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Serum fibrosis markers can predict rapid fibrosis progression after liver transplantation for hepatitis C

โœ Scribed by Surakit Pungpapong; David P. Nunes; Murli Krishna; Raouf Nakhleh; Kyle Chambers; Marwan Ghabril; Rolland C. Dickson; Christopher B. Hughes; Jeffery Steers; Justin H. Nguyen; Andrew P. Keaveny


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
315 KB
Volume
14
Category
Article
ISSN
1527-6465

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โœฆ Synopsis


Although recurrent hepatitis C virus (HCV) after liver transplantation (LT) is universal, a minority of patients will develop cirrhosis within 5 years of surgery, which places them at risk for allograft failure. This retrospective study investigated whether 2 serum fibrosis markers, serum hyaluronic acid (HA) and YKL-40, could be used to predict rapid fibrosis progression (RFP) post-LT. These markers were compared with conventional laboratory tests, histological assessment, and hepatic stellate cell activity (HSCA), a key step in fibrogenesis, as assessed by immunohistochemical staining for alpha-smooth muscle actin. Serum and protocol liver biopsy samples were obtained from 46 LT recipients at means of 5 ฯฎ 2 (biopsy 1) and 39 ฯฎ 6 (biopsy 2) months post-LT, respectively. RFP was defined as an increase in the fibrosis score ี† 2 from biopsy 1 to biopsy 2 (a mean interval of 33 ฯฎ 6 months). The ability of parameters at biopsy 1 to predict RFP was compared with the areas under receiver operating characteristic curves (AUROCs). Of the 46 subjects, 15 developed RFP. Serum HA and YKL-40 performed significantly better than conventional parameters and HSCA in predicting RFP post-LT for HCV at biopsy 1, with AUROCs of 0.89 and 0.92, respectively. The accuracy of serum HA ี† 90 g/L and YKL-40 ี† 200 g/L in predicting RFP at biopsy 1 was 80% and 96%, respectively. In conclusion, we found that elevated levels of serum HA and YKL-40 within the first 6 months after LT accurately predicted RFP. Larger studies evaluating the role of serum HA and YKL-40 in post-LT management are warranted.


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