Department of Gastroenterology, Harran University Hospital, Şanlıurfa, Turkey.
Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University, Stanford, CA, USA.
Hepatology. 2021 Jun;73(6):2099-2109. doi: 10.1002/hep.31797.
Data regarding outcome of COVID-19 in patients with autoimmune hepatitis (AIH) are lacking.
We performed a retrospective study on patients with AIH and COVID-19 from 34 centers in Europe and the Americas. We analyzed factors associated with severe COVID-19 outcomes, defined as the need for mechanical ventilation, intensive care admission, and/or death. The outcomes of patients with AIH were compared to a propensity score-matched cohort of patients without AIH but with chronic liver diseases (CLD) and COVID-19. The frequency and clinical significance of new-onset liver injury (alanine aminotransferase > 2 × the upper limit of normal) during COVID-19 was also evaluated. We included 110 patients with AIH (80% female) with a median age of 49 (range, 18-85) years at COVID-19 diagnosis. New-onset liver injury was observed in 37.1% (33/89) of the patients. Use of antivirals was associated with liver injury (P = 0.041; OR, 3.36; 95% CI, 1.05-10.78), while continued immunosuppression during COVID-19 was associated with a lower rate of liver injury (P = 0.009; OR, 0.26; 95% CI, 0.09-0.71). The rates of severe COVID-19 (15.5% versus 20.2%, P = 0.231) and all-cause mortality (10% versus 11.5%, P = 0.852) were not different between AIH and non-AIH CLD. Cirrhosis was an independent predictor of severe COVID-19 in patients with AIH (P < 0.001; OR, 17.46; 95% CI, 4.22-72.13). Continuation of immunosuppression or presence of liver injury during COVID-19 was not associated with severe COVID-19.
This international, multicenter study reveals that patients with AIH were not at risk for worse outcomes with COVID-19 than other causes of CLD. Cirrhosis was the strongest predictor for severe COVID-19 in patients with AIH. Maintenance of immunosuppression during COVID-19 was not associated with increased risk for severe COVID-19 but did lower the risk for new-onset liver injury during COVID-19.
目前缺乏关于 COVID-19 患者自身免疫性肝炎(AIH)结局的数据。
我们对来自欧洲和美洲 34 个中心的 AIH 和 COVID-19 患者进行了回顾性研究。我们分析了与 COVID-19 严重结局相关的因素,这些结局定义为需要机械通气、入住重症监护病房和/或死亡。将 AIH 患者的结局与未患有 AIH 但患有慢性肝脏疾病(CLD)和 COVID-19 的倾向评分匹配队列的患者进行比较。还评估了 COVID-19 期间新发肝损伤(丙氨酸氨基转移酶>2 倍正常值上限)的频率和临床意义。我们纳入了 110 名 AIH 患者(80%为女性),COVID-19 诊断时的中位年龄为 49(18-85)岁。89 名患者中有 37.1%(33/89)出现新发肝损伤。抗病毒药物的使用与肝损伤相关(P=0.041;比值比,3.36;95%置信区间,1.05-10.78),而 COVID-19 期间继续免疫抑制与较低的肝损伤发生率相关(P=0.009;比值比,0.26;95%置信区间,0.09-0.71)。AIH 和非 AIH CLD 的 COVID-19 严重结局(15.5%与 20.2%,P=0.231)和全因死亡率(10%与 11.5%,P=0.852)的发生率无差异。肝硬化是 AIH 患者 COVID-19 严重结局的独立预测因素(P<0.001;比值比,17.46;95%置信区间,4.22-72.13)。COVID-19 期间继续免疫抑制或存在肝损伤与 COVID-19 严重结局无关。
这项国际多中心研究表明,与其他 CLD 病因相比,AIH 患者 COVID-19 结局无恶化风险。肝硬化是 AIH 患者 COVID-19 严重结局的最强预测因素。COVID-19 期间维持免疫抑制与 COVID-19 严重结局风险增加无关,但可降低 COVID-19 期间新发肝损伤的风险。