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Efficacy and Safety of Immunosuppressive Therapy for PBC-AIH Overlap Syndrome Accompanied by Decompensated Cirrhosis: A Real-World Study

机译:免疫抑制治疗PBC-AIH重叠综合征的疗效和安全性伴随二元肝硬化:真实研究

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摘要

Autoimmune liver disease (AILD) comprises a group of immune-mediated liver diseases that include autoimmune hepatitis (AIH), primary biliary cirrhosis (PBC), and primary sclerosing cholangitis (PSC) [1]. The occurrence of overlapping syndromes at different disease stages (so-called overlap syndromes) is not rare, with PBC-AIH overlap syndrome being the most common [2]. The prevalence of PBC-AIH overlap syndrome is approximately 8-10% in adult patients with either PBC or AIH [3, 4], and this low incidence contributes to imprecise diagnostic criteria; furthermore, no standard therapy is currently available. According to the most recent guidelines based on the results of small studies, a combination of ursodeoxycholic acid (UDCA) and immunosuppressants is often recommended for PBC-AIH in clinical practice [5-7].
机译:自身免疫性肝病(AILD)包括一组免疫介导的肝病,包括自身免疫性肝炎(AIH),原代胆汁肝硬化(PBC)和初级硬化胆管炎(PSC)[1]。 不同疾病阶段(所谓的重叠综合征)的重叠综合征的发生并不罕见,PBC-AIH重叠综合征是最常见的[2]。 PBC-AIH重叠综合征的患病率为PBC或AIH [3,4]的成年患者中约为8-10%,这种低发病率有助于不精确的诊断标准; 此外,目前没有标准治疗。 根据基于小型研究结果的最新指南,通常建议在临床实践中用于PBC-AIH [5-7]的PBC-AIH组合[5-7]。

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