Evidence map›Paper›PMID 27074206›Full record

ArticleJAMA psychiatry2016

Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study.

Carolina Montano, Margaret A Taub, Andrew Jaffe, Eirikur Briem, Jason I Feinberg, Rakel Trygvadottir, Adrian Idrizi, Arni Runarsson, Birna Berndsen, Ruben C Gur and 17 more

Abstract read
In one paragraph

Article in JAMA psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed, 9 pooled it
–field-weighted citation impact
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

105 citing papers in PubMed, 9 syntheses or guidelines pooled it.

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  20. DNA Methylation Patterns Associated with Tinnitus in Young Adults-A Pilot Study.Journal of the Association for Research in Otolaryngology : JARO · 2024
    Article

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

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

27 authors.

Carolina MontanoMedical Scientist Training Program and Predoctoral Training Program in Human Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland2Center for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Margaret A TaubDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Andrew JaffeLieber Institute for Brain Development, Johns Hopkins Medical Campus, Baltimore, Maryland5Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Eirikur BriemCenter for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Jason I FeinbergCenter for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Rakel TrygvadottirCenter for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Adrian IdriziCenter for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Arni RunarssonCenter for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Birna BerndsenCenter for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Ruben C GurNeuropsychiatry Section, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Tyler M MooreNeuropsychiatry Section, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Rodney T PerryDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham.
Doug FugmanRutgers University Cell and DNA Repository, Piscataway, New Jersey.
Sarven SabunciyanStanley Division of Developmental Neurovirology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Robert H YolkenStanley Division of Developmental Neurovirology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Thomas M HydeLieber Institute for Brain Development, Johns Hopkins Medical Campus, Baltimore, Maryland.
Joel E KleinmanLieber Institute for Brain Development, Johns Hopkins Medical Campus, Baltimore, Maryland.
Janet L SobellDepartment of Psychiatry and Behavioral Sciences, Keck School of Medicine of University of Southern California, Los Angeles.
Carlos N PatoDepartment of Psychiatry and Behavioral Sciences, Keck School of Medicine of University of Southern California, Los Angeles.
Michele T PatoDepartment of Psychiatry and Behavioral Sciences, Keck School of Medicine of University of Southern California, Los Angeles.
Rodney C GoDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham.
Vishwajit NimgaonkarDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, Pennsylvania.
Daniel R WeinbergerLieber Institute for Brain Development, Johns Hopkins Medical Campus, Baltimore, Maryland.
David BraffDepartment of Psychiatry, University of California San Diego School of Medicine, La Jolla13VISN22, Mental Illness Research, Education, and Clinical Center, VA Veterans Affairs San Diego Healthcare System, San Diego, California.
Raquel E GurNeuropsychiatry Section, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Margaret Daniele FallinCenter for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, Maryland5Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Andrew P FeinbergCenter for Epigenetics, Johns Hopkins University School of Medicine, Baltimore, Maryland5Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland14Departments of Medicine and Biomedical Engineering, Johns Hopkins U.

Funding

NIMH Center Repository Supporting Stem Cell ResearchU24MH068457 · NIMH · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI BRZUSTOWICZ, LINDA M, KNOWLES, JAMES A · 2003 to 2024
$213.8M
Genomic Psychiatry CohortR01MH085548 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PATO, CARLOS N, PATO, MICHELE T · 2008 to 2012
$16.3M
1/5: A Genome-wide Methylation Scan for Epigenetic Contributions to SchizophreniaU01MH085270 · NIMH · JOHNS HOPKINS UNIVERSITY · PI FEINBERG, ANDREW P. · 2008 to 2012
$9.8M
2/5-A Genome-Wide Methylation Scan for Epigenetic Contributions to SchizophreniaU01MH085264 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GUR, RAQUEL E · 2008 to 2012
$239k
5/5: A Genome-wide Methylation Scan for Epigenetic Contributions to SchizophreniaU01MH085265 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BRAFF, DAVID L. · 2008 to 2012
$191k
3/5: A Genome-Wide Methylation Scan for Epigenetic Contributions to SchizophreniaU01MH085269 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIMGAONKAR, VISHWAJIT LAXMIKANT · 2008 to 2012
$187k
4/5-A Genome-Wide Methylation Scan for Epigenetic Contributions to SchizophreniaU01MH085281 · NIMH · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PERRY, RODNEY T · 2008 to 2012
$181k
NIMH NIH HHS R01 MH085548NIMH NIH HHS U01 MH085264NIMH NIH HHS U01 MH085265NIMH NIH HHS U01 MH085269NIMH NIH HHS U01 MH085270NIMH NIH HHS U01 MH085281NIMH NIH HHS U24 MH068457
6 · The paper itself

Abstract

importanceDNA methylation may play an important role in schizophrenia (SZ), either directly as a mechanism of pathogenesis or as a biomarker of risk.

objectiveTo scan genome-wide DNA methylation data to identify differentially methylated CpGs between SZ cases and controls. DESIGN, SETTING, AND

participantsEpigenome-wide association study begun in 2008 using DNA methylation levels of 456 513 CpG loci measured on the Infinium HumanMethylation450 array (Illumina) in a consortium of case-control studies for initial discovery and in an independent replication set. Primary analyses used general linear regression, adjusting for age, sex, race/ethnicity, smoking, batch, and cell type heterogeneity. The discovery set contained 689 SZ cases and 645 controls (n = 1334), from 3 multisite consortia: the Consortium on the Genetics of Endophenotypes in Schizophrenia, the Project among African-Americans To Explore Risks for Schizophrenia, and the Multiplex Multigenerational Family Study of Schizophrenia. The replication set contained 247 SZ cases and 250 controls (n = 497) from the Genomic Psychiatry Cohort. MAIN OUTCOMES AND MEASURES: Identification of differentially methylated positions across the genome in SZ cases compared with controls.

resultsOf the 689 case participants in the discovery set, 477 (69%) were men and 258 (37%) were non-African American; of the 645 controls, 273 (42%) were men and 419 (65%) were non-African American. In our replication set, cases/controls were 76% male and 100% non-African American. We identified SZ-associated methylation differences at 923 CpGs in the discovery set (false discovery rate, <0.2). Of these, 625 showed changes in the same direction including 172 with P < .05 in the replication set. Some replicated differentially methylated positions are located in a top-ranked SZ region from genome-wide association study analyses. CONCLUSIONS AND RELEVANCE: This analysis identified 172 replicated new associations with SZ after careful correction for cell type heterogeneity and other potential confounders. The overlap with previous genome-wide association study data can provide potential insights into the functional relevance of genetic signals for SZ.

Indexed as

EpigenomicsAdultBlack or African AmericanCpG IslandsDNA MethylationEpigenesis, GeneticFemaleGenetic LociGenetic MarkersGenome-Wide Association StudyHumansMalePhenotypePsychotic DisordersSchizophreniaSex FactorsGenetic Markers

Identifiers

PMID27074206
PMCPMC6353566

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