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

被引:1
作者
Panova-Noeva, Marina [1 ,2 ]
Koeck, Thomas [3 ,4 ]
Schoelch, Corinna [5 ]
Schulz, Andreas [3 ]
Prochaska, Juergen H. [2 ,3 ,4 ]
Michal, Matthias [4 ,6 ]
Strauch, Konstantin [7 ]
Schuster, Alexander K. [8 ]
Lackner, Karl J. [4 ,9 ]
Munzel, Thomas [2 ,4 ,10 ]
Hennige, Anita M. [11 ]
Wild, Philipp S. [2 ,3 ,4 ,12 ]
机构
[1] Boehringer Ingelheim Pharm GmbH & Co KG, Translat Med & Clin Pharmacol, Ingelheim, Germany
[2] Univ Med Ctr, Johannes Gutenberg Univ Mainz, Ctr Thrombosis & Haemostasis, Mainz, Germany
[3] Univ Med Ctr, Johannes Gutenberg Univ Mainz, Ctr Cardiol, Prevent Cardiol & Prevent Med, Mainz, Germany
[4] German Ctr Cardiovasc Res DZHK, Partner Site Rhine Main, Mainz, Germany
[5] Boehringer Ingelheim Pharm GmbH & Co KG, Translat Med & Clin Pharmacol, Biberach, Germany
[6] Univ Med Ctr, Johannes Gutenberg Univ Mainz, Dept Psychosomat Med & Psychotherapy, Mainz, Germany
[7] Univ Med Ctr, Johannes Gutenberg Univ Mainz, Inst Med Biometr Epidemiol & Informat IMBEI, Mainz, Germany
[8] Univ Med Ctr, Johannes Gutenberg Univ Mainz, Dept Ophthalmol, Mainz, Germany
[9] Univ Med Ctr, Johannes Gutenberg Univ Mainz, Inst Clin Chem & Lab Med, Mainz, Germany
[10] Univ Med Ctr, Johannes Gutenberg Univ Mainz, Dept Cardiol Cardiol 1, Mainz, Germany
[11] Boehringer Ingelheim Int GmbH, Therapeut Area Cardiometab & Resp, Biberach, Germany
[12] Inst Mol Biol IMB, Mainz, Germany
基金
欧盟地平线“2020”;
关键词
HEPATOCYTE GROWTH-FACTOR; CORONARY-HEART-DISEASE; INSULIN-RESISTANCE; INTERLEUKIN-6; CONTRIBUTES; CYTOKINES; ROLES; AXIN1; RISK;
D O I
10.1002/oby.24014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveThe objective of this study was to investigate whether an obesity-related inflammatory protein signature (OIPS) is associated with adverse cardiovascular events.MethodsThe 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.ResultsThe 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.ConclusionsThe 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.
引用
收藏
页码:1198 / 1209
页数:12
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