PEDIATRICS Vol. 104 No. 4 Supplement October 1999, pp. 1000-1004
Received May 13, 1999; accepted Jun 22, 1999.

From the * Department of Pediatrics, University of Arkansas for
Medical Sciences, Little Rock, Arkansas; and
Medical Affairs,
Genentech, Inc, South San Francisco, California.
There are few historical data on final or adult
heights after the completion of long-term growth hormone (GH) therapy
in children with GH deficiency (GHD). Adult height has been defined as
that achieved at chronologic ages ranging from 18 to 30 years, at bone ages
13 years (girls) and
15 years (boys), at growth
velocities
1 to 2 cm per 6 to 12 months, at the "cessation of
growth," at "1 year after the completion of pubertal
development," and that at which patients are either "satisfied with
their height" or have attained an "accept adult stature."
Without GH treatment, children with GHD have a mean adult height
standard deviation score of
4.7 (range,
6.1 to
3.9). After treatment, the standard deviation score range from
4.7 to
1.2 (pituitary GH [pitGH] 2-4 times a week) and from
1.4 to
0.5 (recombinant human [rhGH] GH 3 times a week to daily) in women and
from
3.6 to
1.1 (pitGH) and from
1.3 to
0.7 (rhGH) in men.
Because there is no uniformly applied definition of adult height,
comparisons are difficult, but historical data suggest that
posttreatment heights are greater with rhGH than with pitGH.
Using the National Cooperative Growth Study database, we found that the
criteria used to define adult height affected the apparent outcome.
When chronologic age
20 years for men and
18 years for women was
the only criterion, 27% of patients grew
5 cm after having reached
this age. Adding the requirement of advanced puberty before adult
height could be considered to have been attained reduced the proportion
of those who later grew
5 cm to <10%, but also decreased the number
of patients available for analysis. A combination of criteria for adult
height (chronologic and bone age
16 years for boys and
14
years for girls plus advanced puberty plus growth rate of <2 cm per
year) left only 1% of patients with later growth of
5
cm.
This article has been cited by other articles:
![]() |
A J van der Lely Justified and unjustified use of growth hormone Postgrad. Med. J., October 1, 2004; 80(948): 577 - 580. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Coutant, S. Rouleau, F. Despert, N. Magontier, D. Loisel, and J.-M. Limal Growth and Adult Height in GH-Treated Children with Nonacquired GH Deficiency and Idiopathic Short Stature: The Influence of Pituitary Magnetic Resonance Imaging Findings J. Clin. Endocrinol. Metab., October 1, 2001; 86(10): 4649 - 4654. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Kohn, J. R. Julius, and S. L. Blethen Combined Use of Growth Hormone and Gonadotropin-releasing Hormone Analogues: The National Cooperative Growth Study Experience Pediatrics, October 1, 1999; 104(4): 1014 - 1018. [Abstract] [Full Text] |
||||