Smith Steven M, Desai Raj A, Walsh Marta G, Nilles Ester Kim, Shaw Katie, Smith Myra, Chamberlain Alanna M, Derington Catherine G, Bress Adam P, Chuang Cynthia H, Ford Daniel E, Taylor Bradley W, Chandaka Sravani, Patel Lav Parshottambhai, McClay James, Priest Elisa, Fuloria Jyotsna, Doshi Kruti, Ahmad Faraz S, Viera Anthony J, Faulkner Madelaine, O'Brien Emily C, Pletcher Mark J, Cooper-DeHoff Rhonda M
Department of Pharmacotherapy and Translational Research, College of Pharmacy, University of Florida, Gainesville, FL, United States of America.
Department of Pharmaceutical Outcomes and Policy, College of Pharmacy, University of Florida, Gainesville, FL, United States of America.
Am Heart J Plus. 2022 Jan;13:100112. doi: 10.1016/j.ahjo.2022.100112. Epub 2022 Mar 2.
SARS-CoV-2 accesses host cells via angiotensin-converting enzyme-2, which is also affected by commonly used angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs), raising concerns that ACEI or ARB exposure may portend differential COVID-19 outcomes. In parallel cohort studies of outpatient and inpatient COVID-19-diagnosed adults with hypertension, we assessed associations between antihypertensive exposure (ACEI/ARB vs. non-ACEI/ARB antihypertensives, as well as between ACEI- vs. ARB) at the time of COVID-19 diagnosis, using electronic health record data from PCORnet health systems. The primary outcomes were all-cause hospitalization or death (outpatient cohort) or all-cause death (inpatient), analyzed via Cox regression weighted by inverse probability of treatment weights. From February 2020 through December 9, 2020, 11,246 patients (3477 person-years) and 2200 patients (777 person-years) were included from 17 health systems in outpatient and inpatient cohorts, respectively. There were 1015 all-cause hospitalization or deaths in the outpatient cohort (incidence, 29.2 events per 100 person-years), with no significant difference by ACEI/ARB use (adjusted HR 1.01; 95% CI 0.88, 1.15). In the inpatient cohort, there were 218 all-cause deaths (incidence, 28.1 per 100 person-years) and ACEI/ARB exposure was associated with reduced death (adjusted HR, 0.76; 95% CI, 0.57, 0.99). ACEI, versus ARB exposure, was associated with higher risk of hospitalization in the outpatient cohort, but no difference in all-cause death in either cohort. There was no evidence of effect modification across pre-specified baseline characteristics. Our results suggest ACEI and ARB exposure have no detrimental effect on hospitalizations and may reduce death among hypertensive patients diagnosed with COVID-19.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)通过血管紧张素转换酶2进入宿主细胞,而常用的血管紧张素转换酶抑制剂(ACEI)和血管紧张素受体阻滞剂(ARB)也会对其产生影响,这引发了人们对ACEI或ARB暴露可能预示着不同的2019冠状病毒病(COVID-19)结局的担忧。在针对门诊和住院的COVID-19确诊成年高血压患者的平行队列研究中,我们利用PCORnet卫生系统的电子健康记录数据,评估了COVID-19诊断时的降压药暴露情况(ACEI/ARB与非ACEI/ARB降压药之间,以及ACEI与ARB之间)的关联。主要结局为全因住院或死亡(门诊队列)或全因死亡(住院队列),通过治疗权重逆概率加权的Cox回归进行分析。从2020年2月到2020年12月9日,门诊和住院队列分别纳入了来自17个卫生系统的11246名患者(3477人年)和2200名患者(777人年)。门诊队列中有1015例全因住院或死亡(发病率为每100人年29.2例事件),使用ACEI/ARB与否无显著差异(调整后风险比1.01;95%置信区间0.88,1.15)。在住院队列中,有218例全因死亡(发病率为每100人年28.1例),ACEI/ARB暴露与死亡风险降低相关(调整后风险比,0.76;95%置信区间,0.57,0.99)。在门诊队列中,与ARB暴露相比,ACEI暴露与更高的住院风险相关,但在两个队列中全因死亡方面无差异。在预先指定的基线特征中没有效应修饰的证据。我们的结果表明,ACEI和ARB暴露对住院没有不利影响,并且可能降低COVID-19确诊高血压患者的死亡风险。