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Predictors of seropositivity for human herpesvirus type 8 in patients with mild cirrhosis

The high seroprevalence of human herpesvirus type 8 (HHV-8) in moderate or severe cirrhotics appears to be associated with male sex, hepatitis B virus (HBV) infection, alcoholism, and disease severity. The status of HHV-8 infection in mild cirrhotics remains unclear. Plasma samples collected from 93...

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Autores principales: Tseng, Kuo-Chih, Lin, Ming-Nan, Chu, Tang-Yuan, Tsai, Jen-Pi, Su, Cheng-Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520309/
https://www.ncbi.nlm.nih.gov/pubmed/28588294
http://dx.doi.org/10.1038/emi.2017.32
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author Tseng, Kuo-Chih
Lin, Ming-Nan
Chu, Tang-Yuan
Tsai, Jen-Pi
Su, Cheng-Chuan
author_facet Tseng, Kuo-Chih
Lin, Ming-Nan
Chu, Tang-Yuan
Tsai, Jen-Pi
Su, Cheng-Chuan
author_sort Tseng, Kuo-Chih
collection PubMed
description The high seroprevalence of human herpesvirus type 8 (HHV-8) in moderate or severe cirrhotics appears to be associated with male sex, hepatitis B virus (HBV) infection, alcoholism, and disease severity. The status of HHV-8 infection in mild cirrhotics remains unclear. Plasma samples collected from 93 mild cirrhotics and 93 age- and sex-matched healthy controls were analyzed for HHV-8 antibody and HHV-8 DNA. Mild cirrhotics had higher seropositivity for HHV-8 antibodies than healthy controls (P=0.0001). Univariate logistic regression analysis revealed that an age ≥55 years (odds ratio (OR) 2.88, P=0.02), hepatitis C virus (HCV) infection (OR 3.42, P=0.01), and hepatitis activity (OR 4.10, P=0.004) were associated with HHV-8 seropositivity in cirrhotics. Stepwise multivariate logistic regression analysis confirmed that age ≥55 years (adjusted OR (aOR) 1.92, P=0.04) and hepatitis activity (aOR 3.55, P=0.005) were independent factors. The rate of hepatitis activity was higher in HCV-infected than in HBV-infected patients (P<0.0001) and in women than in men (P=0.0001). Cirrhotics who were seropositive for HHV-8 or HCV or had hepatitis activity were significantly older (P=0.02, <0.0001 and <0.0001, respectively). Plasma samples from all participants were negative for HHV-8 DNA. HHV-8 antibody titers in mild cirrhotics also markedly exceeded those in controls (P<0.0001), as did those in patients ≥55 years old vs. younger patients (P=0.01), those in patients with vs. without HCV infection (P=0.0008), and those in patients with vs. without hepatitis activity (P=0.0005). Mild cirrhotics had high HHV-8 seroprevalence and HCV infection, and, in particular, old age and hepatitis activity were predictors.
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spelling pubmed-55203092017-08-21 Predictors of seropositivity for human herpesvirus type 8 in patients with mild cirrhosis Tseng, Kuo-Chih Lin, Ming-Nan Chu, Tang-Yuan Tsai, Jen-Pi Su, Cheng-Chuan Emerg Microbes Infect Original Article The high seroprevalence of human herpesvirus type 8 (HHV-8) in moderate or severe cirrhotics appears to be associated with male sex, hepatitis B virus (HBV) infection, alcoholism, and disease severity. The status of HHV-8 infection in mild cirrhotics remains unclear. Plasma samples collected from 93 mild cirrhotics and 93 age- and sex-matched healthy controls were analyzed for HHV-8 antibody and HHV-8 DNA. Mild cirrhotics had higher seropositivity for HHV-8 antibodies than healthy controls (P=0.0001). Univariate logistic regression analysis revealed that an age ≥55 years (odds ratio (OR) 2.88, P=0.02), hepatitis C virus (HCV) infection (OR 3.42, P=0.01), and hepatitis activity (OR 4.10, P=0.004) were associated with HHV-8 seropositivity in cirrhotics. Stepwise multivariate logistic regression analysis confirmed that age ≥55 years (adjusted OR (aOR) 1.92, P=0.04) and hepatitis activity (aOR 3.55, P=0.005) were independent factors. The rate of hepatitis activity was higher in HCV-infected than in HBV-infected patients (P<0.0001) and in women than in men (P=0.0001). Cirrhotics who were seropositive for HHV-8 or HCV or had hepatitis activity were significantly older (P=0.02, <0.0001 and <0.0001, respectively). Plasma samples from all participants were negative for HHV-8 DNA. HHV-8 antibody titers in mild cirrhotics also markedly exceeded those in controls (P<0.0001), as did those in patients ≥55 years old vs. younger patients (P=0.01), those in patients with vs. without HCV infection (P=0.0008), and those in patients with vs. without hepatitis activity (P=0.0005). Mild cirrhotics had high HHV-8 seroprevalence and HCV infection, and, in particular, old age and hepatitis activity were predictors. Nature Publishing Group 2017-06 2017-06-07 /pmc/articles/PMC5520309/ /pubmed/28588294 http://dx.doi.org/10.1038/emi.2017.32 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Tseng, Kuo-Chih
Lin, Ming-Nan
Chu, Tang-Yuan
Tsai, Jen-Pi
Su, Cheng-Chuan
Predictors of seropositivity for human herpesvirus type 8 in patients with mild cirrhosis
title Predictors of seropositivity for human herpesvirus type 8 in patients with mild cirrhosis
title_full Predictors of seropositivity for human herpesvirus type 8 in patients with mild cirrhosis
title_fullStr Predictors of seropositivity for human herpesvirus type 8 in patients with mild cirrhosis
title_full_unstemmed Predictors of seropositivity for human herpesvirus type 8 in patients with mild cirrhosis
title_short Predictors of seropositivity for human herpesvirus type 8 in patients with mild cirrhosis
title_sort predictors of seropositivity for human herpesvirus type 8 in patients with mild cirrhosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520309/
https://www.ncbi.nlm.nih.gov/pubmed/28588294
http://dx.doi.org/10.1038/emi.2017.32
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