胆道hCGβ是预测原发性硬化性胆管炎患者胆道肿瘤的潜在新标志物

Livers Pub Date : 2021-12-15 DOI:10.3390/livers1040025
H. Koistinen, S. Boyd, J. Arola, K. Jokelainen, R. Koistinen, Anna Lempiäinen, K. Hotakainen, U. Stenman, M. Färkkilä
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引用次数: 1

摘要

原发性硬化性胆管炎(PSC)是一种慢性炎症性疾病,与胆管癌(CCA)风险增加有关。新的标志物,补充或取代CA19-9,迫切需要用于PSC相关胆道肿瘤的筛查。先前的研究表明,血清胰蛋白酶原-2和人绒毛膜促性腺激素β亚基(hCGβ)可能是此类标志物。使用高度特异性的内部免疫测定,我们研究了214名患者胆汁样本中的胰蛋白酶(原)-2和-3、SPINK1和hCGβ,这些患者被转用于内镜逆行胆管造影。我们发现,与没有CCA或重复性发育不良的PSC患者(n=171)相比,1.6年后(中位数为0.1-8.8年)被诊断为CCA的PSC患者,或在刷状细胞学中至少两次观察到胆汁发育不良的患者(n=11),胆汁胰蛋白酶原-2降低(p=0.027),hCGβ升高(p<0.001)。其他研究的标记物在这些组之间没有显示出显著差异。我们的结果值得进一步评估hCGβ作为PSC相关胆道肿瘤的预测标志物。
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Biliary hCGβ Is a Potential Novel Marker for Prediction of Biliary Neoplasia in Primary Sclerosing Cholangitis Patients
Primary sclerosing cholangitis (PSC) is a chronic inflammatory disease, which is associated with an increased risk of cholangiocarcinoma (CCA). Novel markers, to complement or replace CA19-9, are urgently needed for the screening of PSC-associated biliary neoplasia. Previous studies have suggested that serum trypsinogen-2 and human chorionic gonadotropin β-subunit (hCGβ) may serve as such markers. Using highly specific in-house immunoassays, we studied trypsin(ogen)-2 and -3, SPINK1 and hCGβ in bile samples of 214 patients, referred for endoscopic retrograde cholangiography. We found that biliary trypsinogen-2 was decreased (p = 0.027) and hCGβ was elevated (p < 0.001) in PSC patients who were diagnosed 1.6 years (median, range 0.1–8.8 years) later with CCA or in whom biliary dysplasia was observed at least twice in brush cytology (n = 11) as compared to PSC patients without CCA or repeated dysplasia (n = 171). The other studied markers did not show significant differences between these groups. Our results warrant further evaluation of hCGβ as a predictive marker for PSC-associated biliary neoplasia.
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