Evidence map›Paper›PMID 26981576›Full record

Trial reportEBioMedicine2016

Vitamin D, D-dimer, Interferon γ, and sCD14 Levels are Independently Associated with Immune Reconstitution Inflammatory Syndrome: A Prospective, International Study.

Laura W Musselwhite, Bruno B Andrade, Susan S Ellenberg, Ann Tierney, Pablo F Belaunzaran-Zamudio, Adam Rupert, Michael M Lederman, Ian Sanne, Juan G Sierra Madero, Irini Sereti

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in EBioMedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Association between CD4BMC infectious diseases · 2021
    Article
  10. Observational
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Immune Reconstitution Disorders: Spotlight on Interferons.International journal of biomedical investigation · 2019
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 9 institutions in 4 countries.

Laura W MusselwhiteLaboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), 10 Center Drive, Bethesda, MD 20892, USA; Duke Hubert Yeargan Center for Global Health, Duke University, 310 Trent Drive, Duke Box 90518, Durham, NC 27708, USA.
Bruno B AndradeLaboratory of Parasitic Diseases, NIAID, NIH, 50 South Drive, Bethesda, MD 20892, USA; Unidade de Medicina Investigativa, Laboratório Integrado de Microbiologia e Imunorregulação (LIMI), Centro de Pesquisas Gonçalo Moniz (CPqGM), Fundação Oswaldo Cruz (FIOCRUZ), Salvador 40296-710, Brazil; Multinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER Initiative), Brazilian Institute for Tuberculosis Research, José Silveira Foundation, Salvador, Brazil.
Susan S EllenbergCenter for Clinical Epidemiology and Biostatistics, University of Pennsylvania School of Medicine, 611 Blockley Hall, 423 Guardian Drive, Philadelphia, PA 19104-602, USA.
Ann TierneyCenter for Clinical Epidemiology and Biostatistics, University of Pennsylvania School of Medicine, 611 Blockley Hall, 423 Guardian Drive, Philadelphia, PA 19104-602, USA.
Pablo F Belaunzaran-ZamudioDepartamento de Infectología, Instituto Nacional de Ciencias Médicas y Nutrición "Salvador Zubirán", México City, México; División de Investigación, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, México.
Adam RupertLeidos Biomedical Inc., 11951 Freedom Drive, Reston, VA 20190, USA.
Michael M LedermanCase Western Reserve University School of Medicine, 2061 Cornell Rd, Cleveland, OH 44106, USA.
Ian SanneUniversity of Witwatersrand, Johannesburg, South Africa.
Juan G Sierra MaderoDepartamento de Infectología, Instituto Nacional de Ciencias Médicas y Nutrición "Salvador Zubirán", México City, México.
Irini SeretiLaboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), 10 Center Drive, Bethesda, MD 20892, USA.
University of Pennsylvania · USDuke University · USInstituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán · MXLeidos (United States) · USNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USUniversidad Nacional Autónoma de México · MXUniversity of the Witwatersrand · ZAUniversity School · US

Funding

Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI DAVID S METZGER · 1999 to 2026
$78.6M
Case Clinical Trials Unit: Administrative Supplement NOSI AI-20-031.UM1AI069501 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI George Yendewa · 2012 to 2026
$40.4M
Immunopathogenic Mechanisms of Human Immunodeficiency Virus (HIV) DiseaseZIAAI001121 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SERETI, IRINI · 2010 to 2025
$27.2M
Adjunctive immune modulation to improve TB treatmentR21AI110335 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI SUBBIAN, SELVAKUMAR · 2014 to 2015
$437k
Intramural NIH HHSNIAID NIH HHS 1R21AI110335-01NIAID NIH HHS P30 AI045008NIAID NIH HHS UM1 AI069501
6 · The paper itself

Abstract

To determine the immunological profile most important for IRIS prediction, we evaluated 20 baseline plasma biomarkers in Acquired Immunodeficiency Syndrome (AIDS) patients initiating antiretroviral therapy (ART). Patients were enrolled in a randomized, placebo-controlled ART initiation trial in South Africa and Mexico to test whether maraviroc could prevent IRIS. Participants were classified prospectively as having IRIS within 6 months of ART initiation. Twenty plasma biomarkers were measured at study enrollment for 267 participants. Biomarkers were tested for predicting IRIS with adjustment for covariates chosen through forward stepwise selection. Sixty-two participants developed IRIS and of these 19 were tuberculosis (TB)-IRIS. Baseline levels of vitamin D and higher d-dimer, interferon gamma (IFNγ), and sCD14 were independently associated with risk of IRIS in multivariate analyses. TB-IRIS cases exhibited a distinct biosignature from IRIS related to other pathogens, with increased levels of C-reactive protein (CRP), sCD14, IFNγ, and lower levels of Hb that could be captured by a composite risk score. Elevated markers of Type 1 T helper (Th1) response, monocyte activation, coagulation and low vitamin D were independently associated with IRIS risk. Interventions that decrease immune activation and increase vitamin D levels warrant further study.

Indexed as

Acquired Immunodeficiency SyndromeAdultAntiretroviral Therapy, Highly ActiveBiomarkersFemaleFibrin Fibrinogen Degradation ProductsHumansImmune Reconstitution Inflammatory SyndromeInterferon-gammaLipopolysaccharide ReceptorsMaleTh1 CellsVitamin DBiomarkersFibrin Fibrinogen Degradation Productsfibrin fragment DInterferon-gammaLipopolysaccharide ReceptorsVitamin DBiomarkerd-DimerHIVInflammatory cytokineIRISVitamin D

Identifiers

PMID26981576
PMCPMC4776072
OpenAlexW2238913909

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.