Expression and activity of the cytochrome P450 2E1 in patients with nonalcoholic steatosis and steatohepatitis.
Details
Serval ID
serval:BIB_CA37D046B1A6
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Expression and activity of the cytochrome P450 2E1 in patients with nonalcoholic steatosis and steatohepatitis.
Journal
Liver international : official journal of the International Association for the Study of the Liver
ISSN
1478-3223 (Print)
ISSN-L
1478-3223
Publication state
Published
Issued date
08/2007
Peer-reviewed
Oui
Volume
27
Number
6
Pages
764-771
Language
english
Notes
Publication types: Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Abstract
Nonalcoholic steatohepatitis (NASH) and nonalcoholic fatty liver (NAFL) have a different prognosis and should be dealt with differently. The pathogenesis of NASH implicates the overexpression of cytochrome P450 2E1 (CYP2E1). We investigated whether the noninvasive determination of CYP2E1 activity could replace a liver biopsy in order to differentiate NASH from NAFL.
Forty patients referred for suspicion of NASH underwent liver biopsy. In these patients, CYP2E1 activity was determined noninvasively by the 6-hydroxychlorzoxazone/chlorzoxazone (CHZ) ratio (CHZ test). Expression of CYP2E1 on liver slides was assessed by immunohistochemistry, and immunostaining for smooth muscle actin was used to assess the activation of hepatic stellate cells (HSC).
Thirty patients with NASH were compared with 10 subjects with NAFL. No statistically significant difference could be identified for the clinical and biochemical parameters between the two groups. In the histology, steatosis was more important in NASH than in NAFL (P<0.0001). There was no difference either in the activity (CHZ test) or in the expression of CYP2E1 (immunohistochemistry) between patients with NASH and patients with NAFL. The degree of HSC activation was also comparable between the two groups. A positive and significant correlation was found between the activity of CYP2E1 and body mass index (P<0.001) as well as with the degree of steatosis (P=0.008).
For patients suspected to have NASH, noninvasive tests including the determination of the CYP2E1 activity are unable to distinguish them from patients with steatosis.
Forty patients referred for suspicion of NASH underwent liver biopsy. In these patients, CYP2E1 activity was determined noninvasively by the 6-hydroxychlorzoxazone/chlorzoxazone (CHZ) ratio (CHZ test). Expression of CYP2E1 on liver slides was assessed by immunohistochemistry, and immunostaining for smooth muscle actin was used to assess the activation of hepatic stellate cells (HSC).
Thirty patients with NASH were compared with 10 subjects with NAFL. No statistically significant difference could be identified for the clinical and biochemical parameters between the two groups. In the histology, steatosis was more important in NASH than in NAFL (P<0.0001). There was no difference either in the activity (CHZ test) or in the expression of CYP2E1 (immunohistochemistry) between patients with NASH and patients with NAFL. The degree of HSC activation was also comparable between the two groups. A positive and significant correlation was found between the activity of CYP2E1 and body mass index (P<0.001) as well as with the degree of steatosis (P=0.008).
For patients suspected to have NASH, noninvasive tests including the determination of the CYP2E1 activity are unable to distinguish them from patients with steatosis.
Keywords
Adult, Biopsy, Biotransformation, Chlorzoxazone/administration & dosage, Chlorzoxazone/analogs & derivatives, Chlorzoxazone/blood, Chlorzoxazone/pharmacokinetics, Cytochrome P-450 CYP2E1/genetics, Cytochrome P-450 CYP2E1/metabolism, Diagnosis, Differential, Fatty Liver/diagnosis, Fatty Liver/enzymology, Fatty Liver/pathology, Female, Hepatitis/diagnosis, Hepatitis/enzymology, Hepatitis/pathology, Humans, Hydroxylation, Liver/enzymology, Liver/pathology, Male, Middle Aged, Muscle Relaxants, Central/administration & dosage, Muscle Relaxants, Central/blood, Muscle Relaxants, Central/pharmacokinetics, Prognosis
Pubmed
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16/02/2017 12:08
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20/08/2019 15:45