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原发性胆汁性胆管炎中基线胆管减少和治疗反应可预测长期组织学进展。

Baseline ductopenia and treatment response predict long-term histological progression in primary biliary cirrhosis.

机构信息

Liver Centre, Toronto Western Hospital, University Health Network, Ontario, Canada.

出版信息

Am J Gastroenterol. 2010 Oct;105(10):2186-94. doi: 10.1038/ajg.2010.216. Epub 2010 May 25.

Abstract

OBJECTIVES

Laboratory and pathological predictors of future histological progression in primary biliary cirrhosis (PBC) are needed for routine practice and clinical trials. We sought to develop clinically meaningful markers for those with predominantly early disease at risk of progressive liver damage.

METHODS

Patients with PBC (n=69) with a follow-up liver biopsy performed approximately 10 years after initial histological diagnosis were identified and reviewed.

RESULTS

Histological progression in the stage of fibrosis observed in paired liver biopsies from the same patient was associated with the absence of biochemical response to ursodeoxycholic acid (UDCA) at 2 years: alkaline phosphatase (ALP) >1.67 × ULN (upper limit of normal) (P=0.001, odds ratio (OR) 12.14, 95% confidence interval (CI) 2.69-54.74) when defined as an increase in one stage and ALP > 1.76 × ULN (P=0.03, OR 5.07, 95% CI 1.17-21.95) when defined as an increase in two stages. Ductopenia (>50% loss), as formally evaluated through blinded biopsy review of liver tissue obtained at initial diagnosis in a subset of 34 patients, predicted histological progression (P=0.012), along with biochemical response to UDCA (P=0.002). The presence of interface hepatitis in the same biopsies did not.

CONCLUSIONS

Patients with PBC who fail to show a biochemical response to UDCA or who have ductopenia on baseline biopsy progress histologically during extended follow-up. Such patients may benefit from novel treatments, with our exploratory data providing a means of identifying these individuals early in their disease.

摘要

目的

原发性胆汁性肝硬化(PBC)患者需要实验室和病理预测指标,以用于常规临床实践和临床试验。我们旨在为那些早期疾病为主且存在进行性肝损伤风险的患者开发具有临床意义的标志物。

方法

我们确定并回顾了 69 名 PBC 患者的病例,这些患者在初始组织学诊断后大约 10 年进行了随访肝活检。

结果

在同一患者的配对肝活检中观察到纤维化阶段的组织学进展与熊去氧胆酸(UDCA)治疗 2 年后生化应答缺失相关:碱性磷酸酶(ALP)>1.67×正常值上限(ULN)(P=0.001,优势比(OR)12.14,95%置信区间(CI)2.69-54.74),当定义为一个阶段增加时;ALP>1.76×ULN(P=0.03,OR 5.07,95% CI 1.17-21.95),当定义为两个阶段增加时。在 34 名患者的肝组织活检中,通过盲法活检评估,发现胆管减少症(>50%的胆管丢失)预测了组织学进展(P=0.012),同时也预测了 UDCA 的生化应答(P=0.002)。同一活检中存在界面肝炎则不会。

结论

未能对 UDCA 产生生化应答或基线活检中存在胆管减少症的 PBC 患者在随访中会发生组织学进展。这些患者可能受益于新型治疗方法,我们的探索性数据为早期识别这些患者提供了一种方法。

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