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. 2025 Apr 8:S1542-3565(25)00249-6.
doi: 10.1016/j.cgh.2025.02.010. Online ahead of print.

Hepatic Encephalopathy and MELD-Na Predict Treatment Benefit in Autoimmune Hepatitis-related Decompensated Cirrhosis

Pinelopi Arvaniti  1 Sergio Rodríguez-Tajes  2 Marlene Padilla  3 Ignasi Olivas  2 Ezequiel Mauro  4 Cautar El Maimouni  4 Ellina Lytvyak  5 Xavier Verhelst  6 Bastian Engel  7 Richard Taubert  7 Sara Lorente-Pérez  8 Isabel Conde  9 Mar Riveiro-Barciela  10 Juan-Carlos Ruiz-Cobo  10 Carmen Álvarez-Navascués  11 Magdalena Salcedo  12 Judith Gómez  13 Maciej K Janik  14 Beatriz Mateos  15 Cumali Efe  16 Alessandro Granito  17 Elton Dajti  18 Francesco Azzaroli  18 Diana Horta  19 Carmen Vila  20 Inmaculada Castello  21 Indhira Pérez-Medrano  22 Ana Arencibia  23 Alessio Gerussi  24 Tony Bruns  25 Francesca Colaprieto  26 Ana Lleo  26 Natalie Van den Ende  27 Jef Verbeek  27 Álvaro Díaz-González  28 Rosa Ma Morillas  29 Maria Torner-Simó  29 Vanesa Bernal  30 Eva-Maria Fernández  30 Tom J G Gevers  31 Benedetta Terziroli Beretta-Piccoli  32 Elena Gómez  33 Paqui Cuenca  34 Ynte S de Boer  35 Nanda Kerkar  36 David N Assis  37 Rodrigo Liberal  38 Joost P H Drenth  39 Michele M Tana  40 Marcial Sebode  41 Ida Schregel  41 Christoph Schramm  42 Ansgar W Lohse  41 Aldo J Montano-Loza  5 Kalliopi Zachou  43 Alejandra Villamil  3 George N Dalekos  43 María-Carlota Londoño  44 International Autoimmune Hepatitis Group (IAIHG)European Reference Network on Hepatological Diseases (ENR RARE-LIVER)Spanish Registry for Autoimmune and Cholestatic Diseases (ColHai) Registry
Affiliations

Hepatic Encephalopathy and MELD-Na Predict Treatment Benefit in Autoimmune Hepatitis-related Decompensated Cirrhosis

Pinelopi Arvaniti et al. Clin Gastroenterol Hepatol. .

Abstract

Background & aims: Management of patients with autoimmune hepatitis (AIH)-related decompensated cirrhosis is challenging because of the risk of treatment-related complications and lack of clinical recommendations. We investigated the predictive factors for treatment benefit in AIH-related decompensated cirrhosis at diagnosis and developed an algorithm to guide treatment decisions in clinical practice.

Methods: This retrospective, international, multicenter study included 232 patients with histologically confirmed AIH-related decompensated cirrhosis at diagnosis. The sub-hazard ratio (SHR) of mortality was determined by competing risk analysis, considering liver transplantation (LT) as competing event. A decision tree analysis was used to develop a treatment algorithm.

Results: At diagnosis, 89% of patients had ascites, and 41% had overt hepatic encephalopathy (OHE). Treated patients (n = 214; 92%) had higher aminotransferases, bilirubin, and modified hepatic activity index. The SHR of mortality was lower in treated patients (0.438; 95% confidence interval [CI], 0.196-0.981; P = .045). Patients without OHE grade 3/4 and Model for End-Stage Liver Disease-Sodium (MELD-Na) ≤28 at diagnosis were more likely to benefit from treatment. In these patients, a decline in MELD-Na ≥11 after 4 weeks of treatment had a 100% negative predictive value for death/LT. Forty-nine percent of treated patients recompensated during follow-up. Twenty percent of patients had to discontinue treatment, 65% during the first 4 weeks, and only 4% due to infectious complications. OHE ≥grade 2 and MELD-Na at diagnosis predicted the need for treatment discontinuation.

Conclusions: Immunosuppression is beneficial in patients with AIH-related decompensated cirrhosis and active disease. OHE and MELD-Na at diagnosis, along with a decline in MELD-Na at 4 weeks of treatment, are the most important determinants of outcome and can guide treatment decisions.

Keywords: Autoimmune Hepatitis; Decompensated Cirrhosis; Liver Transplant-free Survival; Recompensation.

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