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Updated: Jun 19, 2026

Evaluation of Coronary Flow Reserve After Myocardial Ischemia Reperfusion in Rats
Published on: June 28, 2019
Major depression and coronary flow reserve detected by positron emission tomography
Viola Vaccarino1, John Votaw, Tracy Faber
1Division of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, GA 30306, USA. viola.vaccarino@emory.edu
Insights
Major depressive disorder (MDD) is linked to coronary heart disease (CHD) risk, potentially through shared genetics affecting microvascular function. This study found reduced coronary flow reserve in twins with MDD, suggesting a genetic link to heart disease.
Area of Science:
- Cardiology
- Psychiatry
- Genetics
Background:
- Major depressive disorder (MDD) is associated with coronary heart disease (CHD), but underlying mechanisms remain unclear.
- MDD may increase CHD risk via microvascular circulation changes or shared genetic factors.
- Coronary flow reserve (CFR) is a measure of microvascular function.
Purpose of the Study:
- To investigate the relationship between MDD and CFR.
- To explore potential shared genetic pathways between MDD and microvascular dysfunction.
Main Methods:
- Examined 289 male middle-aged twins, including 106 discordant for MDD and 183 controls.
- Measured CFR using positron emission tomography with (13)N-ammonia for myocardial blood flow.
- Assessed myocardial ischemia using a standard perfusion defect score.
Main Results:
- No significant difference in myocardial ischemia between twins with and without MDD.
- Dizygotic twins with MDD showed a 14% lower CFR compared to their non-MDD brothers (P = .03).
- This association was absent in monozygotic twins, indicating a genetic influence (zygosity-MDD interaction P = .006).
Conclusions:
- Results suggest a shared genetic pathway linking MDD and microvascular dysfunction.
- Common pathophysiological processes may connect MDD and early atherosclerosis development.
Background:
Major depressive disorder (MDD) is associated with coronary heart disease (CHD), but the mechanisms are unclear. The presence of MDD may increase CHD risk by affecting microvascular circulation. It is also plausible that genetic factors influencing MDD may overlap with those for CHD. We sought to examine the relationship between MDD and coronary flow reserve (CFR), the ratio of maximum flow during stress to flow at rest measured in milliliters per minute per gram of tissue.
Methods:
We examined 289 male middle-aged twins, including 106 twins (53 twin pairs) discordant for a lifetime history of MDD and 183 control twins (unrelated to any twins in the experimental group) without MDD. To calculate CFR, we used positron emission tomography with nitrogen 13 ((13)N) ammonia to evaluate myocardial blood flow at rest and after adenosine stress. A standard perfusion defect score was also used to assess myocardial ischemia.
Results:
There was no difference in myocardial ischemia between twins with and without MDD. Among the dizygotic twin pairs discordant for MDD, the CFR was 14% lower in the twins with MDD than in their brothers without MDD (2.36 vs 2.74) (P = .03). This association was not present in the monozygotic discordant pairs who were genetically matched (2.86 vs 2.64) (P = .19). The zygosity-MDD interaction after adjustment was significant (P = .006). The CFR in the dizygotic twins with MDD was also lower than in the control twins.
Conclusions:
Our results provide evidence for a shared genetic pathway between MDD and microvascular dysfunction. Common pathophysiologic processes may link MDD and early atherosclerosis.
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