School of Public Health, University of California, Berkeley, Berkeley, CA, USA.
University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
BMC Med. 2024 Oct 8;22(1):445. doi: 10.1186/s12916-024-03655-x.
Long COVID, also known as post-acute sequelae of COVID-19 (PASC), is a poorly understood condition with symptoms across a range of biological domains that often have debilitating consequences. Some have recently suggested that lingering SARS-CoV-2 virus particles in the gut may impede serotonin production and that low serotonin may drive many Long COVID symptoms across a range of biological systems. Therefore, selective serotonin reuptake inhibitors (SSRIs), which increase synaptic serotonin availability, may be used to prevent or treat Long COVID. SSRIs are commonly prescribed for depression, therefore restricting a study sample to only include patients with depression can reduce the concern of confounding by indication.
In an observational sample of electronic health records from patients in the National COVID Cohort Collaborative (N3C) with a COVID-19 diagnosis between September 1, 2021, and December 1, 2022, and a comorbid depressive disorder, the leading indication for SSRI use, we evaluated the relationship between SSRI use during acute COVID-19 and subsequent 12-month risk of Long COVID (defined by ICD-10 code U09.9). We defined SSRI use as a prescription for SSRI medication beginning at least 30 days before acute COVID-19 and not ending before SARS-CoV-2 infection. To minimize bias, we estimated relationships using nonparametric targeted maximum likelihood estimation to aggressively adjust for high-dimensional covariates.
We analyzed a sample (n = 302,626) of patients with a diagnosis of a depressive condition before COVID-19 diagnosis, where 100,803 (33%) were using an SSRI. We found that SSRI users had a significantly lower risk of Long COVID compared to nonusers (adjusted causal relative risk 0.92, 95% CI (0.86, 0.99)) and we found a similar relationship comparing new SSRI users (first SSRI prescription 1 to 4 months before acute COVID-19 with no prior history of SSRI use) to nonusers (adjusted causal relative risk 0.89, 95% CI (0.80, 0.98)).
These findings suggest that SSRI use during acute COVID-19 may be protective against Long COVID, supporting the hypothesis that serotonin may be a key mechanistic biomarker of Long COVID.
长新冠,也被称为 COVID-19 后急性后遗症(PASC),是一种人们尚未充分了解的病症,其症状涉及一系列生物学领域,且常常带来使人虚弱的后果。最近有人提出,肠道中持续存在的 SARS-CoV-2 病毒颗粒可能会阻碍血清素的产生,而低血清素可能会驱动一系列生物学系统中的长新冠症状。因此,选择性 5-羟色胺再摄取抑制剂(SSRIs),即增加突触血清素可用性的药物,可能被用于预防或治疗长新冠。SSRIs 常用于治疗抑郁症,因此,将研究样本仅限于仅患有抑郁症的患者,可以减少因指示混淆带来的担忧。
在国家 COVID 队列协作组织(N3C)的电子健康记录的观察性样本中,患者在 2021 年 9 月 1 日至 2022 年 12 月 1 日期间被诊断患有 COVID-19,且同时患有合并症抑郁症,这是 SSRIs 使用的主要指征,我们评估了急性 COVID-19 期间使用 SSRIs 与随后 12 个月长新冠(由 ICD-10 代码 U09.9 定义)的风险之间的关系。我们将 SSRIs 使用定义为至少在急性 COVID-19 之前 30 天开始并在 SARS-CoV-2 感染之前未结束的 SSRIs 药物处方。为了最大限度地减少偏差,我们使用非参数靶向最大似然估计来估计关系,以积极调整高维协变量。
我们分析了一个在 COVID-19 诊断之前被诊断患有抑郁症状的患者样本(n=302626),其中 100803 名(33%)患者正在使用 SSRIs。我们发现,与非使用者相比,SSRIs 使用者患长新冠的风险显著降低(调整后的因果相对风险 0.92,95%CI(0.86,0.99)),我们发现了一个类似的关系,比较新的 SSRIs 使用者(急性 COVID-19 前 1 至 4 个月首次使用 SSRIs,且无 SSRIs 使用史)与非使用者(调整后的因果相对风险 0.89,95%CI(0.80,0.98))。
这些发现表明,急性 COVID-19 期间使用 SSRIs 可能对长新冠有保护作用,支持了血清素可能是长新冠关键机制生物标志物的假设。