National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.
Immunoregulation Section, Kidney Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Clin Infect Dis. 2023 Sep 18;77(6):816-826. doi: 10.1093/cid/ciad294.
Identifying individuals with a higher risk of developing severe coronavirus disease 2019 (COVID-19) outcomes will inform targeted and more intensive clinical monitoring and management. To date, there is mixed evidence regarding the impact of preexisting autoimmune disease (AID) diagnosis and/or immunosuppressant (IS) exposure on developing severe COVID-19 outcomes.
A retrospective cohort of adults diagnosed with COVID-19 was created in the National COVID Cohort Collaborative enclave. Two outcomes, life-threatening disease and hospitalization, were evaluated by using logistic regression models with and without adjustment for demographics and comorbidities.
Of the 2 453 799 adults diagnosed with COVID-19, 191 520 (7.81%) had a preexisting AID diagnosis and 278 095 (11.33%) had a preexisting IS exposure. Logistic regression models adjusted for demographics and comorbidities demonstrated that individuals with a preexisting AID (odds ratio [OR], 1.13; 95% confidence interval [CI]: 1.09-1.17; P < .001), IS exposure (OR, 1.27; 95% CI: 1.24-1.30; P < .001), or both (OR, 1.35; 95% CI: 1.29-1.40; P < .001) were more likely to have a life-threatening disease. These results were consistent when hospitalization was evaluated. A sensitivity analysis evaluating specific IS revealed that tumor necrosis factor inhibitors were protective against life-threatening disease (OR, 0.80; 95% CI: .66-.96; P = .017) and hospitalization (OR, 0.80; 95% CI: .73-.89; P < .001).
Patients with preexisting AID, IS exposure, or both are more likely to have a life-threatening disease or hospitalization. These patients may thus require tailored monitoring and preventative measures to minimize negative consequences of COVID-19.
识别出患有严重 2019 年冠状病毒病(COVID-19)结局风险较高的个体,将有助于进行有针对性的、更强化的临床监测和管理。迄今为止,关于预先存在的自身免疫性疾病(AID)诊断和/或免疫抑制剂(IS)暴露对发生严重 COVID-19 结局的影响,证据存在差异。
在国家 COVID 队列协作环境中创建了一个患有 COVID-19 的成年人回顾性队列。使用逻辑回归模型评估危及生命的疾病和住院这两个结局,并分别在调整和不调整人口统计学特征和合并症的情况下进行评估。
在 2453799 名被诊断患有 COVID-19 的成年人中,有 191520 人(7.81%)患有预先存在的 AID 诊断,有 278095 人(11.33%)有预先存在的 IS 暴露。调整人口统计学特征和合并症的逻辑回归模型显示,患有预先存在的 AID(比值比[OR],1.13;95%置信区间[CI]:1.09-1.17;P <.001)、IS 暴露(OR,1.27;95% CI:1.24-1.30;P <.001)或两者兼有(OR,1.35;95% CI:1.29-1.40;P <.001)的个体更有可能发生危及生命的疾病。当评估住院时,得到了一致的结果。一项评估特定 IS 的敏感性分析显示,肿瘤坏死因子抑制剂可预防危及生命的疾病(OR,0.80;95% CI:0.66-0.96;P =.017)和住院(OR,0.80;95% CI:0.73-0.89;P <.001)。
患有预先存在的 AID、IS 暴露或两者兼有的患者更有可能发生危及生命的疾病或住院。这些患者可能需要量身定制的监测和预防措施,以最大限度地减少 COVID-19 的负面后果。