Host genetics and epigenomics of inflammatory bowel disease

Show simple item record

dc.contributor.advisor Claesson, Marcus en Power, E. M. 2021-01-14T11:32:08Z 2021-01-14T11:32:08Z 2019-09-30 2019-09-30
dc.identifier.citation Power, E. M. 2019. Host genetics and epigenomics of inflammatory bowel disease. PhD Thesis, University College Cork. en
dc.identifier.endpage 185 en
dc.description.abstract The overall aim of this thesis was to investigate the interaction between host-genetics and epigenetic profiles in IBD, particularly in CD. This included identifying epigenetic markers in CD patients with frequent relapses and stratifying patients by epigenetic profiles and correlating with gut microbiota profiles. This thesis also investigated genetic variation and its association with IBD, UC and CD. MeQTLs was also investigated to examine the impact of genetic variation on epigenetics. The first study objective included case/control for diseased samples and a second objective was to investigate the active cycle for Crohn’s Disease by comparing paired inflamed and non-inflamed samples. The genetic association analysis found 11 novel SNPs associated with IBD, CD or UC located on Chromosome 6 but did not find any previous IBD susceptibility loci to be significant. The epigenetic analysis based on differential DNA methylation found no significant signals in the case/control analysis. An inflammation factor was found to be present for studies including samples from active areas showing inflammation. MeQTLs analysis showed significant associated loci on genes SMURF1 and GNA12, both genetic susceptibility loci for IBD, CD and UC, and found to be tissue specific for the human gut. Both the epigenetic and meQTL analysis were unable to replicate previous findings from Cooke et al (1) for the inflammation epigenetic analysis and Ventham et al (2) for the epigenetic Case/Control analysis and meQTL study. The analysis examining association between microbiota in the gut and epigenetic changes found three genes SNX18, VWASA and RNF23 to be significantly differentially methylated according to microbiota cluster membership. The cohort for this thesis consisted of 140 cases: 32 controls for genetic analysis and 42 cases:23 controls for epigenetic data. The low power for the genetic analysis (5% power) and epigenetic analysis (4% differential change in methylation at 80% power) suggest that increased sample size is required to increase statistical power. Additional constraints are availability of true healthy samples to act as control samples and biopsy tissue used for biological samples. en
dc.format.mimetype application/pdf en
dc.language.iso en en
dc.publisher University College Cork en
dc.rights © 2019, Emily Maria Power. en
dc.rights.uri en
dc.subject Epigenetics en
dc.subject Genetics en
dc.subject Crohn's disease en
dc.subject Inflammatory bowel disease en
dc.title Host genetics and epigenomics of inflammatory bowel disease en
dc.type Doctoral thesis en
dc.type.qualificationlevel Doctoral en
dc.type.qualificationname PhD - Doctor of Philosophy en
dc.internal.availability Full text not available en
dc.description.version Accepted Version en
dc.contributor.funder University College Cork en
dc.description.status Not peer reviewed en Microbiology en
dc.internal.conferring Spring 2021 en
dc.internal.ricu APC Microbiome Institute en
dc.contributor.advisorexternal Bell, Jordana en
dc.availability.bitstream controlled

Files in this item

This item appears in the following Collection(s)

Show simple item record

© 2019, Emily Maria Power. Except where otherwise noted, this item's license is described as © 2019, Emily Maria Power.
This website uses cookies. By using this website, you consent to the use of cookies in accordance with the UCC Privacy and Cookies Statement. For more information about cookies and how you can disable them, visit our Privacy and Cookies statement