The combined effect of triglyceride–glucose index and high‐sensitivity C‐reactive protein on cardiovascular outcomes in patients with chronic coronary syndrome: A multicenter cohort study

Author:

Li Qinxue1,Song Ying1,Zhang Zheng2,Xu Jingjing1,Liu Zhenyu3,Tang Xiaofang1,Wang Xiaozeng4,Chen Yan1,Zhang Yongzhen5,Zhu Pei1,Guo Xiaogang6,Jiang Lin1,Wang Zhifang7,Liu Ru1,Wang Qingsheng8,Yao Yi1,Feng Yingqing9,Han Yaling4,Yuan Jinqing1ORCID

Affiliation:

1. National Clinical Research Center for Cardiovascular Diseases, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China

2. Department of Cardiology The First Hospital of Lanzhou University Lanzhou China

3. Department of Cardiology, Peking Union Medical College Hospital Chinese Academy of Medical Sciences and Peking Union Medical College Beijing China

4. Department of Cardiology General Hospital of Northern Theater Command Shenyang China

5. Department of Cardiology Peking University Third Hospital Beijing China

6. Department of Cardiology, The First Affiliated Hospital Zhejiang University School of Medicine Zhejiang China

7. Department of Cardiology Xinxiang Central Hospital Xinxiang China

8. Department of Cardiology The First Hospital of Qinhuangdao Qinhuangdao China

9. Department of Cardiology Guangdong Provincial People's Hospital Guangdong China

Abstract

AbstractBackgroundThe triglyceride–glucose (TyG) index and high‐sensitivity C‐reactive protein (hsCRP) are the commonly used biomarkers for insulin resistance and systemic inflammation, respectively. We aimed to investigate the combined association of TyG and hsCRP with the major adverse cardiovascular events (MACE) in patients with chronic coronary syndrome (CCS).MethodsA total of 9421 patients with CCS were included in this study. The primary endpoint was defined as a composite of MACE covering all‐cause death, nonfatal myocardial infarction, and revascularization.ResultsDuring the 2‐year follow‐up period, 660 (7.0%) cases of MACE were recorded. Participants were divided equally into three groups according to TyG levels. Compared with the TyG T1 group, the risk of MACE was significantly higher in the TyG T3 group. It is noteworthy that among patients in the highest tertile of TyG, hsCRP >3 mg/L was significantly associated with an increased risk of MACE, whereas the results were not significant in the medium to low TyG groups. When patients were divided into six groups according to hsCRP and TyG, the Cox regression analysis showed that patients in the TyG T3 and hsCRP >3 mg/L group had a significantly higher risk of MACE than those in the TyG T1 and hsCRP ≤3 mg/L group. However, no significant interaction was found between TyG and hsCRP on the risk of MACE.ConclusionOur study suggests that the concurrent assessment of TyG and hsCRP may be valuable in identifying high‐risk populations and guiding management strategies among CCS patients.image

Publisher

Wiley

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