Polygenic risk of major depressive disorder as a risk factor for venous thromboembolism

Author:

Ward Joey1,Le Ngoc-Quynh2,Suryakant Suryakant3,Brody Jennifer A.4ORCID,Amouyel Philippe5ORCID,Boland Anne67ORCID,Bown Rosemary8ORCID,Cullen Breda1,Debette Stéphanie3,Deleuze Jean-François679,Emmerich Joseph1011,Graham Nicholas1,Germain Marine3,Anderson Jana J.1ORCID,Pell Jill P.1,Lyall Donald M.1,Lyall Laura M.17ORCID,Smith Daniel J.112,Wiggins Kerri L.4ORCID,Soria José Manuel2,Souto Juan Carlos13,Morange Pierre-Emmanuel14,Smith Nicholas L.151617,Trégouët David-Alexandre3ORCID,Sabater-Lleal Maria218ORCID,Strawbridge Rona J.11819ORCID

Affiliation:

1. 1School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom

2. 2Genomics of Complex Disease Unit, Institut d’Investigació Biomèdica Sant Pau, Barcelona, Spain

3. 3University of Bordeaux, INSERM, Bordeaux Population Health Research Center, UMR 1219, Bordeaux, France

4. 4Cardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, WA

5. 5University of Lille, INSERM, CHU Lille, Institut Pasteur de Lille, U1167-RID-AGE-Facteurs de Risque et Déterminants Moléculaires des Maladies Liées au Vieillissement, Lille, France

6. 6Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, Evry, France

7. 7Laboratory of Excellence in Medical Genomics, GENMED, Evry, France

8. 8School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom

9. 9Centre d’Etude du Polymorphisme Humain, Fondation Jean Dausset, Paris, France

10. 10Department of Vascular Medicine, Paris Saint-Joseph Hospital Group, University of Paris, Paris, France

11. 11UMR1153, INSERM CRESS, Paris, France

12. 12Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom

13. 13Unitat d’Hemostàsia i Trombosi, Institut d’Investigació Biomèdica Sant Pau, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

14. 14Aix-Marseille University, INSERM, INRAE, Centre de Recherche en CardioVasculaire et Nutrition, Laboratory of Haematology, CRB Assistance Publique – Hôpitaux de Marseille, HemoVasc, Marseille, France

15. 15Department of Epidemiology, University of Washington, Seattle, WA

16. 16Kaiser Permanente Washington Health Research Institute, Kaiser Permanente Washington, Seattle, WA

17. 17Department of Veterans Affairs Office of Research and Development, Seattle Epidemiologic Research and Information Center, Seattle, WA

18. 18Cardiovascular Medicine Unit, Department of Medicine Solna, Karolinska Institute, Stockholm, Sweden

19. 19Health Data Research UK, Glasgow, United Kingdom

Abstract

Abstract Major depressive disorder (MDD), bipolar disorder (BD), and schizophrenia (SCZ) are associated with an increased risk of cardiovascular diseases, including venous thromboembolism (VTE). The reasons for this are complex and include obesity, smoking, and use of hormones and psychotropic medications. Genetic studies have increasingly provided evidence of the shared genetic risk of psychiatric and cardiometabolic illnesses. This study aimed to determine whether a genetic predisposition to MDD, BD, or SCZ is associated with an increased risk of VTE. Genetic correlations using the largest genome-wide genetic meta-analyses summary statistics for MDD, BD, and SCZ (Psychiatric Genetics Consortium) and a recent genome-wide genetic meta-analysis of VTE (INVENT Consortium) demonstrated a positive association between VTE and MDD but not BD or SCZ. The same summary statistics were used to construct polygenic risk scores for MDD, BD, and SCZ in UK Biobank participants of self-reported White British ancestry. These were assessed for impact on self-reported VTE risk (10 786 cases, 285 124 controls), using logistic regression, in sex-specific and sex-combined analyses. We identified significant positive associations between polygenic risk for MDD and the risk of VTE in men, women, and sex-combined analyses, independent of the known risk factors. Secondary analyses demonstrated that this association was not driven by those with lifetime experience of mental illness. Meta-analyses of individual data from 6 additional independent cohorts replicated the sex-combined association. This report provides evidence for shared biological mechanisms leading to MDD and VTE and suggests that, in the absence of genetic data, a family history of MDD might be considered when assessing the risk of VTE.

Publisher

American Society of Hematology

Subject

Hematology

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