Evidence map›Paper›PMID 25986483›Full record

ArticleArthritis research & therapy2015

A candidate gene study reveals association between a variant of the Peroxisome Proliferator-Activated Receptor Gamma (PPAR-γ) gene and systemic sclerosis.

Roberta Goncalves Marangoni, Benjamin D Korman, Yannick Allanore, Philippe Dieude, Loren L Armstrong, Margarita Rzhetskaya, Monique Hinchcliff, Mary Carns, Sofia Podlusky, Sanjiv J Shah and 6 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Arthritis research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

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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 3 institutions in 1 country.

Roberta Goncalves MarangoniDivision of Rheumatology, Department of Medicine, Northwestern University Feinberg School of Medicine, 240 E. Huron Street, McGaw Pavillion M230, Chicago, IL, USA. roberta.marangoni@northwestern.edu.
Benjamin D KormanDivision of Rheumatology, Department of Medicine, Northwestern University Feinberg School of Medicine, 240 E. Huron Street, McGaw Pavillion M230, Chicago, IL, USA. benjamin-korman@northwestern.edu.
Yannick AllanoreParis Descartes University, INSERM U1016, Institut Cochin, Sorbonne Paris Cité, Paris, France. yannick.allanore@cch.aphp.fr.
Philippe DieudeUniversité Paris 7, INSERM U699, Rhumatologie, Hôpital Bichat, Paris, France. philippe.dieude@bch.aphp.fr.
Loren L ArmstrongDivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. loren-armstrong@northwestern.edu.
Margarita RzhetskayaDivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. m-rzhetskaya@northwestern.edu.
Monique HinchcliffDivision of Rheumatology, Department of Medicine, Northwestern University Feinberg School of Medicine, 240 E. Huron Street, McGaw Pavillion M230, Chicago, IL, USA. m-hinchcliff@northwestern.edu.
Mary CarnsDivision of Rheumatology, Department of Medicine, Northwestern University Feinberg School of Medicine, 240 E. Huron Street, McGaw Pavillion M230, Chicago, IL, USA. m-carns@northwestern.edu.
Sofia PodluskyDivision of Rheumatology, Department of Medicine, Northwestern University Feinberg School of Medicine, 240 E. Huron Street, McGaw Pavillion M230, Chicago, IL, USA. s-podlusky@northwestern.edu.
Sanjiv J ShahDivision of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. sanjiv.shah@northwestern.edu.
Barbara RuizParis Descartes University, INSERM U1016, Institut Cochin, Sorbonne Paris Cité, Paris, France. barbara.ruiz@inserm.fr.
Eric HachullaUniversité Lille II, Médecine Interne, Lille, France. ehachulla@chru-lille.fr.
Kiet TievUniversité Pierre et Marie Curie, Service de Médecine Interne, Hôpital Saint Antoine, Paris, France. kiet.tiev@sat.aphp.fr.
Jean-Luc CracowskiINSERM CIC3, CHU Grenoble, Grenoble, France. Jean-Luc.Cracowski@ujf-grenoble.fr.
John VargaDivision of Rheumatology, Department of Medicine, Northwestern University Feinberg School of Medicine, 240 E. Huron Street, McGaw Pavillion M230, Chicago, IL, USA. j-varga@northwestern.edu.
M Geoffrey HayesDivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. ghayes@northwestern.edu.
Institut Cochin · FRSorbonne Université · FRUniversité de Lille · FR

Funding

Career Development in Women's Health (CDWH)K12HD055884 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DUNAIF, ANDREA E · 2007 to 2016
$4.2M
Predictive Ability of Gene Expression Signatures In Skin as SSc BiomarkersK23AR059763 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HINCHCLIFF, MONIQUE EVANGELINE · 2013 to 2015
$390k
NIAMS NIH HHS K23 AR059763NICHD NIH HHS K12 HD055884
6 · The paper itself

Abstract

introductionThe multifunctional nuclear receptor peroxisome proliferator-activated receptor gamma (PPAR-γ) has potent anti-fibrotic effects, and its expression and activity are impaired in patients with systemic sclerosis (SSc). We investigated PPAR-γ gene (PPARG) single nucleotide polymorphisms (SNPs) associated with SSc.

methodsTag SNPs spanning PPARG were genotyped in a European ancestry US discovery cohort comprising 152 SSc patients and 450 controls, with replication of our top signal in a European cohort (1031 SSc patients and 1014 controls from France). Clinical parameters and disease severity were analyzed to evaluate clinical associations with PPARG variants.

resultsIn the discovery cohort, a single PPARG intronic SNP (rs10865710) was associated with SSc (p=0.010; odds ratio=1.52 per C allele, 95% confidence interval 1.10-2.08). This association was replicated in the French validation cohort (p=0.052; odds ratio=1.16 per C allele, 95% confidence interval 1.00-1.35). Meta-analysis of both cohorts indicated stronger evidence for association (p=0.002; odds ratio=1.22 per C allele, 95% confidence interval 1.07-1.40). The rs10865710 C allele was also associated with pulmonary arterial hypertension in the French SSc cohort (p=0.002; odds ratio=2.33 per C allele, 95% confidence interval 1.34-4.03).

conclusionsA PPARG variant is associated with susceptibility to SSc, consistent with a role of PPAR-γ in the pathogenesis of SSc.

Indexed as

Gene Expression RegulationGenetic Predisposition to DiseaseAdultAllelesEuropeFemaleGenotypeHumansIncidenceMaleMiddle AgedPeroxisome Proliferator-Activated ReceptorsPolymorphism, Single NucleotidePPAR gammaRisk FactorsRNAPeroxisome Proliferator-Activated ReceptorsPPAR gammaRNA

Identifiers

PMID25986483
PMCPMC4437446
OpenAlexW1588555436

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Registered trials

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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.