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High blood glucose levels are associated with fibrosis/cirrhosis progression in chronic hepatitis C.

Authors :
Abdelkader RY
Abdelrazek MA
Attallah A
Farid K
El-Far M
Source :
Journal of immunoassay & immunochemistry [J Immunoassay Immunochem] 2021 Nov 02; Vol. 42 (6), pp. 559-570. Date of Electronic Publication: 2021 Apr 22.
Publication Year :
2021

Abstract

Chronic hepatitis C (CHC) leads eventually to liver fibrosis, advanced hepatic disease and related deaths. Therefore, it is very important to assess clinical risk factors associated with rapid CHC and hepatic fibrosis progression. Former studies reported diabetes mellitus synergistic interactions with other host factors to fibrosis progression. Here, we aimed to evaluate the association between elevated blood glucose levels and CHC progression according to METAVIR system in patients chronically infected with HCV-genotype 4 and to evaluate the correlation between elevated glucose levels and liver- and viral-related biochemical parameters. A total of 160 patients with CHC (80 with liver fibrosis and 80 with cirrhosis) and 40 healthy volunteers, negative for HCV, were included. Our results revealed that cirrhotic patients had high ( P = .0001) fasting (169.1 ± 50.2 mg/dL), postprandial (208 (123-320) mg/dL), and random (176.8 ± 51 mg/dL) glucose levels compared to patients with liver fibrosis (105.0 ± 32, 120 (105-135), and 113.5 ± 35 mg/dL, respectively). Mean serum fasting, postprandial and random glucose levels were significantly ( P = .0001) increased with an increase in fibrosis stages, F1< F2< F3< F4. Blood glucose levels were also significantly ( P < .05) correlated with liver disease related biological parameters and HCV-Ab titer. In conclusion, our results highlighted the fibrogenic impact of elevated glucose levels on CHC patients.

Details

Language :
English
ISSN :
1532-4230
Volume :
42
Issue :
6
Database :
MEDLINE
Journal :
Journal of immunoassay & immunochemistry
Publication Type :
Academic Journal
Accession number :
33886414
Full Text :
https://doi.org/10.1080/15321819.2021.1911813