Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Division of Gastroenterology Hepatology and Nutrition, The Hospital for Sick Children and the University of Toronto, Toronto, Ontario, Canada.
Liver Int. 2024 Aug;44(8):1797-1807. doi: 10.1111/liv.15943. Epub 2024 May 3.
Autoimmune hepatitis (AIH) in children presenting in acute liver failure (ALF) can be fatal and often requires liver transplantation (LTx). This individual patient data meta-analysis (IPD) aims to examine management and outcomes of this population, given the lack of large cohort studies on paediatric AIH first presenting as ALF (AIH-ALF).
A systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Review and Meta-Analyses of IPD statement using PubMed and Excerpta Medica dataBASE, and included English studies published between 2000 and 2020. The study included patients under 21 years of age, diagnosed with type 1 or 2 AIH and presenting with ALF. Data extracted included clinical and biochemical characteristics, interventions, and outcomes.
Three hundred and thirty eligible patients from 61 studies were identified, with an additional five patients from our institution. The majority were female (66.8%), with a median age of 10. Overall, 59.7% achieved native liver survival (NLS), 35% underwent LTx, and 5% died before LTx. The use of corticosteroids with non-steroid immunomodulators increased the likelihood of NLS by 2.5-fold compared to corticosteroids alone. AIH-1 was associated with 3.3-fold odds for NLS, compared to AIH-2. However, on multivariate analysis, only AIH-1 was identified as an independent predictor for NLS (OR 3.8 [95% CI 1.03-14.2], p = .04).
While corticosteroids and non-steroid immunomodulators treatment may offer enhanced probability of achieving NLS, treatment regimens for AIH-ALF may need to consider patient-specific factors, especially AIH type. This highlights the potential for NLS in AIH-ALF and suggest a need to identify biomarkers which predict the need for combination immunosuppression to avoid LTx.
儿童自身免疫性肝炎(AIH)并发急性肝衰竭(ALF)可能是致命的,往往需要进行肝移植(LTx)。本项个体患者数据荟萃分析(IPD)旨在针对这一人群的管理和结局进行研究,因为目前缺乏关于儿童 AIH 首次表现为 ALF(AIH-ALF)的大型队列研究。
根据个体患者数据荟萃分析的首选报告项目声明,使用 PubMed 和 Excerpta Medica dataBASE 进行了系统评价,纳入了 2000 年至 2020 年期间发表的英语研究。研究纳入了年龄在 21 岁以下、诊断为 1 型或 2 型 AIH 并伴有 ALF 的患者。提取的数据包括临床和生化特征、干预措施和结局。
从 61 项研究中确定了 330 名符合条件的患者,另有 5 名患者来自我们的机构。大多数患者为女性(66.8%),中位年龄为 10 岁。总体而言,59.7%的患者实现了自体肝存活(NLS),35%的患者接受了 LTx,5%的患者在接受 LTx 前死亡。与单独使用皮质类固醇相比,皮质类固醇联合非甾体免疫调节剂可使 NLS 的可能性增加 2.5 倍。与 AIH-2 相比,AIH-1 使 NLS 的可能性增加了 3.3 倍。然而,多变量分析显示,只有 AIH-1 是 NLS 的独立预测因素(OR 3.8 [95%CI 1.03-14.2],p=0.04)。
虽然皮质类固醇和非甾体免疫调节剂治疗可能会提高实现 NLS 的可能性,但 AIH-ALF 的治疗方案可能需要考虑患者的具体因素,尤其是 AIH 类型。这突出了 AIH-ALF 中实现 NLS 的潜力,并表明需要确定预测需要联合免疫抑制以避免 LTx 的生物标志物。