Peak bone mass, which can be defined as the amount of bony tissue pres
ent at the end of the skeletal maturation, is an important determinant
of osteoporotic fracture risk. Measurement of bone mass development.
The bone mass of a given part of the skeleton is directly dependent up
on both its volume or size and the density of the mineralized tissue c
ontained within the periosteal envelope. The techniques of single-1 an
d dual-energy photon or X-ray absorptiometry measure the so-called 'ar
eal' or 'surface' bone mineral density (BMD), a variable which has bee
n shown to be directly related to bone strength. Bone mass gain during
puberty. During puberty the gender difference in bone mass becomes ex
pressed. This difference appears to be essentially due to a more prolo
nged bone maturation period in males than in females, with a larger in
crease in bone size and cortical thickness. Puberty affects bone size
much more than the volumetric mineral density. There is no significant
sex difference in the volumetric trabecular density at the end of pub
ertal maturation. During puberty, the accumulation rate in areal BMD a
t both the lumbar spine and femoral neck levels increases to four- to
sixfold over a 3- and 4-year period in females and males, respectively
. Change in bone mass accumulation rate is less marked in long bone di
aphyses. There is an asynchrony between the gain in statural height an
d bone mass growth. This phenomenon may be responsible for the occurre
nce of a transient period of a relative increase in bone fragility tha
t may account for the pattern of fracture incidence during adolescence
. Variance in peak bone mass. At the beginning of the third decade the
re is a large variability in the normal values of areal BMD in the axi
al and appendicular skeleton. This large variance, which is observed a
t sites particularly susceptible to osteoporotic fractures such as lum
bar spine and femoral neck, is barely reduced after correction for sta
tural height, and does not appear to increase substantially during adu
lt life. The height-independent broad variance in bone mass develops d
uring puberty at sites such as lumbar spine and femoral neck, where th
e accretion rate is markedly increased. Time of peak bone mass attainm
ent. Despite the fact that a majority of studies did not indicate that
bone mass continues to accumulate significantly during the third and
fourth decades, it has been generally accepted that peak bone mass at
any skeletal site is attained in both sexes during the mid-thirties. H
owever, recent studies indicate that in healthy Caucasian females with
apparently adequate intakes of energy and calcium, bone mass accumula
tion can virtually be completed before the end of the second decade, f
or both lumbar spine and femoral neck. It is possible that both geneti
c and environmental factors could influence the time of peak bone mass
achievement. Determinants of peaks bone mass. Several variables, more
or less independent, are supposed to influence bone mass accumulation
during growth; heredity, sex, dietary components, endocrine factors,
mechanical forces, and exposure to risk factors. Quantitatively, the m
ost prominent factor appears to be the genetic determinant, as estimat
ed by studies comparing monozygotic and dizygotic twins. That heredity
is not to be the only determinant of peak bone mass is of practical i
nterest, since environmental factors can be modified. With respect to
nutrition, the quantitative importance of calcium intake in bone mass
accumulation during growth, particularly at sites prone to osteoporoti
c fractures, remains to be clearly determined. The same can be said fo
r the impact of physical activity. Finally, the crucial years when the
se external factors will be particularly effective on bone mass accumu
lation remain to be determined by longitudinal prospective studies in
order to produce credible and well targeted recommendations for the se
tting up of osteoporosis prevention programs aimed at maximizing peak
bone mass.