Major Depressive Disorder Impacts Peripheral Artery Disease Risk Through Intermediary Risk Factors

Author:

Shakt Gabrielle12ORCID,Tsao Noah L.12,Levin Michael G.13ORCID,Walker Venexia24ORCID,Kember Rachel L.15ORCID,Klarin Derek67ORCID,Tsao Phil68ORCID,Voight Benjamin F.1910ORCID,Scali Salvatore T.11ORCID,Damrauer Scott M.1210ORCID

Affiliation:

1. Corporal Michael Crescenz VA Medical Center Philadelphia PA USA

2. Department of Surgery, Perelman School of Medicine University of Pennsylvania Philadelphia PA USA

3. Department of Medicine, Perelman School of Medicine University of Pennsylvania Philadelphia PA USA

4. Medical Research Council Integrative Epidemiology Unit University of Bristol Bristol United Kingdom

5. Department of Psychiatry, Perelman School of Medicine University of Pennsylvania Philadelphia PA USA

6. VA Palo Alto Health Care System Palo Alto CA USA

7. Division of Vascular Surgery Stanford University Palo Alto CA USA

8. Department of Medicine Stanford University School of Medicine Stanford CA USA

9. Department of Systems Pharmacology and Translational Therapeutics University of Pennsylvania Philadelphia PA USA

10. Department of Genetics, Perelman School of Medicine University of Pennsylvania Philadelphia PA USA

11. Malcolm Randall VA Medical Center Gainesville FL USA

Abstract

Background Major depressive disorder (MDD) has been identified as a causal risk factor for multiple forms of cardiovascular disease. Although observational evidence has linked MDD to peripheral artery disease (PAD), causal evidence of this relationship is lacking. Methods and Results Inverse variance weighted 2‐sample Mendelian randomization was used to test the association the between genetic liability for MDD and genetic liability for PAD. Genetic liability for MDD was associated with increased genetic liability for PAD (odds ratio [OR], 1.17 [95% CI, 1.06–1.29]; P =2.6×10 −3 ). Genetic liability for MDD was also associated with increased genetically determined lifetime smoking ( β =0.11 [95% CI, 0.078–0.14]; P =1.2×10 −12 ), decreased alcohol intake ( β =−0.078 [95% CI, −0.15 to 0]; P =0.043), and increased body mass index ( β =0.10 [95% CI, 0.02–0.19]; P =1.8×10 −2 ), which in turn were associated with genetic liability for PAD (smoking: OR, 2.81 [95% CI, 2.28–3.47], P =9.8×10 −22 ; alcohol: OR, 0.77 [95% CI, 0.66–0.88]; P =1.8×10 −4 ; body mass index: OR, 1.61 [95% CI, 1.52–1.7]; P =1.3×10 −57 ). Controlling for lifetime smoking index, alcohol intake, and body mass index with multivariable Mendelian randomization completely attenuated the association between genetic liability for MDD with genetic liability for PAD. Conclusions This work provides evidence for a possible causal association between MDD and PAD that is dependent on intermediate risk factors, adding to the growing body of evidence suggesting that effective management and treatment of cardiovascular diseases may require a composite of physical and mental health interventions.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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