NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE248260 Query DataSets for GSE248260
Status Public on Mar 06, 2024
Title Brain and Blood Transcriptome Profiles Delineate Common Genetic Pathways across Suicidal Ideation and Suicide II
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Human genetic studies indicate that suicidal ideation and behavior are both heritable. Most studies have examined associations between aberrant gene expression and suicide behavior, but behavior risk is linked to severity of suicidal ideation. Through a gene network approach, this study investigates how gene co-expression patterns are associated with suicidal ideation and severity using RNA-seq data in peripheral blood from 46 live participants with elevated suicidal ideation and 46 with no ideation. Associations with presence of suicidal ideation were found within 18 co-expressed modules (p<0.05), as well as in 3 co-expressed modules associated with suicidal ideation severity (p<0.05, not explained by severity of depression). Suicidal ideation presence and severity-related gene modules with enrichment of genes involved in defense against microbial infection, inflammation, and adaptive immune response were identified, and investigated using RNA-seq data from postmortem brain that revealed gene expression differences with moderate effect sizes in suicide decedents vs. non-suicides in white matter, but not gray matter. Findings support a role of brain and peripheral blood inflammation in suicide risk, showing that suicidal ideation presence and severity are associated with an inflammatory signature detectable in blood and brain, indicating a biological continuity between ideation and suicidal behavior that may underlie a common heritability.
 
Overall design Prefrontal cortical regions, specifically the ventral white matter (BA 47), from frozen brain sections were used for RNA-seq assays. The cohort consisted of 15 suicide decedents, and 9 non-psychiatric non-suicide controls who died of accidental causes and were all free of gross neuropathology.
 
Contributor(s) Shengnan S, Qingkun L, Zhaoyu W, Yung-yu H, Elizabeth SM, Andrew J. D, Gorazd R, Yongchao G, Hanga G, J John M, Fatemeh H
Citation(s) 38278992
Submission date Nov 20, 2023
Last update date Mar 28, 2024
Contact name Fatemeh Haghighi
E-mail(s) fatemeh.haghighi@mssm.edu
Organization name Icahn School of Medicine at Mount Sinai
Department Neuroscience
Lab Haghighi Lab
Street address 1425 Madison Ave, 9-20D
City New York
State/province NY
ZIP/Postal code 10029
Country USA
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (24)
GSM7910375 104A
GSM7910376 109A
GSM7910377 131A
Relations
BioProject PRJNA1043124

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE248260_white_matter_count_matrix.csv.gz 1.3 Mb (ftp)(http) CSV
SRA Run SelectorHelp
Raw data are available in SRA

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap