NYCTHEMERAL PROFILE OF NONSPECTRAL HEART-RATE-VARIABILITY MEASURES INWOMEN AND MEN - DESCRIPTION OF A NORMAL SAMPLE AND 2 SUDDEN CARDIAC-ARREST SUBSAMPLES
R. Burr et al., NYCTHEMERAL PROFILE OF NONSPECTRAL HEART-RATE-VARIABILITY MEASURES INWOMEN AND MEN - DESCRIPTION OF A NORMAL SAMPLE AND 2 SUDDEN CARDIAC-ARREST SUBSAMPLES, Journal of electrocardiology, 27, 1994, pp. 54-62
Heart rate variability (HRV), a noninvasive systemic index of the cent
ral autonomic nervous system, demonstrates considerable within-subject
variability, including a strong systematic 24-hour nycthemeral (or le
ss precisely, circadian) component. Recent interest in the timing of s
udden cardiac arrest (SCA), especially the pronounced morning rise in
sudden deaths, has motivated research into coincident dynamic phenomen
a in HRV indices of central autonomic nervous system activity. In this
study, statistical (nonspectral) HRV measures (SD and %RR50) were sum
marized for consecutive 15-minute blocks from 24-hour Holter electroca
rdiogram tapes. Six subgroups were scrutinized: women and men respecti
vely in three clinical strata (normal subjects [n = 85 women and 40 me
n], SCA with no current or prior myocardial infarction [MI] [n = 9 wom
en and 31 men], SCA with old MI [n = 7 women and 48 men]). Significant
nycthemeral effects were observable for all HRV measures in five of t
he six groups, with a dramatic fall in HRV during the hours of the mor
ning with the highest phenomenologic incidence of SCA. Both strata of
SCA subjects had much lower HRV than the normal subjects. This effect
was strongest during the night-time hours, particularly for a purporte
d index of vagal tone (%RR50). For reasons that are not known, the nin
e female SCA survivors who had no current or previous MI presented ver
y distinct 24-hour patterns for the HRV measures studied. Twenty-four-
hour profiles of shea-term statistical HRV provide a rich field for th
e observation of within-subject adaptations of the central autonomic n
ervous system inputs to the heart in both normal and clinical subgroup
s.