Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Mar 24:13:848274.
doi: 10.3389/fendo.2022.848274. eCollection 2022.

Components of Metabolic Syndrome in Youth With Classical Congenital Adrenal Hyperplasia

Affiliations
Review

Components of Metabolic Syndrome in Youth With Classical Congenital Adrenal Hyperplasia

Mimi S Kim et al. Front Endocrinol (Lausanne). .

Abstract

Classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most common primary adrenal insufficiency in children, involving cortisol deficiency, hyperandrogenism, and cardiometabolic risk. Prior studies have reported that youth with classical CAH have a higher prevalence of the components of metabolic syndrome: obesity, hypertension, elevated fasting blood glucose, and dyslipidemia. Yet, the incidence of the complete metabolic syndrome itself in children and adolescents with CAH is relatively rare. Traditional cardiometabolic risk factors can surface early in children with classical CAH, and continue to present and evolve over the lifetime, although it is only recently that reports of Type 2 diabetes and adverse cardiac events have begun to surface in adults affected by this condition. The pathophysiology underlying the increased prevalence of cardiometabolic risk factors in patients with CAH is not well-understood, with disease treatments and androgen excess having been studied to date. The aim of this review is to evaluate the recent literature on traditional cardiometabolic risk factors in youth with classical CAH, and to consider non-traditional risk factors/biomarkers for subclinical atherosclerosis, inflammation, and insulin resistance. A better understanding of these traditional and non-traditional risk factors in youth with CAH could help guide treatment options and prevent the onset of metabolic syndrome in adulthood, reducing overall patient morbidity.

Keywords: adolescents; cardiovascular disease risk; children; congenital adrenal hyperplasia; metabolic syndrome; pediatric obesity; pediatrics.

PubMed Disclaimer

Conflict of interest statement

MG receives research support from Novo Nordisk, Adrenas Therapeutics, Neurocrine Biosciences, and Spruce Biosciences. MG serves on advisory boards or as a consultant for Adrenas Therapeutics, Ascendis, Eton Pharmaceuticals, Novo Nordisk, and Pfizer; serves on data safety monitoring boards for Ascendis and Saniona/Medpace; serves as an adjudication committee member for ICON Clinical Research, LLC/Aeterna Zentaris; and receives royalties from McGraw-Hill and UpToDate. MK receives research support from Neurocrine Biosciences and Spruce Biosciences. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Cardiometabolic risk factors in youth with classical CAH due to 21-hydroxylase deficiency. Traditional and non-traditional cardiometabolic risk factors observed in youth with classical CAH. *Figure created with Biorender.

Similar articles

Cited by

References

    1. Merke DP, Auchus RJ. Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. N Engl J Med (2020) 383(13):1248–61. doi: 10.1056/NEJMra1909786 - DOI - PubMed
    1. Witchel SF. Congenital Adrenal Hyperplasia. J Pediatr Adolesc Gynecol (2017) 30(5):520–34. doi: 10.1016/j.jpag.2017.04.001 - DOI - PMC - PubMed
    1. Weiss R, Dziura J, Burgert TS, Tamborlane WV, Taksali SE, Yeckel CW, et al. . Obesity and the Metabolic Syndrome in Children and Adolescents. N Engl J Med (2004) 350(23):2362–74. doi: 10.1056/NEJMoa031049 - DOI - PubMed
    1. Cornean RE, Hindmarsh PC, Brook CG. Obesity in 21-Hydroxylase Deficient Patients. Arch Dis Child (1998) 78(3):261–3. doi: 10.1136/adc.78.3.261 - DOI - PMC - PubMed
    1. Finkielstain GP, Kim MS, Sinaii N, Nishitani M, Van Ryzin C, Hill SC, et al. . Clinical Characteristics of a Cohort of 244 Patients With Congenital Adrenal Hyperplasia. J Clin Endocrinol Metab (2012) 97(12):4429–38. doi: 10.1210/jc.2012-2102 - DOI - PMC - PubMed