医学
危险系数
比例危险模型
内科学
置信区间
急性冠脉综合征
临床终点
胃肠病学
单变量分析
多元分析
心肌梗塞
随机对照试验
作者
Qi Xi,Yanan Zhang,Yijia Wang,Sun Jiayi,Ruiyue Yang,Siming Wang,Jun Dong,Wenxiang Chen,Fusui Ji,Xue Yu
标识
DOI:10.1016/j.atherosclerosis.2024.117552
摘要
Background and aims The immuno-inflammatory response is a crucial early step in the development of acute coronary syndrome (ACS). In this study, we investigated whether immunoglobulin M (IgM) in the body's initial immune response can predict the prognosis of patients with ACS. Methods This prospective cohort study enrolled 1556 ACS patients at Beijing Hospital between March 2017 and October 2020. All patients underwent coronary angiography (CAG). The serum IgM concentration and biochemical indicators were evaluated prior to CAG. The primary endpoint was the composite endpoint of major adverse cardiovascular and cerebrovascular events (MACCEs). Multivariate Cox proportional hazards models was used to explore the association between IgM levels and the endpoint. Results The average serum IgM levels of the population was 61.3 (42.6 - 88.4) mg/dL. During the median follow-up period of 55 months, 150 MACCEs occurred. Kaplan-Meier analysis showed that low serum IgM levels were associated with occurrence of MACCEs (log-rank p = 0.009). Univariate Cox proportional hazards models showed that low serum IgM ( ≤ 78.05mg/dL) was associated with MACCEs (hazard ratio (HR) 1.648, 95% confidence interval (CI): 1.129-2.406, p = 0.010). In patients with IgM ≤ 78.05mg/dL, the HR for partially adjusted MACCEs events was 1.576 (95% CI: 1.075-2.310) and 1.930 (95% CI: 1.080-3.449) after adjusting for multiple covariates. The subgroup analysis showed that for patients in ≤ 24 BMI, never smoking and non-dyslipidemia subgroup, the lower serum IgM levels was significantly associated with the risk of MACCEs (pinteraction < 0.001, pinteraction = 0.037, pinteraction = 0.024, respectively). Conclusions Low serum IgM levels was independently associated with MACCEs in ACS patients, especially for patients without obesity, smoking and dyslipidemia.
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