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肥胖相关炎症蛋白特征与心血管临床结局:来自古腾堡健康研究的结果。

Obesity-related inflammatory protein signature in cardiovascular clinical outcomes: results from the Gutenberg Health Study.

机构信息

Translational Medicine and Clinical Pharmacology, Boehringer Ingelheim Pharma GmbH & Co. KG, Ingelheim, Germany.

Center for Thrombosis and Haemostasis, University Medical Center, Johannes Gutenberg University Mainz, Mainz, Germany.

出版信息

Obesity (Silver Spring). 2024 Jun;32(6):1198-1209. doi: 10.1002/oby.24014. Epub 2024 Apr 25.

Abstract

OBJECTIVE

The objective of this study was to investigate whether an obesity-related inflammatory protein signature (OIPS) is associated with adverse cardiovascular events.

METHODS

The Olink Target 96 Inflammation panel was performed in 6662 participants from the population-based Gutenberg Health Study (GHS). The OIPS was selected by a logistic regression model, and its association with cardiovascular outcomes was evaluated by Cox regression analysis. The GHS-derived OIPS was externally validated in the MyoVasc study.

RESULTS

The identified OIPS entailed 21 proteins involved in chemokine activity, tumor necrosis factor (TNF) receptor binding, and growth factor receptor binding. The signature revealed a novel positive association of axis inhibition protein 1 with obesity. The OIPS was associated with increased risk of all-cause and cardiac deaths, major adverse cardiovascular events, and incident coronary artery disease, independent of clinical covariates and established risk instruments. A BMI-stratified analysis confirmed the association of OIPS with increased death in those with obesity and overweight and with increased risk for coronary artery disease in those with obesity. The association of OIPS with increased risk of all-cause and cardiac deaths was validated in the MyoVasc cohort.

CONCLUSIONS

The OIPS showed a significant association with adverse clinical outcomes, particularly in those with overweight and obesity, and represents a promising tool for identifying patients at higher risk for worse cardiovascular outcomes.

摘要

目的

本研究旨在探讨肥胖相关炎症蛋白谱(OIPS)是否与不良心血管事件相关。

方法

在基于人群的哥廷根健康研究(GHS)中,对 6662 名参与者进行了 Olink 靶向 96 炎症面板检测。通过逻辑回归模型选择 OIPS,并通过 Cox 回归分析评估其与心血管结局的关系。GHS 衍生的 OIPS 在 MyoVasc 研究中进行了外部验证。

结果

确定的 OIPS 涉及 21 种参与趋化因子活性、肿瘤坏死因子(TNF)受体结合和生长因子受体结合的蛋白质。该标志物揭示了轴抑制蛋白 1 与肥胖之间存在新的正相关关系。OIPS 与全因死亡和心脏死亡、主要不良心血管事件和新发冠状动脉疾病的风险增加相关,独立于临床协变量和既定风险工具。BMI 分层分析证实,OIPS 与肥胖和超重人群死亡风险增加以及肥胖人群冠心病风险增加相关。OIPS 与全因和心脏死亡风险增加的相关性在 MyoVasc 队列中得到了验证。

结论

OIPS 与不良临床结局显著相关,特别是在超重和肥胖人群中,代表了一种有前途的工具,可以识别心血管结局较差风险较高的患者。

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