Zhou Shangxun, Qiu Miaohan, Wang Kexin, Duan Yixuan, Liu Daoshen, Xu Ying, Mu Xuefei, Li Jing, Li Yi, Han Yaling
State Key Laboratory of Frigid Zone Cardiovascular Disease, Cardiovascular Research Institute and Department of Cardiology, General Hospital of Northern Theater Command, Shenyang, China.
The Department of Cardiology, Xijing Hospital, Air Force Medical University, Xi'an, China.
PLoS One. 2025 May 28;20(5):e0322281. doi: 10.1371/journal.pone.0322281. eCollection 2025.
This research aimed to explore the association of high-sensitivity C-reactive protein to albumin ratio (CAR) with death events in community-based patients with coronary heart disease (CHD).
624 CHD participants were followed for 36 months using data from the 2015-2018 National Health and Nutrition Examination Survey (NHANES). The CAR was dichotomized at 0.075 mg/g to stratify inflammation levels. Relationships between CAR, high-sensitivity C-reactive protein (hsCRP), albumin (ALB) and all-cause and cardiac death in all participants and subgroups were analyzed using restricted cubic spline (RCS), Kaplan-Meier survival curves and Cox proportional hazards models.
Both CAR and hsCRP showed positive correlations with all-cause and cardiac death risk while ALB exhibited a U-shaped correlation with all-cause death risk but a negative correlation with cardiac death risk. The high-CAR group had higher risks of all-cause (P = 0.04) and cardiac death (P = 0.02). The hazard ratios (HR) (95% confidence intervals (CI)) for all-cause death was 1.77 (1.15-2.74) (P = 0.010), while it was 2.99 (1.44-6.22) (P = 0.003) for cardiac death. No significant interaction was observed in subgroup analyses.
A CAR threshold of 0.075 mg/g effectively distinguished between high and low inflammation risks. Elevated CAR significantly increased the risk of all-cause and cardiac death in community CHD patients.
本研究旨在探讨基于社区的冠心病(CHD)患者中高敏C反应蛋白与白蛋白比值(CAR)与死亡事件之间的关联。
利用2015 - 2018年国家健康与营养检查调查(NHANES)的数据,对624名冠心病参与者进行了36个月的随访。将CAR以0.075 mg/g进行二分法划分,以分层炎症水平。使用受限立方样条(RCS)、Kaplan - Meier生存曲线和Cox比例风险模型分析了所有参与者及亚组中CAR、高敏C反应蛋白(hsCRP)、白蛋白(ALB)与全因死亡和心源性死亡之间的关系。
CAR和hsCRP均与全因死亡和心源性死亡风险呈正相关,而ALB与全因死亡风险呈U型相关,但与心源性死亡风险呈负相关。高CAR组全因死亡(P = 0.04)和心源性死亡(P = 0.02)风险更高。全因死亡的风险比(HR)(95%置信区间(CI))为1.77(1.15 - 2.74)(P = 0.010),而心源性死亡的风险比为2.99(1.44 - 6.22)(P = 0.003)。亚组分析未观察到显著的交互作用。
CAR阈值为0.075 mg/g能有效区分高炎症风险和低炎症风险。CAR升高显著增加了社区冠心病患者的全因死亡和心源性死亡风险。