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November 18, 2019 7:00 am
Though young age at the time of Kasai and surgical experience have been identified as factors in the long-term outcome of patients with biliary atresia (BA), why is it that some with timely intervention still fail to respond? Conceptually, I’ve considered those who had progressive disease as probably having an intrahepatic component of their biliary disease that a Kasai operation cannot help.
New research (Z Luo, P Shivakumar, R Mourya, S Gutta, JA Bezerra. Gastroenterol 2019; 157: 1138-52) identifies genetic factors that are likely a more powerful predictor of Kasai response then the traditional clinical factors.
The science in this study is fascinating –combining genetic heat maps, and survival curves. The prediction with a 14-gene signature is amplified with serum total bilirubin at 3 months post-Kasai. In addition, these studies are combined with a mouse model treated with N-acetylcysteine (NAC). Histologic changes were then assessed.
Key findings:
My take: This 14-gene signature has the potential to change our approach to children with BA. Also, when evaluating surgical success rate, these underlying genetic factors will need to be incorporated.
Related blog posts:
Posted by gutsandgrowth
Categories: Pediatric Gastroenterology Liver Disease
Tags: biliary atresia, N-acetylcysteine, outcome
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By 2020 AASLD President: Jorge Bezerra | gutsandgrowth on January 2, 2021 at 9:00 am