Evidence map›Paper›PMID 24776767›Full record

ArticlePloS one2014

The DNA methylome and transcriptome of different brain regions in schizophrenia and bipolar disorder.

Yun Xiao, Cynthia Camarillo, Yanyan Ping, Tania Bedard Arana, Hongying Zhao, Peter M Thompson, Chaohan Xu, Bin Brenda Su, Huihui Fan, Javier Ordonez and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Epigenetic Control in Schizophrenia.Sub-cellular biochemistry · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Differentially methylated regions in bipolar disorder and suicide.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2019
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Hypermethylation ofOxidative medicine and cellular longevity · 2018
    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

17 authors at 3 institutions in 3 countries.

Yun XiaoCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Cynthia CamarilloThe Center of Excellence in Neuroscience, Texas Tech University Health Science Center, El Paso, Texas, United States of America.
Yanyan PingCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Tania Bedard AranaDepartments of Psychiatry, Texas Tech University Health Science Center, El Paso, Texas, United States of America.
Hongying ZhaoCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Peter M ThompsonSouthwest Brain Bank, Department of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States of America.
Chaohan XuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Bin Brenda SuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Huihui FanCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Javier OrdonezThe Center of Excellence in Neuroscience, Texas Tech University Health Science Center, El Paso, Texas, United States of America.
Li WangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Chunxiang MaoUniversity of Toronto, Toronto, Canada.
Yunpeng ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Dianne CruzSouthwest Brain Bank, Department of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States of America.
Michael A EscamillaDepartments of Psychiatry, Texas Tech University Health Science Center, El Paso, Texas, United States of America; The Center of Excellence in Neuroscience, Texas Tech University Health Science Center, El Paso, Texas, United States of America.
Xia LiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Chun XuDepartments of Psychiatry, Texas Tech University Health Science Center, El Paso, Texas, United States of America; College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China; The Center of Excellence in Neuroscience, Texas Tech University Health Science Center, El Paso, Texas, United States of America.
Texas Tech University · USHarbin Medical University · CNThe University of Texas Health Science Center at San Antonio · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extensive changes in DNA methylation have been observed in schizophrenia (SC) and bipolar disorder (BP), and may contribute to the pathogenesis of these disorders. Here, we performed genome-scale DNA methylation profiling using methylated DNA immunoprecipitation followed by sequencing (MeDIP-seq) on two brain regions (including frontal cortex and anterior cingulate) in 5 SC, 7 BP and 6 normal subjects. Comparing with normal controls, we identified substantial differentially methylated regions (DMRs) in these two brain regions of SC and BP. To our surprise, different brain regions show completely distinct distributions of DMRs across the genomes. In frontal cortex of both SC and BP subjects, we observed widespread hypomethylation as compared to normal controls, preferentially targeting the terminal ends of the chromosomes. In contrast, in anterior cingulate, both SC and BP subjects displayed extensive gain of methylation. Notably, in these two brain regions of SC and BP, only a few DMRs overlapped with promoters, whereas a greater proportion occurs in introns and intergenic regions. Functional enrichment analysis indicated that important psychiatric disorder-related biological processes such as neuron development, differentiation and projection may be altered by epigenetic changes located in the intronic regions. Transcriptome analysis revealed consistent dysfunctional processes with those determined by DMRs. Furthermore, DMRs in the same brain regions from SC and BP could successfully distinguish BP and/or SC from normal controls while differentially expressed genes could not. Overall, our results support a major role for brain-region-dependent aberrant DNA methylation in the pathogenesis of these two disorders.

Indexed as

DNA MethylationTranscriptomeBipolar DisorderBrainFemaleHumansMaleOrgan SpecificitySchizophreniaSequence Analysis, DNASequence Analysis, RNA

Identifiers

PMID24776767
PMCPMC4002434
OpenAlexW2072801868

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.