Evidence map›Paper›PMID 25828994›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2015

Concurrent Anemia and Elevated C-Reactive Protein Predicts HIV Clinical Treatment Failure, Including Tuberculosis, After Antiretroviral Therapy Initiation.

Rupak Shivakoti, Wei-Teng Yang, Nikhil Gupte, Sima Berendes, Alberto La Rosa, Sandra W Cardoso, Noluthando Mwelase, Cecilia Kanyama, Sandy Pillay, Wadzanai Samaneka and 13 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% of its field
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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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

23 authors at 16 institutions in 8 countries.

Rupak ShivakotiDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Wei-Teng YangDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Nikhil GupteDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Sima BerendesMalawi College of Medicine-Johns Hopkins University Research Project, Blantyre.
Alberto La RosaAsociacion Civil Impacta Salud y Educacion, Lima, Peru.
Sandra W CardosoSTD/AIDS Clinical Research Laboratory, Instituto de Pesquisa Clinica Evandro Chagas, Fundacao Oswaldo Cruz, Rio de Janeiro, Brazil.
Noluthando MwelaseDepartment of Medicine, University of Witwatersrand, Johannesburg, South Africa.
Cecilia KanyamaUniversity of North Carolina Lilongwe, Malawi.
Sandy PillayDurban International Clinical Research Site, Durban University of Technology, South Africa.
Wadzanai SamanekaUniversity of Zimbabwe Clinical Research Centre, Harare.
Cynthia RiviereLes Centres GHESKIO, Port-Au-Prince, Haiti.
Patcharaphan SugandhavesaResearch Institute for Health Sciences, Chiang Mai, Thailand.
Brento SantosHospital Nossa Senhora de Conceição, Porto Alegre, Brazil.
Selvamuthu PoongulaliY. R. Gaitonde Center for AIDS Research and Education, Chennai.
Srikanth TripathyNational AIDS Research Institute, Pune, India.
Robert C BollingerDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Judith S CurrierDepartment of Medicine, University of California, Los Angeles.
Alice M TangDepartment of Public Health and Community Medicine, Tufts University School of Medicine, Boston, Massachusetts.
Richard D SembaDepartment of Ophthalmology, Johns Hopkins University School of Medicine.
Parul ChristianDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Thomas B CampbellDepartment of Medicine, Division of Infectious Diseases, University of Colorado School of Medicine, Aurora.
Amita GuptaDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
New Work Concept Sheet 319 and The Prospective Evaluation of Antiretrovirals in Resource-Limited Settings Study Team
Johns Hopkins University · USJohns Hopkins Medicine · USAsociación Civil Impacta Salud y Educación · PEDurban University of Technology · ZAFundação Oswaldo Cruz · BRGheskio Centers · HTHospital Nossa Senhora da Conceição · BRLilongwe University of Agriculture and Natural Resources · MWNational AIDS Research Institute · INTufts University · USUniversity of California, Los Angeles · USUniversity of Colorado Denver · USUniversity of Malawi · MWUniversity of the Witwatersrand · ZAUniversity of Zimbabwe · ZWYR Gaitonde Centre for AIDS Research and Education · IN

Funding

Leadership and Operations Center (LOC), AIDS Clinical Trials Group (ACTG); LOC 1/UM1AI068636 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph J Eron, RAJESH T GANDHI · 2011 to 2026
$1073.1M
Statistical and Data Management Center (SDMC), AIDS Clinical Trials Group (ACTG)UM1AI068634 · NIAID · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Marlene Ann Cooper, Michael David Hughes · 2011 to 2026
$246.6M
Validation, CLIA and Qualification (VQC): Enhancing the RS ratio as a tool for AIDS Clinical Trial Group (ACTG) tuberculosis trialsUM1AI106701 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Grace M Aldrovandi · 2014 to 2026
$116.8M
University of North Carolina Global HIV Prevention and Treatment Clinical Trials Unit 2024 SupplementUM1AI069423 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph J Eron, MINA CHRISTINE HOSSEINIPOUR · 2012 to 2026
$71.8M
Impact of Malnutrition on HIV Treatment Failure in Resource-Limited SettingsR01AI080417 · NIAID · JOHNS HOPKINS UNIVERSITY · PI GUPTA, AMITA · 2009 to 2012
$2.3M
NIAID NIH HHS R01 AI080417NIAID NIH HHS UM1 AI068634NIAID NIH HHS UM1 AI068636NIAID NIH HHS UM1 AI106701
6 · The paper itself

Abstract

backgroundAnemia is a known risk factor for clinical failure following antiretroviral therapy (ART). Notably, anemia and inflammation are interrelated, and recent studies have associated elevated C-reactive protein (CRP), an inflammation marker, with adverse human immunodeficiency virus (HIV) treatment outcomes, yet their joint effect is not known. The objective of this study was to assess prevalence and risk factors of anemia in HIV infection and to determine whether anemia and elevated CRP jointly predict clinical failure post-ART.

methodsA case-cohort study (N = 470 [236 cases, 234 controls]) was nested within a multinational randomized trial of ART efficacy (Prospective Evaluation of Antiretrovirals in Resource Limited Settings [PEARLS]). Cases were incident World Health Organization stage 3, 4, or death by 96 weeks of ART treatment (clinical failure). Multivariable logistic regression was used to determine risk factors for pre-ART (baseline) anemia (females: hemoglobin <12.0 g/dL; males: hemoglobin <13.0 g/dL). Association of anemia as well as concurrent baseline anemia and inflammation (CRP ≥ 10 mg/L) with clinical failure were assessed using multivariable Cox models.

resultsBaseline anemia prevalence was 51% with 15% prevalence of concurrent anemia and inflammation. In analysis of clinical failure, multivariate-adjusted hazard ratios were 6.41 (95% confidence interval [CI], 2.82-14.57) for concurrent anemia and inflammation, 0.77 (95% CI, .37-1.58) for anemia without inflammation, and 0.45 (95% CI, .11-1.80) for inflammation without anemia compared to those without anemia and inflammation.

conclusionsART-naive, HIV-infected individuals with concurrent anemia and inflammation are at particularly high risk of failing treatment, and understanding the pathogenesis could lead to new interventions. Reducing inflammation and anemia will likely improve HIV disease outcomes. Alternatively, concurrent anemia and inflammation could represent individuals with occult opportunistic infections in need of additional screening.

Indexed as

AdultAgedAnemiaAnti-Retroviral AgentsCase-Control StudiesC-Reactive ProteinFemaleHIV InfectionsHumansIncidenceMaleMiddle AgedProspective StudiesRisk FactorsTreatment FailureYoung AdultAnti-Retroviral AgentsC-Reactive Proteinanemiaantiretroviral therapyCRPHIVinflammation

Identifiers

PMID25828994
PMCPMC4542913
OpenAlexW2167606981

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.