Gastroenterology Unit, Department of Medicine, King Abdul Aziz University Hospital, Jeddah, Saudi Arabia.
Saudi J Gastroenterol. 2010 Apr-Jun;16(2):95-9. doi: 10.4103/1319-3767.61235.
BACKGROUND/AIM: Autoimmune hepatitis (AIH) is a common cause of end-stage liver disease worldwide. It is a disease prevalent in children and adults, with female predominance and variable clinical presentations. AIH has favorable responses to steroids and immunomodulators. Diagnosis of AIH is based on clinical and laboratory criteria, as suggested by the International Autoimmune Hepatitis Group. Data on the disease pattern of AIH from the Middle East countries is scarce.
In this retrospective analysis, we studied clinical and laboratory features, immunological data, radiological findings, liver biopsy findings and response to therapy in patients with AIH from the hepatology clinics of King Abdul Aziz, University Hospital, Jeddah, from 1994 to 2008.
We diagnosed 41 patients with AIH, and 33 were included in the analysis. The mean age was 32.3 years, with female predominance of 75.7%. De-compensated cirrhosis at presentation was found in 45.5% of the patients. Acute hepatitis was associated with significantly higher levels of the serum ALT and bilirubin (P=0.001 and P=0.03, respectively). All our patients had type 1 AIH. Treatment with prednisolone and azathioprine resulted in complete or partial remission in majority of the patients (54.8%). However, patients with advanced disease showed a poorer response to treatment (P=0.016). Six patients with poor compliance had relapse of AIH. Two patients had a flare of the disease during pregnancy, and they responded well with prednisolone. The longest follow-up was 14 years and the shortest was 2 months. Four patients died from liver disease.
AIH patients in Saudi Arabia are likely to present with advanced disease at a young age and would have a poorer response to therapy as compared with patients in other countries worldwide.
背景/目的:自身免疫性肝炎(AIH)是全球范围内导致终末期肝病的常见原因。它是一种在儿童和成人中普遍存在的疾病,以女性为主,临床表现多样。AIH 对类固醇和免疫调节剂有良好的反应。AIH 的诊断基于临床和实验室标准,如国际自身免疫性肝炎组所建议的。来自中东国家的 AIH 疾病模式数据很少。
在这项回顾性分析中,我们研究了 1994 年至 2008 年期间来自吉达阿卜杜勒阿齐兹国王大学医院肝病诊所的 AIH 患者的临床和实验室特征、免疫学数据、影像学发现、肝活检结果以及对治疗的反应。
我们诊断了 41 例 AIH 患者,其中 33 例纳入分析。平均年龄为 32.3 岁,女性占 75.7%。就诊时失代偿性肝硬化占 45.5%。急性肝炎与血清 ALT 和胆红素水平显著升高相关(P=0.001 和 P=0.03)。我们所有的患者均为 1 型 AIH。泼尼松龙和硫唑嘌呤治疗使大多数患者(54.8%)完全或部分缓解。然而,晚期疾病患者的治疗反应较差(P=0.016)。6 例依从性差的患者 AIH 复发。2 例妊娠期间疾病发作,泼尼松龙治疗效果良好。最长随访时间为 14 年,最短为 2 个月。4 例患者死于肝病。
与全球其他国家的患者相比,沙特阿拉伯的 AIH 患者可能在年轻时就出现晚期疾病,并且对治疗的反应较差。