Hepatitis B virus infection in HIV-positive individuals in the UK collaborative HIV cohort (UK CHIC) study

Hepatitis B virus (HBV) infection is an increasingly important cause of morbidity and mortality in HIV-infected adults. This study aimed to determine the prevalence and incidence of HBV in the UK CHIC Study, a multicentre observational cohort. 12 HIV treatment centres were included. Of 37,331 patien...

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Veröffentlicht in:PloS one 2012-11, Vol.7 (11), p.e49314-e49314
Hauptverfasser: Price, Huw, Bansi, Loveleen, Sabin, Caroline A, Bhagani, Sanjay, Burroughs, Andrew, Chadwick, David, Dunn, David, Fisher, Martin, Main, Janice, Nelson, Mark, Pillay, Deenan, Rodger, Alison, Taylor, Chris, Gilson, Richard
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container_issue 11
container_start_page e49314
container_title PloS one
container_volume 7
creator Price, Huw
Bansi, Loveleen
Sabin, Caroline A
Bhagani, Sanjay
Burroughs, Andrew
Chadwick, David
Dunn, David
Fisher, Martin
Main, Janice
Nelson, Mark
Pillay, Deenan
Rodger, Alison
Taylor, Chris
Gilson, Richard
description Hepatitis B virus (HBV) infection is an increasingly important cause of morbidity and mortality in HIV-infected adults. This study aimed to determine the prevalence and incidence of HBV in the UK CHIC Study, a multicentre observational cohort. 12 HIV treatment centres were included. Of 37,331 patients, 27,450 had at least one test (HBsAg, anti-HBs or anti-HBc) result post-1996 available. 16,043 were white, 8,130 black and 3,277 other ethnicity. Route of exposure was homosexual sex 15,223 males, heterosexual sex 3,258 males and 5,384 females, injecting drug use 862 and other 2,723. The main outcome measures used were the cumulative prevalence and the incidence of HBV coinfection. HBV susceptible patients were followed up until HBsAg and/or anti-HBc seroconversion incident infection, evidence of vaccination or last visit. Poisson regression was used to determine associated factors. 25,973 had at least one HBsAg test result. Participants with HBsAg results were typically MSM (57%) and white (59%) (similar to the cohort as a whole). The cumulative prevalence of detectable HBsAg was 6.9% (6.6 to 7.2%). Among the 3,379 initially HBV-susceptible patients, the incidence of HBV infection was 1.7 (1.5 to 1.9)/100 person-years. Factors associated with incident infection were older age and IDU. The main limitation of the study was that 30% of participants did not have any HBsAg results available. However baseline characteristics of those with results did not differ from those of the whole cohort. Efforts are on-going to improve data collection. The prevalence of HBV in UK CHIC is in line with estimates from other studies and low by international standards. Incident infection continued to occur even after entry to the cohort, emphasising the need to ensure early vaccination.
doi_str_mv 10.1371/journal.pone.0049314
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This study aimed to determine the prevalence and incidence of HBV in the UK CHIC Study, a multicentre observational cohort. 12 HIV treatment centres were included. Of 37,331 patients, 27,450 had at least one test (HBsAg, anti-HBs or anti-HBc) result post-1996 available. 16,043 were white, 8,130 black and 3,277 other ethnicity. Route of exposure was homosexual sex 15,223 males, heterosexual sex 3,258 males and 5,384 females, injecting drug use 862 and other 2,723. The main outcome measures used were the cumulative prevalence and the incidence of HBV coinfection. HBV susceptible patients were followed up until HBsAg and/or anti-HBc seroconversion incident infection, evidence of vaccination or last visit. Poisson regression was used to determine associated factors. 25,973 had at least one HBsAg test result. Participants with HBsAg results were typically MSM (57%) and white (59%) (similar to the cohort as a whole). The cumulative prevalence of detectable HBsAg was 6.9% (6.6 to 7.2%). 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Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Price, Huw</au><au>Bansi, Loveleen</au><au>Sabin, Caroline A</au><au>Bhagani, Sanjay</au><au>Burroughs, Andrew</au><au>Chadwick, David</au><au>Dunn, David</au><au>Fisher, Martin</au><au>Main, Janice</au><au>Nelson, Mark</au><au>Pillay, Deenan</au><au>Rodger, Alison</au><au>Taylor, Chris</au><au>Gilson, Richard</au><au>Tavis, John E.</au><aucorp>UK Collaborative HIV Cohort Hepatitis Group, Steering Committee</aucorp><aucorp>UK Collaborative HIV Cohort Hepatitis Group, Steering Committee</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis B virus infection in HIV-positive individuals in the UK collaborative HIV cohort (UK CHIC) study</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012-11-07</date><risdate>2012</risdate><volume>7</volume><issue>11</issue><spage>e49314</spage><epage>e49314</epage><pages>e49314-e49314</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Hepatitis B virus (HBV) infection is an increasingly important cause of morbidity and mortality in HIV-infected adults. This study aimed to determine the prevalence and incidence of HBV in the UK CHIC Study, a multicentre observational cohort. 12 HIV treatment centres were included. Of 37,331 patients, 27,450 had at least one test (HBsAg, anti-HBs or anti-HBc) result post-1996 available. 16,043 were white, 8,130 black and 3,277 other ethnicity. Route of exposure was homosexual sex 15,223 males, heterosexual sex 3,258 males and 5,384 females, injecting drug use 862 and other 2,723. The main outcome measures used were the cumulative prevalence and the incidence of HBV coinfection. HBV susceptible patients were followed up until HBsAg and/or anti-HBc seroconversion incident infection, evidence of vaccination or last visit. Poisson regression was used to determine associated factors. 25,973 had at least one HBsAg test result. Participants with HBsAg results were typically MSM (57%) and white (59%) (similar to the cohort as a whole). The cumulative prevalence of detectable HBsAg was 6.9% (6.6 to 7.2%). Among the 3,379 initially HBV-susceptible patients, the incidence of HBV infection was 1.7 (1.5 to 1.9)/100 person-years. Factors associated with incident infection were older age and IDU. The main limitation of the study was that 30% of participants did not have any HBsAg results available. However baseline characteristics of those with results did not differ from those of the whole cohort. Efforts are on-going to improve data collection. The prevalence of HBV in UK CHIC is in line with estimates from other studies and low by international standards. Incident infection continued to occur even after entry to the cohort, emphasising the need to ensure early vaccination.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23145150</pmid><doi>10.1371/journal.pone.0049314</doi><oa>free_for_read</oa></addata></record>
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subjects Acquired immune deficiency syndrome
Adults
AIDS
AIDS treatment
Analysis
Antigens
Antiretroviral drugs
Biology
Care and treatment
Cohort Studies
Coinfection - epidemiology
Collaboration
Data collection
Datasets
Drug therapy
Epidemiology
Female
Females
Health aspects
Hepatitis
Hepatitis B
Hepatitis B - complications
Hepatitis B - epidemiology
Hepatitis B surface antigen
HIV
HIV Infections - complications
HIV patients
Homosexuality
Hospitals
Human immunodeficiency virus
Humans
Immunization
Incidence
Infections
Infectious diseases
International standardization
International standards
Laboratories
Liver diseases
Male
Males
Medicine
Minority & ethnic groups
Morbidity
Mortality
Patients
Poisson density functions
Population
Prevalence
Seroconversion
Sex
Sexually transmitted diseases
Statistical analysis
STD
United Kingdom - epidemiology
Vaccination
Vaccination - statistics & numerical data
Viruses
title Hepatitis B virus infection in HIV-positive individuals in the UK collaborative HIV cohort (UK CHIC) study
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