Suppr超能文献

三级医疗机构自身免疫性肝病的谱及真实世界治疗经验

Spectrum of Autoimmune Liver Disease and Real-World Treatment Experience from a Tertiary Care Hospital.

作者信息

Taneja Sunil, Mehtani Rohit, De Arka, Mitra Suvradeep, Rathi Sahaj, Verma Nipun, Premkumar Madhumita, Minz Ranjana, Duseja Ajay, Das Ashim, Singh Virendra, Dhiman Radha K, Chawla Yogesh K

机构信息

Department of Hepatology, Post Graduate Institute of Medical Education & Research, Chandigarh, India.

Department of Immunopathology, Post Graduate Institute of Medical Education & Research, Chandigarh, India.

出版信息

J Clin Exp Hepatol. 2023 Mar-Apr;13(2):241-251. doi: 10.1016/j.jceh.2022.11.002. Epub 2022 Nov 10.

Abstract

BACKGROUND AND AIMS

Autoimmune liver disease (AILD) comprises of autoimmune hepatitis (AIH), primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC) with a spectrum of overlap amongst the three. We analyzed the spectrum and treatment outcomes of patients with AILD presenting to a tertiary care center in India.

METHODS

A retrospective analysis of AILD patients from June 2008 to April 2021 was performed. The diagnosis was based on clinical, biochemical, imaging, serological, and histological characteristics. Eligible patients received treatment depending on the disease stage. Biochemical response to treatment was defined as normalization of AST, ALT, bilirubin, and immunoglobulin G levels at 6 months in AIH, normalization of total bilirubin and/or albumin at 1 year in PBC and decrease in alkaline phosphatase (ALP) levels by 40% in PSC.

RESULTS

Two hundred seventy-five patients were analyzed. AIH (58.54%) was most common, followed by an overlap of AIH-PBC (24%) and AIH-PSC (6.54%), PSC (6.18%), and PBC (4.72%). Most patients presented in 3rd or 4th decade, except PBC which occurred predominantly in 5th decade. The majority of patients were females (72.72%). Jaundice was the most common presentation seen in 60% of patients. Cirrhosis was present in 57.47% of patients. Patients with overlap had more pruritus (54.76 vs 6.83%), fatigue (63.1% vs 49.7%), hepatomegaly (52.4% vs 25.5%), and higher ALP (80.9% vs 37.7%) than patients with AIH alone. Acute presentation was seen in 33 patients (13.5%) with most having AIH flare. Five patients had acute liver failure (ALF) and 9 had acute-on-chronic liver failure (ACLF). ALF was associated with 80% mortality while 55.56% of patients with ACLF had a complete biochemical response to immunosuppression. Among patients with AIH and/or overlap who received immunosuppression, a complete biochemical response to immunosuppression was seen in 60.69% of patients. High ALT (OR 1.001 [1.000-1.003],  = 0.034), high albumin (OR 1.91 [1.05-3.48],  = 0.034) and low fibrosis on biopsy (OR 0.54 [0.33-0.91],  = 0.020) predicted complete response.

CONCLUSION

AIH is the most common AILD followed by overlap syndromes, PSC and PBC in our cohort. Biochemical response to immunosuppression is seen in 60% of patients with AIH & low fibrosis score on histopathology predicts a complete response.

摘要

背景与目的

自身免疫性肝病(AILD)包括自身免疫性肝炎(AIH)、原发性胆汁性胆管炎(PBC)和原发性硬化性胆管炎(PSC),这三种疾病之间存在一系列重叠情况。我们分析了在印度一家三级医疗中心就诊的AILD患者的情况及治疗结果。

方法

对2008年6月至2021年4月期间的AILD患者进行回顾性分析。诊断基于临床、生化、影像学、血清学和组织学特征。符合条件的患者根据疾病阶段接受治疗。治疗的生化反应在AIH中定义为6个月时AST、ALT、胆红素和免疫球蛋白G水平恢复正常,在PBC中定义为1年时总胆红素和/或白蛋白恢复正常,在PSC中定义为碱性磷酸酶(ALP)水平降低40%。

结果

共分析了275例患者。AIH最为常见(58.54%),其次是AIH - PBC重叠(24%)和AIH - PSC重叠(6.54%)、PSC(6.18%)和PBC(4.72%)。大多数患者在第三或第四个十年发病,但PBC主要发生在第五个十年。大多数患者为女性(72.72%)。黄疸是最常见的表现,60%的患者出现黄疸。57.47%的患者存在肝硬化。与单纯AIH患者相比,重叠综合征患者有更多瘙痒(54.76%对6.83%)、疲劳(63.1%对49.7%)、肝肿大(52.4%对25.5%)以及更高的ALP水平(80.9%对37.7%)。33例患者(13.5%)呈急性表现,多数为AIH发作。5例患者发生急性肝衰竭(ALF),9例患者发生慢加急性肝衰竭(ACLF)。ALF的死亡率为80%,而55.56%的ACLF患者对免疫抑制有完全生化反应。在接受免疫抑制的AIH和/或重叠综合征患者中,60.69%的患者对免疫抑制有完全生化反应。高ALT(OR 1.001 [1.000 - 1.003],P = 0.034)、高白蛋白(OR 1.91 [1.05 - 3.48],P = 0.034)以及活检时低纤维化(OR 0.54 [0.33 - 0.91],P = 0.020)预示着完全反应。

结论

在我们的队列中,AIH是最常见的AILD,其次是重叠综合征、PSC和PBC。60%的AIH患者对免疫抑制有生化反应,组织病理学纤维化评分低预示着完全反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e46c/10025584/e8e4fae0d56d/ga1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验