Disrupted Circadian Rhythm of Epinephrine in Males With Youth-Onset Type 2 Diabetes.

catecholamine circadian rhythm type 2 diabetes

Journal

Journal of the Endocrine Society
ISSN: 2472-1972
Titre abrégé: J Endocr Soc
Pays: United States
ID NLM: 101697997

Informations de publication

Date de publication:
15 Dec 2022
Historique:
received: 16 11 2022
entrez: 12 1 2023
pubmed: 13 1 2023
medline: 13 1 2023
Statut: epublish

Résumé

Blood pressure and plasma catecholamines normally decline during sleep and rapidly increase in early morning. This is blunted in adults with type 2 diabetes (T2D). We hypothesize that increased sympatho-adrenal activity during sleep differentiates youth with T2D from nondiabetic obese youth and lean youth. Fasting spot morning and 24-hour urines were collected in obese adolescents with and without T2D, and normal-weight controls. Fractionated free urine catecholamines (epinephrine, norepinephrine, and dopamine) were measured, and the ratio of fasting spot morning to 24-hour catecholamines was calculated. Urinary 24-hour catecholamine levels were comparable across the 3 groups. Fasting morning epinephrine and the ratio of fasting morning/24-hour epinephrine were higher in youth with T2D ( Circadian rhythm in catecholamines is disrupted in youth-onset T2D, with a blunted overnight fall in urinary epinephrine in males. Conversely, fasting morning norepinephrine and dopamine levels were lower in obese females with or without T2D. Higher nocturnal catecholamines in males with T2D might associate with, or predispose to, hypertension and cardiovascular complications. Lower catecholamine excretion in females with obesity might serve an adaptive, protective role.

Identifiants

pubmed: 36632209
doi: 10.1210/jendso/bvac190
pii: bvac190
pmc: PMC9825134
doi:

Types de publication

Journal Article

Langues

eng

Pagination

bvac190

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society.

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Auteurs

Stephanie Giessner (S)

General Pediatrics, Duke University Medical Center, Durham, NC 27710, USA.

Megan E Ramaker (ME)

Duke Molecular Physiology Institute (DMPI), Duke University Medical Center, Durham, NC 27701, USA.

Kathryn Blew (K)

Division of Pediatric Endocrinology and Diabetes, Duke University Medical Center, Durham, NC 27710, USA.

Matthew L Crawford (ML)

Department of Research and Development, LabCorp, Burlington, NC 27215, USA.

Russell P Grant (RP)

Department of Research and Development, LabCorp, Burlington, NC 27215, USA.

James R Bain (JR)

Duke Molecular Physiology Institute (DMPI), Duke University Medical Center, Durham, NC 27701, USA.
Sarah W. Stedman Nutrition and Metabolism Center, Duke University Medical Center, Durham, NC 27705, USA.
Division of Endocrinology, Metabolism, and Nutrition, Duke University Medical Center, Durham, NC 27710, USA.

Michael Muehlbauer (M)

Duke Molecular Physiology Institute (DMPI), Duke University Medical Center, Durham, NC 27701, USA.
Sarah W. Stedman Nutrition and Metabolism Center, Duke University Medical Center, Durham, NC 27705, USA.

Nina Jain (N)

Division of Endocrinology, Department of Pediatrics, University of North Carolina, Chapel Hill, NC 27514, USA.

Daniel S Hsia (DS)

Clinical Trials Unit, Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.

Sarah Armstrong (S)

Division of General Pediatrics and Adolescent Health, Duke University Medical Center, Durham, NC 27710, USA.
Department of Family Medicine and Community Health, Duke University Medical Center, Durham, NC 27710, USA.
Department of Population Health Sciences, Duke University Medical Center, Durham, NC 27701, USA.
Duke Clinical Research Institute, Duke University Medical Center, Durham, NC 27701, USA.

Michael Freemark (M)

Duke Molecular Physiology Institute (DMPI), Duke University Medical Center, Durham, NC 27701, USA.
Division of Pediatric Endocrinology and Diabetes, Duke University Medical Center, Durham, NC 27710, USA.

Pinar Gumus Balikcioglu (P)

Duke Molecular Physiology Institute (DMPI), Duke University Medical Center, Durham, NC 27701, USA.
Division of Pediatric Endocrinology and Diabetes, Duke University Medical Center, Durham, NC 27710, USA.
Sarah W. Stedman Nutrition and Metabolism Center, Duke University Medical Center, Durham, NC 27705, USA.

Classifications MeSH