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Frielitz-Wagner, I.V.* ; Mattutat, J.* ; Frielitz, F.S.* ; Scheuermann, K.* ; Gesing, J.* ; Marheineke, D.* ; Löffler, D.S.* ; Kiess, W.* ; Körner, A.

Diurnal rythm of Nampt is gender and weight dependent.

Obes. Res. Clin. Pract. 18, 181-188 (2024)
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RESEARCH AIM: Nicotinamide phosphoribosyltransferase (Nampt) is an adipocytokine that is elevated in obesity, type 2 diabetes and increased levels are associated with inflammatory processes. Nampt serum concentrations have been suggested to follow a diurnal rhythm peaking in the afternoon in lean males. However, no data exists regarding the effects of gender and body weight. MATERIAL AND METHODS: We measured Nampt serum levels over 24 h in a cohort of healthy individuals living with either normal weight or obesity. Furthermore, effects of meals, oral glucose tolerance test and physical exercise on Nampt concentrations were evaluated. Correlation analyses to other hormonal- and lab parameters and anthropometric measurements were performed. RESULTS: Nampt showed a diurnal rhythm with increased levels at daytime and a peak in the early afternoon. This diurnal rhythm was significant for all groups but obese males. The Nampt amplitude, measured both relatively and absolutely, was significantly higher in females than in males. Meals did not influence Nampt serum levels, whereas physical exercise and an OGTT did significantly influence Nampt serum levels. CONCLUSION: In conclusion, we found gender specific differences in Nampt amplitude and coefficient variation with both being higher in females. The circadian rhythm of Nampt was independent of gender in healthy lean individuals, whereas it was disturbed in men with obesity.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Diurnal Rhythm ; Nampt ; Obesity; Plasma Visfatin Concentrations; Adipokine; Glucose; Obese; Fat
Language english
Publication Year 2024
HGF-reported in Year 2024
ISSN (print) / ISBN 1871-403X
e-ISSN 1878-0318
Quellenangaben Volume: 18, Issue: 3, Pages: 181-188 Article Number: , Supplement: ,
Publisher Elsevier
Publishing Place 125 London Wall, London, England
Reviewing status Peer reviewed
Institute(s) Helmholtz Institute for Metabolism, Obesity and Vascular Research (HI-MAG)
POF-Topic(s) 30201 - Metabolic Health
Research field(s) Helmholtz Diabetes Center
PSP Element(s) G-506503-001
Grants Integrated Research and Treatment Centre (IFB) Adiposity Diseases
Federal Ministry of Education and Research (BMBF) , Germany
European Regional Development Fund (ERFD) by means of the Free State of Saxony
LIFE (Leipzig Research Center for Civilization Diseases, Universitat Leipzig) - European Union
German Research Foundation (DFG)
Scopus ID 85197444230
PubMed ID 38960771
Erfassungsdatum 2024-07-24