a decline of >30% of renal function or worsening status of albuminuria) were followed. Associations of sTNFR1 levels and cardiovascular, renal, and cardiorenal composite events were analyzed in regression models presented by hazard ratio (HR) and 95% confidence interval (95% CI).

Results: Among 370 subjects, 42 cardiovascular and 86 renal composite events occurred. Higher sTNFR1 levels were related to higher frequency and risks of cardiovascular composite events (HR 1.07, 95% CI 1.01-1.13, p = 0.009) and renal composite events (HR 1.05, 95% CI 1.02-1.09, p < 0.001). Occurrences of cardiovascular composite events were not predicted by precedential renal composite events. sTNFR1 levels were proved to be associated with risks of cardiorenal composite events in Cox regression sequential models (adjusted HR 1.04, 95% CI 1.00-1.08, p = 0.03). The results were consistent in all subgroup analyses.

Conclusion: Levels of sTNFR1 were associated with cardiorenal complications of T2DM and the predictabilities of TNFR1 levels were better than precedential cardiovascular or renal events.

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CiteScore
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