Differentiating IgG4-related Sclerosing Cholangitis from Primary Sclerosing Cholangitis: A Comprehensive Systematic Review and Meta-analysis of Diagnostic Features.

Mark C Wang,Albert C Chong,Erick Cruz Grave,Andrew Tarakji,Kabir Rahal,Lucas Nastaskin,Abby Kunitsky,Karin J Saric,Helen Lee,Ara Sahakian,James L Buxbaum
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Abstract

INTRODUCTION Immunoglobulin G4-related sclerosing cholangitis (IgG4-SC) and primary sclerosing cholangitis (PSC) are cholestatic disorders which may be difficult to differentiate. Importantly, PSC is an untreatable progressive fibroinflammatory disease, whereas IgG4-SC responds to immunosuppression if recognized in a timely manner. This systematic review and meta-analysis aimed to identify and define the performance of clinical, biochemical, radiographic, and histologic features to differentiate between these two diseases. METHODS A systematic search for comparative studies of IgG4-SC and PSC through November 2023 (with repeat evaluation for interval literature in December 2024) was performed and data extraction performed in duplicate. Pooled proportions, odds ratios (OR), means, and standardized mean differences of pertinent diagnostic features were calculated using random-effects inverse-variance models. RESULTS We identified thirty-eight studies comparing patients with IgG4-SC and PSC. IgG4-SC patients were more likely to have pancreatic disease (p <0.001) but less likely to have inflammatory bowel disease (p<0.001) than those with PSC. Serum IgG4 was significantly higher in IgG4-SC (p<0.001), as anticipated. Radiographically, IgG4-SC demonstrated long distal strictures (p=0.02) and symmetric ductal thickening (p<0.001), whereas PSC showed a beaded appearance (p=0.038). With the exception of IgG4 staining, histologic features including periductal fibrosis were similar between these entities, though sample size was limited for these features. DISCUSSION Our meta-analysis shows that IgG4-SC and PSC present with similar clinical and radiographic features and possibly comparable histology. A history of unusual pancreatitis and elevated IgG4 (serum or tissue) prompt assessment for more specific radiographic features which if present warrant a therapeutic treatment trial.
鉴别igg4相关的硬化性胆管炎与原发性硬化性胆管炎:诊断特征的综合系统回顾和荟萃分析
免疫球蛋白g4相关的硬化性胆管炎(IgG4-SC)和原发性硬化性胆管炎(PSC)是难以区分的胆汁淤积性疾病。重要的是,PSC是一种无法治疗的进行性纤维炎性疾病,而IgG4-SC如果及时识别,则对免疫抑制有反应。本系统综述和荟萃分析旨在识别和定义临床、生化、放射学和组织学特征的表现,以区分这两种疾病。方法系统检索截至2023年11月IgG4-SC和PSC的比较研究(2024年12月对区间文献进行重复评价),并分两份提取数据。使用随机效应反方差模型计算相关诊断特征的合并比例、优势比(OR)、均值和标准化均值差异。结果:我们确定了38项比较IgG4-SC和PSC患者的研究。IgG4-SC患者比PSC患者更容易患胰腺疾病(p<0.001),但更不容易患炎症性肠病(p<0.001)。正如预期的那样,血清IgG4在IgG4- sc中显著升高(p<0.001)。影像学上,IgG4-SC表现为远端狭窄(p=0.02)和对称导管增厚(p<0.001),而PSC表现为串珠状外观(p=0.038)。除了IgG4染色外,这些实体之间的组织学特征包括管周纤维化是相似的,尽管这些特征的样本量有限。我们的荟萃分析显示,IgG4-SC和PSC具有相似的临床和影像学特征,并且可能具有相似的组织学。不寻常的胰腺炎病史和IgG4(血清或组织)升高,及时评估更具体的放射学特征,如果存在的话,需要进行治疗性治疗试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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