Extract

To the editor:

We read with great interest the paper by Shulman et al. (1). The authors report the beneficial effect of 1-yr recombinant human (rh) GH treatment on cardiac mass and function in children with classical GH deficiency (GHD). These findings have important clinical implications in the long-term follow-up because there is a well-established relationship between GHD and increased cardiovascular mortality in untreated adults (2). We would like, however, to make some comments.

In the study, 10 young children with a relatively early onset of GHD at a median age of less than 5 yr were treated with rhGH at a dose of 0.3 mg/kg·wk for 12 months; seven had structural abnormalities of the hypothalamic-pituitary axis, a diagnosis compatible with permanent GHD. Their main findings consisted in increased left ventricular mass indexed by body surface area, height or height2.7 after 1 yr of rhGH therapy. The trophic effect of GH on the heart was confirmed, but the results raise questions about the long-term safety of subjects with childhood onset GHD treated at the above-mentioned dose.

You do not currently have access to this article.