Severe infections as risk factors for acute myocardial infarction: a nationwide, Danish cohort study from 1987-2018

医学 心肌梗塞 内科学 危险系数 肺炎 心内膜炎 相对风险 比例危险模型 队列研究 丹麦语 泌尿系统 置信区间 哲学 语言学
作者
E. Pedersen,Harman Yonis,Gertrud Baunbæk Egelund,Nicolai Lohse,Christian Torp‐Pedersen,Birgitte Lindegaard,Andreas Vestergaard Jensen
出处
期刊:European Journal of Preventive Cardiology [Oxford University Press]
标识
DOI:10.1093/eurjpc/zwae344
摘要

Abstract Aims Infections have been associated with acute myocardial infarction (AMI), but differences in risk between infection types and age groups are unclear. This study aims to investigate whether infections are associated with subsequent AMI and whether the risk differs across infection sites and age groups. Methods Nationwide registers were used to include 702596 adults hospitalized between 1987-2018 with either; pneumonia (n=344319), urinary tract infection (UTI) (n=270101), soft tissue/bone infection (n=66718), central nervous system infection (CNS) (n=17025), or endocarditis (n=4433). Patients were sex- and age-matched with two unexposed controls. Outcome was first-time AMI within ten years. A time-dependent cox proportional hazards model with cut-offs at 30 and 90 days was used for calculating adjusted hazard ratios (HR). Results Pneumonia, UTI, and soft tissue/bone infection were associated with increased relative rates of AMI compared to matched, unexposed controls. Highest relative rates were found within the first 0-30 days post-exposure; Pneumonia: HR 3.39 (95% CI 3.15-3.65), UTI: HR 2.44 (95% CI 2.21-2.70), Soft tissue/bone infection: HR 1.84 (95% CI 1.45-2.33). Relative rates decreased over time but remained significantly elevated throughout the follow-up period and was increased in all age groups. No association was found for CNS infection and for endocarditis only at 31-90 days, HR 2.28 (95% CI 1.20-4.33). Conclusion Acute infections are associated with increased relative rates of AMI across different infection sites and age groups with higher relative rates found for pneumonia. This indicates that some infections may act as a trigger for AMI with a site and/or pathogen specific risk.
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