Associations of ITPA gene polymorphisms with outcomes among chronic hepatitis C patients treated with Peg-interferon/ribavirin: A 5-year follow-up study.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
27 Oct 2023
Historique:
medline: 2 11 2023
pubmed: 31 10 2023
entrez: 31 10 2023
Statut: ppublish

Résumé

To investigate associations between inosine triphosphatase (ITPA) gene polymorphisms and long-term outcomes among chronic hepatitis C (CHC) patients in Northeast China treated with Peg-interferon (IFN)/ribavirin (RBV). CHC patients who received Peg-IFN-2a/RBV treatment during between 2011 and 2013 at 5 hepatitis centers in Northeast China were enrolled. ITPA single nucleotide polymorphisms rs1127354 and rs7270101 from all patients were detected and their associations with 5-year outcomes were analyzed. A total of 635 patients, including 421 infected with hepatitis C virus (HCV) genotype 1 and 214 infected with non-genotype 1 were included. No significant differences were observed in the distribution frequencies of ITPA rs1127354 variants and ITPase activity between patients with HCV genotype 1 and non-genotype 1. In patients who received more than 80% of the planned RBV dose, the 5-year virological response rate and the improvement in liver fibrosis were higher in those with ITPA rs1127354 non-CC with ITPase activity <25% compared with these outcomes in patients with ITPA rs1127354 CC with 100% ITPase activity. Multiple regression analysis revealed that HCV genotype non-1, low baseline HCV ribose nucleic acid (RNA) levels (≤4 × 105 IU/mL), interleukin-28B rs12979860 CC genotype, low baseline liver fibrosis (Fibroscan 0-2), and ITPA rs1127354 non-CC genotype were independent predictors for a high long-term virological response rate, whereas interleukin-28B rs12979860 CC genotype, ITPA rs1127354 non-CC genotype, and low baseline liver fibrosis were independent predictors for improvement of liver fibrosis. ITPA rs1127354 polymorphisms is predictors of long-term outcomes in CHC patients treated with Peg-IFN/RBV.

Identifiants

pubmed: 37904484
doi: 10.1097/MD.0000000000035508
pii: 00005792-202310270-00140
pmc: PMC10615403
doi:

Substances chimiques

Ribavirin 49717AWG6K
Antiviral Agents 0
Pyrophosphatases EC 3.6.1.-
Interferons 9008-11-1
Interleukins 0
ITPA protein, human EC 3.6.1.9

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e35508

Informations de copyright

Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc.

Déclaration de conflit d'intérêts

The authors have no funding and conflicts of interest to disclose.

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Auteurs

Zhenhua Liu (Z)

Department of Cardiovascular Medicine, The Third Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, China.

Yanxin Wang (Y)

Department of Cardiovascular Medicine, The Third Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, China.

Hongyu Li (H)

Department of Cardiovascular Medicine, The Third Affiliated Hospital of Changchun University of Chinese Medicine, Changchun, China.

Xinyu Wang (X)

Jilin Institute for Drug Control, Changchun, China.

Xue Wang (X)

College of Food Science and Engineering, Northwest A&F University, Yangling, Shanxi, PR China.

Xinwei Xu (X)

Huanan Agricultural Technology Extension Center, Huarong, China.

Chunyu Ma (C)

Sichuan Tianzow Breeding Co., Ltd, Chongqing, China.

Jiangbin Wang (J)

Department of Digestive, China-Japan Union Hospital Affiliated to Jilin University, Changchun, China.

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Classifications MeSH