Evidence map›Paper›PMID 36323703›Full record

SynthesisNature communications2022

Shared genetic risk factors and causal association between psoriasis and coronary artery disease.

Matthew T Patrick, Qinmengge Li, Rachael Wasikowski, Nehal Mehta, Johann E Gudjonsson, James T Elder, Xiang Zhou, Lam C Tsoi

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
5.6field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it, 66 citations in OpenAlex.

  1. Pooled it
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  13. Review
  14. Psoriasis.Nature reviews. Disease primers · 2025
    Review
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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

8 authors at 3 institutions in 1 country.

Matthew T PatrickDepartment of Dermatology, Michigan Medicine, University of Michigan, Michigan, MI, USA.ORCID 0000-0002-6174-9002
Qinmengge LiDepartment of Biostatistics, School of Public Health, University of Michigan, Michigan, MI, USA.
Rachael WasikowskiDepartment of Dermatology, Michigan Medicine, University of Michigan, Michigan, MI, USA.ORCID 0000-0003-3544-3023
Nehal MehtaSection of Inflammation and Cardiometabolic Disease, National Heart, Lung, and Blood Institute, National Institutes of Health, Michigan, MD, USA.
Johann E GudjonssonDepartment of Dermatology, Michigan Medicine, University of Michigan, Michigan, MI, USA.ORCID 0000-0002-0080-0812
James T ElderDepartment of Dermatology, Michigan Medicine, University of Michigan, Michigan, MI, USA.
Xiang ZhouDepartment of Biostatistics, School of Public Health, University of Michigan, Michigan, MI, USA.ORCID 0000-0002-4331-7599
Lam C TsoiDepartment of Dermatology, Michigan Medicine, University of Michigan, Michigan, MI, USA. alextsoi@med.umich.edu.ORCID 0000-0003-1627-5722
Michigan Medicine · USUniversity of Michigan · USNational Institutes of Health · US

Funding

University of Michigan Skin Biology and Diseases Resource-based CenterP30AR075043 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Johann Eli Gudjonsson · 2019 to 2026
$6.6M
Genetic and Genomic Dissection of Psoriatic ArthritisR01AR063611 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD, GLADMAN, DAFNA D · 2012 to 2023
$6.2M
Functional Genomics of PsoriasisR01AR065183 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 2013 to 2016
$1.7M
Integrative Biology Approach to Identify and Characterize Roles of lncRNAs Associated with Psoriasis PathologyK01AR072129 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TSOI, LAM CHEUNG · 2017 to 2021
$500k
NIAMS NIH HHS K01 AR072129NIAMS NIH HHS P30 AR075043NIAMS NIH HHS R01 AR063611NIAMS NIH HHS R01 AR065183
6 · The paper itself

Abstract

Psoriasis and coronary artery disease (CAD) are related comorbidities that are well established, but whether a genetic basis underlies this is not well studied. We apply trans-disease meta-analysis to 11,024 psoriasis and 60,801 CAD cases, along with their associated controls, identifying one opposing and three shared genetic loci, which are confirmed through colocalization analysis. Combining results from Bayesian credible interval analysis with independent information from genomic, epigenomic, and spatial chromatin organization, we prioritize genes (including IFIH1 and IL23A) that have implications for common molecular mechanisms involved in psoriasis and CAD inflammatory signaling. Chronic systemic inflammation has been associated with CAD and myocardial infarction, and Mendelian randomization analysis finds that CAD as an exposure can have a significant causal effect on psoriasis (OR = 1.11; p = 3×10

Indexed as

Coronary Artery DiseasePsoriasisBayes TheoremGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansInflammationMendelian Randomization AnalysisPolymorphism, Single NucleotideRisk Factors

Identifiers

PMID36323703
PMCPMC9630428
OpenAlexW4307984318

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.