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DC Field | Value | Language |
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dc.contributor.author | Amy E. Greer | en_US |
dc.contributor.author | San San Ou | en_US |
dc.contributor.author | Ethan Wilson | en_US |
dc.contributor.author | Estelle Piwowar-Manning | en_US |
dc.contributor.author | Michael S. Forman | en_US |
dc.contributor.author | Marybeth McCauley | en_US |
dc.contributor.author | Theresa Gamble | en_US |
dc.contributor.author | Cholticha Ruangyuttikarn | en_US |
dc.contributor.author | Mina C. Hosseinipour | en_US |
dc.contributor.author | Nagalingeswaran Kumarasamy | en_US |
dc.contributor.author | Mulinda Nyirenda | en_US |
dc.contributor.author | Beatriz Grinsztejn | en_US |
dc.contributor.author | Jose Henrique Pilotto | en_US |
dc.contributor.author | Natthapol Kosashunhanan | en_US |
dc.contributor.author | Marineide Gonçalves De Melo | en_US |
dc.contributor.author | Joseph Makhema | en_US |
dc.contributor.author | Victor Akelo | en_US |
dc.contributor.author | Ravindre Panchia | en_US |
dc.contributor.author | Sharlaa Badal-Faesen | en_US |
dc.contributor.author | Ying Q. Chen | en_US |
dc.contributor.author | Myron S. Cohen | en_US |
dc.contributor.author | Susan H. Eshleman | en_US |
dc.contributor.author | Chloe L. Thio | en_US |
dc.contributor.author | Alexandra Valsamakis | en_US |
dc.date.accessioned | 2018-09-05T03:50:44Z | - |
dc.date.available | 2018-09-05T03:50:44Z | - |
dc.date.issued | 2017-01-01 | en_US |
dc.identifier.issn | 10779450 | en_US |
dc.identifier.issn | 15254135 | en_US |
dc.identifier.other | 2-s2.0-85026363946 | en_US |
dc.identifier.other | 10.1097/QAI.0000000000001511 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85026363946&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/57839 | - |
dc.description.abstract | © 2017 Wolters Kluwer Health, Inc. All rights reserved. Objective: Data comparing hepatitis B virus (HBV) infection in HIV-infected [HIV(+)], and HIV-uninfected [HIV(2)] individuals recruited into the same study are limited. HBV infection status and chronic hepatitis B (cHB) were characterized in a multinational clinical trial: HIV Prevention Trials Network (HPTN 052). Method: HBV infection status at enrollment was compared between HIV(+) (N = 1241) and HIV(-) (N = 1232) from 7 HBV-endemic countries. Hepatitis B e antigen and plasma HBV DNA were determined in cHB. Median CD4, median plasma HIV RNA, and prevalence of transaminase elevation were compared in HIV(+) with and without cHB. Significance was assessed with x2Fisher exact and median tests. Results: Among all participants, 33.6% had HBV exposure without cHB (8.9% isolated HBV core antibody, "HBcAb"; 24.7% HBcAb and anti-HB surface antibody positive, "recovered"), 4.3% had cHB, 8.9% were vaccinated, and 53.5% were uninfected. Data were similar among HIV(+) and HIV(2) except for isolated HBcAb, which was more prevalent in HIV(+) than HIV(2) [10.1% vs. 7.7%, P = 0.046]. Median HBV DNA trended higher in HIV(+) than in HIV(2). In HIV (+) with cHB versus those without cHB, transaminase elevations were more prevalent (alanine aminotransferase # grade 2, 12% vs. 5.2%, P = 0.037; aspartate aminotransferase # grade 2, 26% vs. 6.0%, P, 0.001), CD4 trended lower, and HIV RNA was similar. Conclusions: HBV infection status did not differ by HIV infection status. HIV co-infection was associated with isolated HBcAb and a trend of increased HBV DNA. In HIV, cHB was associated with mild transaminase elevations and a trend toward lower CD4. | en_US |
dc.subject | Medicine | en_US |
dc.title | Comparison of hepatitis b virus infection in HIV-infected and HIV-uninfected participants enrolled in a multinational clinical trial: HPTN 052 | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Journal of Acquired Immune Deficiency Syndromes | en_US |
article.volume | 76 | en_US |
article.stream.affiliations | Johns Hopkins Hospital | en_US |
article.stream.affiliations | Fred Hutchinson Cancer Research Center | en_US |
article.stream.affiliations | The Johns Hopkins School of Medicine | en_US |
article.stream.affiliations | FHI 360 | en_US |
article.stream.affiliations | FHI 360 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | The University of North Carolina at Chapel Hill | en_US |
article.stream.affiliations | University of North Carolina Project Malawi | en_US |
article.stream.affiliations | VHS Medical Centre India | en_US |
article.stream.affiliations | University of Malawi College of Medicine | en_US |
article.stream.affiliations | Fundacao Oswaldo Cruz | en_US |
article.stream.affiliations | Hospital Geral de Rio de Janeiro | en_US |
article.stream.affiliations | Hospital Nossa Senhora da Conceicao | en_US |
article.stream.affiliations | Botswana Harvard AIDS Institute Partnership | en_US |
article.stream.affiliations | Kenya Medical Research Institute | en_US |
article.stream.affiliations | Center for Disease Control | en_US |
article.stream.affiliations | University of Witwatersrand | en_US |
article.stream.affiliations | Johns Hopkins University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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