Table 3:
Our top 4 priorities for genetic studies of MD
Priority | Opportunity |
---|---|
Increase the sample sizes available for GWAS of MD, including cases meeting full DSM or ICD criteria for major depressive disorder | Improved knowledge of genetic architecture, more accurate genetic prediction, greater numbers of genetic instruments to discover modifiable environmental factors. Identification of genetic variants contributing to more severe and persistent clinically-defined definitions |
Greater inclusion of diverse ancestries and low and middle-income countries | Representative inclusion of global ethnicities and cultures; improved fine-mapping of causal variants; stronger causal inferences based on consistently identified associations in different contexts |
Integration with electronic medical records | Ability to examine longitudinal associations with clinical symptoms, treatment response and comorbid physical conditions; enables stratification of depression based on clinical factors; provides a platform for recruitment to clinical trials and observational studies |
Developing the neurosciences of polygenic disorders | To identify the intermediate molecular, cellular, and systems biology of MD through simultaneous modelling of many low-penetrance risk alleles |