G. Hargitai et al., Growth patterns and final height in congenital adrenal hyperplasia due to classical 21-hydroxylase deficiency - Results of a multicenter study, HORMONE RES, 55(4), 2001, pp. 161-171
Background. Longitudinal growth and bone age (BA) development are the most
important clinical parameters for monitoring adequate glucocorticoid replac
ement in children with congenital adrenal hyperplasia (CAH). Aim of the Stu
dy. To analyze the growth pattern of patients treated for CAH of the salt w
asting (SW) and simple virilizing (SV) clinical forms; to evaluate final he
ight as compared to reference data and individual target height; to evaluat
e the course of BA development. Patients and Methods: A large database of 5
98 patients with CAH was created in 5 Central European countries and growth
data of 341 treated patients with 21-hydroxylase deficiency were analyzed
retrospectively. The patients were of Caucasian origin. Centiles were const
ructed in a cross-sectional manner and an additional longitudinal analysis
was performed in order to evaluate the pubertal growth spurt by applying pa
rticular statistical methods (Preece-Baines model). Results: The growth of
SW CAH patients was impaired in infancy and early childhood (0-3 years of a
ge), but followed normal patterns in childhood until puberty. In contrast,
children with SV CAH had normal patterns of growth in infancy and early chi
ldhood and were considerably taller than healthy references during childhoo
d. In the longitudinal study, peak height velocity in both boys and girls w
as normal, but it occurred at an earlier age than in the standard populatio
n. The final height of patients with CAH was reduced in comparison to both
the reference and the individual target height. No correlations were found
between final height and age at the start of the therapy in SV patients or
between final height and year of birth. BA was advanced in both types of CA
H, but more accelerated in SV patients. Conclusion: Characteristic growth p
atterns for treated SV and SW CAH children were identified, with a normal p
ubertal growth spurt and reduced final height being observed. Copyright (C)
2001 S. Karger AG, Basel.