Abstract
THE PERSISTENTQUESTION Should clonidine be used to ac celerate growth in children with short stature? is critically addressed by Toy and Middleton. As they point out, the factors affecting linear growth are complex and incom pletely understood. It is clear, however, that one important factor required for normal growth is the adequate release of pituitary growth hormone (GH). Since its discovery in 1979 as a useful pharmacologic agent to stimulate pituitary GH release,' the selective alpha.-adrenergic agonist cloni dine has been used extensively to acutely measure pituitary GH-producing capabilities. This property of clonidine has also raised substantial interest regarding its use for the treatment of short stature. The mechanisms by which clo nidine exerts this effect on GH release remain unknown, but are believed to be a result of direct stimulation of GH releasing hormone.! Many uncontrolled studies reviewed by Toy and Mid dleton have described a relationship between short-term clonidine administration and an increase in patient growth velocity. In addition, Volta et al. recently reported the re sults of their controlled, randomly assigned study that com pared the effects of placebo, levodopa, GH, and clonidine on growth velocity in children. These investigators demon strated an overall increase in the growth velocity for the six-month study period in children who received GH or clonidine. However, there appeared to be only a small per centage of individuals treated with clonidine (20 percent) who demonstrated an increased height velocity greater than 2 crn/y compared with controls.' In another recently published study, Esteban et al. concluded that clonidine in creased growth velocity >2 crn/y in 65 percent of 88 chil dren studied.' Nevertheless, and despite the opinions of
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