Abbas Zaigham, Asim Muhammad, Saeed Alina, Siddiqui Basit, Abbas Minaam
Gastroenterology and Hepatology, Dr. Ziauddin University Hospital, Karachi, PAK.
Gastroenterology, Dr. Ziauddin University Hospital, Karachi, PAK.
Cureus. 2021 Nov 21;13(11):e19789. doi: 10.7759/cureus.19789. eCollection 2021 Nov.
Background The autoimmune illnesses that affect the liver include autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC), and overlap syndrome. In our patients, we aimed to address the complete spectrum of autoimmune liver disorders, clinical presentation, and autoantibodies. Methods The study included all the patients diagnosed with autoimmune liver disorder irrespective of age, gender, and ethnic background presented at the liver clinic of the hospital in the last two years. The diagnosis was based on characteristic clinical and laboratory findings, the presence of one or more characteristic autoantibodies, and/or histological abnormalities. The diagnosis of AIH was further validated by revised International AIH Group criteria using a scoring calculator. The diagnostic criteria for PBC required the presence of chronic elevation of alkaline phosphatase (ALP) with positive antimitochondrial antibody (AMA) or positive PBC-specific anti-nuclear antibodies (ANA) (sp-100, gp-210) tests and/or compatible histology. The patients of AIH-PBC overlap syndrome fulfilled the criteria for AIH in the setting of PBC. Patients having liver involvement in other autoimmune disorders were included in the study. Results The total number of patients was 124; 83 (67%) were females; mean age ± standard error of mean (SEM) was 44.97 ± 1.47 years with a range of 09-84 years. Type-1 AIH was seen in 68 (54.8%) patients, type-2 AIH in 10 (8.1%) patients, PBC in 22 (17.7%) patients, overlap of PBC with AIH in 10 (8.1%) patients, IgG4 disease in four (3.2%) patients, psoriasis-specific immune hepatitis in four (3.2%) patients, celiac disease-related hepatitis in three (2.4%) patients, sarcoidosis in two (1.6%) patients, and ichthyosis-associated hepatitis in one (0.8%) patient. There was a high prevalence of cirrhosis (50%) at the time of presentation; 19% of patients had decompensated liver disease. ANA was positive in 52/68 cases of AIH type-1, but anti-smooth muscle antibody (ASMA) was reactive only in nine cases and anti-soluble liver antigen (SLA) in five cases. There was no female preponderance in type-2 AIH (M:F = 6:4). AMA was reactive in 25 (78%) cases of PBC and overlap syndrome. Antibodies prevalent in PBC (AMA-M2, AMA-M2-3E, sp-100, gp-210, anti-Ro52) were also seen in some cases of AIH, though they did not fulfill the criteria of the overlap syndrome. Conclusion There is an unmet need for the early diagnosis of autoimmune liver diseases and the initiation of appropriate management to prevent complications.
影响肝脏的自身免疫性疾病包括自身免疫性肝炎(AIH)、原发性胆汁性胆管炎(PBC)、原发性硬化性胆管炎(PSC)和重叠综合征。在我们的患者中,我们旨在全面研究自身免疫性肝病的范围、临床表现和自身抗体。
该研究纳入了过去两年在医院肝病门诊就诊的所有被诊断为自身免疫性肝病的患者,无论其年龄、性别和种族背景如何。诊断基于特征性的临床和实验室检查结果、一种或多种特征性自身抗体的存在和/或组织学异常。AIH的诊断通过使用评分计算器的修订国际AIH小组标准进一步验证。PBC的诊断标准要求碱性磷酸酶(ALP)持续升高,同时抗线粒体抗体(AMA)阳性或PBC特异性抗核抗体(ANA)(sp-100、gp-210)检测阳性和/或组织学相符。AIH-PBC重叠综合征患者在PBC的背景下符合AIH的标准。有肝脏受累的其他自身免疫性疾病患者也纳入了研究。
患者总数为124例;83例(67%)为女性;平均年龄±平均标准误差(SEM)为44.97±1.47岁,年龄范围为09-84岁。68例(54.8%)患者为1型AIH,10例(8.1%)患者为2型AIH,22例(17.7%)患者为PBC,10例(8.1%)患者为PBC与AIH重叠,4例(3.2%)患者为IgG4病,4例(3.2%)患者为银屑病特异性免疫性肝炎,3例(2.4%)患者为乳糜泻相关性肝炎,2例(1.6%)患者为结节病,1例(0.8%)患者为鱼鳞病相关性肝炎。就诊时肝硬化的患病率很高(50%);19%的患者有失代偿性肝病。在68例1型AIH患者中,52例ANA阳性,但抗平滑肌抗体(ASMA)仅9例呈反应性,抗可溶性肝抗原(SLA)5例呈反应性。2型AIH中无女性优势(男:女 = 6:4)。25例(78%)PBC和重叠综合征患者AMA呈反应性。在一些AIH病例中也发现了PBC中常见的抗体(AMA-M2、AMA-M2-3E、sp-100、gp-210、抗Ro52),尽管它们不符合重叠综合征的标准。
自身免疫性肝病的早期诊断以及启动适当的治疗以预防并发症仍存在未满足的需求。