Evidence map›Paper›PMID 29867928›Full record

ArticleFrontiers in immunology2018

Polymorphism rs1385129 Within Glut1 Gene

Jesse J R Masson, Catherine L Cherry, Nicholas M Murphy, Isabel Sada-Ovalle, Tabinda Hussain, Riya Palchaudhuri, Jeffrey Martinson, Alan L Landay, Baki Billah, Suzanne M Crowe and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 34% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Human mutation · 2026
    Article
  5. Article
  6. Genetic signatures ofFrontiers in immunology · 2024
    Observational
  7. Review
  8. Review
  9. Frontiers in pharmacology · 2021
    Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
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 at 7 institutions in 4 countries.

Jesse J R MassonCentre for Biomedical Research, Burnet Institute, Melbourne, VIC, Australia.
Catherine L CherryCentre for Biomedical Research, Burnet Institute, Melbourne, VIC, Australia.
Nicholas M MurphyMonash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC, Australia.
Isabel Sada-OvalleUnidad de Investigación Instituto Nacional de Enfermedades Respiratorias, Mexico City, Mexico.
Tabinda HussainDepartment of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia.
Riya PalchaudhuriCentre for Biomedical Research, Burnet Institute, Melbourne, VIC, Australia.
Jeffrey MartinsonDepartment of Immunology-Microbiology, Rush University Medical Centre, Chicago, IL, United States.
Alan L LandayDepartment of Immunology-Microbiology, Rush University Medical Centre, Chicago, IL, United States.
Baki BillahSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Suzanne M CroweCentre for Biomedical Research, Burnet Institute, Melbourne, VIC, Australia.
Clovis S PalmerCentre for Biomedical Research, Burnet Institute, Melbourne, VIC, Australia.
Monash University · AUBurnet Institute · AURush University Medical Center · USAustralian Regenerative Medicine Institute · AUInstituto Nacional de Enfermedades Respiratorias · MXMonash IVF · AUUniversity of the Witwatersrand · ZA

Funding

University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI EDWIN ROBERTO ORELLANA · 1988 to 2026
$104.9M
NIAID NIH HHS P30 AI027757
6 · The paper itself

Abstract

Untreated HIV infection is associated with progressive CD4+ T cell depletion, which is generally recovered with combination antiretroviral therapy (cART). However, a significant proportion of cART-treated individuals have poor CD4+ T cell reconstitution. We investigated associations between HIV disease progression and CD4+ T cell glucose transporter-1 (Glut1) expression. We also investigated the association between these variables and specific single nucleotide polymorphisms (SNPs) within the Glut1 regulatory gene AKT (rs1130214, rs2494732, rs1130233, and rs3730358) and in the Glut1-expressing gene SLC2A1 (rs1385129 and rs841853) and antisense RNA 1 region SLC2A1-AS1 (rs710218). High CD4+Glut1+ T cell percentage is associated with rapid CD4+ T cell decline in HIV-positive treatment-naïve individuals and poor T cell recovery in HIV-positive individuals on cART. Evidence suggests that poor CD4+ T cell recovery in treated HIV-positive individuals is linked to the homozygous genotype (GG) associated with SLC2A1 SNP rs1385129 when compared to those with a recessive allele (GA/AA) (odds ratio = 4.67;

Indexed as

AdultAnti-Retroviral AgentsCD4 Lymphocyte CountCD4-Positive T-LymphocytesCohort StudiesDisease ProgressionGlucose Transporter Type 1HIV InfectionsHumansMaleMiddle AgedPolymorphism, Single NucleotideProto-Oncogene Proteins c-aktYoung AdultAKT1 protein, humanAnti-Retroviral AgentsGlucose Transporter Type 1Proto-Oncogene Proteins c-aktSLC2A1 protein, humanAKTCD4+ T cellsGlut1HIVimmune activationimmune reconstitutionimmunometabolismSLC2A1

Identifiers

PMID29867928
PMCPMC5966582
OpenAlexW2803356256

What OpenQuestion holds

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LicenceCC BY
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.