Identification of Epigenetic Methylation Signatures With Clinical Value in Crohn's Disease. Issue 10 (October 2019)
- Record Type:
- Journal Article
- Title:
- Identification of Epigenetic Methylation Signatures With Clinical Value in Crohn's Disease. Issue 10 (October 2019)
- Main Title:
- Identification of Epigenetic Methylation Signatures With Clinical Value in Crohn's Disease
- Authors:
- Moret-Tatay, Inés
Cerrillo, Elena
Sáez-González, Esteban
Hervás, David
Iborra, Marisa
Sandoval, Juan
Busó, Enrique
Tortosa, Luis
Nos, Pilar
Beltrán, Belén - Abstract:
- Abstract : INTRODUCTION: DNA methylation is an epigenetic mechanism that regulates gene expression and represents an important link between genotype, environment, and disease. It is a reversible and inheritable mechanism that could offer treatment targets. We aimed to assess the methylation changes on specific genes previously associated with Crohn's disease (CD) and to study their possible associations with the pathology. METHODS: We included 103 participants and grouped them into 2 cohorts (a first [n = 31] and a second validation [n = 72] cohort), with active CD (aCD) and inactive CD (iCD) and healthy participants (CTR). DNA was obtained from the peripheral blood and analyzed by the Agena platform. The selected genes were catalase ( CAT ), α-defensin 5 ( DEFA5 ), FasR, FasL, tumor necrosis factor ( TNF ), TNFRSF1A, TNFRSF1B, PPA2, ABCB1, NOD2, PPARγ, and PKCζ . We used the elastic net algorithm and R software. RESULTS: We studied 240 CpGs. Sixteen CpGs showed differential methylation profiles among aCD, iCD, and CTR. We selected for validation those with the greatest differences: DEFA5 CpG_11; CpG_13; CAT CpG_31.32; TNF CpG_4, CpG_12; and ABCB1 CpG_21. Our results validated the genes DEFA5 (methylation gain) and TNF (methylation loss) with P values < 0.001. In both cases, the methylation level was maintained and did not change with CD activity (aCD vs iCD). The subanalysis comparison between aCD and iCD showed significant differential methylation profiles in other CpGs:Abstract : INTRODUCTION: DNA methylation is an epigenetic mechanism that regulates gene expression and represents an important link between genotype, environment, and disease. It is a reversible and inheritable mechanism that could offer treatment targets. We aimed to assess the methylation changes on specific genes previously associated with Crohn's disease (CD) and to study their possible associations with the pathology. METHODS: We included 103 participants and grouped them into 2 cohorts (a first [n = 31] and a second validation [n = 72] cohort), with active CD (aCD) and inactive CD (iCD) and healthy participants (CTR). DNA was obtained from the peripheral blood and analyzed by the Agena platform. The selected genes were catalase ( CAT ), α-defensin 5 ( DEFA5 ), FasR, FasL, tumor necrosis factor ( TNF ), TNFRSF1A, TNFRSF1B, PPA2, ABCB1, NOD2, PPARγ, and PKCζ . We used the elastic net algorithm and R software. RESULTS: We studied 240 CpGs. Sixteen CpGs showed differential methylation profiles among aCD, iCD, and CTR. We selected for validation those with the greatest differences: DEFA5 CpG_11; CpG_13; CAT CpG_31.32; TNF CpG_4, CpG_12; and ABCB1 CpG_21. Our results validated the genes DEFA5 (methylation gain) and TNF (methylation loss) with P values < 0.001. In both cases, the methylation level was maintained and did not change with CD activity (aCD vs iCD). The subanalysis comparison between aCD and iCD showed significant differential methylation profiles in other CpGs: TNF, FAS, ABCB1, CAT, and TNFRS1BF genes. DISCUSSION: The methylation status of DEFA5 and TNF genes provides a signature biomarker that characterizes patients with CD and supports the possible implication of the environment and the immune system in CD pathogenesis. … (more)
- Is Part Of:
- Clinical and translational gastroenterology. Volume 10:Issue 10(2019)
- Journal:
- Clinical and translational gastroenterology
- Issue:
- Volume 10:Issue 10(2019)
- Issue Display:
- Volume 10, Issue 10 (2019)
- Year:
- 2019
- Volume:
- 10
- Issue:
- 10
- Issue Sort Value:
- 2019-0010-0010-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-10
- Subjects:
- Stomach -- Diseases -- Periodicals
Intestines -- Diseases -- Periodicals
Gastroenterology
Gastrointestinal Diseases
Liver Diseases
Intestines -- Diseases
Stomach -- Diseases
Periodical
Periodicals
Fulltext
Internet Resources
Periodicals
Electronic journals
616.33 - Journal URLs:
- http://bibpurl.oclc.org/web/52768 ↗
http://www.nature.com/ctg ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/1564/ ↗
https://journals.lww.com/ctg/pages/default.aspx ↗
http://www.nature.com/ ↗ - DOI:
- 10.14309/ctg.0000000000000083 ↗
- Languages:
- English
- ISSNs:
- 2155-384X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 15903.xml