Department of Internal Medicine University of Michigan Ann Arbor MI.
Division of Cardiology Department of Internal Medicine University of Michigan Ann Arbor MI.
J Am Heart Assoc. 2021 Dec 21;10(24):e023535. doi: 10.1161/JAHA.121.023535. Epub 2021 Dec 10.
Background Use of angiotensin-converting enzyme inhibitors and angiotensin receptor blockers (ACEi/ARB) is thought to affect COVID-19 through modulating levels of angiotensin-converting enzyme 2, the cell entry receptor for SARS-CoV2. We sought to assess the association between ACEi/ARB, biomarkers of inflammation, and outcomes in patients hospitalized for COVID-19. Methods and Results We leveraged the ISIC (International Study of Inflammation in COVID-19), identified patients admitted for symptomatic COVID-19 between February 1, 2020 and June 1, 2021 for COVID-19, and examined the association between in-hospital ACEi/ARB use and all-cause death, need for ventilation, and need for dialysis. We estimated the causal effect of ACEi/ARB on the composite outcomes using marginal structural models accounting for serial blood pressure and serum creatinine measures. Of 2044 patients in ISIC, 1686 patients met inclusion criteria, of whom 398 (23.6%) patients who were previously on ACEi/ARB received at least 1 dose during their hospitalization for COVID-19. There were 215 deaths, 407 patients requiring mechanical ventilation, and 124 patients who required dialysis during their hospitalization. Prior ACEi/ARB use was associated with lower levels of soluble urokinase plasminogen activator receptor and C-reactive protein. In multivariable analysis, in-hospital ACEi/ARB use was associated with a lower risk of the composite outcome of in-hospital death, mechanical ventilation, or dialysis (adjusted hazard ratio 0.49, 95% CI [0.36-0.65]). Conclusions In patients hospitalized for COVID-19, ACEi/ARB use was associated with lower levels of inflammation and lower risk of in-hospital outcomes. Clinical trials will define the role of ACEi/ARB in the treatment of COVID-19. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT04818866.
背景 使用血管紧张素转化酶抑制剂和血管紧张素受体阻滞剂(ACEi/ARB)被认为通过调节血管紧张素转化酶 2(SARS-CoV2 的细胞进入受体)的水平来影响 COVID-19。我们试图评估 ACEi/ARB、炎症生物标志物与 COVID-19 住院患者结局之间的关联。
方法和结果 我们利用了 ISIC(COVID-19 中的国际炎症研究),确定了 2020 年 2 月 1 日至 2021 年 6 月 1 日期间因 COVID-19 住院的有症状 COVID-19 患者,并检查了住院期间使用 ACEi/ARB 与全因死亡、需要通气和需要透析之间的关联。我们使用考虑连续血压和血清肌酐测量值的边际结构模型估计 ACEi/ARB 对复合结局的因果效应。在 ISIC 的 2044 名患者中,1686 名患者符合纳入标准,其中 398(23.6%)名之前使用 ACEi/ARB 的患者在 COVID-19 住院期间至少接受了 1 剂治疗。住院期间有 215 例死亡,407 例患者需要机械通气,124 例患者需要透析。先前使用 ACEi/ARB 与可溶性尿激酶型纤溶酶原激活物受体和 C 反应蛋白水平降低相关。多变量分析显示,住院期间使用 ACEi/ARB 与住院期间死亡、机械通气或透析的复合结局风险降低相关(调整后的危险比 0.49,95%CI [0.36-0.65])。
结论 在因 COVID-19 住院的患者中,ACEi/ARB 的使用与炎症水平降低和住院结局风险降低相关。临床试验将确定 ACEi/ARB 在 COVID-19 治疗中的作用。