Section of Infectious Diseases, Department of Internal Medicine, Taipei City Hospital, Taipei, Taiwan.
Department of Health Care Management, National Taipei University of Nursing and Health Sciences, Taipei, Taiwan.
J Acquir Immune Defic Syndr. 2019 Mar 1;80(3):255-263. doi: 10.1097/QAI.0000000000001917.
Although the HIV can cause myocardial inflammation, the association of HIV infection with subsequent development of heart failure (HF) has not been extensively studied. This nationwide cohort study aimed to determine the risk of incident HF in people living with HIV/AIDS (PLWHA).
We identified PLWHA using the Taiwan Centers for Disease Control and Prevention HIV Surveillance System. An age- and sex-matched control group without HIV infection was selected from the Taiwan National Health Insurance Research Database for comparison. All patients were followed up until December 2014 and were observed for a new diagnosis of HF. A time-dependent Cox proportional hazards model was used to determine the association of HIV and highly active antiretroviral therapy with incident HF, with death as a competing risk event.
Of the 120,765 patients (24,153 PLWHA and 96,612 matched controls), 641 (0.53%) had incident HF during a mean follow-up period of 5.84 years, including 192 (0.79%) PLWHA and 449 (0.46%) controls. Time to diagnosis of incident HF was significantly shorter in PLWHA than in those without HIV infection (P < 0.001, the log-rank test). After adjusting for age, sex, and comorbidities, HIV infection was found to be an independent risk factor for incident HF (adjusted hazard ratio, 1.52; 95% confidence interval: 1.27 to 1.82). As the duration of highly active antiretroviral therapy increased, the risk of HF decreased (P = 0.014).
HIV infection was an independent risk factor for incident HF. Clinicians need to be aware of the higher risk of HF in PLWHA.
虽然 HIV 可引起心肌炎症,但 HIV 感染与心力衰竭(HF)的后续发展之间的关联尚未得到广泛研究。本项全国性队列研究旨在确定人类免疫缺陷病毒/艾滋病(PLWHA)患者中 HF 发病的风险。
我们使用台湾疾病管制署的 HIV 监测系统确定 PLWHA。从台湾全民健康保险研究数据库中选择年龄和性别匹配的未感染 HIV 的对照组进行比较。所有患者均随访至 2014 年 12 月,观察 HF 的新诊断情况。使用时间依赖性 Cox 比例风险模型来确定 HIV 和高效抗逆转录病毒治疗与 HF 发病的关联,以死亡作为竞争风险事件。
在 120765 例患者(24153 例 PLWHA 和 96612 例匹配对照)中,有 641 例(0.53%)在平均 5.84 年的随访期间发生 HF,其中 192 例(0.79%)为 PLWHA,449 例(0.46%)为对照组。PLWHA 的 HF 诊断时间明显短于无 HIV 感染患者(P < 0.001,对数秩检验)。在调整年龄、性别和合并症后,发现 HIV 感染是 HF 发病的独立危险因素(调整后的危险比,1.52;95%置信区间:1.27 至 1.82)。随着高效抗逆转录病毒治疗时间的延长,HF 的风险降低(P = 0.014)。
HIV 感染是 HF 发病的独立危险因素。临床医生需要意识到 PLWHA 发生 HF 的风险更高。