Cryptogenic chronic hepatitis: looking for an ideal diagnostic algorithm

G. G. L. Cançado, Aline Coelho Rocha Candolo, M. J. Nardelli, P. M. Zitelli, D. Mazo, C. Oliveira, M. Cunha-Silva, R. D. Greca, R. C. Araújo, Amanda Sacha Paulino Tolentino Alustau, C. Couto, Gabriel Rezende de Lima Roque, A. Farias, F. Carrilho, M. Pessoa
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Abstract

Cryptogenic chronic hepatitis is a growing cause of liver transplants, affecting 5%–15% of patients with chronic liver diseases. This study aimed to identify underlying causes of cryptogenic liver disease in a Brazilian cohort and propose a new diagnostic algorithm, including investigation for metabolic-dysfunction-associated fatty liver disease (MAFLD) and lysosomal acid lipase deficiency (LAL-D).A retrospective analysis was conducted on 326 patients with presumed cryptogenic hepatitis.Using Czaja’s algorithm, non-alcoholic fatty liver disease was diagnosed in 21.3% of patients, while alpha-1 antitrypsin deficiency, alcoholic liver disease, autoimmune hepatitis, hemochromatosis, biliary-related hepatitis, viral hepatitis, Budd–Chiari syndrome, glycogenosis, drug-induced liver injury, and Wilson’s disease were diagnosed in smaller proportions (< 3.5% each). LAL-D was found in 1% of patients, and 53.6% of patients remained with cryptogenic hepatitis. The etiology of the liver disease in a subset of patients undergoing liver transplantation was updated post hoc based on explant histology, and non-alcoholic steatohepatitis was found in 52.5% of patients. By incorporating the concept of MAFLD, the new algorithm could diagnose 49.1% of patients, reducing the number of individuals without an etiological diagnosis by 11.4%.One-third of patients with initially presumed cryptogenic liver disease were diagnosed with MAFLD. LAL-D should be considered in patients with chronic liver disease of unknown etiology. The updated diagnostic algorithm proposed in this study could improve diagnostic accuracy and aid in the management of patients with cryptogenic hepatitis.
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隐源性慢性肝炎:寻找理想的诊断算法
隐源性慢性肝炎是肝移植的一个日益严重的原因,影响5%-15%的慢性肝病患者。本研究旨在确定巴西队列中隐源性肝病的潜在原因,并提出一种新的诊断算法,包括代谢功能障碍相关脂肪肝(MAFLD)和溶酶体酸性脂肪酶缺乏症(LAL-D)的调查。对326例推测为隐源性肝炎的患者进行了回顾性分析。使用Czaja算法,21.3%的患者被诊断为非酒精性脂肪性肝病,而α-1抗胰蛋白酶缺乏症、酒精性肝病、自身免疫性肝炎、血色素沉着症、胆道相关肝炎、病毒性肝炎、布-加综合征、糖原生成病、药物性肝损伤和Wilson病的诊断比例较小(各<3.5%)。在1%的患者中发现LAL-D,53.6%的患者仍患有隐源性肝炎。根据外植体组织学,对接受肝移植的一部分患者的肝病病因进行了事后更新,52.5%的患者发现了非酒精性脂肪性肝炎。通过引入MAFLD的概念,新算法可以诊断49.1%的患者,将没有病因诊断的患者数量减少11.4%。三分之一的最初推测为隐源性肝病的患者被诊断为MAFLD。病因不明的慢性肝病患者应考虑LAL-D。本研究中提出的更新诊断算法可以提高诊断准确性,并有助于管理隐源性肝炎患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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