Assistance Publique-Hopitaux de Paris, DMU Psychiatrie et Addictologie, Hôpital Corentin-Celton, Institut de Psychiatrie et Neurosciences de Paris (IPNP), INSERM, UMR_S1266, Université de Paris, Paris, France.
Department of Psychobiology and Behavioural Sciences Methods, Faculty of Psychology, Universidad Complutense de Madrid, Pozuelo de Alarcón, Madrid, Spain.
Clin Pharmacol Ther. 2021 Dec;110(6):1498-1511. doi: 10.1002/cpt.2317. Epub 2021 Jul 2.
Several medications commonly used for a number of medical conditions share a property of functional inhibition of acid sphingomyelinase (ASM), or FIASMA. Preclinical and clinical evidence suggest that the ASM/ceramide system may be central to severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) infection. We examined the potential usefulness of FIASMA use among patients hospitalized for severe coronavirus disease 2019 (COVID-19) in an observational multicenter study conducted at Greater Paris University hospitals. Of 2,846 adult patients hospitalized for severe COVID-19, 277 (9.7%) were taking an FIASMA medication at the time of their hospital admission. The primary end point was a composite of intubation and/or death. We compared this end point between patients taking vs. not taking an FIASMA medication in time-to-event analyses adjusted for sociodemographic characteristics and medical comorbidities. The primary analysis was a Cox regression model with inverse probability weighting (IPW). Over a mean follow-up of 9.2 days (SD = 12.5), the primary end point occurred in 104 patients (37.5%) receiving an FIASMA medication, and 1,060 patients (41.4%) who did not. Despite being significantly and substantially associated with older age and greater medical severity, FIASMA medication use was significantly associated with reduced likelihood of intubation or death in both crude (hazard ratio (HR) = 0.71, 95% confidence interval (CI) = 0.58-0.87, P < 0.001) and primary IPW (HR = 0.58, 95%CI = 0.46-0.72, P < 0.001) analyses. This association remained significant in multiple sensitivity analyses and was not specific to one particular FIASMA class or medication. These results show the potential importance of the ASM/ceramide system in COVID-19 and support the continuation of FIASMA medications in these patients. Double-blind controlled randomized clinical trials of these medications for COVID-19 are needed.
几种常用于多种医疗状况的药物具有抑制酸性鞘磷脂酶(ASM)或 FIASMA 的功能。临床前和临床证据表明,ASM/神经酰胺系统可能是严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染的核心。我们在巴黎大区大学附属医院进行的一项观察性多中心研究中,研究了 FIASMA 在因严重 2019 年冠状病毒病(COVID-19)住院的患者中的潜在用途。在 2846 名因严重 COVID-19 住院的成年患者中,有 277 名(9.7%)在入院时正在服用 FIASMA 药物。主要终点是插管和/或死亡的复合终点。我们在时间事件分析中比较了接受和未接受 FIASMA 药物治疗的患者的主要终点,该分析调整了社会人口统计学特征和合并症。主要分析是使用逆概率加权(IPW)的 Cox 回归模型。在平均 9.2 天(标准差=12.5)的随访期间,接受 FIASMA 药物治疗的患者中有 104 人(37.5%)发生了主要终点,而未接受 FIASMA 药物治疗的患者中有 1060 人(41.4%)发生了主要终点。尽管 FIASMA 药物的使用与年龄较大和医疗严重程度显著相关,但在未校正(风险比(HR)=0.71,95%置信区间(CI)=0.58-0.87,P<0.001)和主要 IPW(HR=0.58,95%CI=0.46-0.72,P<0.001)分析中,FIASMA 药物的使用与插管或死亡的可能性降低显著相关。在多项敏感性分析中,这种关联仍然显著,并且不限于特定的 FIASMA 类别或药物。这些结果表明 ASM/神经酰胺系统在 COVID-19 中的重要性,并支持继续在这些患者中使用 FIASMA 药物。需要针对这些药物治疗 COVID-19 的双盲对照随机临床试验。