Genome-wide association analysis within The Manitoba Personalized Lifestyle Research study

dc.contributor.authorBadurally Adam, Bibi Taskeen
dc.contributor.examiningcommitteeMyrie, Semone (Food and Human Nutritional Sciences)
dc.contributor.examiningcommitteeMackay, Dylan (Food and Human Nutritional Sciences)
dc.contributor.examiningcommitteeTaylor, James (Food and Human Nutiritional Sciences)
dc.contributor.supervisorEck, Peter
dc.contributor.supervisorHu, Pingzhao
dc.date.accessioned2025-01-21T16:58:04Z
dc.date.available2025-01-21T16:58:04Z
dc.date.issued2024-12-19
dc.date.submitted2024-12-19T01:09:27Zen_US
dc.degree.disciplineFood and Human Nutritional Sciences
dc.degree.levelMaster of Science (M.Sc.)
dc.description.abstractOverall Abstract Background: Obesity is a major public health challenge worldwide and in Manitoba. An estimated 40-70% of obesity is heritable; however, these genetic associations are poorly investigated in the Manitoban adult population using the “gold standard” Dual Energy X-Ray Absorptiometry (DXA) to assess obesity phenotypes. The Manitoba Personalized Lifestyle Research (TMPLR) project enabled a genetic association study in middle-aged Manitobans. Obesity phenotypes considered are total, gynoid, android, arms, legs, and trunk fat mass. Objectives: 1. Perform a systematic review to determine genes associated with obesity phenotypes assessed by DXA in middle-aged cohorts. 2. Develop a “pipeline” to conduct Genome-Wide Association Studies (GWAS) within the TMPLR. 3. Conduct a GWAS on obesity phenotypes within TMPLR. 4. Compare the genes from the systematic review to those from TMPLR data analysis. Methods: The Covidence platform was used for the systematic review. Publications up to July 2023 sourced from Embase and Medline. The methods for the TMPLR project have been published. A GWAS pipeline was established using the Biodata Catalyst bioinformatics platform and the Seven Bridges R studio version 4.1. Results: Out of 94 and 25 studies obtained from Medline and Embase respectively, 14 studies met the eligibility criteria and 13 genes were identified that are associated with obesity-related phenotypes. No significant genome-wide association with obesity was established in the TMPLR cohort. However, 23 loci have had suggestive associations with the obesity phenotypes. Conclusion: There is a lack of high-quality genetic studies that use DXA data and adult populations. No genome-wide associations were reported in TMPLR, likely due to the limited sample size of the cohort. However, a bioinformatics pipeline to analyze genome-wide associations in TMPLR cohort is established and can be used for larger cohorts, such as UK biobanks.
dc.description.noteFebruary 2025
dc.description.sponsorshipBiodata Catalyst Pilot Funds
dc.identifier.urihttp://hdl.handle.net/1993/38840
dc.language.isoeng
dc.subjectObesity
dc.subjectGenome-Wide Association Studies (GWAS)
dc.subjectManitoba Personalized Lifestyle Research (TMPLR)
dc.subjectDual-Energy X-Ray Absorptiometry (DXA)
dc.subjectGenetics
dc.titleGenome-wide association analysis within The Manitoba Personalized Lifestyle Research study
local.subject.manitobayes
project.funder.nameResearch Manitoba
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