Ml. Loro et al., Early identification of children predisposed to low peak bone mass and osteoporosis later in life, J CLIN END, 85(10), 2000, pp. 3908-3918
The amount of bone that is gained during adolescence is the main contributo
r to peak bone mass, which, in turn, is a major determinant of osteoporosis
and fracture risk in the elderly. We examined whether computed tomography
measurements for the density and the volume of bone in the axial and the ap
pendicular skeletons could be tracked through puberty in 40 healthy white c
hildren (20 girls and 29 boys). Longitudinal measurements of the cross-sect
ional area and cancellous hone density of the vertebral bodies and the cros
s-sectional and cortical bone areas of the femurs at the beginning of puber
ty accounted for 62-92% of the variations seen at sexual maturity; on avera
ge, 3 yr later. When baseline values for these bone traits were divided int
o quartiles, a linear relation across Tanner stages of sexual development w
as observed for each quartile in both girls and boys. The regression lines
differed among quartiles for each trait, paralleled each other, and did not
overlap. Thus, we are now in a position to identify those children who are
genetically prone to develop low values for peak bone mass and toward whom
osteoporosis prevention trials should be geared.