Three-year data from a comparative study with recombinant human growth hormone in the treatment of short stature in young children with intrauterine growth retardation

被引:35
作者
Fjellestad-Paulsen, A
Czernichow, P
Brauner, R
Bost, M
Colle, M
Lebouc, JY
Lecornu, M
Leheup, B
Limal, JM
Raux, MC
Toublanc, JE
Rappaport, R
机构
[1] Hop Robert Debre, Dept Paediat Endocrinol, F-75019 Paris, France
[2] Hop Necker Enfants Malad, Paris, France
[3] Hop Trousseau, F-75571 Paris, France
[4] Hop St Vincent de Paul, Paris, France
[5] Ctr Hosp Reg Nord, Grenoble, France
[6] Hop Sud, Rennes, France
[7] Ctr Hosp Reg, Rennes, France
[8] Hop Brabois, Nancy, France
关键词
growth hormone treatment; intrauterine growth retardation; short stature;
D O I
10.1080/08035259850158209
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Growth acceleration and bone maturation were studied for 3 y in 69 children with severe short stature and a history of intrauterine growth retardation (IUGR), to determine the effect of treatment with recombinant human growth hormone (r-hGH). The patients were enrolled in an open, multicentre trial and were randomly allocated to either the treated group (Group I)or the control group (Group 2). The children in Group 1 were treated daily with 0.2 IU/kg/body weight (0.067 mg/kg) s.c., during 3 y and the children in Group 2 started the study with a 1-y observation period followed by a 3-y treatment period. At birth, their mean weight standard deviation score (SDS) was -2.5 and their mean length SDS -3.5. At baseline, the patients were prepubertal, non-GH deficient, with no known dysmorphic features. Mean age was 4.5 y, bone age was 3.3 y, height SDS was -3.4, height velocity (HV) SDS was -1.6, and body mass index SDS was -1.4. After I y of treatment, linear HV in Group 1 increased in comparison with the pre-treatment period (from 5.7 +/- 2.0 to 10.1 +/- 1.7 cm/y; p < 0.001) and with the first year of observation in Group 2 (p < 0.001). Increased KV was sustained during the second and third year of treatment and was significantly higher than at baseline. A similar growth pattern was seen during the 3 y of CH treatment in Group 2. Mean height SDS for chronological age increased by 2.0 +/- 0.7 in the two groups after 3 y of treatment. HV after 1 y of treatment was negatively correlated with growth velocity at baseline. Bone age remained retarded but increased with a mean of almost 4 y after 3 y of treatment in both groups. Even at a dose that is three times the replacement dose treatment with r-hGH was well tolerated. From these results, we conclude that r-hGH treatment over 3 y can induce sustained catch-up growth in young children with severe shea stature and a history of IUGR. Long-term studies are needed to assess ultimate effects on final height.
引用
收藏
页码:511 / 517
页数:7
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