Recombinant growth hormone for children and adolescents with Turner syndrome.

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Baxter L, Bryant J, Cave CB, Milne R.
 
Cochrane Database of Systematic Reviews 2007, Issue 1. Art. No.: CD003887. DOI: 10.1002/14651858.CD003887.pub2


The purpose of this review was to assess the effects of recombinant growth hormone in children and adolescents with Turner Syndrome. Turner syndrome (TS) is a genetic disorder affecting the sexual development and appearance of girls and women. Women with TS are much shorter than normal women within their respective populations (by about 21 cm or eight inches). Recombinant human growth hormone (hGH) has been used to increase growth and final height in girls who have Turner syndrome.


This review analyzed randomized controlled clinical trials which were identified from a search of MEDLINE, EMBASE, The Cochrane Library, LILACS, BIOSIS, Science Citation Index and reference lists. The reviewers assessed studies for methodological quality and extracted data from four studies which were carried out in children with TS before achieving final height. The selected studies administered growth hormone for a minimum of six months and compared the data with a placebo or no treatment control condition. The primary outcomes were final height and growth. Secondary outcomes included bone age, quality of life, cognitive performance, and adverse effects.


The trials included 365 participants. Only one trial reported final height in 61 treated women to be 148 cm versus 141 cm in 43 untreated women. Short-term growth velocity was greater in treated than untreated girls after one year and two years. Skeletal maturity was not accelerated by treatment with recombinant growth hormone (hGH). Adverse effects were minimally reported.
The reviewers concluded that recombinant human growth hormone (hGH) doses between 0.3 to 0.375 mg/kg/wk increase short-term growth in girls with Turner syndrome by approximately three cm in the first year and two cm in the second year of treatment.

 Treatment in one trial increased final height by approximately six cm over an untreated control group. Despite this increase, the final height of treated women was still outside the normal range.



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