Severe Infection and Risk of Cardiovascular Disease: A Multicohort Study

医学 危险系数 人口 心肌梗塞 内科学 前瞻性队列研究 队列研究 疾病 比例危险模型 队列 可归因风险 冲程(发动机) 生命银行 相对风险 流行病学 置信区间 生物信息学 环境卫生 机械工程 工程类 生物
作者
Pyry N Sipilä,Joni V Lindbohm,Mark Hamer,Nelli Heikkilä,Jussi Vahtera,Sakari Suominen,Ari Väänänen,Aki Koskinen,Solja T Nyberg,Seppo Meri,Jaana Pentti,Charlotte Warren-Gash,Andrew C Hayward,Mika Kivimäki
出处
期刊:Circulation [Ovid Technologies (Wolters Kluwer)]
被引量:1
标识
DOI:10.1161/circulationaha.122.061183
摘要

BACKGROUND: The excess risk of cardiovascular disease associated with a wide array of infectious diseases is unknown. We quantified the short- and long-term risk of major cardiovascular events in people with severe infection and estimated the population-attributable fraction. METHODS: We analyzed data from 331 683 UK Biobank participants without cardiovascular disease at baseline (2006–2010) and replicated our main findings in an independent population from 3 prospective cohort studies comprising 271 533 community-dwelling participants from Finland (baseline 1986–2005). Cardiovascular risk factors were measured at baseline. We diagnosed infectious diseases (the exposure) and incident major cardiovascular events after infections, defined as myocardial infarction, cardiac death, or fatal or nonfatal stroke (the outcome) from linkage of participants to hospital and mortality registers. We computed adjusted hazard ratios (HRs) and 95% CIs for infectious diseases as short- and long-term risk factors for incident major cardiovascular events. We also calculated population-attributable fractions for long-term risk. RESULTS: In the UK Biobank (mean follow-up, 11.6 years), 54 434 participants were hospitalized for an infection, and 11 649 had an incident major cardiovascular event at follow-up. Relative to participants with no record of infectious disease, those who were hospitalized experienced increased risk of major cardiovascular events, largely irrespective of the subtype of infection. This association was strongest during the first month after infection (HR, 7.87 [95% CI, 6.36–9.73]), but remained elevated during the entire follow-up (HR, 1.47 [95% CI, 1.40–1.54]). The findings were similar in the replication cohort (HR, 7.64 [95% CI, 5.82–10.03] during the first month; HR, 1.41 [95% CI, 1.34–1.48] during mean follow-up of 19.2 years). After controlling for traditional cardiovascular risk factors, the population-attributable fraction for severe infections and major cardiovascular events was 4.4% in the UK Biobank and 6.1% in the replication cohort. CONCLUSIONS: Infections severe enough to require hospital treatment were associated with increased risks for major cardiovascular disease events immediately after hospitalization. A small excess risk was also observed in the long-term, but residual confounding cannot be excluded.
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