Master of Arts (MA)
First Committee Member
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Bipolar disorder (BP), a severe mental disorder characterized by recurring manic and depressive episodes, has been shown to have a strong genetic underpinning. Current theory suggests that it is the summation of risk alleles, spread across the entirety of the genome, which contributes to the development of BP, as well as other polygenic traits. The comorbid nature of these polygenic traits are often problematic for diagnosticians as the symptomology of the disorders may vary substantially between individuals and can create diagnostic confusion. To alleviate issues such as these, a more objective measure, to be used alongside current diagnostic procedures, is needed. To accomplish this, researchers have begun to turn their attention towards an ever increasing body of publicly available genetic data.
Recently, polygenic risk scores have been implemented in genetic risk prediction. Genome-wide association study (GWAS) summary statistics, derived on a plethora of psychiatric disorders, are readily accessible and provide a cost efficient strategy for generating risk scores. In this study, we attempted to not only predict the diagnosis of bipolar disorder utilizing publicly available genotype information, but to also improve upon current methodology by showing that the inclusion of risk scores calculated on comorbid traits can benefit the accuracy and generalizability of the classification model. While the results reported herein are mixed, this study provides strong support for the feasibility of genetic prediction of psychiatric disorders. This approach was, to our knowledge, entirely novel and the first time it had been implemented in practice.
Bioinformatics | Genetics | Psychology
University of Nevada, Las Vegas
Mize, Travis, "Multi-Polygenic Risk Score Prediction Model for Bipolar Disorder" (2019). UNLV Theses, Dissertations, Professional Papers, and Capstones. 3738.
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