Notes
First, we performed a Genome-Wide Association Study (GWAS) on an anhedonia phenotype that identified 11 regions of the genome. The phenotype was based on the question of how many days in the past two weeks the respondent didn't get pleasure form things they usually enjoyed with the responses were grouped into the proportion of days in the last two weeks. We then correlated the summary statistics of the GWAS with GWAS summary statistics for psychiatric pathologies. The final thing we did was created polygenic risk scores and found that genetic loading for anhedonia associated with poorer brain white matter integrity, smaller total grey matter volume, and smaller volumes of brain regions linked to reward and pleasure processing, including orbito-frontal cortex.
Application 6553
Genome-wide association studies of mental health.
The primary aim of this research is to identify genetic associations with a) major depression plus mania/bipolar disorder, and b) vulnerability to depression and other negative mood states (as measured by neuroticism score). These aims will be achieved by conducting genome-wide association studies (GWAS), making use of data from the UK Biobank genotyping project. This project is linked to previous analyses our team have undertaken on Biobank data in the areas of mood disorder, cognitive function, cardiometabolic disease and ethnicity and meets Biobank?s stated purpose of improving the prevention, diagnosis and treatment of illnesses by identifying genetic risk factors for common mental disorders, as well as genetic risk factors for trait-like vulnerability to these disorders (neuroticism). Insights from this work will lead to a better understanding of disease processes in depression, better approaches to diagnosis and ultimately the development of new treatments. This work will consist of genome-wide association studies (GWAS), making use of data from the UK Biobank genotyping project. These GWAS studies on depression and neuroticism will make use of phenotypic and genetic data on all Biobank participants (full cohort).
Lead investigator: | Dr Rona Strawbridge |
Lead institution: | University of Glasgow |
9 related Returns
Return ID | App ID | Description | Archive Date |
3883 | 6553 | Carotid Intima-Media: Thickness Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UK Biobank | 29 Sep 2021 |
3885 | 6553 | Exploring the Role of Contactins across Psychological, Psychiatric and Cardiometabolic Traits within UK Biobank | 29 Sep 2021 |
3886 | 6553 | Genetic variation in CADM2 as a link between psychological traits and obesity | 29 Sep 2021 |
1963 | 6553 | Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia | 4 Feb 2020 |
1981 | 6553 | Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort | 10 Feb 2020 |
2524 | 6553 | Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide | 23 Oct 2020 |
2121 | 6553 | Polygenic risk for schizophrenia and season of birth within the UK Biobank cohort | 10 Mar 2020 |
3888 | 6553 | The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function | 29 Sep 2021 |
3884 | 6553 | The overlap of genetic susceptibility to schizophrenia and cardiometabolic disease can be used to identify metabolically diferent groups of individuals | 29 Sep 2021 |