@article{oai:kanazawa-u.repo.nii.ac.jp:00014362,
 author = {Kakuda, Yuko and Harada, Kenichi and Nakanuma, Yasuni},
 issue = {2},
 journal = {Journal of Clinical Pathology},
 month = {Feb},
 note = {Aims: The canals of Hering (CoH), which are the most peripherally located bile drainage pathway, are considered a niche of hepatic progenitor cells. Recently, CoH loss has been described as an early feature of primary biliary cirrhosis (PBC). We investigated the correlation between CoH loss and the histopathological variables of PBC. Methods: Liver biopsy specimens from 62 PBC patients (M:F=8:54, age=58±12 years) were evaluated prior to ursodeoxycholic acid treatment. Liver biopsies of patients with normal liver (n=11), chronic viral hepatitis (n=36) and non-alcoholic fatty liver disease (n=13) were used as controls. The number of CoH per definite area of hepatic parenchyma (c to p ratio) was calculated in individual cases. We compared the c to p ratios of PBC patients with that of controls and analysed the correlations with histological variables and clinical features. Results: The c to p ratios in PBC patients with mild and extensive fibrosis were lower than those in controls with each degree of fibrosis. The c to p ratios were negatively correlated with stage, fibrosis, bile duct loss, orcein-positive granule deposition and hepatitis activities in PBC (p<0.01) and with alkaline phosphatase and total bilirubin levels at liver biopsies (p<0.05). Conclusions: The number of CoH was low in early stages and further decreased with stage progression in PBC. CoH loss, reflecting a reduced supply of progenitor cells to the biliary tree, may be involved in the histological progression of PBC. © 2015, BMJ Publishing Group. All rights reserved., kenichih@med.kanazawa-u.ac.jp},
 pages = {141--147},
 title = {Canals of Hering loss relates to the progression of the histological stages of primary biliary cirrhosis},
 volume = {68},
 year = {2015}
}