Evidence map›Paper›PMID 24508837›Full record

ArticleJournal of acquired immune deficiency syndromes (1999)2014

Association between HIV-1 tropism and CCR5 human haplotype E in a Caucasian population.

Kristi Huik, Radko Avi, Helen Uibopuu, Merit Pauskar, Tõnu Margus, Tõnis Karki, Tõnu Krispin, Piret Kool, Kristi Rüütel, Ave Talu and 6 more

Open access · greenAbstract read
In one paragraph

Article in Journal of acquired immune deficiency syndromes (1999), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. CCR2, CCR5, and CXCL12 variation and HIV/AIDS in Papua New Guinea.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2015
    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

16 authors at 6 institutions in 2 countries.

Kristi Huik*Department of Microbiology, Faculty of Medicine, University of Tartu, Tartu, Estonia; †West-Tallinn Hospital Laboratories, Tallinn, Estonia; ‡Department of Bioinformatics, Institute of Molecular and Cell Biology, University of Tartu and Estonian Biocentre, Tartu, Estonia; §Tartu Prison Hospital, Tartu, Estonia; ‖National Institute for Health Development, Tallinn, Estonia; ¶Department of Public Health, Faculty of Medicine, University of Tartu, Tartu, Estonia; #Department of Medicine, University of Texas Health Science Center, San Antonio, TX; and **Veterans Administration Research Center for AIDS and HIV-1 Infection, and ††Center for Personalized Medicine, South Texas Veterans Health Care System, San Antonio, TX.
Radko Avi
Helen Uibopuu
Merit Pauskar
Tõnu Margus
Tõnis Karki
Tõnu Krispin
Piret Kool
Kristi Rüütel
Ave Talu
Katri Abel-Ollo
Anneli Uusküla
Andrew Carrillo
Weijing He
Sunil K Ahuja
Irja Lutsar
University of Tartu · EENational Institute for Health Development · EEThe University of Texas Health Science Center at San Antonio · USEast Tallinn Central Hospital · EETartu University Hospital · EEUnited States Department of Veterans Affairs · US

Funding

Risk Factors for HIV/AIDS in Drug UsersR01DA003574 · NIDA · NEW YORK UNIVERSITY · PI DES JARLAIS, DON C, MCKNIGHT, COURTNEY · 1986 to 2025
$16.2M
Host Genetic Determinants of HIV PathogenesisR37AI046326 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI AHUJA, SUNIL K · 2005 to 2014
$7.8M
Center for Personalized Medicine: Systems of Biology of Inflammation and ImmunityIP1CX000875 · VA · SOUTH TEXAS VETERANS HEALTH CARE SYSTEM · PI AHUJA, SEEMA SINGH, AHUJA, SUNIL K · 2014 to 2017
–
CSRD VA IP1 CX000875NIAID NIH HHS R37 AI046326NIAID NIH HHS R37AI046326NIDA NIH HHS R01 DA003574NIDA NIH HHS R01DA03574
6 · The paper itself

Abstract

backgroundThe influence of the diversity of CCR5 on HIV susceptibility and disease progression has been clearly demonstrated but how the variability of this gene influences the HIV tropism is poorly understood. We investigated whether CCR5 haplotypes are associated with HIV tropism in a Caucasian population.

methodsWe evaluated 161 HIV-positive subjects in a cross-sectional study. CCR5 haplotypes were derived after genotyping 9 CCR2-CCR5 polymorphisms. The HIV subtype was determined by phylogenetic analysis using the maximum likelihood method and viral tropism by the genotypic tropism assay (geno2pheno). Associations between CCR5 haplotypes and viral tropism were determined using logistic regression analyses. Samples from 500 blood donors were used to evaluate the representativeness of HIV-positives in terms of CCR5 haplotype distribution.

resultsThe distribution of CCR5 haplotypes was similar in HIV-positive subjects and blood donors. The majority of viruses (93.8%) belonged to HIV-1 CRF06_cpx; 7.5% were X4, and the remaining were R5 tropic. X4 tropic viruses were over represented among people with CCR5 human haplotype E (HHE) compared with those without this haplotype (13.0% vs 1.4%; P = 0.006). People possessing CCR5 HHE had 11 times increased odds (odds ratio = 11.00; 95% confidence interval: 1.38 to 87.38) of having X4 tropic viruses than those with non-HHE. After adjusting for antiretroviral (ARV) therapy, neither the presence of HHE nor the use of ARV was associated with X4 tropic viruses.

conclusionsOur results suggest that CCR5 HHE and ARV treatment might be associated with the presence of HIV-1 X4 tropic viruses.

Indexed as

Genetic Predisposition to DiseaseViral TropismAdultCross-Sectional StudiesEstoniaFemaleGenetic Association StudiesHaplotypesHIV-1HIV InfectionsHumansLogistic ModelsMalePhylogenyPolymorphism, Single NucleotideReceptors, CCR5CCR5 protein, humanReceptors, CCR5

Identifiers

PMID24508837
PMCPMC4146654
OpenAlexW2049090787

What OpenQuestion holds

Textmetadata
LicenceTDM
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.