High-dose growth hormone treatment of short children born small for gestational age

作者
Francis de Zegher,M Maes,Sharron Erna Gargosky,Claudine Heinrichs,Marc V Du Caju,Georges Thiry,Jean De Schepper,Margarita Craen,Luc Breysem,Annika Löfström,P Jönsson,Jean-Pierre Bourguignon,Paul Malvaux,Ron G. Rosenfeld
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [Oxford University Press]
卷期号:81 (5): 1887-1892 被引量:110
标识
DOI:10.1210/jc.81.5.1887
摘要

The effect of GH administration was evaluated over 2 yr in 50 short, prepubertal, non-GH deficient children born small for gestational age, who had been randomly allocated to a group receiving no treatment or daily sc GH treatment at a dose of 0.2 or 0.3 IU/kg. At the start of the study, mean age was 5.2 yr, bone age was 4.0 yr, height SDS was -3.5, height velocity SDS was -0.8, weight SDS was -2.7, and body mass index SDS was -1.9. Catch-up growth was observed in none of the untreated and all of the treated children. The response to GH treatment included a near doubling of growth velocity and of weight gain and a mean height increment of more than 2 SDS. GH treatment was associated with a distinct acceleration of bone maturation. The differences between the growth responses evoked by the two GH doses were minor. The prepubertal GH-induced catch-up growth was associated with elevated serum concentrations of insulin, insulin-like growth factor-I, insulin-like growth factor binding protein-3, and osteocalcin, whereas insulin-like growth factor-II levels remained unaltered. GH treatment was well tolerated. In conclusion, high-dose GH administration over 2 yr is emerging as a potential therapy to increase the short stature that results from insufficient catch-up growth in young children born small for gestational age. The long-term impact of this approach remains to be delineated.
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