M. Rooney et al., Bone mineral content and bone mineral metabolism: Changes after growth hormone treatment in juvenile chronic arthritis, J RHEUMATOL, 27(4), 2000, pp. 1073-1081
Objective. To determine whether growth, hormone (rhGH) affects bone mineral
metabolism and bone mineral content (BMC, g/cm) in a therapeutic trial of
recombinant growth hormone in growth retarded children with juvenile chroni
c arthritis (JCA) treated with steroid.
Methods. BMC was measured in 20 children (of whom 17 were treated with cort
icosteroid) before and after one year of rhGH. Children were randomized to
receive either low dose (12 IU/m(2)/week) or high dose (24 IU/m(2)/week) fo
r one year. Three monthly assessments were made of disease activity and ant
hropomorphic measurements. Blood and urine samples were also obtained to me
asure indicators of disease activity, bone remodeling, and vitamin D and pa
rathyroid hormone (PTH) status.
Results. BMC increased during the treatment period and correlated with incr
easing height. Osteocalcin levels, normally indicators of bone formation, i
ncreased after rhGH treatment and correlated significantly with height velo
city, particularly for the high dose treatment group. In contrast, osteocal
cin levels were negatively correlated with C-reactive protein levels, both
before and during treatment. Height velocity, vitamin D, PTH, and osteocalc
in levels were significantly lower than age matched controls before treatme
nt.
Conclusion. Steroid treated children with both JCA and severe growth retard
ation have reduced vitamin D, PTH, and osteocalcin levels. After treatment
with rhGH, height velocity increased, as did BMC. Growth hormone might be a
useful adjunct in the treatment of severe growth retardation and osteoporo
sis in children with JCA. The longterm benefits of rhGH in the treatment of
osteoporosis remain unclear.