Long-term effects of growth hormone treatment on growth and puberty in patients with chronic renal insufficiency

被引:66
|
作者
Hokken-Koelega, A
Mulder, P
De Jong, R
Lilieu, M
Donckerwolcke, R
Groothof, J
机构
[1] Sophia Childrens Hosp, Dept Pediat, Div Endocrinol, NL-3015 GJ Rotterdam, Netherlands
[2] Erasmus Univ, Dept Epidemiol & Biostat, NL-3000 DR Rotterdam, Netherlands
[3] Radboud Univ Hosp, Dept Pediat, Div Nephrol, Nijmegen, Netherlands
[4] Univ Utrecht Hosp, Wilhelmina Childrens Hosp, Utrecht, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
关键词
long-term growth hormone therapy; growth; puberty; chronic renal insufficiency;
D O I
10.1007/s004670000340
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Several prospective trials have shown that recombinant human growth hormone (GH) accelerates growth significantly during the first years of therapy, but the effects of long-term GH therapy with regard to longterm growth response and safety have not yet been established. Forty-five Dutch prepubertal children [28 boys, 17 girls, mean (SD) age 7.8 (3.4) years] with chronic renal insufficiency (CRI) and severe growth retardation started GH therapy between 1988 and 1991 within one of the randomized Dutch trials. Long-term GH therapy, in this study a maximum of 8 years, resulted in a sustained and significant improvement of height standard deviation score (SDS) compared with baseline values (P<0.001). The mean height SDS reached the lower end (-2 SDS) of the normal growth chart after 3 years of GH therapy. During the following years the mean height SDS gradually increased, thereby approaching the mean target height SDS after 6 years of GH therapy. Three factors were significantly associated with the height SDS after 4 years of GH therapy: height SDS at the start (+) of therapy, age at the start of therapy (-), and the duration of dialysis treatment (-). Bone maturation did not accelerate during longterm GH therapy. Children on a conservative regimen at the start of GH therapy had no accelerated deterioration of renal function during 6 years of GH therapy. The average daily GH dose administered over the years had no significant influence on the glomerular filtration rate after 4 years. GH therapy had no adverse effects or significant effect on parathyroid hormone concentration, nor were there any radiological signs of renal osteodystrophy. Puberty started at a median age, within the normal range, of 12.4 years in boys and 12.0 years in girls, respectively. Long-term GH therapy leads to a sustained improvement in height SDS in children with growth retardation secondary to CRI, resulting in a normalization of height in accordance with their target height SDS, without evidence of deleterious effects on renal function or bone maturation. A GH dosage of 4 IU/m(2) per day appears efficient and safe. Our long-term data show that final height will be within the normal target height range when GH therapy is continued for many years.
引用
收藏
页码:701 / 706
页数:6
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