2008Sichuan Medical JournalRequires access

The study of therapeutic effect of recombinant humen growth hormone in children with turner syndrome.

Sun Xiao-mei

Open publisher page 0 citations

Abstract

Objective To assese the efficacy of recombinant human growth hormone in promoting the growth in children with Turner syndrome.Methods 60 children with Turner syndrome were treated with subcutaneous injection of rhGH(0.15~0.18IU/(kg·d)daily before sleep for 3~18months.Results The growth velocity of these children increased from(2.33±0.71)cm to(8.51±1.31)cm after 3 months treatment,to(8.37±0.88) cm after 6 months treatment,to(7.56±1.35) cm after 12 months treatment.and to(7.18±1.89) cm after 24 months treatment.There were significant diference in the growth velocity before and after treatment(P0.05).There were no change in the mean body weight and BA during the whole course of rhGH therapy.During the course of rhGH therapy,no remarkable adverse effect was found,except that fewer patients suffered fromlocal reactions in injection sites and slight increasement of the erum ALT levels.Conclusion rhGH appears to be an effective and safe drug for promoting the growth in children with Turner syndrome.

About this research paper

What this paper is about

Objective To assese the efficacy of recombinant human growth hormone in promoting the growth in children with Turner syndrome.Methods 60 children with Turner syndrome were treated with subcutaneous injection of rhGH(0.15~0.18IU/(kg·d)daily before sleep for 3~18months.Results The growth velocity of these children increased from(2.33±0.71)cm to(8.51±1.31)cm after 3 months treatment,to(8.37±0.88) cm after 6 months treatment,to(7.56±1.35) cm after 12 months treatment.and to(7.18±1.89) cm after 24 months treatment.There were significant diference in the growth velocity before and after treatment(P0.05).There were no change in the mean body weight and BA during the whole course of rhGH therapy.During the course of rhGH therapy,no remarkable adverse effect was found,except that fewer patients suffered fromlocal reactions in injection sites and slight increasement of the erum ALT levels.Conclusion rhGH appears to be an effective and safe drug for promoting the growth in children with Turner syndrome.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To assese the efficacy of recombinant human growth hormone in promoting the growth in children with Turner syndrome.Methods 60 children with Turner syndrome were treated with subcutaneous injection of rhGH(0.15~0.18IU/(kg·d)daily before sleep for 3~18months.Results The growth velocity of these children increased from(2.33±0.71)cm to(8.51±1.31)cm after 3 months treatment,to(8.37±0.88) cm after 6 months treatment,to(7.56±1.35) cm after 12 months treatment.and to(7.18±1.89) cm after 24 months treatment.There were significant diference in the growth velocity before and after treatment(P0.05).There were no change in the mean body weight and BA during the whole course of rhGH therapy.During the course of rhGH therapy,no remarkable adverse effect was found,except that fewer patients suffered fromlocal reactions in injection sites and slight increasement of the erum ALT levels.Conclusion rhGH appears to be an effective and safe drug for promoting the growth in children with Turner syndrome.

Key concepts: Medicine, Turner syndrome, Human growth hormone, Growth velocity, Adverse effect, Growth hormone, Recombinant DNA, Growth hormone treatment

Related papers

Back to paper searchBrowse research topicsOriginal source
The study of therapeutic effect of recombinant humen growth hormone in children with turner syndrome. — Research Paper | ScholarLens