Evidence map›Paper›PMID 36243721›Full record

ArticleNature communications2022

Genetic variants associated with psychiatric disorders are enriched at epigenetically active sites in lymphoid cells.

Mary-Ellen Lynall, Blagoje Soskic, James Hayhurst, Jeremy Schwartzentruber, Daniel F Levey, Gita A Pathak, Renato Polimanti, Joel Gelernter, Murray B Stein, Gosia Trynka and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

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  19. Anti-inflammatory Drugs in the Treatment of Depression.Current topics in behavioral neurosciences · 2024
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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

12 authors at 5 institutions in 3 countries.

Mary-Ellen LynallDepartment of Psychiatry, Herchel Smith Building of Brain & Mind Sciences, Cambridge Biomedical Campus, University of Cambridge, Cambridge, CB2 0SZ, UK. mel41@cam.ac.uk.ORCID 0000-0002-1939-7525
Blagoje SoskicWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID 0000-0003-3173-4528
James HayhurstOpen Targets, Wellcome Genome Campus, Hinxton, UK.
Jeremy SchwartzentruberWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Daniel F LeveyVA Connecticut Healthcare System, West Haven, CT, USA.ORCID 0000-0001-8431-9569
Gita A PathakVA Connecticut Healthcare System, West Haven, CT, USA.
Renato PolimantiVA Connecticut Healthcare System, West Haven, CT, USA.ORCID 0000-0003-0745-6046
Joel GelernterVA Connecticut Healthcare System, West Haven, CT, USA.ORCID 0000-0002-4067-1859
Murray B SteinVA San Diego Healthcare System, San Diego, CA, USA.ORCID 0000-0001-9564-2871
Gosia TrynkaWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID 0000-0002-6955-9529
Menna R ClatworthyMolecular Immunity Unit, University of Cambridge Department of Medicine, Cambridge, UK.
Ed BullmoreDepartment of Psychiatry, Herchel Smith Building of Brain & Mind Sciences, Cambridge Biomedical Campus, University of Cambridge, Cambridge, CB2 0SZ, UK.
Yale University · USUniversity of Cambridge · GBWellcome Sanger Institute · GBOpen Targets · GBUniversity of California San Diego · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
BLRD VA IK2 BX005058Medical Research Council MC_G0802534Medical Research Council MR/S006257/1NCATS NIH HHS UL1 TR001863Wellcome Trust WT206194
6 · The paper itself

Abstract

Multiple psychiatric disorders have been associated with abnormalities in both the innate and adaptive immune systems. The role of these abnormalities in pathogenesis, and whether they are driven by psychiatric risk variants, remains unclear. We test for enrichment of GWAS variants associated with multiple psychiatric disorders (cross-disorder or trans-diagnostic risk), or 5 specific disorders (cis-diagnostic risk), in regulatory elements in immune cells. We use three independent epigenetic datasets representing multiple organ systems and immune cell subsets. Trans-diagnostic and cis-diagnostic risk variants (for schizophrenia and depression) are enriched at epigenetically active sites in brain tissues and in lymphoid cells, especially stimulated CD4

Indexed as

Mental DisordersSchizophreniaCatalytic DomainGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLymphocytesPolymorphism, Single Nucleotide

Identifiers

PMID36243721
PMCPMC9569335
OpenAlexW4306290733

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.