Evidence map›Paper›PMID 21681054›Full record

ArticleAIDS (London, England)2011

Association of polymorphisms in the LEDGF/p75 gene (PSIP1) with susceptibility to HIV-1 infection and disease progression.

Paradise Madlala, Rik Gijsbers, Frauke Christ, Anneleen Hombrouck, Lise Werner, Koleka Mlisana, Ping An, Salim S Abdool Karim, Cheryl A Winkler, Zeger Debyser and 1 more

Open access · greenAbstract read
In one paragraph

Article in AIDS (London, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  3. Identification of novel nuclear targets of human thioredoxin 1.Molecular & cellular proteomics : MCP · 2014
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  5. Interrogating HIV integrase for compounds that bind--a SAMPL challenge.Journal of computer-aided molecular design · 2014
    Article
  6. Article
  7. Article
  8. HIV Drug Resistance and the Advent of Integrase Inhibitors.Current infectious disease reports · 2013
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. 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

11 authors at 3 institutions in 2 countries.

Paradise MadlalaHIV Pathogenesis Programme, University of KwaZulu-Natal, Durban, South Africa.
Rik Gijsbers
Frauke Christ
Anneleen Hombrouck
Lise Werner
Koleka Mlisana
Ping An
Salim S Abdool Karim
Cheryl A Winkler
Zeger Debyser
Thumbi Ndung'u
KU Leuven · BEUniversity of KwaZulu-Natal · ZACentre for the AIDS Programme of Research in South Africa · ZA

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
Identification of Genetic Factors Associated with Infectious DiseasesZIABC010297 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WINKLER, CHERYL · 2009 to 2022
$6.3M
CCR NIH HHS HHSN261200800001CIntramural NIH HHSNCI NIH HHS HHSN261200800001ENIAID NIH HHS N01-AI-15422NIAID NIH HHS R01-AI067073NIAID NIH HHS U19 AI051794NIAID NIH HHS U19 AI 51794
6 · The paper itself

Abstract

objectiveLEDGF/p75, encoded by the PSIP1 gene, interacts with HIV-1 integrase and targets HIV-1 integration into active genes. We investigated the influence of polymorphisms in PSIP1 on HIV-1 acquisition and disease progression in black South Africans.

methodsIntegrase binding domain of LEDGF/p75 was sequenced in 126 participants. Four haplotype tagging SNPs rs2277191, rs1033056, rs12339417 and rs10283923 referred to as SNP1, SNP2, SNP3 and SNP4, respectively, and one exonic SNP rs61744944 (SNP5, Q472L) were genotyped in 195 HIV-1 seronegative, 52 primary and 403 chronically infected individuals using TaqMan assays. LEDGF/p75 expression was quantified by real-time RT-PCR. The impact of Q472L mutation on the interaction with HIV_1 IN was measured by AlphaScreen.

resultsrs2277191 (SNP1) A was more frequent among seropositives (P = 0.06, Fisher's exact test). Among individuals followed longitudinally SNP1A trended towards association with higher likelihood of HIV-1 acquisition [relative hazard (RH) = 2.21, P = 0.08; Cox model] and it was also associated with rapid disease progression (RH = 5.98, P = 0.04; Cox model) in the recently infected (primary infection) cohort. rs12339417 (SNP3)C was associated with slower decline of CD4(+) T cells (P = 0.02) and lower messenger RNA (mRNA) levels of LEDGF/p75 (P < 0.01). Seroconverters had higher preinfection mRNA levels of LEDGF/p75 (P < 0.01) and these levels decreased after HIV-1 infection (P = 0.02).

conclusionsGenetic variants of PSIP1 may affect HIV-1 outcomes. Further studies are needed to confirm the effect of genetic variation of PSIP1 on HIV-1 pathogenesis in different cohorts.

Indexed as

MutationPolymorphism, Single NucleotideAdaptor Proteins, Signal TransducingDisease ProgressionGenetic Predisposition to DiseaseHIV-1HIV InfectionsHumansIntegrasesReverse Transcriptase Polymerase Chain ReactionTranscription FactorsAdaptor Proteins, Signal TransducingIntegrasesPSIP1 protein, humanTranscription Factors

Identifiers

PMID21681054
PMCPMC3233670
OpenAlexW2128468606

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.