EFFECT OF GROWTH ON VARIABILITY OF LEFT-VENTRICULAR MASS - ASSESSMENTOF ALLOMETRIC SIGNALS IN ADULTS AND CHILDREN AND THEIR CAPACITY TO PREDICT CARDIOVASCULAR RISK
G. Desimone et al., EFFECT OF GROWTH ON VARIABILITY OF LEFT-VENTRICULAR MASS - ASSESSMENTOF ALLOMETRIC SIGNALS IN ADULTS AND CHILDREN AND THEIR CAPACITY TO PREDICT CARDIOVASCULAR RISK, Journal of the American College of Cardiology, 25(5), 1995, pp. 1056-1062
Objectives. We sought to determine whether growth influences the relat
ion between left ventricular mass and body size and whether use of dif
ferent body size indexes affects the ability of ventricular mass to pr
edict complications of hypertension. Background. Allometric (or growth
) signals between left ventricular mass and height have recently been
reported to improve previous approaches for normalization of ventricul
ar mass for body size. Methods. Residuals of left ventricular mass-hei
ght(2.7) relations were analyzed in a learning series of 611 normotens
ive, normal weight subjects 4 months to 70 years old and, separately,
in 383 children (<17 years old) and 228 adults. Ten year cardiovascula
r morbidity in a test series of 253 hypertensive adults was compared w
ith groups with normal or high baseline left ventricular mass normaliz
ed for body weight, height, body surface area and allometric powers of
height. Results. The dispersion of residuals of ventricular mass vers
us height(2.7) increased with increasing height or age in children but
not in adults, suggesting that the effect of other variables on ventr
icular growth increases during body growth and stabilizes in adulthood
. Therefore, we derived separate allometric signals for adults (predic
ted ventricular mass = 45.4 x height(2.13), r = 0.48) and children (32
.3 x height(2.3), r = 0.85) (both p < 0.0001), Patients with left vent
ricular hypertrophy had 3.3 times higher cardiac risk with elevated le
ft ventricular mass/height(2.7) (p < 0.001), 2.6 to 2.7 times higher r
isk with left ventricular mass indexed for height, height(2.13) and bo
dy surface area (all p < 0.01) and 1.7 times the risk with ventricular
mass/weight (p > 0.1). Conclusions. These results show the following:
1) Variability of left ventricular mass in relation to height increas
es during human growth; 2) allometric signals of left ventricular mass
versus height are lower in adults and children than those obtained ac
ross the entire age spectrum; 3) height-based indexes of left ventricu
lar mass at least maintain and may enhance prediction of cardiac risk
by hypertensive left ventricular hypertrophy; and 4) the allometric si
gnal derived across the entire spectrum of age appears to be more usef
ul for prediction of cardiovascular risk than that computed in adults.