Cited by 22Sexual Differentiation and DisordersAdrenal Hormones and DisordersOvarian function and disorders

Absence of clinically relevant growth acceleration in untreated children with non-classical congenital adrenal hyperplasia

Pijnenburg-Kleizen, Karijn J., Borm, George F., Otten, Barto J., Schott, Dina A., van den Akker, Erica L., Stokvis-Brantsma, Wilhelmina H., Voorhoeve, Paul G., Bakker, Boudewijn +1 more·2012·Hormone Research in Paediatrics

Abstract

BACKGROUND/AIMS: In classical congenital adrenal hyperplasia (CAH), elevation of adrenal androgens leads to accelerated growth and bone maturation with compromised adult height. In untreated children with non-classical CAH (NC-CAH), in which adrenal androgens are generally only slightly increased, growth velocity may not be significantly elevated. METHODS: Twenty-four patients were included and divided into a symptomatic and an asymptomatic group. Height was expressed as height standard deviation scores (HSDS) and corrected for target height (HSDS-THSDS). Bone maturation was expressed as bone age acceleration (BA(c) = bone age - calendar age). Linear mixed models with random factor patient were used for the analysis of growth and bone age. RESULTS: In symptomatic patients (n = 17), HSDS-THSDS only slightly increased by 0.06 SDS per year (95% CI 0.02-0.10). Mean BA(c) was 2.21 years (SDS 0.66, p < 0.0001). In asymptomatic patients (n = 7), no significant growth acceleration or BA(c) was found. CONCLUSIONS: In untreated NC-CAH children, growth acceleration is small and generally not visible on their growth charts. BA(c) is more pronounced. Therefore, the absence of an increase in growth velocity does not exclude the diagnosis of NC-CAH. When considering this diagnosis, bone age acceleration should also be taken into account.

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Crossref · 10.1159/000337217

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  • No general guidelines exist for the management and follow-up of patients with NC CAH, and the overall evidence of recommendations for NC CAH is low.

    “In contrast to classic CAH, no general guidelines exist for the management and follow-up of these patients and the overall evidence of recommendations for NC CAH is low (134,342,417-419).”

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References 18 · Cited by 22

Authors
Pijnenburg-Kleizen, K. J., Borm, G. F., Otten, B. J., Schott, D. A., van den Akker, E. L., Stokvis-Brantsma, W. H., Voorhoeve, P. G., Bakker, B., & Claahsen-van der Grinten, H. L.
Affiliations
  • Radboud University Medical Center (NL)
  • Canisius-Wilhelmina Ziekenhuis (NL)
  • Reinier de Graaf Hospital (NL)
Venue
Hormone Research in Paediatrics
Publisher
S. Karger AG
Published
2012
Volume
77
Issue
3
Pages
164-169
ISSN
  • 1663-2818 (ISSN-L)
  • 1663-2826
OpenAlex
W2109325625
Cited by
22
References
18
Citations by year
2026: 1 · 2025: 1 · 2024: 4 · 2022: 2 · 2021: 2 · 2020: 3 · 2019: 1 · 2014: 2 · 2013: 3 · 2012: 2
FWCI
0.90
Type
journal article
Language
en
Open access
closed
Locations
  • Hormone Research in Paediatrics (publishedVersion)
  • PubMed (publishedVersion)
  • Research Publications (Maastricht University) (publishedVersion)
  • EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
  • EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
  • Radboud Repository (Radboud University) (submittedVersion)
  • Research Publications (Maastricht University) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
  • Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
Keywords
non-classical congenital adrenal hyperplasia, growth acceleration, untreated children, adrenal androgens, height standard deviation score, target height, skeletal maturation
MeSH terms
Adrenal Hyperplasia, Congenital, Age Determination by Skeleton, Bone Development, Child, Child, Preschool, Female, Humans, Male

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