TY - JOUR
T1 - Components of heart rate variability measured during healing of acute myocardial infarction
AU - Bigger, J. Thomas
AU - Kleiger, Robert E.
AU - Fleiss, Joseph L.
AU - Rolnitzky, Linda M.
AU - Steinman, Richard C.
AU - Miller, J. Philip
N1 - Funding Information:
From the Division of Cardiology, Department of Medicine, and ’ Division of Biostatistics, School of Public Health Columbia Uni-Rec ently we reported that heart rate (HR) variability, versity, New York and the Arrhythmia Control Unit, the Cohn-n-1 defined as the standard deviation of all normal RR (or bia-Presbyterian Medical Center, New York, and the Depart-N-N) intervals in a &hour continuous electrocardio- ment of Medicine and Division of Biostatistics, Washington Uni-gram recording made 11 f 3 days after acute myocar- versity School of Medicine, St. Louis, Missouri. This study was dial infarction, predicted long-term survival.1 Low HR supported in part by grants HL-22982 and HL-70204 from the variability was the strongest predictor of mortality National Heart, Lung, and Blood Institute and by grant RR-among the Holter variables measured, i.e., HR, ven- 00845 from the Research Resources Administration, Bethesda, tricular arrhythmia frequency or repetitive ventricular Maryland; and by funds from the Gebbie Foundation, James-arrhythmias. HR variability remained a significant town, New York, Merck, Sharp and Dohme Research Laborato-predictor of mortality after adjusting for clinical and ries, West Point, Pennsylvania, and the Winthrop and Chernow demographic variables, other Holter features, includ- Foundations, New York, New York. Manuscript received July ing HR and ventricular arrhythmias, and left ventricu- 28,1987;r evised manuscript received and accepted October 15, lar ejection fraction. Our hypothesis to explain this 1987. finding is that decreased HR variability correlates Address for reprints: J. Thomas Bigger, Jr., MD, Division of with decreased vagal nervous activity or increased Cardiology, Columbia University, 830 West 188th Street, New sympathetic nervous activity that may predispose the York, New York 10032. heart to ventricular fibrillation. The current study elu- *Committee members and enrolling cidated the causeso f differences in HR and in compo- the Appendix. nents of HR variability between patients with low and
PY - 1988/2/1
Y1 - 1988/2/1
N2 - A high degree of heart rate (HR) variability is found in persons with normal hearts, whereas low HR variability can be found in patients with severe coronary artery disease, congestive heart failure and diabetic neuropathy. Two weeks after acute myocardial infarction, low HR variability predicted reduced long-term survival even after adjusting for clinical risk indicators, left ventricular ejection fraction, HR and ventricular arrhythmias. The present study elucidated the causes of differences in HR and HR variability between patients with low and high HR variability. In a matched-pair study, 10 patients with low HR variability (24-hour standard deviation of N-N intervals <50 ms) were randomly selected. For each of these 10 patients, a control patient with high HR variability (24-hour standard deviation of N-N intervals ≥100 ms), matched for age, left ventricular ejection fraction and rales in the coronary care unit was selected. Patients who were taking either digitalis or β-adrenergic blocking drugs were excluded. Analysis of 24-hour electrocardiograms showed that for the tew HR variability group compared with the high: (1) the daytime and nighttime average HR was faster; (2) the difference between daytime and nighttime HR was less; (3) the proportion of differences >50 ms between successive N-N Intervals was smaller; and (4) the number of HR "spkes" per day (Increase In HR ≥10 beats/min, lasting from 3 to 15 minutes) was less. These findings Indicate that parasympathetic nervous activity is substantially reduced in patients with tow HR variability compared with control patients. Low parasympathetic activity or high sympathetic activity decreases the electrical ventricular fibrillation threshold and increases the probability of ventricular fibrillation during myocardial ischemia, and may explain the association between low HR variability and mortality after acute myocardial infarction.
AB - A high degree of heart rate (HR) variability is found in persons with normal hearts, whereas low HR variability can be found in patients with severe coronary artery disease, congestive heart failure and diabetic neuropathy. Two weeks after acute myocardial infarction, low HR variability predicted reduced long-term survival even after adjusting for clinical risk indicators, left ventricular ejection fraction, HR and ventricular arrhythmias. The present study elucidated the causes of differences in HR and HR variability between patients with low and high HR variability. In a matched-pair study, 10 patients with low HR variability (24-hour standard deviation of N-N intervals <50 ms) were randomly selected. For each of these 10 patients, a control patient with high HR variability (24-hour standard deviation of N-N intervals ≥100 ms), matched for age, left ventricular ejection fraction and rales in the coronary care unit was selected. Patients who were taking either digitalis or β-adrenergic blocking drugs were excluded. Analysis of 24-hour electrocardiograms showed that for the tew HR variability group compared with the high: (1) the daytime and nighttime average HR was faster; (2) the difference between daytime and nighttime HR was less; (3) the proportion of differences >50 ms between successive N-N Intervals was smaller; and (4) the number of HR "spkes" per day (Increase In HR ≥10 beats/min, lasting from 3 to 15 minutes) was less. These findings Indicate that parasympathetic nervous activity is substantially reduced in patients with tow HR variability compared with control patients. Low parasympathetic activity or high sympathetic activity decreases the electrical ventricular fibrillation threshold and increases the probability of ventricular fibrillation during myocardial ischemia, and may explain the association between low HR variability and mortality after acute myocardial infarction.
UR - http://www.scopus.com/inward/record.url?scp=0023713704&partnerID=8YFLogxK
U2 - 10.1016/0002-9149(88)90917-4
DO - 10.1016/0002-9149(88)90917-4
M3 - Article
C2 - 3341195
AN - SCOPUS:0023713704
SN - 0002-9149
VL - 61
SP - 208
EP - 215
JO - The American journal of cardiology
JF - The American journal of cardiology
IS - 4
ER -