NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE112611 Query DataSets for GSE112611
Status Public on Apr 03, 2018
Title Blood-Derived DNA Methylation Signatures of Crohn’s Disease and Severity of Intestinal Inflammation
Organism Homo sapiens
Experiment type Methylation profiling by array
Summary Crohn’s disease is a relapsing inflammatory disorder with a variable clinical course. While most patients present with purely an inflammatory phenotype (B1) at diagnosis, a subgroup (~20%) rapidly progresses to complicated disease manifestations that include stricturing (B2) within 5 years. DNA methylation is a key epigenetic mechanism that can regulate gene expression and thereby influence the development and progression of complex diseases. Site-specific DNA methylation differences have been reported in peripheral blood of patients with Crohn’s disease, but investigation of the temporal relationship between methylation and disease is required to establish whether the methylome plays a causal role and can be leveraged for therapeutic benefits. To this end, we conducted an epigenome-wide study of methylation (~850K sites) in peripheral blood at diagnosis and during follow-up from the RISK pediatric Crohn’s disease inception cohort. While some methylation changes associated with Crohn’s disease might be causal, in peripheral blood the vast majority are found to be a transient consequence of inflammation and thus a symptom of disease.
 
Overall design DNA methylation was assessed in peripheral blood from pediatric non-IBD controls and patients with Crohn's disease at two time points - at diagnosis and follow-up. Peripheral blood DNA was extracted, bisulfite converted and genome-wide DNA methylation was interrogated using the HumanMethylationEPIC BeadChip (Illumina).
 
Contributor(s) Somineni HK, Venkateswaran S, Kilaru V, Marigorta UM, Mo A, Okou DT, Kellermayer R, Mondal K, Cobb D, Walters TD, Griffiths A, Noe JD, Crandall WV, Rosh JR, Mack DR, Heyman MB, Baker SS, Stephens MC, Baldassano RN, Markowitz JF, Dubinsky MC, Cho J, Hyams JS, Denson LA, Gibson G, Cutler DJ, Conneely KN, Smith AK, Kugathasan S
Citation(s) 30779925, 35172000
Submission date Apr 02, 2018
Last update date Apr 19, 2022
Contact name Alicia Smith
E-mail(s) aksmit3@emory.edu
Organization name Emory University
Street address 101 Woodruff Circle
City Atlanta
ZIP/Postal code 30322
Country USA
 
Platforms (1)
GPL21145 Infinium MethylationEPIC
Samples (402)
GSM3074028 13-040_At Dx
GSM3074029 13-040_24M
GSM3074030 01-093
Relations
BioProject PRJNA448454

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
GSE112611_RAW.tar 161.2 Mb (http)(custom) TAR
GSE112611_beta_values.txt.gz 2.5 Gb (ftp)(http) TXT
GSE112611_methlyated_unmethylated.txt.gz 1.5 Gb (ftp)(http) TXT
Processed data are available on Series record

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