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Published on: April 15, 2020
Shared mechanisms between coronary heart disease and depression: findings from a large UK general population-based
Golam M Khandaker1,2, Verena Zuber3, Jessica M B Rees4
1Department of Psychiatry, University of Cambridge, Cambridge, UK.
Insights
Shared environmental factors, not genetics, largely explain the link between coronary heart disease (CHD) and depression. However, triglycerides, IL-6, and CRP may be causal risk factors for depression.
Area of Science:
- Cardiovascular Medicine
- Psychiatry
- Genetics
Background:
- Comorbidity between coronary heart disease (CHD) and depression is well-documented.
- Underlying shared mechanisms between CHD and depression remain unclear.
Purpose of the Study:
- To investigate shared genetic and environmental factors contributing to CHD-depression comorbidity.
- To assess potential causal relationships between cardiovascular risk factors, CHD, and depression using Mendelian randomization.
Main Methods:
- Analysis of 367,703 UK Biobank participants of European ancestry.
- Assessment of family history of heart disease and CHD genetic risk scores.
- Mendelian randomization analyses for triglycerides, IL-6, and CRP in relation to depression.
Main Results:
- Family history of heart disease increased depression risk by 20%.
- CHD genetic risk score did not associate with depression risk.
- Triglycerides, IL-6, and CRP showed likely causal links to depression.
Conclusions:
- Comorbidity between depression and CHD is primarily driven by shared environmental factors.
- Triglycerides, IL-6, and CRP represent potential therapeutic targets for depression.
Abstract:
While comorbidity between coronary heart disease (CHD) and depression is evident, it is unclear whether the two diseases have shared underlying mechanisms. We performed a range of analyses in 367,703 unrelated middle-aged participants of European ancestry from UK Biobank, a population-based cohort study, to assess whether comorbidity is primarily due to genetic or environmental factors, and to test whether cardiovascular risk factors and CHD are likely to be causally related to depression using Mendelian randomization. We showed family history of heart disease was associated with a 20% increase in depression risk (95% confidence interval [CI] 16-24%, p < 0.0001), but a genetic risk score that is strongly associated with CHD risk was not associated with depression. An increase of 1 standard deviation in the CHD genetic risk score was associated with 71% higher CHD risk, but 1% higher depression risk (95% CI 0-3%; p = 0.11). Mendelian randomization analyses suggested that triglycerides, interleukin-6 (IL-6), and C-reactive protein (CRP) are likely causal risk factors for depression. The odds ratio for depression per standard deviation increase in genetically-predicted triglycerides was 1.18 (95% CI 1.09-1.27; p = 2 × 10-5); per unit increase in genetically-predicted log-transformed IL-6 was 0.74 (95% CI 0.62-0.89; p = 0.0012); and per unit increase in genetically-predicted log-transformed CRP was 1.18 (95% CI 1.07-1.29; p = 0.0009). Our analyses suggest that comorbidity between depression and CHD arises largely from shared environmental factors. IL-6, CRP and triglycerides are likely to be causally linked with depression, so could be targets for treatment and prevention of depression.
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