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Increased Abdominal Adiposity in Adolescents and Young Adults With Classical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Overview
Specialty Endocrinology
Date 2015 Jun 11
PMID 26062016
Citations 28
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Abstract

Context: Childhood obesity rates in congenital adrenal hyperplasia (CAH) exceed the high rates seen in normal children, potentially increasing their risk of cardiovascular disease (CVD). Abdominal adiposity, in particular visceral adipose tissue (VAT), is strongly associated with metabolic syndrome and CVD. However, it remains unknown whether VAT is increased in CAH.

Objective: The objective of the study was to determine whether adolescents and young adults with classical CAH have more VAT and sc adipose tissue (SAT) than matched controls and whether VAT and SAT are associated with biomarkers of metabolic syndrome, inflammation, and hyperandrogenism in CAH.

Design/setting: This was a cross-sectional study at a tertiary center.

Participants: CAH subjects (n = 28; 15.6 ± 3.2 y; 15 females) were matched for age, sex, ethnicity, and body mass index to healthy controls (n = 28; 16.7 ± 2.3 y; 15 females).

Main Outcome Measures: VAT and SAT, using computed tomography imaging and serum biomarkers associated with CVD risk, were measured. Data are reported as mean ± SD.

Results: Both VAT (43.8 ± 45.5 cm(2)) and SAT (288.1 ± 206.5 cm(2)) were higher in CAH subjects than controls (VAT 26.4 ± 29.6 cm(2) and SAT 226.3 ± 157.5 cm(2); both P < .001). The VAT to SAT ratio was also higher in CAH subjects (0.15 ± 0.07) than controls (0.12 ± 0.06; P < .05). Within CAH, measures of obesity (waist to height ratio, fat mass) and inflammation (plasminogen activator inhibitor-1, high-sensitivity C-reactive protein, leptin) correlated strongly with VAT and SAT. In addition, homeostasis model assessment of insulin resistance, and low-density lipoprotein correlated with abdominal adiposity. There were no sex differences for VAT or SAT in CAH subjects.

Conclusions: CAH adolescents and young adults have increased abdominal adiposity, with a higher proportion of proinflammatory VAT than SAT. An improved understanding of the mechanism of obesity in CAH may lead to targeted prevention and therapeutics in this high-risk population.

Citing Articles

Metabolic Syndrome Spectrum in Children with Classic Congenital Adrenal Hyperplasia-A Comprehensive Review.

Panic Zaric S, Milenkovic T, Todorovic S, Mitrovic K, Cvetkovic D, Cehic M Metabolites. 2025; 15(2).

PMID: 39997713 PMC: 11857733. DOI: 10.3390/metabo15020089.


Clinical Manifestations and Treatment Challenges in Infants and Children With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Nokoff N, Buchanan C, Barker J J Clin Endocrinol Metab. 2025; 110(Supplement_1):S13-S24.

PMID: 39836622 PMC: 11749889. DOI: 10.1210/clinem/dgae563.


Challenges in Adolescent and Adult Males With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Claahsen-van der Grinten H, Adriaansen B, Falhammar H J Clin Endocrinol Metab. 2025; 110(Supplement_1):S25-S36.

PMID: 39836620 PMC: 11749911. DOI: 10.1210/clinem/dgae718.


Long-Read Sequencing Identifying the Genetic Complexity of Congenital Adrenal Hyperplasia in the Pedigree.

Chen X, Zhao J, Li D, Xi N, Yi D, Yan M Mol Genet Genomic Med. 2024; 12(11):e70029.

PMID: 39575462 PMC: 11582476. DOI: 10.1002/mgg3.70029.


Proof of concept for a superior therapeutic index of corticosterone compared with hydrocortisone in patients with congenital adrenal hyperplasia.

Kyle C, Boyle L, Nixon M, Homer N, Simpson J, Rutter A Eur J Endocrinol. 2024; 191(6):535-544.

PMID: 39546623 PMC: 11606648. DOI: 10.1093/ejendo/lvae144.


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