Evidence map›Paper›PMID 39215251›Full record

ArticleBMC infectious diseases2024

Hepatitis B prevalence and risk factors among adults living with HIV in South Africa: a clinic-based cohort study.

Megana Shivakumar, Caitlin A Moe, Ashley Bardon, Meighan Krows, Sabina Govere, Mahomed Yunus S Moosa, Connie Celum, Paul K Drain

Abstract read
In one paragraph

Article in BMC infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Megana ShivakumarDepartment of Global Health, University of Washington, 908 Jefferson St., 12th floor, Seattle, WA, 98104, USA.
Caitlin A MoeDepartment of Global Health, University of Washington, 908 Jefferson St., 12th floor, Seattle, WA, 98104, USA.
Ashley BardonGlobal Health Center, Washington University, St. Louis, USA.
Meighan KrowsDepartment of Global Health, University of Washington, 908 Jefferson St., 12th floor, Seattle, WA, 98104, USA.
Sabina GovereAIDS Healthcare Foundation, Durban, South Africa.
Mahomed Yunus S MoosaDepartment of Infectious Diseases, University of KwaZulu-Natal, Durban, South Africa.
Connie CelumDepartment of Global Health, University of Washington, 908 Jefferson St., 12th floor, Seattle, WA, 98104, USA.
Paul K DrainDepartment of Global Health, University of Washington, 908 Jefferson St., 12th floor, Seattle, WA, 98104, USA. pkdrain@uw.edu.

Funding

The impact of HIV viral diversity and cellular immunity on HIV pathogenesisP30AI060354 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI ARTHUR Y KIM · 2004 to 2026
$94.4M
Clinic-based Screening to Prevent HIV-associated Cryptococcal MortalityK23AI108293 · NIAID · UNIVERSITY OF WASHINGTON · PI DRAIN, PAUL K · 2014 to 2018
$928k
NIAID NIH HHS K23 AI108293NIAID NIH HHS P30 AI060354
6 · The paper itself

Abstract

backgroundPeople living with HIV (PLHIV) may have concurrent Hepatitis B Virus (HBV) infection, and certain antiretroviral therapies are recommended for HBV-HIV co-infected individuals. Routine screening for Hepatitis B virus may influence management of antiretroviral therapy for PLHIV, but risk factors for co-infection have not been well defined. The objective of this study was to identify risk factors for HBV infection among PLHIV in South Africa.

methodsWe conducted a cross-sectional analysis of a prospective, clinic-based cohort study of adults seeking HIV testing from 2013-2017 in Umlazi township, South Africa. Patients newly diagnosed with HIV were enrolled and subsequently tested for Hepatitis B surface antigen positive (HBsAg +). We used a Poisson linear regression model to assess which factors, pertaining to sociodemographic status, medical history, clinical symptoms, mental health were associated with HBV.

resultsAmong 3,105 PLHIV participants in South Africa, 6% were positive for HBV. Males had a higher HBV prevalence (10.4%) than females (5.2%). Within the HBV-positive group, the mean age was 33.2 years, with 38.3% females and 43.9% having completed high school or higher. About 39.9% reported alcohol use, 24.7% had a smoking history, and 8.3% reported substance use in the past year. Older participants born before 1995, when routine infant HBV vaccination was introduced, were more likely to have HBV. In multivariable analyses, smoking history increased HBV risk in females (aPR = 2.58; 95% CI 1.47-2.52), while alcohol use decreased HBV risk in males (aPR = 0.36; 95% CI 0.19-0.70).

conclusionsIn a South African cohort, roughly one in 16 PLHIV had HBV co-infection, and this rate was higher in males. The most prominent risk factors for HBV infection in PLHIV were alcohol use, higher income, and smoking history, which may help inform targeted treatment and prevention strategies. Creating HBV-specific screening and prevention strategies for PLHIV may be useful for reducing HBV infections.

Indexed as

Hepatitis BHIV InfectionsAdultCohort StudiesCoinfectionCross-Sectional StudiesFemaleHepatitis B virusHumansMaleMiddle AgedPrevalenceProspective StudiesRisk FactorsSouth AfricaYoung AdultCo-infectionHBVHIVRisk factors

Identifiers

PMID39215251
PMCPMC11365233

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.