Altered Cortisol Metabolism Increases Nocturnal Cortisol Bioavailability in Prepubertal Children With Type 1 Diabetes Mellitus.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2021
Historique:
received: 16 07 2021
accepted: 22 11 2021
entrez: 31 12 2021
pubmed: 1 1 2022
medline: 17 2 2022
Statut: epublish

Résumé

Disturbances in the activity of the hypothalamus-pituitary-adrenal axis could lead to functional alterations in the brain of diabetes patients. In a later perspective of investigating the link between the activity of the hypothalamus-pituitary-adrenal axis and the developing brain in children with diabetes, we assessed here nocturnal cortisol metabolism in prepubertal children with type 1 diabetes mellitus (T1DM). Prepubertal patients (aged 6-12 years) diagnosed with T1DM at least 1 year previously were recruited, along with matched controls. Nocturnal urine samples were collected, with saliva samples taken at awakening and 30 minutes after awakening. All samples were collected at home over 5 consecutive days with no detectable nocturnal hypoglycaemia. The State-Trait Anxiety Inventory (trait scale only) and Child Depression Inventory were also completed. Glucocorticoid metabolites in the urine, salivary cortisol (sF) and cortisone (sE) were measured by liquid chromatography-tandem mass spectrometry. Metabolic data were analysed by logistic regression, adjusting for sex, age, BMI and trait anxiety score. Urine glucocorticoid metabolites were significantly lower in T1DM patients compared to controls. 11β-hydroxysteroid dehydrogenase type 1 activity was significantly higher, while 11β-hydroxysteroid dehydrogenase type 2, 5(α+β)-reductase and 5α-reductase levels were all lower, in T1DM patients compared to controls. There was a significant group difference in delta sE level but not in delta sF level between the time of awakening and 30 minutes thereafter. Our findings suggest that altered nocturnal cortisol metabolism and morning HPA axis hyperactivity in children with T1DM leads to greater cortisol bioavailability and lower cortisol production as a compensatory effect. This altered nocturnal glucocorticoid metabolism when cortisol production is physiologically reduced and this HPA axis hyperactivity question their impact on brain functioning.

Identifiants

pubmed: 34970219
doi: 10.3389/fendo.2021.742669
pmc: PMC8712331
doi:

Substances chimiques

Glucocorticoids 0
Membrane Proteins 0
11-beta-Hydroxysteroid Dehydrogenase Type 1 EC 1.1.1.146
11-beta-Hydroxysteroid Dehydrogenase Type 2 EC 1.1.1.146
3-Oxo-5-alpha-Steroid 4-Dehydrogenase EC 1.3.99.5
SRD5A2 protein, human EC 1.3.99.5
Cortisone V27W9254FZ
Hydrocortisone WI4X0X7BPJ

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

742669

Informations de copyright

Copyright © 2021 Brossaud, Corcuff, Vautier, Bergeron, Valade, Lienhardt, Moisan and Barat.

Déclaration de conflit d'intérêts

The 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.

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Auteurs

Julie Brossaud (J)

Nuclear Medicine, Hospital of Bordeaux, Pessac, France.
Université de Bordeaux, INRAE, Bordeaux INP, NutriNeuro, Bordeaux, France.

Jean-Benoît Corcuff (JB)

Nuclear Medicine, Hospital of Bordeaux, Pessac, France.
Université de Bordeaux, INRAE, Bordeaux INP, NutriNeuro, Bordeaux, France.

Vanessa Vautier (V)

Pediatric Endocrinology and DiaBEA Unit, Hôpital des Enfants, Hospital of Bordeaux, Bordeaux, France.

Aude Bergeron (A)

Pediatric Endocrinology and DiaBEA Unit, Hôpital des Enfants, Hospital of Bordeaux, Bordeaux, France.

Aurelie Valade (A)

Paediatric Unit, Hospital of Bayonne, Bayonne, France.

Anne Lienhardt (A)

Paediatric Unit, Hospital of Limoges, Limoges, France.

Marie-Pierre Moisan (MP)

Université de Bordeaux, INRAE, Bordeaux INP, NutriNeuro, Bordeaux, France.

Pascal Barat (P)

Université de Bordeaux, INRAE, Bordeaux INP, NutriNeuro, Bordeaux, France.
Pediatric Endocrinology and DiaBEA Unit, Hôpital des Enfants, Hospital of Bordeaux, Bordeaux, France.

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