Growth hormone therapy for children born small for gestational age: Height gain is less dose dependent over the long term than over the short term

被引:73
作者
de Zegher, F
Hokken-Koelega, A
机构
[1] Katholieke Univ Leuven, Louvain, Belgium
[2] Erasmus Univ, Med Ctr, Rotterdam, Netherlands
关键词
growth hormone; small for gestational age; growth; intrauterine growth retardation; short stature; adult height;
D O I
10.1542/peds.2004-1934
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background. Approximately 3% of children are born small for gestational age (SGA), and similar to 10% of SGA children maintain a small body size throughout childhood and often into adult life. Among short SGA children, growth hormone (GH) therapy increases short-term growth in a dose-dependent manner; experience with long-term therapy is limited. Objective. To delineate the dose dependency of long-term height gain among short SGA children receiving GH therapy. Methods. We performed an epianalysis of the first adult height data for SGA children ( n = 28) enrolled in 3 randomized trials comparing the growth-promoting efficacy of 2 continuous GH regimens ( 33 or 67 mu g/kg per day for similar to 10 years, starting at similar to 5 years of age); in addition, we performed a meta-analysis of the adult height results published previously and those presented here. Results. Epianalysis outcomes ( n = 28) suggested that adult height increased more with a higher-dose regimen than with a lower-dose regimen. In the meta-analysis ( n = 82), the higher-dose regimen was found to elicit a long-term height gain superior to that achieved with the lower-dose regimen by a mean of 0.4 SD ( similar to 1 inch). Children who were shorter at the start of therapy experienced more long-term height gain. Conclusions. These findings confirm GH therapy as an effective and safe approach to reduce the adult height deficit that short SGA children otherwise face. In addition, the first meta-analysis indicated that height gain is less dose dependent over the long term than over the short term, at least within the dose range explored to date. For SGA children whose stature is not extremely short, current data support the use of a GH dose of similar to 33 mu g/kg per day from start to adult height, particularly if treatment starts at a young age; shorter children ( for example, height below - 3 SD) might benefit from an approach in which short-term catch-up growth is achieved with a higher dose (>= 50 mu g/kg per day) and long-term growth to adult height is ensured with a GH dose of similar to 33 mu g/kg per day. Because GH-induced accelerations of height and weight gain evolve in parallel, the dose tapering from >= 50 mu g/kg to similar to 33 mu g/kg can be accomplished by simply maintaining the absolute GH dose ( in micrograms) while the child gains weight ( in kilograms). With this algorithm, more growth-responsive children taper their GH dose down to similar to 33 mu g/kg per day more quickly.
引用
收藏
页码:e458 / e462
页数:5
相关论文
共 23 条
[1]  
[Anonymous], [No title captured]
[2]  
Boguszewski M, 1998, ACTA PAEDIATR, V87, P257
[3]   DOSE-DEPENDENT CATCH-UP GROWTH AFTER 2 YEARS OF GROWTH-HORMONE TREATMENT IN INTRAUTERINE GROWTH-RETARDED CHILDREN [J].
CHATELAIN, P ;
JOB, JC ;
BLANCHARD, J ;
DUCRET, JP ;
OLIVIER, M ;
SAGNARD, L ;
VANDERSCHUERENLODEWEYCKX, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (06) :1454-1460
[4]   ADULT HEIGHT IN CHILDREN WITH PREPUBERTAL SHORT STATURE SECONDARY TO INTRAUTERINE GROWTH-RETARDATION [J].
CHAUSSAIN, JL ;
COLLE, M ;
DUCRET, JP .
ACTA PAEDIATRICA, 1994, 83 :72-73
[5]   Short stature associated with intrauterine growth retardation: Final height of untreated and growth hormone-treated children [J].
Coutant, R ;
Carel, JC ;
Letrait, M ;
Bouvattier, C ;
Chatelain, P ;
Coste, J ;
Chaussain, JL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (04) :1070-1074
[6]   Growth hormone treatment of short children born small for gestational age:: Growth responses with continuous and discontinuous regimens over 6 years [J].
de Zegher, F ;
Albertsson-Wikland, K ;
Wollmann, HA ;
Chatelain, P ;
Chaussain, JL ;
Löfström, A ;
Jonsson, B ;
Rosenfeld, RG .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (08) :2816-2821
[7]   High-dose growth hormone (GH) treatment in non-GH-deficient children born small for gestational age induces growth responses related to pre-treatment GH secretion and associated with a reversible decrease in insulin sensitivity [J].
De Zegher, F ;
Ong, K ;
Van Helvoirt, M ;
Mohn, A ;
Woods, K ;
Dunger, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (01) :148-151
[8]   Growth hormone treatment of short children born small for gestational age: Metanalysis of four independent, randomized, controlled, multicentre studies [J].
deZegher, F ;
AlbertssonWikland, K ;
Wilton, P ;
Chatelain, P ;
Jonsson, B ;
Lofstrom, A ;
Butenandt, O ;
Chaussain, JL .
ACTA PAEDIATRICA, 1996, 85 :27-31
[9]   High-dose growth hormone treatment of short children born small for gestational age [J].
deZegher, F ;
Maes, M ;
Gargosky, SE ;
Heinrichs, C ;
DuCaju, MVL ;
Thiry, G ;
DeSchepper, J ;
Craen, M ;
Breysem, L ;
Lofstrom, A ;
Jonsson, P ;
Bourguignon, JP ;
Malvaux, P ;
Rosenfeld, RG .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (05) :1887-1892
[10]  
deZegher F, 1997, ACTA PAEDIATR, V86, P207