As the result of accelerated growth, the final height of infants born with
low birth weight (LBW) is near to the normal. Limited data are available ab
out the bone density and bone turnover just after completion of skeletal de
velopment. We have investigated the bone turnover and bone density in 49 ap
parently healthy young LBW men (age 19-21 years: 21 born small for gestatio
nal age (SGA) and 28 appropriate for gestational age (AGA)) and in 16 age-m
atched controls. Bone mineral density of lumbar spine, femoral neck, and ra
dius midshaft. the markers of calcium homeostasis, biochemical parameters o
f bone turnover as serum osteocalcin (OC), and urinary pyridinoline (PYD) a
nd deoxypyridinoline (DPD) levels were measured. Bone mineral densities of
LBW subjects were not altered. Serum calcium (SGA: 2.44 +/- 0.15: AGA: 2.41
+/- 0.17, control: 2.25 +/- 0.09 mmol/liter, P < 0.05). OC (SGA: 23.4 +/-
9.9; AGA: 20.8 +/- 7.6: control: 13.3 +/- 4.6 ng/ml. P < 0.01), total alkal
ine phosphatase (AP) (SGA: 201 +/- 61: AGA: 193 +/- 81, control: 117 +/- 34
IU/liter, P < 0.01), and urinary DPD/creat (ln.values: SGA: 3.10 +/- 0.48;
AGA: 3.17 +/- 0.46; control: 2.58 +/- 0.57 nmol/mmol, P < 0.05) were highe
r, whereas fractional excretion of calcium (SGA: 0.94 +/- 0.470; AGA: 1.03
+/- 0.51, control: 1.31 +/- 0.75%, P < 0.05) was lower in both SGA and AGA
groups. PTH and 25OHD were not different. Significant correlation was obtai
ned between seCa, OC, AP, DPD and birth weight of the subjects, but feCa co
rrelated inversely to the birth weight. It was concluded that the bone turn
over of LBW men is accelerated, but well balanced in young adulthood. Furth
er investigation is needed to de scribe the possible link between accelerat
ed bone turnover and hormonal homeostasis of LBW subjects.