Evidence map›Paper›PMID 30573655›Full record

SynthesisAnnals of the rheumatic diseases2019

Genome-wide meta-analysis reveals shared new

Marialbert Acosta-Herrera, Martin Kerick, David González-Serna, Myositis Genetics Consortium, Scleroderma Genetics Consortium, Cisca Wijmenga, Andre Franke, Peter K Gregersen, Leonid Padyukov, Jane Worthington and 4 more

Open access · hybridAbstract readMeta-Analysis
In one paragraph

Synthesis in Annals of the rheumatic diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 5 pooled it
7.8field-weighted citation impact, top 2% 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

70 citing papers in PubMed, 5 syntheses or guidelines pooled it, 116 citations in OpenAlex.

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10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 9 institutions in 6 countries.

Marialbert Acosta-Herrera *Institute of Parasitology and Biomedicine López-Neyra, IPBLN-CSIC, PTS Granada, Granada, Spain m.acostaherrera@ipb.csic.es javiermartin@ipb.csic.es.
Martin KerickInstitute of Parasitology and Biomedicine López-Neyra, IPBLN-CSIC, PTS Granada, Granada, Spain.
David González-SernaInstitute of Parasitology and Biomedicine López-Neyra, IPBLN-CSIC, PTS Granada, Granada, Spain.
Myositis Genetics Consortium
Scleroderma Genetics Consortium
Cisca WijmengaDepartment of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
Andre FrankeInstitute of Clinical Molecular Biology, Christian-Albrechts-University of Kiel, Kiel, Germany.
Peter K GregersenRobert S Boas Center for Genomics and Human Genetics, Feinstein Institute for Medical Research, Manhasset, New York, USA.
Leonid PadyukovRheumatology Unit, Department of Medicine, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
Jane WorthingtonManchester NIHR Biomedical Research Centre, The University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
Timothy James VyseDivision of Genetics and Molecular Medicine, King's College London, London, UK.
Marta Eugenia Alarcón-RiquelmeCentre for Genomics and Oncological Research (GENYO), Pfizer-University of Granada-Andalusian Regional Government, Granada, Spain.
Maureen D MayesDepartment of Internal Medicine, Division of Rheumatology, The University of Texas Health Science Center-Houston, Houston, Texas, USA.
Javier Martin *Institute of Parasitology and Biomedicine López-Neyra, IPBLN-CSIC, PTS Granada, Granada, Spain m.acostaherrera@ipb.csic.es javiermartin@ipb.csic.es.
Instituto de Parasitología y Biomedicina "López - Neyra" · ESFeinstein Institute for Medical Research · USKarolinska University Hospital · SEKiel University · DEKing's College London · GBNIHR Manchester Biomedical Research Centre · GBPfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research · ESThe University of Texas Health Science Center at Houston · USUniversity of Groningen · NL

Funding

Environmental/genetic Risk Factors and Pathogenesis of Autoimmune DiseaseZIAES101074 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI RIDER, LISA · 2009 to 2025
$34.6M
Genetics and Pathogenesis of SclerodermaZIAAR041209 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI GOURH, PRAVITT · 2019 to 2024
$6.3M
Pathogenesis And Genetic/environmental Risk Factors ForZ01ES101074 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI MILLER, FREDERICK · 2002 to 2008
$2.7M
Intramural NIH HHS Z01 ES101074Medical Research Council G0100594Medical Research Council G0600237Medical Research Council G0901461Medical Research Council MR/M004600/1
6 · The paper itself

Abstract

objectiveImmune-mediated inflammatory diseases (IMIDs) are heterogeneous and complex conditions with overlapping clinical symptoms and elevated familial aggregation, which suggests the existence of a shared genetic component. In order to identify this genetic background in a systematic fashion, we performed the first cross-disease genome-wide meta-analysis in systemic seropositive rheumatic diseases, namely, systemic sclerosis, systemic lupus erythematosus, rheumatoid arthritis and idiopathic inflammatory myopathies.

methodsWe meta-analysed ~6.5 million single nucleotide polymorphisms in 11 678 cases and 19 704 non-affected controls of European descent populations. The functional roles of the associated variants were interrogated using publicly available databases.

resultsOur analysis revealed five shared genome-wide significant independent

conclusionsWe have identified shared new risk

Indexed as

Adultalpha KaryopherinsArthritis, RheumatoidFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLim KinasesLupus Erythematosus, SystemicMaleMembrane ProteinsMyositisPolymorphism, Single NucleotideQuantitative Trait LociRepressor ProteinsRheumatic Diseasesalpha KaryopherinsKPNA4 protein, humanLIMK1 protein, humanLim KinasesMembrane ProteinsNAB1 protein, humanPRR12 protein, humanRepressor Proteinsautoimmune diseasesautoimmunitygene polymorphism

Identifiers

PMID30573655
PMCPMC6800208
OpenAlexW2905951514

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.