Depression as an independent determinant of decreased heart rate variability in patients post myocardial infarction
Insights
Depression significantly lowers heart rate variability (HRV) in myocardial infarction (MI) patients, independent of other clinical factors. This autonomic nervous system derangement may worsen cardiac outcomes post-MI.
Area of Science:
- Cardiology
- Psychiatry
- Autonomic Neuroscience
Background:
- Depression is a known risk factor for cardiac events and mortality after myocardial infarction (MI).
- The autonomic nervous system (ANS) plays a crucial role in cardiovascular regulation and recovery post-MI.
Purpose of the Study:
- To investigate the role of the autonomic nervous system, specifically heart rate variability (HRV), in mediating the increased cardiac risk associated with depression in post-MI patients.
Main Methods:
- A study group of 95 non-depressed and 53 depressed post-MI patients was assessed three months after MI.
- Depressive symptoms were measured using the Beck Depression Inventory (BDI).
- Autonomic nervous system activity was evaluated by analyzing 24-hour ambulatory electrocardiographic recordings to assess heart rate variability (HRV).
Main Results:
- Depression was associated with significantly lower longer-range HRV (SDANN, very-low-frequency, and low-frequency power).
- Higher age and lower left ventricular ejection fraction (<0.40) were also linked to reduced HRV.
- Even after adjusting for age and ejection fraction, depression remained independently associated with decreased HRV.
Conclusions:
- Post-MI patients with depression exhibit reduced longer-range HRV compared to those without depression.
- This autonomic derangement associated with depression may contribute to the adverse cardiac outcomes observed in these patients.
- The findings support the hypothesis that depression exacerbates autonomic dysfunction, negatively impacting prognosis after myocardial infarction.
Objective:
Depression is associated with an increased risk of cardiac morbidity and mortality in patients following myocardial infarction (MI). Our objective was to investigate the potential role of the autonomic nervous system in mediating this detrimental effect.
Methods:
The study group consisted of 95 consecutive post-MI patients without depression and 53 post-MI patients with depression. Depressive symptoms were assessed by the Beck Depression Inventory (BDI). Activity of the autonomic nervous system was assessed by analysing heart rate variability (HRV) using 24-hour ambulatory electrocardiographic recordings as obtained three months post MI.
Results:
Higher age, female gender and left ventricular ejection fraction <0.40 were associated with lower HRV (SDANN, and very-low-frequency and low-frequency power, but not RMSSD and high-frequency power), as was depression. In the multivariate analysis, age and left ventricular ejection fraction but not gender emerged to be independently associated with HRV. After adjustment for these two covariates, depression remained significantly associated with low HRV.
Conclusions:
Patients with depression in the present post-MI study are characterised by decreased longer-range HRV compared with the patients without depression, independent of other clinical variables. This observation supports the concept that one of the mechanisms underlying the detrimental effect of depression on post-MI prognosis may be that depression adds to the autonomic derangement post MI.
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