From infancy through young adulthood the activity of bone formation pr
edominates, resulting in a steady accumulation of bone mass. As the ra
te of growth changes with age, so skeletal modeling progresses through
phases of different intensity with time. This is paralleled by concom
itant changes in bone and calcium metabolism. Bone modeling and skelet
al consolidation probably result from a complex sequence of hormonal c
hanges in interaction with nutritional factors. However, current knowl
edge of the role, sequence, and genetic regulation of hormonal events
during puberty, and of the response of bone tissue in interaction with
nutrition is limited. This interaction is now beginning to be elucida
ted. The importance of this interaction with regard to fracture epidem
iology in children and peak bone mass acquisition has been discussed.