Phenome-wide screening of the putative causal determinants of depression using genetic data. Issue 17 (8th April 2022)
- Record Type:
- Journal Article
- Title:
- Phenome-wide screening of the putative causal determinants of depression using genetic data. Issue 17 (8th April 2022)
- Main Title:
- Phenome-wide screening of the putative causal determinants of depression using genetic data
- Authors:
- Aman, Asma M
García-Marín, Luis M
Thorp, Jackson G
Campos, Adrian I
Cuellar-Partida, Gabriel
Martin, Nicholas G
Rentería, Miguel E - Abstract:
- Abstract: Depression is one of the most common mental health disorders and one of the top causes of disability throughout the world. The present study sought to identify putative causal associations between depression and hundreds of complex human traits through a genome-wide screening of genetic data and a hypothesis-free approach. We leveraged genome-wide association studies summary statistics for depression and 1504 complex traits and investigated potential causal relationships using the latent causal variable method. We identified 559 traits genetically correlated with depression risk at FDR < 5%. Of these, 46 were putative causal genetic determinants of depression, including lifestyle factors, diseases of the nervous system, respiratory disorders, diseases of the musculoskeletal system, traits related to the health of the gastrointestinal system, obesity, vitamin D levels and the use of prescription medications, among others. No phenotypes were identified as potential outcomes of depression. Our results suggest that genetic liability to multiple complex traits may contribute to a higher risk for depression. In particular, we show a putative causal genetic effect of pain, obesity and inflammation on depression. These findings provide novel insights into the potential causal determinants of depression and should be interpreted as testable hypotheses for future studies to confirm, which may facilitate the design of new prevention strategies to reduce depression's burden.
- Is Part Of:
- Human molecular genetics. Volume 31:Issue 17(2022)
- Journal:
- Human molecular genetics
- Issue:
- Volume 31:Issue 17(2022)
- Issue Display:
- Volume 31, Issue 17 (2022)
- Year:
- 2022
- Volume:
- 31
- Issue:
- 17
- Issue Sort Value:
- 2022-0031-0017-0000
- Page Start:
- 2887
- Page End:
- 2898
- Publication Date:
- 2022-04-08
- Subjects:
- Human molecular genetics -- Periodicals
Human chromosome abnormalities -- Periodicals
572.8 - Journal URLs:
- http://hmg.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/hmg/ddac081 ↗
- Languages:
- English
- ISSNs:
- 0964-6906
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4336.198000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23173.xml