Effect of androgen excess and glucocorticoid exposure on metabolic risk profiles in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.


Journal

The Journal of steroid biochemistry and molecular biology
ISSN: 1879-1220
Titre abrégé: J Steroid Biochem Mol Biol
Pays: England
ID NLM: 9015483

Informations de publication

Date de publication:
03 2020
Historique:
received: 25 07 2019
revised: 06 11 2019
accepted: 11 11 2019
pubmed: 16 11 2019
medline: 7 7 2020
entrez: 16 11 2019
Statut: ppublish

Résumé

Data on cardiovascular morbidity in adults with congenital adrenal hyperplasia (CAH) is sparse. We therefore aimed to determine the role of androgen control and glucocorticoid therapy on metabolic health. For that purpose, we included 90 patients (N = 39 men, N = 51 women) with classic CAH due to 21-hydroxylase deficiency (N = 61 salt wasting, N = 29 simple virilizing) and an equal number of controls matched for age, sex, BMI and smoking-habits. We could show that there was no difference in intima-media-thickness between patients and controls and only one patient fulfilled all criteria of the metabolic syndrome. CAH men presented with an increased relative body fat mass in comparison to controls (25.6 % vs. 22.1 %; p = 0.011) while this was not true for CAH women. Body fat was lower in those taking hydrocortisone instead of synthetic glucocorticoids (B = -3.27; p = 0.048). While arterial hypertension was rare, 54 % of patients had an impaired systolic drop at night or were classified as non-dippers (17 %). Impaired dipping was not associated with evening glucocorticoid and fludrocortisone intake but mediated by sodium levels. Insulin resistance was more common in CAH women (B = 1.689; p = 0.036) and in those with poor androgen control (B = 0.823; p = 0.046). In summary, we could show that good cardiovascular health outcome in adult CAH patients can be achieved. Hydrocortisone is superior in terms of body composition. It is yet unclear how non-dipping will translate into cardiovascular morbidity in the long-term.

Identifiants

pubmed: 31730799
pii: S0960-0760(19)30438-8
doi: 10.1016/j.jsbmb.2019.105540
pii:
doi:

Substances chimiques

Androgens 0
CYP21A1P pseudogene, human 0
Glucocorticoids 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

105540

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest All authors have declared that no conflict of interest exists.

Auteurs

Luisa Paizoni (L)

Medizinische Klinik and Poliklinik IV, Klinikum der Universität München, LMU München, Munich, Germany.

Matthias K Auer (MK)

Medizinische Klinik and Poliklinik IV, Klinikum der Universität München, LMU München, Munich, Germany.

Heinrich Schmidt (H)

Abteilung für Pädiatrische Endokrinologie, Dr. von Hauner'sches Kinderspital, Klinikum der Universität München, LMU München, Munich, Germany.

Angela Hübner (A)

Klinik für Kinder- und Jugendmedizin, Universitätsklinikum Dresden, Technische Universität Dresden, Dresden, Germany.

Martin Bidlingmaier (M)

Medizinische Klinik and Poliklinik IV, Klinikum der Universität München, LMU München, Munich, Germany.

Nicole Reisch (N)

Medizinische Klinik and Poliklinik IV, Klinikum der Universität München, LMU München, Munich, Germany. Electronic address: Nicole.reisch@med.uni-muenchen.de.

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Classifications MeSH