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Prognostic significance of inflammation in patients with coronary artery disease at low residual inflammatory risk

Patients with coronary artery disease (CAD) at low residual inflammatory risk are often overlooked in research and practice. This study examined the associations between fourteen inflammatory indicators and all-cause mortality in 5,339 CAD patients with baseline high-sensitivity C-reactive protein (...

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Detalles Bibliográficos
Autores principales: Li, Tianyu, Wang, Peizhi, Wang, Xiaozeng, Liu, Zhenyu, Zhang, Zheng, Zhang, Yongzhen, Wang, Zhifang, Feng, Yingqing, Wang, Qingsheng, Guo, Xiaogang, Tang, Xiaofang, Xu, Jingjing, Song, Ying, Chen, Yan, Xu, Na, Yao, Yi, Liu, Ru, Zhu, Pei, Han, Yaling, Yuan, Jinqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10628835/
https://www.ncbi.nlm.nih.gov/pubmed/37942015
http://dx.doi.org/10.1016/j.isci.2023.108060
Descripción
Sumario:Patients with coronary artery disease (CAD) at low residual inflammatory risk are often overlooked in research and practice. This study examined the associations between fourteen inflammatory indicators and all-cause mortality in 5,339 CAD patients with baseline high-sensitivity C-reactive protein (hsCRP) <2 mg/L who received percutaneous coronary intervention and statin and aspirin therapy. The median follow-up time was 2.1 years. Neutrophil-derived systemic inflammatory response index (SIRI) yielded the strongest and most robust association with all-cause mortality among all indicators. Lower hsCRP remained to be associated with a lower risk of all-cause mortality. A newly developed comprehensive inflammation score (CIS) showed better predictive performance than other indicators, which was validated by an independent external cohort. In conclusion, neutrophil-derived indicators, particularly SIRI, strongly predicted all-cause mortality independent of hsCRP in CAD patients at low residual inflammatory risk. CIS may help identify individuals with inflammation burdens that cannot be explained by hsCRP alone.