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

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Obesity Pub Date : 2024-04-25 DOI:10.1002/oby.24014
Marina Panova-Noeva, Thomas Koeck, Corinna Schoelch, Andreas Schulz, Jürgen H. Prochaska, Matthias Michal, Konstantin Strauch, Alexander K. Schuster, Karl J. Lackner, Thomas Münzel, Anita M. Hennige, Philipp S. Wild
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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.

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心血管临床结果中与肥胖相关的炎症蛋白特征:古腾堡健康研究的结果。
目的本研究旨在探讨肥胖相关炎症蛋白特征(OIPS)是否与不良心血管事件有关。方法对基于人群的古腾堡健康研究(GHS)的6662名参与者进行了Olink Target 96炎症面板分析。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预后的关系。结果发现,OIPS包含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。该特征揭示了轴抑制蛋白 1 与肥胖的新的正相关性。OIPS与全因死亡和心源性死亡、主要不良心血管事件和冠状动脉疾病风险的增加有关,不受临床协变量和既定风险工具的影响。体重指数分层分析证实,OIPS 与肥胖和超重者死亡风险增加以及肥胖者冠状动脉疾病风险增加有关。结论:OIPS 与不良临床预后有显著关联,尤其是在超重和肥胖患者中,是识别心血管预后较差的高风险患者的有效工具。
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来源期刊
Obesity
Obesity 医学-内分泌学与代谢
CiteScore
11.70
自引率
1.40%
发文量
261
审稿时长
2-4 weeks
期刊介绍: Obesity is the official journal of The Obesity Society and is the premier source of information for increasing knowledge, fostering translational research from basic to population science, and promoting better treatment for people with obesity. Obesity publishes important peer-reviewed research and cutting-edge reviews, commentaries, and public health and medical developments.
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