Effects of hepatitis C virus genotypes and viral load on glucose and lipid metabolism after sustained virological response with direct-acting antivirals
- PMID: 37222317
- PMCID: PMC10204843
- DOI: 10.1590/1806-9282.20221163
Effects of hepatitis C virus genotypes and viral load on glucose and lipid metabolism after sustained virological response with direct-acting antivirals
Erratum in
-
ERRATUM.Rev Assoc Med Bras (1992). 2023 Jul 24;69(7):e20221163ERRATUM. doi: 10.1590/1806-9282.20221163ERRATUM. Rev Assoc Med Bras (1992). 2023. PMID: 37493811 Free PMC article.
Abstract
Objective: The objective of this study, carried out at the university hospital of the Federal University of Rio Grande, was to assess whether the treatment of chronic hepatitis C with direct-acting antivirals and the sustained virological response will affect the metabolic influences of the hepatitis C virus and whether these effects will vary according to genotypes and virus load.
Methods: This is an intervention pre-post study, carried out from March 2018 to December 2019, evaluating 273 hepatitis C virus patients treated with direct-acting antivirals. Inclusion criteria included being monoinfected with hepatitis C virus and achieving sustained virological response . Exclusion criteria included the presence of decompensated cirrhosis or co-infected with hepatitis B virus or human immunodeficiency virus. Genotypes, genotype 1 subtypes, and hepatitis C virus viral load were analyzed. Glucose metabolism was evaluated by the Homeostasis Model Assessment-insulin resistance indices: Homeostasis Model Assessment-β, TyG, and HbA1c, measured at the beginning of treatment and in sustained virological response. Statistical analysis with a T test by paired comparison of the means of the variables in the pretreatment and in the sustained virological response.
Results: Homeostasis Model Assessment-insulin resistance analysis: there were no significant differences between pretreatment and sustained virological response. Homeostasis Model Assessment-β analysis: significant increase in genotype 1 patients (p<0.028). TyG index analysis: significant increase in genotype 1b (p<0.017), genotype 3 (p<0.024), and genotype non-1 with low viral load (p<0.039). HbA1c analysis: significant decrease in genotype 3 (p<0.001) and genotype non-1 patients with low viral load (p<0.005).
Conclusion: We detected significant metabolic influences after sustained virological response: impairment in lipid profile and improvements in the glucose metabolism. We found significant differences in genotype dependence, genotype 1 subtypes, and viral load.
Conflict of interest statement
Conflicts of interest: the authors declare there is no conflicts of interest.
Similar articles
-
Hepatitis C virus eradication by direct antiviral agents improves glucose tolerance and reduces post-load insulin resistance in nondiabetic patients with genotype 1.Liver Int. 2018 Jul;38(7):1206-1211. doi: 10.1111/liv.13669. Epub 2018 Jan 19. Liver Int. 2018. PMID: 29265719
-
Impact of hepatitis C virus eradication with direct-acting antivirals on glycidic metabolism.Arch Endocrinol Metab. 2023 Mar 30;67(3):314-322. doi: 10.20945/2359-3997000000543. Epub 2022 Dec 1. Arch Endocrinol Metab. 2023. PMID: 36468927 Free PMC article.
-
Factors That Influence the Virological Response in Patients with Chronic Hepatitis C Treated with Pegylated Interferon and Ribavirin.Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017 Mar 1;38(1):25-33. doi: 10.1515/prilozi-2017-0003. Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2017. PMID: 28593897
-
Therapy of chronic hepatitis C virus infection in the era of direct-acting and host-targeting antiviral agents.J Infect. 2014 Jan;68(1):1-20. doi: 10.1016/j.jinf.2013.08.019. Epub 2013 Sep 4. J Infect. 2014. PMID: 24012819 Review.
-
[Significance of hepatitis C virus baseline polymorphism during the antiviral therapy].Orv Hetil. 2015 May 24;156(21):849-54. doi: 10.1556/650.2015.30180. Orv Hetil. 2015. PMID: 26038992 Review. Hungarian.
References
-
- Ferreira CT, Silveira TR. Hepatites virais: aspectos da epidemiologia e da prevenção. Rev Bras Epidemiol. 2004;7(4):473–487. doi: 10.1590/S1415-790X2004000400010. - DOI
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical