Am. Boot et al., Bone mineral density, bone metabolism and body composition of children with chronic renal failure, with and without growth hormone treatment, CLIN ENDOCR, 49(5), 1998, pp. 665-672
OBJECTIVE Osteopenia has been reported in adult patients with chronic renal
failure (CRF), only a few studies have been performed in children. The obj
ective of this study was to evaluate bone mineral density (BMD), bone turno
ver, body composition in children with CRF and to study the effect of GH on
these variables.
DESIGN Two groups were identified: patients with growth retardation who rec
eived GH (GH-group) and patients most of whom were not growth retarded who
did not receive GH (no-GH-group). After an observation period of 6 months,
the patients in the GH-group started GH treatment. Patients were studied ev
ery 6 months during 18 months.
PATIENTS Thirty-six prepubertal patients (27 boys and 9 girls), mean age 7.
9 years, with CRF participated in the study. The GH-group consisted of 17 p
atients of whom 14 completed one year treatment. The no-GH-group consisted
of 19 patients, of whom 16 were followed for 6 months, 14 for 12 months and
13 for 18 months.
MEASUREMENTS Lumbar spine BMD, total body BMD and body composition were ass
essed by dual energy X-ray absorptiometry, compared to age-and sex-matched
reference values of the same population and expressed as standard deviation
scores (SDS), BMD of appendicular bone was measured by quantitative microd
ensitometry (QMD). Blood samples were obtained to assess bone metabolism an
d growth factors.
RESULTS Baseline mean lumbar spine and total body BMD SDS of ail patients w
ere not significantly different from normal. Mean lumbar spine and total bo
dy BMD SDS did not change significantly in the GH-group during GH treatment
. The change of QMD at the midshaft during the first 6 months of GH treatme
nt was significantly smaller than during the observation period (P< 0.01).
Height SDS and biochemical markers of both bone formation and bone resorpti
on increased significantly during GH treatment; 1,25-dihydroxyvitamin D rem
ained stable. Lean tissue mass increased (P<0.001) and percentage body fat
decreased (P< 0.01) during GH treatment. BMD, the biochemical markers of bo
ne turnover which are independent of renal function, and body composition r
emained stable in the no-GH-group.
CONCLUSIONS Mean lumbar spine and total body BMD of children with chronic r
enal failure did not differ from healthy controls. The lack of a GH-induced
increase in 1,25-dihydroxyvitamin D levels, probably due to treatment with
alpha-calcidol, might be linked to the absence of a response in BMD during
GH treatment in children with chronic renal failure.