AP-HP.Centre-Université de Paris, Hôpital Corentin-Celton, Département Médico-Universitaire de Psychiatrie et Addictologie, 92130, Issy-les-Moulineaux, France.
INSERM, Institut de Psychiatrie et Neurosciences de Paris, UMR_S1266, Paris, France.
Mol Psychiatry. 2021 Sep;26(9):5199-5212. doi: 10.1038/s41380-021-01021-4. Epub 2021 Feb 4.
A prior meta-analysis showed that antidepressant use in major depressive disorder was associated with reduced plasma levels of several pro-inflammatory mediators, which have been associated with severe COVID-19. Recent studies also suggest that several antidepressants may inhibit acid sphingomyelinase activity, which may prevent the infection of epithelial cells with SARS-CoV-2, and that the SSRI fluoxetine may exert in-vitro antiviral effects on SARS-CoV-2. We examined the potential usefulness of antidepressant use in patients hospitalized for COVID-19 in an observational multicenter retrospective cohort study conducted at AP-HP Greater Paris University hospitals. Of 7230 adults hospitalized for COVID-19, 345 patients (4.8%) received an antidepressant within 48 h of hospital admission. The primary endpoint was a composite of intubation or death. We compared this endpoint between patients who received antidepressants and those who did not in time-to-event analyses adjusted for patient characteristics, clinical and biological markers of disease severity, and other psychotropic medications. The primary analysis was a multivariable Cox model with inverse probability weighting. This analysis showed a significant association between antidepressant use and reduced risk of intubation or death (HR, 0.56; 95% CI, 0.43-0.73, p < 0.001). This association remained significant in multiple sensitivity analyses. Exploratory analyses suggest that this association was also significant for SSRI and non-SSRI antidepressants, and for fluoxetine, paroxetine, escitalopram, venlafaxine, and mirtazapine (all p < 0.05). These results suggest that antidepressant use could be associated with lower risk of death or intubation in patients hospitalized for COVID-19. Double-blind controlled randomized clinical trials of antidepressant medications for COVID-19 are needed.
一项先前的荟萃分析表明,在重度抑郁症中使用抗抑郁药与几种促炎介质的血浆水平降低有关,而这些介质与严重的 COVID-19 有关。最近的研究还表明,几种抗抑郁药可能抑制酸性鞘磷脂酶的活性,从而可能阻止 SARS-CoV-2 感染上皮细胞,并且 SSRI 氟西汀可能对 SARS-CoV-2 发挥体外抗病毒作用。我们在 AP-HP 大巴黎大学医院进行的一项观察性多中心回顾性队列研究中,研究了 COVID-19 住院患者使用抗抑郁药的潜在作用。在 7230 名因 COVID-19 住院的成年人中,有 345 名(4.8%)在入院后 48 小时内接受了抗抑郁药。主要终点是插管或死亡的复合终点。我们在时间事件分析中比较了接受抗抑郁药和未及时接受抗抑郁药的患者的这一终点,该分析调整了患者特征、疾病严重程度的临床和生物学标志物以及其他精神药物。主要分析是使用逆概率加权的多变量 Cox 模型进行的。该分析显示,使用抗抑郁药与插管或死亡风险降低显著相关(HR,0.56;95%CI,0.43-0.73,p<0.001)。在多次敏感性分析中,该关联仍然显著。探索性分析表明,这种关联对于 SSRI 和非 SSRI 抗抑郁药以及氟西汀、帕罗西汀、依地普仑、文拉法辛和米氮平也具有显著意义(均 p<0.05)。这些结果表明,在 COVID-19 住院患者中,使用抗抑郁药可能与较低的死亡或插管风险相关。需要进行 COVID-19 抗抑郁药物的双盲对照随机临床试验。