Evidence map›Paper›PMID 25038116›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2014

Rapid disease progression in HIV-1 subtype C-infected South African women.

Koleka Mlisana, Lise Werner, Nigel J Garrett, Lyle R McKinnon, Francois van Loggerenberg, Jo-Ann S Passmore, Clive M Gray, Lynn Morris, Carolyn Williamson, Salim S Abdool Karim and 1 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–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

33 citing papers in PubMed.

  1. Trial
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  5. Long-term non-progression and risk factors for disease progression among children living with HIV in Botswana and Uganda: A retrospective cohort study.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2024
    Article
  6. Article
  7. Article
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  10. Addressing an HIV cure in LMIC.Retrovirology · 2021
    Review
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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

11 authors.

Koleka MlisanaCentre for the AIDS Programme of Research in South Africa Department of Medical Microbiology, University of KwaZulu-Natal, Durban National Health Laboratory Service, Johannesburg, South Africa.
Lise WernerCentre for the AIDS Programme of Research in South Africa.
Nigel J GarrettCentre for the AIDS Programme of Research in South Africa.
Lyle R McKinnonCentre for the AIDS Programme of Research in South Africa.
Francois van LoggerenbergCentre for the AIDS Programme of Research in South Africa The Global Health Network, Centre for Tropical Medicine, University of Oxford, United Kingdom.
Jo-Ann S PassmoreCentre for the AIDS Programme of Research in South Africa National Health Laboratory Service, Johannesburg, South Africa Divisions of Immunology and Medical Virology, Institute of Infectious Diseases and Molecular Medicine, Faculty of Health Sciences, University of Cape Town.
Clive M GrayNational Health Laboratory Service, Johannesburg, South Africa Divisions of Immunology and Medical Virology, Institute of Infectious Diseases and Molecular Medicine, Faculty of Health Sciences, University of Cape Town.
Lynn MorrisAIDS Virus Research Unit, National Institute for Communicable Diseases, Johannesburg, South Africa.
Carolyn WilliamsonCentre for the AIDS Programme of Research in South Africa National Health Laboratory Service, Johannesburg, South Africa Divisions of Immunology and Medical Virology, Institute of Infectious Diseases and Molecular Medicine, Faculty of Health Sciences, University of Cape Town.
Salim S Abdool KarimCentre for the AIDS Programme of Research in South Africa Columbia University, New York, New York.
Centre for the AIDS Programme of Research in South Africa (CAPRISA) 002 Study Team

Funding

The Viral Set Point in HIV-1 Subtype C InfectionU19AI051794 · NIAID · UNIVERSITY OF KWAZULU-NATAL · PI ABDOOL KARIM, SALIM S · 2002 to 2007
$22.5M
ENHANCING, TRAINING, RESEARCH CAPACITY AND EXPERTISE IN HIV CARE-ENTREER24TW008863 · FIC · UNIVERSITY OF KWAZULU-NATAL · PI BOBAT, RAZIYA, HAMMER, SCOTT M · 2010 to 2015
$8.6M
FIC NIH HHS R24 TW008863NIAID NIH HHS AI51794NIAID NIH HHS U19 AI051794
6 · The paper itself

Abstract

backgroundWhereas human immunodeficiency virus (HIV) subtype B-infected individuals generally progress to AIDS within 8-10 years, limited data exist for other clades, especially from Africa. We investigated rates of HIV disease progression of clade C-infected South African women.

methodsProspective seroincidence cohorts in KwaZulu-Natal were assessed for acute HIV infection monthly (n = 245) or every 3 months (n = 594) for up to 4 years. Rapid disease progression was defined as CD4 decline to <350 cells/µL by 2 years postinfection. Serial clinical and laboratory assessments were compared using survival analysis and logistic regression models.

resultsSixty-two women were identified at a median of 42 days postinfection (interquartile range, 34-59), contributing 282 person-years of follow-up. Mean CD4 count dropped by 39.6% at 3 months and 46.7% at 6 months postinfection in women with preinfection measurements. CD4 decline to <350 cells/µL occurred in 31%, 44%, and 55% of women at 1, 2, and 3 years postinfection, respectively, and to <500 cells/µL in 69%, 79%, and 81% at equivalent timepoints. Predictors of rapid progression were CD4 count at 3 months postinfection (hazard ratio [HR], 2.07; 95% confidence interval [CI], 1.31-3.28; P = .002), setpoint viral load (HR, 3.82; 95% CI, 1.51-9.67; P = .005), and hepatitis B coinfection (HR, 4.54; 95% CI, 1.31-15.69; P = .017). Conversely, presence of any of HLAB*1302, B*27, B*57, B*5801, or B*8101 alleles predicted non-rapid progression (HR, 0.19; 95% CI, .05-.74; P = .016).

conclusionsNearly half of subtype C-infected women progressed to a CD4 count <350 cells/µL within 2 years of infection. Implementing 2013 World Health Organization treatment guidelines (CD4 count <500 cells/µL) would require most individuals to start antiretroviral therapy within 1 year of HIV infection.

Indexed as

HIV-1AdultCD4 Lymphocyte CountDisease ProgressionFemaleHIV InfectionsHumansProspective StudiesSeroepidemiologic StudiesSouth AfricaSurvival AnalysisViral LoadYoung Adultacute HIV infectionHIV disease progressionsubtype Cviral loadwomen

Identifiers

PMID25038116
PMCPMC4271037

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.