Cousins Henry C, Altman Russ B
Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA, USA.
Department of Bioengineering, Stanford University, Stanford, CA, USA.
medRxiv. 2023 Mar 2:2023.02.28.23286515. doi: 10.1101/2023.02.28.23286515.
Spironolactone has been proposed as a potential modulator of SARS-CoV-2 cellular entry. We aimed to measure the effect of spironolactone use on the risk of adverse outcomes following COVID-19 hospitalization.
We performed a retrospective cohort study of COVID-19 outcomes for patients with or without exposure to spironolactone, using population-scale claims data from the Komodo Healthcare Map. We identified all patients with a hospital admission for COVID-19 in the study window, defining treatment status based on spironolactone prescription orders. The primary outcomes were progression to respiratory ventilation or mortality during the hospitalization. Odds ratios (OR) were estimated following either 1:1 propensity score matching (PSM) or multivariable regression. Subgroup analysis was performed based on age, gender, body mass index (BMI), and dominant SARS-CoV-2 variant.
Among 898,303 eligible patients with a COVID-19-related hospitalization, 16,324 patients (1.8%) had a spironolactone prescription prior to hospitalization. 59,937 patients (6.7%) met the ventilation endpoint, and 26,515 patients (3.0%) met the mortality endpoint. Spironolactone use was associated with a significant reduction in odds of both ventilation (OR 0.82; 95% CI: 0.75-0.88; p < 0.001) and mortality (OR 0.88; 95% CI: 0.78-0.99; p = 0.033) in the PSM analysis, supported by the regression analysis. Spironolactone use was associated with significantly reduced odds of ventilation for all age groups, men, women, and non-obese patients, with the greatest protective effects in younger patients, men, and non-obese patients.
Spironolactone use was associated with a protective effect against ventilation and mortality following COVID-19 infection, amounting to up to 64% of the protective effect of vaccination against ventilation and consistent with an androgen-dependent mechanism. The findings warrant initiation of large-scale randomized controlled trials to establish a potential therapeutic role for spironolactone in COVID-19 patients.
螺内酯已被提出作为严重急性呼吸综合征冠状病毒2(SARS-CoV-2)细胞进入的潜在调节剂。我们旨在衡量使用螺内酯对新型冠状病毒肺炎(COVID-19)住院后不良结局风险的影响。
我们利用来自科莫多医疗地图的大规模索赔数据,对暴露于或未暴露于螺内酯的患者的COVID-19结局进行了一项回顾性队列研究。我们确定了研究窗口内所有因COVID-19住院的患者,并根据螺内酯处方订单确定治疗状态。主要结局是住院期间进展为呼吸通气或死亡。在1:1倾向评分匹配(PSM)或多变量回归后估计比值比(OR)。根据年龄、性别、体重指数(BMI)和主要的SARS-CoV-2变体进行亚组分析。
在898303例符合条件的与COVID-19相关住院患者中,16324例患者(1.8%)在住院前有螺内酯处方。59937例患者(6.7%)达到通气终点,26515例患者(3.0%)达到死亡终点。在PSM分析中,使用螺内酯与通气(OR 0.82;95%CI:0.75-0.88;p<0.001)和死亡(OR 0.88;95%CI:0.78-0.99;p = 0.033)的几率显著降低相关,回归分析也支持这一结果。使用螺内酯与所有年龄组、男性、女性和非肥胖患者通气几率的显著降低相关,在年轻患者、男性和非肥胖患者中保护作用最大。
使用螺内酯与COVID-19感染后对通气和死亡的保护作用相关,高达疫苗接种对通气保护作用的64%,且与雄激素依赖机制一致。这些发现值得开展大规模随机对照试验,以确定螺内酯在COVID-19患者中的潜在治疗作用。