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Evaluation of bi-directional causal association between depression and cardiovascular diseases: a Mendelian randomization study.
Li, Gloria Hoi-Yee; Cheung, Ching-Lung; Chung, Albert Kar-Kin; Cheung, Bernard Man-Yung; Wong, Ian Chi-Kei; Fok, Marcella Lei Yee; Au, Philip Chun-Ming; Sham, Pak-Chung.
  • Li GH; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong.
  • Cheung CL; Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong.
  • Chung AK; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong.
  • Cheung BM; Department of Psychiatry, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong.
  • Wong IC; Department of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong.
  • Fok MLY; Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong.
  • Au PC; Research Department of Practice and Policy, School of Pharmacy, University College London, London, UK.
  • Sham PC; Central and North West London NHS Foundation Trust, London, UK.
Psychol Med ; 52(9): 1765-1776, 2022 07.
Article en En | MEDLINE | ID: mdl-33032663
ABSTRACT

BACKGROUND:

Depression and cardiovascular disease (CVD) are associated with each other but their relationship remains unclear. We aim to determine whether genetic predisposition to depression are causally linked to CVD [including coronary artery disease (CAD), myocardial infarction (MI), stroke and atrial fibrillation (AF)].

METHODS:

Using summary statistics from the largest genome-wide association studies (GWAS) or GWAS meta-analysis of depression (primary

analysis:

n = 500 199), broad depression (help-seeking behavior for problems with nerves, anxiety, tension or depression; secondary

analysis:

n = 322 580), CAD (n = 184 305), MI (n = 171 875), stroke (n = 446 696) and AF (n = 1 030 836), genetic correlation was tested between two depression phenotypes and CVD [MI, stroke and AF (not CAD as its correlation was previously confirmed)]. Causality was inferred between correlated traits by Mendelian Randomization analyses.

RESULTS:

Both depression phenotypes were genetically correlated with MI (depression rG = 0.169; p = 9.03 × 10-9; broad depression rG = 0.123; p = 1 × 10-4) and AF (depression rG = 0.112; p = 7.80 × 10-6; broad depression rG = 0.126; p = 3.62 × 10-6). Genetically doubling the odds of depression was causally associated with increased risk of CAD (OR = 1.099; 95% CI 1.031-1.170; p = 0.004) and MI (OR = 1.146; 95% CI 1.070-1.228; p = 1.05 × 10-4). Adjustment for blood lipid levels/smoking status attenuated the causality between depression and CAD/MI. Null causal association was observed for CVD on depression. A similar pattern of results was observed in the secondary analysis for broad depression.

CONCLUSIONS:

Genetic predisposition to depression may have positive causal roles on CAD/MI. Genetic susceptibility to self-awareness of mood problems may be a strong causal risk factor of CAD/MI. Blood lipid levels and smoking may potentially mediate the causal pathway. Prevention and early diagnosis of depression are important in the management of CAD/MI.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Accidente Cerebrovascular Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies / Screening_studies / Systematic_reviews Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Accidente Cerebrovascular Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies / Screening_studies / Systematic_reviews Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article