The current adult heights of hypopituitary children treated with recombinan
t human growth hormone (rGH) now range between -1.5 to -0.7 height SD score
s (Ht SDS) of control populations. These height outcomes are markedly bette
r than those observed after treatment with pituitary derived human growth h
ormone (-4.7 to -2.0 Ht SDS). Although treatment with rGH has not yielded a
dult heights that are equal to genetic target heights, the discrepancy is m
uch less now than in previous decades. Higher rGH dose, longer duration of
treatment, early age at diagnosis, correction of height deficit before onse
t of puberty, and daily rGH injections have had beneficial effects on final
adult heights. The current dosing regimens (0.3 to 0.18 mg/kg/week) have n
ot had an adverse effect on bone maturation and have not stimulated an earl
ier onset of puberty. Although height gains in puberty are less than contro
ls, a majority of treated subjects reach heights within the normal range fo
r adults. Higher doses of rGH during puberty have been studied in limited n
umbers of adolescents with positive effects; however, standard dosing will
likely continue to be used because of financial considerations and safety c
oncerns. Further improvements in adult heights are likely to be reported wh
en the youngest children who began rGH in 1985 complete their growth.