The Unique Role of 11-Oxygenated C19 Steroids in Both Premature Adrenarche and Premature Pubarche.


Journal

Hormone research in paediatrics
ISSN: 1663-2826
Titre abrégé: Horm Res Paediatr
Pays: Switzerland
ID NLM: 101525157

Informations de publication

Date de publication:
2020
Historique:
received: 23 09 2020
accepted: 20 11 2020
pubmed: 3 2 2021
medline: 9 11 2021
entrez: 2 2 2021
Statut: ppublish

Résumé

Recent studies have shown 11-oxygenated androgens (11oAs) are the dominant androgens in premature adrenarche (PA). Our objective was to compare 11oAs and conventional androgens in a well-defined cohort of children with PA or premature pubarche (PP) and correlate these androgens with metabolic markers. A prospective cross-sectional study was conducted at a university hospital. Fasting early morning serum steroids (including 11oAs) and metabolic biomarkers were compared and their correlations determined in children ages 3-8 years (F) or 3-9 years (M) with PA or PP (5 M and 15 F) and healthy controls (3 M and 8 F). There were no differences between PA, PP, and controls or between PA and PP subgroups for sex, BMI z-score, or criteria for childhood metabolic syndrome. Dehydroepiandrosterone sulfate (DHEAS) was elevated only in the PA subgroup, as defined. 11oAs were elevated versus controls in PA and PP although no differences in 11oAs were noted between PA and PP. Within the case cohort, there was high correlation of T and A4 with 11-ketotestosterone and 11β-hydroxyandrostenedione. While lipids did not differ, median insulin and HOMA-IR were higher but not statistically different in PA and PP. PA and PP differ only by DHEAS and not by 11oAs or insulin sensitivity, consistent with 11oAs - rather than DHEAS - mediating the phenotypic changes of pubarche. Case correlations suggest association of 11oAs with T and A4. These data are the first to report the early morning steroid profiles including 11oAs in a well-defined group of PA, PP, and healthy children.

Identifiants

pubmed: 33530089
pii: 000513236
doi: 10.1159/000513236
pmc: PMC7965256
mid: NIHMS1657921
doi:

Substances chimiques

Androgens 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

460-469

Subventions

Organisme : NIDDK NIH HHS
ID : T32 DK065522
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001873
Pays : United States

Informations de copyright

© 2021 S. Karger AG, Basel.

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Auteurs

Brittany K Wise-Oringer (BK)

Division of Pediatric Endocrinology, Diabetes and Metabolism, Columbia University Irving Medical Center, New York, New York, USA.

Anne Claire Burghard (AC)

Division of Pediatric Endocrinology, Diabetes and Metabolism, Columbia University Irving Medical Center, New York, New York, USA.

Patrick O'Day (P)

Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.

Abeer Hassoun (A)

Division of Pediatric Endocrinology, Diabetes and Metabolism, Columbia University Irving Medical Center, New York, New York, USA.

Aviva B Sopher (AB)

Division of Pediatric Endocrinology, Diabetes and Metabolism, Columbia University Irving Medical Center, New York, New York, USA.

Ilene Fennoy (I)

Division of Pediatric Endocrinology, Diabetes and Metabolism, Columbia University Irving Medical Center, New York, New York, USA.

Kristen M Williams (KM)

Division of Pediatric Endocrinology, Diabetes and Metabolism, Columbia University Irving Medical Center, New York, New York, USA.

Patricia M Vuguin (PM)

Division of Pediatric Endocrinology, Diabetes and Metabolism, Columbia University Irving Medical Center, New York, New York, USA.

Renu Nandakumar (R)

Irving Institute for Clinical and Translational Research, Columbia University Irving Medical Center, New York, New York, USA.

Donald J McMahon (DJ)

Division of Endocrinology, Columbia University Irving Medical Center, New York, New York, USA.

Richard J Auchus (RJ)

Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Department of Pharmacology, University of Michigan, Ann Arbor, Michigan, USA.

Sharon E Oberfield (SE)

Division of Pediatric Endocrinology, Diabetes and Metabolism, Columbia University Irving Medical Center, New York, New York, USA, seo8@cumc.columbia.edu.

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