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DOI 10.1038/s41598-020-76875-9

Медицинская библиотека · Scientific reports · 2020

Decreased circulating clusterin reflects severe liver complications after hepatoportoenterostomy of biliary atresia.

Udomsinprasert Wanvisa, Poovorawan Yong, Chongsrisawat Voranush, Vejchapipat Paisarn, Honsawek Sittisak

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

This study aimed to determine whether circulating levels of clusterin (CLU), an extracellular chaperone implicated in cholestatic and fibrotic processes, are associated with clinical parameters of post-operative BA patients and could serve as a BA biomarker. Ninety-six BA patients and 56 healthy controls were recruited. Circulating CLU levels were measured using enzyme-linked immunosorbent assay. Circulating CLU levels were significantly reduced in BA patients - especially those with worse outcomes including jaundice, severe liver fibrosis, and late-stage of hepatic dysfunction. Multivariate linear regression analysis revealed that circulating CLU levels were negatively associated with outcome parameters indicating jaundice status, degree of fibrosis, and liver dysfunction, but positively correlated with serum albumin and platelet number of BA patients. Lower circulating CLU levels were considerably associated with poor survival of post-operative BA patients. Receiver-operating characteristic curve analysis demonstrated a diagnostic value of circulating CLU as a non-invasive indicator for poor outcomes of BA patients (AUC = 0.85), with a sensitivity of 81.5% and a specificity of 73.5%. All findings indicate that reduced circulating CLU might reflect poor outcomes of BA patients and have potential as a novel biomarker for the disease severity following Kasai-operation.

Для цитирования: Udomsinprasert Wanvisa, Poovorawan Yong, Chongsrisawat Voranush, Vejchapipat Paisarn, Honsawek Sittisak. Decreased circulating clusterin reflects severe liver complications after hepatoportoenterostomy of biliary atresia.. Scientific reports. 2020. DOI: 10.1038/s41598-020-76875-9.

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