Higher macrophage superoxide anion production in coronary artery disease (CAD) patients with Type D personality
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Published on: April 3, 2017
Claudia Zuccarella-Hackl1, Roland von Känel2, Livia Thomas3
1Biological and Health Psychology, University of Bern, Bern, Switzerland; Department of Clinical Research, University of Bern, Bern, Switzerland.
Insights
Type D personality is linked to worse outcomes in heart disease patients. Individuals with Type D showed increased macrophage superoxide anion production, a key factor in atherosclerosis.
Area of Science:
- Cardiology
- Psychosomatic Medicine
- Immunology
Background:
- Type D personality is an independent risk factor for poor cardiac prognosis and increased mortality in cardiovascular disease (CVD).
- The precise mechanisms linking Type D personality to adverse CVD outcomes remain unclear.
- Macrophages are crucial in the development of atherosclerosis, the underlying process in coronary artery disease (CAD).
Purpose of the Study:
- To investigate macrophage superoxide anion production in male CAD patients with and without Type D personality.
- To explore the association between Type D personality, its subscales (negative affectivity, social inhibition), and macrophage activity in CAD patients.
Main Methods:
- Studied 20 male CAD patients with Type D and 20 age-matched male CAD patients without Type D.
- Assessed Type D personality using the DS14 questionnaire, measuring negative affectivity and social inhibition.
- Measured macrophage superoxide anion production via the WST-1 assay, controlling for confounders.
Main Results:
- CAD patients with Type D exhibited significantly higher macrophage superoxide anion production compared to those without Type D (p<0.001).
- Both negative affectivity and social inhibition, as well as their interaction, were independently associated with increased superoxide anion production.
- These findings remained significant after controlling for classical CVD risk factors, atherosclerosis severity, and psychological factors.
Conclusions:
- CAD patients with Type D personality demonstrate elevated macrophage superoxide anion production.
- This heightened macrophage activity may represent a key mechanism contributing to the increased morbidity and mortality observed in Type D CAD patients.
Background:
Type D personality (Type D) is an independent psychosocial risk factor for poor cardiac prognosis and increased mortality in patients with cardiovascular disease (CVD), but the involved mechanisms are poorly understood. Macrophages play a pivotal role in atherosclerosis, the process underlying coronary artery disease (CAD). We investigated macrophage superoxide anion production in production in CAD patients with and without Type D.
Methods And Results:
We studied 20 male CAD patients with Type D (M:66.7±9.9years) and 20 age-matched male CAD patients without Type D (M:67.7±8.5years). Type D was measured using the DS14 questionnaire with the two subscales 'negative affectivity' and 'social inhibition'. We assessed macrophage superoxide anion production using the WST-1 assay. All analyses were controlled for potential confounders. CAD patients with Type D showed higher superoxide anion production compared to CAD patients without Type D (F(1,38)=15.57, p<0.001). Complementary analyses using the Type D subscales 'negative affectivity' and 'social inhibition', and their interaction as continuous measures, showed that both Type D subscales (negative affectivity: (ß=0.48, p=0.002, R(2)=0.227); social inhibition: (ß=0.46, p=0.003, R(2)=0.208)) and their interaction (ß=0.36, p=0.022, R(2)=0.130) were associated with higher WST-1 reduction scores. Results remained significant when controlling for classical CVD risk factors (i.e. body mass index, mean arterial blood pressure), atherosclerosis severity (i.e. intima media thickness, presence of carotid plaques), and psychological factors (depressive symptom severity, chronic stress).
Conclusions:
Our results indicate higher macrophage superoxide anion production in CAD patients with Type D compared to those without Type D. This may suggest a mechanism contributing to increased morbidity and mortality in CAD patients with Type D.
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