S. Guzzetti et al., ALTERED DYNAMICS OF THE CIRCADIAN RELATIONSHIP BETWEEN SYSTEMIC ARTERIAL-PRESSURE AND CARDIAC SYMPATHETIC DRIVE EARLY ON IN MILD HYPERTENSION, Clinical science, 86(2), 1994, pp. 209-215
This study was designed to test the hypothesis that simultaneous non-i
nvasive assessment of the circadian variations in both intermittent ar
terial pressure and the continuous 24 h changes of spectral markers of
cardiac neural control could provide new information on cardiovascula
r regulatory mechanisms, in hypertensive patients and normotensive sub
jects. To test this hypothesis we studied 18 subjects with mild hypert
ension and II normotensive subjects in whom we recorded simultaneously
non-invasive intermittent arterial pressure and Holter electrocardiog
ram for 24 h. We also studied the same subjects during resting and sta
nding conditions in the clinical laboratory. 2. The normalized power o
f the low-frequency (similar to 0.1 Hz) spectral component of R-R inte
rval variability, considered mainly a marker of sympathetic drive to t
he sino-atrial node, was, at rest, significantly higher in the hyperte
nsive than in the normotensive subjects, as already reported. Moreover
, the values of the low-frequency component at rest recorded in the cl
inical laboratory were significantly correlated with those obtained fr
om ambulatory recording during night rest. The decrease in the values
of arterial pressure during the night-time was accompanied by a reduct
ion in the power of the low-frequency component only in the case of no
rmotensive subjects. Accordingly, the slope of the regression of the l
ow-frequency component as a function of systolic arterial pressure dur
ing ambulatory recordings was steep in normotensive subjects and fiat
in hypertensive subjects. 3. The computer analysis of Holter recording
s combined with ambulatory arterial pressure monitoring seems to provi
de a new method with which to quantify the early changes in cardiovasc
ular regulatory mechanisms that could help to identify individuals at
higher risk.