A. Simon et al., DETECTION OF PRECLINICAL ATHEROSCLEROSIS MAY OPTIMIZE THE MANAGEMENT OF HYPERTENSION, American journal of hypertension, 10(7), 1997, pp. 813-824
Because of the limited ability of blood pressure elevation to predict
risk, the mass drug treatment of hypertension above an arbitrary thres
hold may result in many subjects being overtreated. One potential way
to overcome this problem is to noninvasively detect preclinical athero
sclerosis. Hypertension has been shown to be associated with I) increa
sed intima-media thickness and more frequent plaques in extracoronary
arteries, 2) more frequent calcifications in coronary arteries, 3) inc
reased wall rigidity in the aorta and peripheral arteries, and 4) impa
ired endothelium dependent vasodilation and abnormal blood rheology, w
hich are capable of promoting the conversion of atherosclerosis into a
therothrombosis. The prognostic significance of these markers of precl
inical atherosclerosis is supported by evidence of their association w
ith numerous risk factors, and prevalence and incidence of cardiovascu
lar damages. Preclinical arterial lesions also constitute ideal target
s to test whether antihypertensive treatment can reverse or slow down
arterial disease, and whether such a reversal produces better preventi
on than simply lowering blood pressure. Finally, the detection of athe
rosclerosis applied to large populations of mildly hypertensive subjec
ts safely and at relatively low cost could help to better target the p
harmacological treatment, given that a substantial proportion of subje
cts without evidence of preclinical disease may be suitable for nondru
g treatment. (C) 1997 American Journal of Hypertension, Ltd.