Molinsky Rebecca L, Shah Amil, Yuzefpolskaya Melana, Yu Bing, Misialek Jeffrey R, Bohn Bruno, Vock David, MacLehose Richard, Borlaug Barry A, Colombo Paolo C, Ndumele Chiadi E, Ishigami Junichi, Matsushita Kunihiro, Lutsey Pamela L, Demmer Ryan T
Division of Epidemiology and Community Health, School of Public Health University of Minnesota Minneapolis MN USA.
Cardiovascular Imaging Program, Departments of Medicine and Radiology Brigham and Women's Hospital, Harvard Medical School Boston MA USA.
J Am Heart Assoc. 2025 Feb 4;14(3):e033877. doi: 10.1161/JAHA.123.033877. Epub 2025 Jan 30.
The immune response to infections may become dysregulated and promote myocardial damage contributing to heart failure (HF). We examined the relationship between infection-related hospitalization (IRH) and HF, HF with preserved ejection fraction, and HF with reduced ejection fraction.
We studied 14 468 adults aged 45 to 64 years in the ARIC (Atherosclerosis Risk in Communities) Study who were HF free at visit 1 (1987-1989). IRH was identified using select () codes in hospital discharge records and was treated as a time-varying exposure. HF incidence was defined as the first occurrence of either a hospitalization that included an () discharge code of 428 (428.0-428.9) among the primary or secondary diagnoses or a death certificate with an code of 428 or an () code of I50 among any of the listed diagnoses or underlying causes of death. We used multivariable-adjusted Cox proportional hazards models to assess the association between IRH and incident HF, HF with reduced ejection fraction, and HF with preserved ejection fraction. Median follow-up time was 27 years, 55% were women, 26% were Black, mean age at baseline was 54±6 years, 46% had an IRH, and 3565 had incident HF. Hazard ratio (HR) for incident HF events among participants who had an IRH compared with those who did not was 2.35 (95% CI, 2.19-2.52). This relationship was consistent across different types of infections. Additionally, IRH was associated with both HF with reduced ejection fraction and HF with preserved ejection fraction: 1.77 (95% CI, 1.35-2.32) and 2.97 (95% CI, 2.36-3.75), respectively.
IRH was associated with incident HF, HF with reduced ejection fraction, and HF with preserved ejection fraction. IRH might represent a modifiable risk factor for HF pathophysiology.
对感染的免疫反应可能会失调,并促进心肌损伤,进而导致心力衰竭(HF)。我们研究了感染相关住院(IRH)与HF、射血分数保留的HF以及射血分数降低的HF之间的关系。
我们在社区动脉粥样硬化风险(ARIC)研究中对14468名年龄在45至64岁之间的成年人进行了研究,这些人在首次就诊(1987 - 1989年)时没有HF。IRH通过医院出院记录中的特定()代码确定,并被视为随时间变化的暴露因素。HF发病率定义为在主要或次要诊断中首次出现包含()出院代码428(428.0 - 428.9)的住院治疗,或在任何列出的诊断或潜在死因中有代码428的死亡证明,或有代码I50的()代码。我们使用多变量调整的Cox比例风险模型来评估IRH与新发HF、射血分数降低的HF以及射血分数保留的HF之间的关联。中位随访时间为27年,55%为女性,26%为黑人,基线平均年龄为54±6岁,46%有IRH,3565人发生了新发HF。与未发生IRH的参与者相比,发生IRH的参与者发生HF事件的风险比(HR)为2.35(95%CI,2.19 - 2.52)。这种关系在不同类型的感染中是一致的。此外,IRH与射血分数降低的HF和射血分数保留的HF均相关:分别为1.77(95%CI,1.35 - 2.32)和2.97(95%CI,2.36 - 3.75)。
IRH与新发HF、射血分数降低的HF以及射血分数保留的HF相关。IRH可能是HF病理生理学中一个可改变的危险因素。