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  4. Colchicine to prevent cardiovascular death after an acute myocardial infarction.
 
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Colchicine to prevent cardiovascular death after an acute myocardial infarction.

Journal
Journal of the Formosan Medical Association = Taiwan yi zhi
Journal Volume
124
Journal Issue
11
Start Page
1077
End Page
1083
ISSN
0929-6646
Date Issued
2025-11
Author(s)
Chang, Yu-Ching
Yeh, Lo-Chia
TING TSE LIN  
CHING-CHANG HUANG  
CHI-SHENG HUNG  
Yang, Yen-Yun
Chuang, Shu-Lin
LIAN-YU LIN  
Lin, Lung-Chun  
HSIEN-LI KAO  
YEN-HUNG LIN  
DOI
10.1016/j.jfma.2024.11.014
URI
https://pubmed.ncbi.nlm.nih.gov/39627074/
https://scholars.lib.ntu.edu.tw/handle/123456789/724658
Abstract
Clinical and experimental evidence have demonstrated the protective benefits of colchicine in acute myocardial infarction (AMI) through its potential anti-inflammatory effect. However, investigations on the Asian population are limited. This retrospective longitudinal cohort study used electronic medical records from a tertiary medical center in Taiwan. Patients with their first AMI from the emergency department between 2010 and 2020 were included. The outcomes included all-cause death, hospitalization for heart failure, stroke, and emergency admission for angina. Propensity-score matching (PSM, 5 to 1) and Cox's proportional hazards regression model were used to estimate hazard ratios (HRs). A total of 2841 patients with their first admission for AMI were identified, of which 176 (6.2%) received colchicine and 2665 (93.8%) did not. After a median follow-up of 21.4 months, the incidence of all-cause death was significantly reduced in the colchicine group (HR, 0.560; 95% confidence interval [CI], 0.361-0.862; P = 0.008), driven by the significant risk reduction of cardiovascular death (HR, 0.291; 95% CI, 0.142-0.613; P = 0.001). There was no significant difference of other outcomes. After PSM, the protective effect remained in the colchicine group compared with non-users (HR, 0.331; 95% CI, 0.162-0.690; P = 0.003). The relationship between endpoints and various time-to-treatment initiation showed a significant reduction in the risk of all-cause death for whom colchicine was initiated < Day 3 compared with placebo. Low-dose colchicine led to a significantly lower risk of cardiovascular death than non-users among patients with a recent myocardial infarction. They benefit from early, in-hospital initiation of colchicine after AMI.
Subjects
Acute myocardial infarction
Cardiovascular death
Colchicine
SDGs

[SDGs]SDG3

Type
journal article

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