Evidence map›Paper›PMID 34893534›Full record

ArticleJournal of the American Society of Nephrology : JASN2022

GWAS in Mice Maps Susceptibility to HIV-Associated Nephropathy to the

Nicholas J Steers, Yask Gupta, Vivette D D'Agati, Tze Y Lim, Natalia DeMaria, Anna Mo, Judy Liang, Kelsey O Stevens, Dina F Ahram, Wan Yee Lam and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Collapsing glomerulopathy: unraveling varied pathogeneses.Current opinion in nephrology and hypertension · 2023
    Review
  3. 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

14 authors at 2 institutions in 1 country.

Nicholas J SteersDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Yask GuptaDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Vivette D D'AgatiDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York.
Tze Y LimDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Natalia DeMariaDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Anna MoDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.ORCID 0000-0002-3902-4769
Judy LiangDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Kelsey O StevensDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Dina F AhramDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Wan Yee LamDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Mihai GageaDepartment of Veterinary Medicine and Surgery, University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Lalitha NagarajanDepartment of Genetics, University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Simone Sanna-CherchiDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Ali G GharaviDivision of Nephrology, Department of Medicine, Columbia University Irving Medical Center, New York, New York.
Columbia University Irving Medical Center · USThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo gain insight into the pathogenesis of collapsing glomerulopathy, a rare form of FSGS that often arises in the setting of viral infections, we performed a genome-wide association study (GWAS) among inbred mouse strains using a murine model of HIV-1 associated nephropathy (HIVAN).

methodsWe first generated F1 hybrids between HIV-1 transgenic mice on the FVB/NJ background and 20 inbred laboratory strains. Analysis of histology, BUN, and urinary NGAL demonstrated marked phenotypic variation among the transgenic F1 hybrids, providing strong evidence for host genetic factors in the predisposition to nephropathy. A GWAS in 365 transgenic F1 hybrids generated from these 20 inbred strains was performed.

resultsWe identified a genome-wide significant locus on chromosome 13-C3 and multiple additional suggestive loci. Crossannotation of the Chr. 13 locus, including single-cell transcriptomic analysis of wildtype and HIV-1 transgenic mouse kidneys, nominated

conclusionsThese findings demonstrate the utility of GWAS in mice to uncover host genetic factors for rare kidney traits and suggest

Indexed as

AIDS-Associated NephropathyAnimalsDisease Models, AnimalDNA-Binding ProteinsFemaleGenetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyGlomerulosclerosis, Focal SegmentalMaleMiceMice, TransgenicDNA-Binding ProteinsSsbp2 protein, mousecollapsing glomerulopathyfocal segmental glomerulosclerosisHIV nephropathymurine GWASSsbp2

Identifiers

PMID34893534
PMCPMC8763192
OpenAlexW4200406988

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.