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Myocardial infarction and post-traumatic stress disorder: frequency, outcome, and atherosclerotic mechanisms
Marie-Louise Gander1, Roland von Känel
1Division of Psychosomatic Medicine/Department of General Internal Medicine, University Hospital Berne, Switzerland.
Insights
Post-traumatic stress disorder (PTSD) affects 14.7% of myocardial infarction (MI) survivors and may increase cardiovascular disease risk. Further research is needed to confirm PTSD as an atherogenic risk factor.
Area of Science:
- Cardiology
- Psychiatry
- Immunology
Background:
- Post-traumatic stress disorder (PTSD) can emerge after myocardial infarction (MI).
- The role of PTSD as a risk factor for cardiovascular disease (CVD) remains unclear.
- Biological pathways linking PTSD and atherosclerosis require elucidation.
Purpose of the Study:
- To determine the prevalence of PTSD in patients post-MI.
- To examine the association between PTSD and cardiovascular outcomes.
- To investigate inflammatory markers in PTSD related to atherosclerosis.
Main Methods:
- A critical review of 31 English-language studies was conducted.
- Studies were identified through PubMed searches and bibliography reviews.
- The review focused on PTSD prevalence, cardiovascular endpoints, and inflammatory changes.
Main Results:
- The pooled prevalence of PTSD post-MI was 14.7% across 13 studies (827 patients).
- PTSD was associated with increased cardiovascular readmission and mortality risk in some studies.
- Elevated inflammatory markers, including cytokines and C-reactive protein, were observed in PTSD patients, suggesting a pro-inflammatory state.
Conclusions:
- PTSD develops frequently in post-MI patients.
- Evidence suggests PTSD may be an atherogenic risk factor.
- Further research in larger cohorts is necessary to confirm these findings and explore underlying mechanisms.
Background:
Post-traumatic stress disorder (PTSD) may develop in the aftermath of an acute myocardial infarction (MI). Whether PTSD is a risk factor for cardiovascular disease (CVD) is elusive. The biological mechanisms linking PTSD with atherosclerosis are unclear.
Design:
A critical review of 31 studies in the English language pursuing three aims: (i) to estimate the prevalence of PTSD in post-MI patients; (ii) to investigate the association of PTSD with cardiovascular endpoints; and (iii) to search for low-grade systemic inflammatory changes in PTSD pertinent to atherosclerosis.
Methods:
We located studies by PubMed electronic library search and through checking the bibliographies of these sources.
Results:
The weighted prevalence of PTSD after MI was 14.7% (range 0-25%; a total of 13 studies and 827 post-MI patients). Two studies reported a prospective association between PTSD and an increased risk of cardiovascular readmission in post-MI patients and of cardiovascular mortality in combat veterans, respectively. In a total of 11 studies, patients with PTSD had increased rates of physician-rated and self-reported cardiovascular diseases. Various cytokines and C-reactive protein were investigated in a total of seven studies suggesting that PTSD confers a pro-inflammatory state.
Conclusions:
Increasing evidence suggests that PTSD specifically related to MI develops considerably frequently in post-MI patients. More research is needed in larger cohorts applying a population design to substantiate findings suggesting PTSD is an atherogenic risk factor and to understand better the suspected behavioural and biological mechanisms involved.
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