K. Otsuka et al., PREDICTIVE VALUE OF BLOOD-PRESSURE DIPPING AND SWINGING WITH REGARD TO VASCULAR-DISEASE RISK, Clinical drug investigation, 11(1), 1996, pp. 20-31
This prospective 6-year follow-up study of 176 patients treated with a
ntihypertensive drugs investigates the extent to which an excessive ci
rcadian blood pressure (BP) amplitude (above the 90th percentile of ge
nder- and age-matched peers) contributes to the risk of adverse vascul
ar outcomes (coronary events, ischaemic stroke, renal failure and reti
nal bleeding). The results are compared with those based on the standa
rd deviation (SD) of BP and a measure of 'dipping' (night-time vs dayt
ime BP difference). A relative risk invariably larger than unity is fo
und for 'over-swingers', that is for patients with an excessive circad
ian BP amplitude, and with one exception also for patients with an SD
in the upper decile of the distribution, A classification of patients
as dippers vs non-dippers does not detect any statistically significan
t difference in the incidence of adverse vascular outcomes in the samp
le investigated. A combination of ambulatory or manual BP monitoring a
nd chronobiological data analysis and interpretation facilitates the d
iagnosis of an excessive circadian BP amplitude and can serve to guide
the timing of treatment, not only for lowering BP but also to reduce
BP variability in particular, an excessive circadian amplitude. The la
tter condition, and an SD in the upper decile of the distribution, in
this order, were associated with the largest increase in risk for isch
aemic stroke and nephropathy. The excessive circadian BP amplitude con
stitutes an a priori no-win situation in the case of reliance upon con
ventional casual measurements, since in this condition, the BP is elev
ated only during part of the day. Thus, if casual BP measurements are
taken when pressures are acceptable, the patient is likely to be left
untreated, but would remain at a very high risk of developing vascular
disease, Conversely, should the patient be examined when pressures ar
e high, drugs may be prescribed that may lower the BP too much when gi
ven at the wrong time when, unknowingly, pressures are already spontan
eously low and may barely suffice for perfusion. Since some antihypert
ensive drugs can reduce both BP and BP variability, further studies ar
e required in order to examine whether treatment aimed at reducing an
excessive circadian BP amplitude improves prognosis in subjects with h
igh BP variability.