4.8 Article

Serum YKL-40 is increased in patients with hepatic fibrosis

Journal

JOURNAL OF HEPATOLOGY
Volume 32, Issue 6, Pages 911-920

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S0168-8278(00)80095-1

Keywords

alcoholic liver disease; HC gp-39; liver fibrogenesis; liver fibrosis; YKL-40

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Background/Aims: YKL-40, a mammalian member of the chitinase family, is a lectin that binds heparin and chitin, The function of YKL-40 is unknown, but it may function in tissue remodelling. The aims of this study were to assess the level of circulating YKL-40 in patients with various kinds and degree of chronic liver disease and its possible relation to liver fibrosis, Methods: Serum YKL-40 levels were determined by radioimmunoassay in 129 patients with suspected liver disease and related to histological findings and immunohistochemical staining of YKL-40 in a liver biopsy taken simultaneously with the blood sample. Results: The median serum YKL-40 was highest in patients with alcoholic cirrhosis (532 mu g/I), in particular in patients with additional alcoholic hepatitis (740 mu g/I). Patients with alcoholic cirrhosis, post-hepatitic cirrhosis (425 mu g/I) and non-cirrhotic fibrosis (330 mu g/I ) had significantly higher serum YKL-40 than normal subjects (102 mu g/I), patients with fatty liver (195 mu g/I) or patients with viral hepatitis without fibrosis (174 mu g/I). Serum YKL-40 was significantly (p<0.001) related to the degree of liver fibrosis with the highest levels in patients with moderate (466 mu g/I) to severe (676 mu g/I) fibrosis. Serum YKL-40 was also increased (p=0.018) in patients with slight fibrosis (270 mu g/I) compared to patients without fibrosis, Immunohistochemical analysis demonstrated positive staining for YKL-40 antigen in areas with fibrosis, particularly areas with active fibrogenesis, YKL-40 staining was never found in hepatocytes, Conclusions: Our study indicates that the increased serum YKL-40 in patients with liver disease of various degree and aetiology seems to reflect fibrosis and fibrogenesis.

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