Evidence map›Paper›PMID 36327221›Full record

ArticlePLoS genetics2022

COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection.

Yuxuan Wang, Suri Guga, Kejia Wu, Zoe Khaw, Konstantinos Tzoumkas, Phil Tombleson, Mary E Comeau, Carl D Langefeld, Deborah S Cunninghame Graham, David L Morris and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 21 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

11 authors at 3 institutions in 2 countries.

Yuxuan WangDepartment of Medical & Molecular Genetics, King's College London, London, United Kingdom.ORCID 0000-0002-5539-0654
Suri GugaDepartment of Medical & Molecular Genetics, King's College London, London, United Kingdom.
Kejia WuDepartment of Medical & Molecular Genetics, King's College London, London, United Kingdom.
Zoe KhawDepartment of Medical & Molecular Genetics, King's College London, London, United Kingdom.ORCID 0000-0001-8930-3486
Konstantinos TzoumkasDepartment of Medical & Molecular Genetics, King's College London, London, United Kingdom.ORCID 0000-0003-2739-7004
Phil TomblesonNIHR GSTFT/KCL Biomedical Research Centre, London, United Kingdom.
Mary E ComeauDepartment of Biostatistics and Data Science and Center for Precision Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, United States of America.
Carl D LangefeldDepartment of Biostatistics and Data Science and Center for Precision Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, United States of America.
Deborah S Cunninghame GrahamDepartment of Medical & Molecular Genetics, King's College London, London, United Kingdom.ORCID 0000-0002-3066-6693
David L MorrisDepartment of Medical & Molecular Genetics, King's College London, London, United Kingdom.ORCID 0000-0002-1754-8932
Timothy J VyseDepartment of Medical & Molecular Genetics, King's College London, London, United Kingdom.ORCID 0000-0003-1123-1464
King's College London · GBWake Forest University · USUCL Biomedical Research Centre · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome wide association studies show there is a genetic component to severe COVID-19. We find evidence that the genome-wide genetic association signal with severe COVID-19 is correlated with that of systemic lupus erythematosus (SLE), having formally tested this using genetic correlation analysis by LD score regression. To identify the shared associated loci and gain insight into the shared genetic effects, using summary level data we performed meta-analyses, a local genetic correlation analysis and fine-mapping using stepwise regression and functional annotation. This identified multiple loci shared between the two traits, some of which exert opposing effects. The locus with most evidence of shared association is TYK2, a gene critical to the type I interferon pathway, where the local genetic correlation is negative. Another shared locus is CLEC1A, where the direction of effects is aligned, that encodes a lectin involved in cell signaling, and the anti-fungal immune response. Our analyses suggest that several loci with reciprocal effects between the two traits have a role in the defense response pathway, adding to the evidence that SLE risk alleles are protective against infection.

Indexed as

Autoimmune DiseasesCOVID-19Lupus Erythematosus, SystemicGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPolymorphism, Single Nucleotide

Identifiers

PMID36327221
PMCPMC9632821
OpenAlexW4308045435

What OpenQuestion holds

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LicenceCC BY
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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.