Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/144702
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dc.titleGENETIC EPIDEMIOLOGY INVESTIGATION OF CORONARY ARTERY DISEASESEVERITY: IDENTIFICATION OF RISK FACTORS AND ASSOCIATED GENETIC VARIANTS
dc.contributor.authorZHANG QIANYUN
dc.date.accessioned2018-07-09T18:00:22Z
dc.date.available2018-07-09T18:00:22Z
dc.date.issued2018-01-26
dc.identifier.citationZHANG QIANYUN (2018-01-26). GENETIC EPIDEMIOLOGY INVESTIGATION OF CORONARY ARTERY DISEASESEVERITY: IDENTIFICATION OF RISK FACTORS AND ASSOCIATED GENETIC VARIANTS. ScholarBank@NUS Repository.
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/144702
dc.description.abstractIntroduction Coronary artery disease (CAD) is one of the top killers worldwide. Yet few studies have identified the non-genetic and genetic risk factors for CAD severity, especially in Singaporean population. Methods Subjects from the Singapore CAD Genetics Study (SCADGENS) were classified by multiple vessels diseased (MVD) status. Logistic regression was applied to identify the non-genetic risk factors, and Genome-wide association study (GWAS) was applied for the genetic tests. Results Diabetes (P=0.007) and dyslipidemia (P=0.016) were significantly associated with an increased risk of MVD in smokers. All of the top 9 hits were from chromosome 13 and none of them attained the GWAS significance level of 5.00x10-8. The major allele of the top hit rs875589 is associated with risk, and might interact with ethnicity. Conclusion We identified non-genetic risk factors, as well as an ethnicity-interactive variant that is close to genome-wide significance for CAD severity in Singaporean population.
dc.language.isoen
dc.subjectCoronary artery disease severity, risk factors, genetic factors, GWAS, Singaporean population
dc.typeThesis
dc.contributor.departmentPAEDIATRICS
dc.contributor.supervisorHeng Chew Kiat
dc.contributor.supervisorSoong Tuck Wah
dc.description.degreeMaster's
dc.description.degreeconferredMASTER OF SCIENCE (RSH-SOM)
dc.identifier.orcid0000-0001-5477-1589
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