Evidence map›Paper›PMID 35922419›Full record

SynthesisTranslational psychiatry2022

Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder.

Sonia Hesam-Shariati, Bronwyn J Overs, Gloria Roberts, Claudio Toma, Oliver J Watkeys, Melissa J Green, Kerrie D Pierce, Howard J Edenberg, Holly C Wilcox, Emma K Stapp and 6 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Translational psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 19% 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, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Quo Vadis translational neuroscience?Translational neuroscience · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Research progress in mitochondrial quality control in schizophrenia.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Article
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 6 institutions in 3 countries.

Sonia Hesam-ShariatiNeuroscience Research Australia, Sydney, NSW, Australia.
Bronwyn J OversNeuroscience Research Australia, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0002-7138-5556
Gloria RobertsSchool of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
Claudio TomaNeuroscience Research Australia, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0003-3901-7507
Oliver J WatkeysNeuroscience Research Australia, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0003-2575-9243
Melissa J GreenNeuroscience Research Australia, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0002-9361-4874
Kerrie D PierceNeuroscience Research Australia, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0003-0636-4836
Howard J EdenbergDepartment of Medical and Molecular Genetics, Indiana University, Indianapolis, IN, USA.ORCID http://orcid.org/0000-0003-0344-9690
Holly C WilcoxChild Psychiatry & Public Health, Johns Hopkins University, Baltimore, MD, USA.
Emma K StappJohns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.ORCID http://orcid.org/0000-0003-0628-0704
Melvin G McInnisDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.ORCID http://orcid.org/0000-0002-0375-6247
Leslie A HulvershornDepartment of Psychiatry, Stark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, IN, USA.
John I NurnbergerDepartment of Medical and Molecular Genetics, Indiana University, Indianapolis, IN, USA.ORCID http://orcid.org/0000-0002-7674-1767
Peter R SchofieldNeuroscience Research Australia, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0003-2967-9662
Philip B MitchellSchool of Psychiatry, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia.
Janice M FullertonNeuroscience Research Australia, Sydney, NSW, Australia. j.fullerton@neura.edu.au.ORCID http://orcid.org/0000-0003-4014-4490
UNSW Sydney · AUIndiana University School of MedicineJohns Hopkins University · USNeuroscience Research Australia · AUIndiana University – Purdue University Indianapolis · USUniversity of Michigan · US

Funding

Adolescents at High Risk for Familial Bipolar DisorderR01MH068009 · NIMH · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI NURNBERGER, JOHN I · 2005 to 2009
$1.7M
Adolescents at High Risk for Familial Bipolar Disorder.R01MH068006 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MCINNIS, MELVIN G · 2005 to 2009
$1.4M
Adolescents at High Risk For Familial Bipolar DisorderR01MH073151 · NIMH · WASHINGTON UNIVERSITY · PI GLOWINSKI, ANNE L · 2005 to 2009
$1.3M
NIMH NIH HHS MH068006NIMH NIH HHS MH073151NIMH NIH HHS MH68009NIMH NIH HHS R01 MH068006NIMH NIH HHS R01 MH068009NIMH NIH HHS R01 MH073151
6 · The paper itself

Abstract

Environmental factors contribute to risk of bipolar disorder (BD), but how environmental factors impact the development of psychopathology within the context of elevated genetic risk is unknown. We herein sought to identify epigenetic signatures operating in the context of polygenic risk for BD in young people at high familial risk (HR) of BD. Peripheral blood-derived DNA was assayed using Illumina PsychArray, and Methylation-450K or -EPIC BeadChips. Polygenic risk scores (PRS) were calculated using summary statistics from recent genome-wide association studies for BD, major depressive disorder (MDD) and cross-disorder (meta-analysis of eight psychiatric disorders). Unrelated HR participants of European ancestry (n = 103) were stratified based on their BD-PRS score within the HR-population distribution, and the top two quintiles (High-BD-PRS; n = 41) compared against the bottom two quintiles (Low-BD-PRS; n = 41). The High-BD-PRS stratum also had higher mean cross-disorder-PRS and MDD-PRS (ANCOVA p = 0.035 and p = 0.024, respectively). We evaluated DNA methylation differences between High-BD-PRS and Low-BD-PRS strata using linear models. One differentially methylated probe (DMP) (cg00933603; p = 3.54 × 10

Indexed as

Bipolar DisorderMajor Depressive DisorderAdolescentEpigenesis, GeneticGenetic Predisposition to DiseaseGenome-Wide Association StudyHLA AntigensHumansMultifactorial InheritanceValine-tRNA LigaseHLA AntigensValine-tRNA LigaseVARS2 protein, human

Identifiers

PMID35922419
PMCPMC9349272
OpenAlexW4289593693

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.