慢性肝病(包括自身免疫性肝炎/重叠综合征和并发其他肝病的自身免疫性肝炎)中的国际自身免疫性肝炎评分修订版。

Panagiotis A Papamichalis, Kalliopi Zachou, George K Koukoulis, Aikaterini Veloni, Efthimia G Karacosta, Lampros Kypri, Ioannis Mamaloudis, Stella Gabeta, Eirini I Rigopoulou, Ansgar W Lohse, George N Dalekos
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引用次数: 0

摘要

研究背景我们进行了一项研究,以确定国际自身免疫性肝炎组织(IAHG)评分在非自身免疫性肝炎(AIH)肝病、AIH/重叠综合征以及AIH与其他肝病并存病例中的实用性和诊断价值:我们对 423 例肝病患者进行了 IAHG 评分,其中不包括 AIH、AIH/重叠综合征和 AIH 并发其他肝病的患者,即慢性乙型肝炎患者(n = 109)、慢性丙型肝炎患者(n = 95)、慢性丁型肝炎患者(n = 4)、慢性丙型肝炎(95 例)、慢性丁型肝炎(4 例)、胆汁淤积性肝病(28 例)、非酒精性脂肪肝(55 例)、自身免疫性胆汁淤积性肝病(77 例)、原因不明的肝脏疾病(32 例)和其他肝脏疾病(23 例)。此外,还调查了24名伴有各种肝脏疾病的AIH患者,包括10名AIH/重叠综合征患者和14名同时患有其他肝脏疾病的AIH患者。43名AIH患者组成对照组:该评分的特异性为 98.1%,而揭示 AIH/重叠综合征患者或 AIH 并发其他肝病患者 AIH 的敏感性仅为 50%和 78.6%。在二元逻辑回归模型中,存在其他自身免疫性疾病(p < 0.001)、组织学总分(p < 0.001)和自身抗体阳性(p < 0.05)被认为是预测AIH/重叠综合征或AI并发其他肝病的独立因素:IAHG评分系统对排除慢性肝病患者的AIH有很好的特异性,但对排除AIH/重叠综合征或AIH并发其他肝病的敏感性不高。如果在没有肝炎病毒标记物的情况下出现其他自身免疫性疾病或自身抗体标记物,医生就应该警惕可能存在 "纯粹 "的 AIH 或与其他肝脏疾病(AIH/重叠综合征或并发其他肝脏疾病的 AIH)相关的 AIH。在这些情况下,肝组织学检查似乎至关重要,必须始终将其纳入肝病患者的检查中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The revised international autoimmune hepatitis score in chronic liver diseases including autoimmune hepatitis/overlap syndromes and autoimmune hepatitis with concurrent other liver disorders.

The revised international autoimmune hepatitis score in chronic liver diseases including autoimmune hepatitis/overlap syndromes and autoimmune hepatitis with concurrent other liver disorders.

Background: We conducted a study in order to determine the usefulness and diagnostic value of International Autoimmune Hepatitis Group (IAHG) score in non-autoimmune hepatitis (AIH) hepatic disorders as well as in AIH/overlap syndromes and in cases with coexistence of AIH and other liver diseases.

Methods: We applied the IAHG score in 423 patients with liver diseases excluding patients with AIH, AIH/overlap syndromes and AIH with concurrent other liver disease namely, patients with chronic hepatitis B (n = 109), chronic hepatitis C (n = 95), chronic hepatitis D (n = 4), alchoholic liver disease (n = 28), non-alcoholic fatty liver disease (n = 55), autoimmune cholestatic liver diseases (n = 77), liver disorders of undefined origin (n = 32) and with miscellaneous hepatic disorders (n = 23). 24 patients with AIH associated with any kind of liver disorder including 10 patients with AIH/overlap syndromes and 14 AIH with concurrent other liver disease were also investigated. 43 patients with AIH consisted the control group.

Results: The specificity of the score was 98.1% while the sensitivity in unmasking AIH in patients with either AIH/overlap syndromes or AIH with concurrent other liver diseases was only 50% and 78.6%. In the binary logistic regression model, the presence of other autoimmune diseases (p < 0.001), the total histological score (p < 0.001) and positivity for autoantibodies (p < 0.05) were identified as independent predictors for the presnce of AIH/ovea syndromes o AI with concurren other liver diseass.

Conclusion: The IAHG scoring system has very good specificity for excluding AIH in patients with chronic liver diseases but not that sensitivity in order to unmask AIH/overlap syndromes or AIH with concurrent other liver diseases. The presence of other autoimmune diseases or autoantibody markers in the absence of hepatitis viral markers should alarm physicians for the possible presence of AIH either as "pure" AIH or in association with other liver disorders (AIH/overlap syndromes or AIH with concurrent other liver diseases). Under these conditions, liver histology seems essential and it must always be included in the work up of hepatic patients.

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