Cargando…
Up-regulation of Plasma Hexosylceramide (d18:1/18:1) Contributes to Genotype 2 Virus Replication in Chronic Hepatitis C: A 20-Year Cohort Study
The aim of the present study was to explore the relationship between plasma sphingolipids and hepatitis C virus (HCV) replication in chronic hepatitis C (CHC) patients. A cohort of 120 treatment-naïve CHC patients was included. Liver biopsies and the Scheuer scoring system were used to assess hepati...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907656/ https://www.ncbi.nlm.nih.gov/pubmed/27281078 http://dx.doi.org/10.1097/MD.0000000000003773 |
_version_ | 1782437571211558912 |
---|---|
author | Zhang, Jin-Yan Qu, Feng Li, Jun-Feng Liu, Mei Ren, Feng Zhang, Jing-Yun Bian, Dan-Dan Chen, Yu Duan, Zhong-Ping Zhang, Jin-Lan Zheng, Su-Jun |
author_facet | Zhang, Jin-Yan Qu, Feng Li, Jun-Feng Liu, Mei Ren, Feng Zhang, Jing-Yun Bian, Dan-Dan Chen, Yu Duan, Zhong-Ping Zhang, Jin-Lan Zheng, Su-Jun |
author_sort | Zhang, Jin-Yan |
collection | PubMed |
description | The aim of the present study was to explore the relationship between plasma sphingolipids and hepatitis C virus (HCV) replication in chronic hepatitis C (CHC) patients. A cohort of 120 treatment-naïve CHC patients was included. Liver biopsies and the Scheuer scoring system were used to assess hepatic inflammatory activity. Blood biochemical indicators, HCV-RNA load, and immunological markers were also measured. Forty-four plasma sphingolipids were identified and quantified using high-performance liquid chromatography–tandem mass spectrometry. The hexosylceramide (HexCer) (d18:1/18:1) level was significantly different between patients with a low HCV load (<10(6) IU/mL) and a high HCV load (≥10(6) IU/mL), and it was positively correlated with the HCV-RNA load (r = 0.337, P = 0.001) in CHC patients. Additionally, the plasma HexCer (d18:1/18:1) level (odds ratio 1.302, 95% confidence interval 1.129–1.502) was an independent factor for a high HCV-RNA load. For patients with hepatic inflammation grade ≤2 or HCV genotype 2, HexCer (d18:1/18:1) was independently related to a high HCV-RNA load. Plasma HexCer (d18:1/18:1) might be involved in the high viral replication level in chronic HCV infection, especially for CHC patients with genotype 2. |
format | Online Article Text |
id | pubmed-4907656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-49076562016-07-28 Up-regulation of Plasma Hexosylceramide (d18:1/18:1) Contributes to Genotype 2 Virus Replication in Chronic Hepatitis C: A 20-Year Cohort Study Zhang, Jin-Yan Qu, Feng Li, Jun-Feng Liu, Mei Ren, Feng Zhang, Jing-Yun Bian, Dan-Dan Chen, Yu Duan, Zhong-Ping Zhang, Jin-Lan Zheng, Su-Jun Medicine (Baltimore) 4500 The aim of the present study was to explore the relationship between plasma sphingolipids and hepatitis C virus (HCV) replication in chronic hepatitis C (CHC) patients. A cohort of 120 treatment-naïve CHC patients was included. Liver biopsies and the Scheuer scoring system were used to assess hepatic inflammatory activity. Blood biochemical indicators, HCV-RNA load, and immunological markers were also measured. Forty-four plasma sphingolipids were identified and quantified using high-performance liquid chromatography–tandem mass spectrometry. The hexosylceramide (HexCer) (d18:1/18:1) level was significantly different between patients with a low HCV load (<10(6) IU/mL) and a high HCV load (≥10(6) IU/mL), and it was positively correlated with the HCV-RNA load (r = 0.337, P = 0.001) in CHC patients. Additionally, the plasma HexCer (d18:1/18:1) level (odds ratio 1.302, 95% confidence interval 1.129–1.502) was an independent factor for a high HCV-RNA load. For patients with hepatic inflammation grade ≤2 or HCV genotype 2, HexCer (d18:1/18:1) was independently related to a high HCV-RNA load. Plasma HexCer (d18:1/18:1) might be involved in the high viral replication level in chronic HCV infection, especially for CHC patients with genotype 2. Wolters Kluwer Health 2016-06-10 /pmc/articles/PMC4907656/ /pubmed/27281078 http://dx.doi.org/10.1097/MD.0000000000003773 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 4500 Zhang, Jin-Yan Qu, Feng Li, Jun-Feng Liu, Mei Ren, Feng Zhang, Jing-Yun Bian, Dan-Dan Chen, Yu Duan, Zhong-Ping Zhang, Jin-Lan Zheng, Su-Jun Up-regulation of Plasma Hexosylceramide (d18:1/18:1) Contributes to Genotype 2 Virus Replication in Chronic Hepatitis C: A 20-Year Cohort Study |
title | Up-regulation of Plasma Hexosylceramide (d18:1/18:1) Contributes to Genotype 2 Virus Replication in Chronic Hepatitis C: A 20-Year Cohort Study |
title_full | Up-regulation of Plasma Hexosylceramide (d18:1/18:1) Contributes to Genotype 2 Virus Replication in Chronic Hepatitis C: A 20-Year Cohort Study |
title_fullStr | Up-regulation of Plasma Hexosylceramide (d18:1/18:1) Contributes to Genotype 2 Virus Replication in Chronic Hepatitis C: A 20-Year Cohort Study |
title_full_unstemmed | Up-regulation of Plasma Hexosylceramide (d18:1/18:1) Contributes to Genotype 2 Virus Replication in Chronic Hepatitis C: A 20-Year Cohort Study |
title_short | Up-regulation of Plasma Hexosylceramide (d18:1/18:1) Contributes to Genotype 2 Virus Replication in Chronic Hepatitis C: A 20-Year Cohort Study |
title_sort | up-regulation of plasma hexosylceramide (d18:1/18:1) contributes to genotype 2 virus replication in chronic hepatitis c: a 20-year cohort study |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907656/ https://www.ncbi.nlm.nih.gov/pubmed/27281078 http://dx.doi.org/10.1097/MD.0000000000003773 |
work_keys_str_mv | AT zhangjinyan upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT qufeng upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT lijunfeng upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT liumei upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT renfeng upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT zhangjingyun upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT biandandan upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT chenyu upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT duanzhongping upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT zhangjinlan upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy AT zhengsujun upregulationofplasmahexosylceramided181181contributestogenotype2virusreplicationinchronichepatitisca20yearcohortstudy |