Yu Chen, Haoyu Wen, You Li, Weituo Zhang, Tianyu Mao, Chenyi Jiang, Huayang Zhang, Yujie Zhou, Xiting Pu, Bo Li, Jun Zhang, Li Yan, Min Lian, Li Sheng, Canjie Guo, Qixia Wang, Qi Miao, Jing Hua, Hai Li, Ruqi Tang, Christopher L Bowlus, M Eric Gershwin, Zhengrui You, Xiao Xiao, Xiong Ma
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引用次数: 0
Abstract
Background & aims: In this study, we aimed to evaluate the incidence, predictors, and prognostic significance of recompensation in autoimmune hepatitis (AIH)-related decompensated cirrhosis following immunosuppressive therapy (IST).
Methods: We retrospectively analyzed patients with AIH at first decompensation. Recompensation, defined using modified Baveno VII criteria, required clinical resolution (≥12 months without ascites, variceal bleeding, or hepatic encephalopathy, with liver function restored to Child-Pugh A) along with aetiological suppression (complete biochemical response under IST). Predictors of recompensation were identified using multivariate regression, and survival outcomes were compared among compensated, recompensated, and non-recompensated groups.
Results: A total of 258 patients with AIH-related decompensated cirrhosis were included (median follow-up: 47 months, IQR 28-75). Clinical resolution was achieved by 124 patients (48.1%), while 68 patients (30.9% of 220 treated with IST) met criteria for recompensation. Predictors of recompensation included ascites as the only complication (hazard ratio [HR] 14.40, 95% CI 4.17-49.64, p <0.001), lower IgG levels (HR 0.90, 95% CI 0.89-0.96, p <0.001), higher bilirubin levels (HR 1.04, 95% CI 1.00-1.08, p = 0.030), and higher platelet counts (HR 1.01, 95% CI 1.00-1.01, p = 0.039). Patients achieving recompensation experienced a significantly reduced risk of liver transplantation or death (HR 0.07, 95% CI 0.01-0.50, p = 0.009), with survival outcomes comparable to those of compensated patients.
Conclusions: Recompensation was achieved in approximately one-third of patients with AIH-related decompensated cirrhosis undergoing IST, leading to markedly improved transplant-free survival. Predictors of recompensation included having ascites as the sole complication, lower IgG levels, higher bilirubin levels, and higher platelet counts.
Impact and implications: The predictors and long-term prognostic implications of recompensation in patients with autoimmune hepatitis (AIH)-related decompensated cirrhosis remain unclear. This study demonstrates that recompensation is achievable in patients with AIH-related decompensated cirrhosis and is associated with significant long-term benefits, including improved survival and reduced transplantation needs. We identified ascites (as the sole decompensating event), lower IgG levels, higher bilirubin levels and higher platelet counts as independent predictors of recompensation. These findings can be used by clinicians to identify the patients most likely to benefit from immunosuppressive therapy.
背景与目的:在本研究中,我们旨在评估免疫抑制治疗(IST)后自身免疫性肝炎(AIH)相关失代偿肝硬化再代偿的发生率、预测因素和预后意义。方法:回顾性分析首次失代偿的AIH患者。再补偿,使用改良的Baveno VII标准定义,需要临床缓解(≥12个月无腹水、静脉曲张出血或肝性脑病,肝功能恢复到Child-Pugh A)以及病因抑制(IST下完全生化反应)。使用多变量回归确定再补偿的预测因素,并比较补偿组、补偿组和未补偿组的生存结果。结果:共纳入258例aih相关失代偿性肝硬化患者(中位随访:47个月,IQR 28-75)。124例患者(48.1%)达到临床缓解,而68例患者(220例IST治疗中的30.9%)符合再补偿标准。再代偿的预测因素包括腹水是唯一的并发症(危险比[HR] 14.40, 95% CI 4.17-49.64, p 0.001)、较低的IgG水平(危险比0.90,95% CI 0.89-0.96, p 0.001)、较高的胆红素水平(危险比1.04,95% CI 1.00-1.08, p = 0.030)和较高的血小板计数(危险比1.01,95% CI 1.00-1.01, p = 0.039)。获得再补偿的患者肝移植或死亡风险显著降低(HR 0.07, 95% CI 0.01-0.50, p = 0.009),生存结果与获得补偿的患者相当。结论:大约三分之一的aih相关失代偿肝硬化患者接受了IST治疗,获得了再代偿,显著提高了无移植生存期。再代偿的预测因素包括腹水是唯一的并发症,较低的IgG水平,较高的胆红素水平和较高的血小板计数。影响和意义:自身免疫性肝炎(AIH)相关失代偿性肝硬化患者再代偿的预测因素和长期预后意义尚不清楚。该研究表明,aih相关失代偿性肝硬化患者可以实现再代偿,并具有显著的长期益处,包括提高生存率和减少移植需求。我们确定腹水(作为唯一的失代偿事件),较低的IgG水平,较高的胆红素水平和较高的血小板计数作为再代偿的独立预测因子。这些发现可以被临床医生用来确定最有可能从免疫抑制治疗中获益的患者。
期刊介绍:
JHEP Reports is an open access journal that is affiliated with the European Association for the Study of the Liver (EASL). It serves as a companion journal to the highly respected Journal of Hepatology.
The primary objective of JHEP Reports is to publish original papers and reviews that contribute to the advancement of knowledge in the field of liver diseases. The journal covers a wide range of topics, including basic, translational, and clinical research. It also focuses on global issues in hepatology, with particular emphasis on areas such as clinical trials, novel diagnostics, precision medicine and therapeutics, cancer research, cellular and molecular studies, artificial intelligence, microbiome research, epidemiology, and cutting-edge technologies.
In summary, JHEP Reports is dedicated to promoting scientific discoveries and innovations in liver diseases through the publication of high-quality research papers and reviews covering various aspects of hepatology.