Mj. Niemela et al., EFFECT OF BETA-BLOCKADE ON HEART-RATE-VARIABILITY IN PATIENTS WITH CORONARY-ARTERY DISEASE, Journal of the American College of Cardiology, 23(6), 1994, pp. 1370-1377
Objectives. This study assessed the effects of beta-blockade on heart
rate variability in patients with coronary artery disease and determin
ed whether the effects of metoprolol in a controlled-release formulati
on and atenolol differ with regard to electrocardiographic measures of
cardiac autonomic control. Background. Low heart rate variability is
common in coronary artery disease and is associated with increased mor
tality. Beta-adrenergic blocking drugs may increase heart rate variabi
lity in healthy subjects, but there is limited knowledge of whether th
ey are able to modify heart rate variability in patients with uncompli
cated coronary artery disease. Methods. In a randomly allocated, doubl
e-blind crossover study with three 2-week treatment periods, 200 mg of
controlled release metoprolol once a day, 100 mg of atenolol once a d
ay or placebo once a day were administered in 18 male patients with st
able coronary artery disease. The 24-h heart rate variability was meas
ured in both the time and frequency domains. Results. Beta-blockade in
duced a significant increase in heart rate variability, but no signifi
cant differences were found between atenolol and metoprolol. The avera
ge 24-h high frequency power increased by 64% after atenolol and by 62
% after metoprolol. The root mean square successive difference of norm
al RR intervals increased by 70% after atenolol and by 62% after metop
rolol, and the standard deviations of RR intervals increased by 20% an
d 16%, respectively. Beta-blockade had no significant effects on the a
mplitude of the circadian rhythm of heart rate variability, although b
oth metoprolol and atenolol blunted the abrupt decrease of high freque
ncy power after arousal. Conclusions. Beta blockade by metoprolol and
atenolol enhance the heart rate variability in patients with coronary
artery disease. This may contribute to the protective effects of beta-
blockade in ischemic heart disease.