Frequency of prediabetes in individuals with increased adiposity and metabolically healthy or unhealthy phenotypes.

estimated glucose disposal rate impaired fasting glucose impaired glucose tolerance insulin‐resistance metabolically healthy obesity

Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
08 May 2024
Historique:
revised: 21 04 2024
received: 01 03 2024
accepted: 22 04 2024
medline: 9 5 2024
pubmed: 9 5 2024
entrez: 9 5 2024
Statut: aheadofprint

Résumé

To utilize the estimated glucose disposal rate (eGDR) index of insulin sensitivity, which is based on readily available clinical variables, namely, waist circumference, hypertension and glycated haemoglobin, to discriminate between metabolically healthy and unhealthy phenotypes, and to determine the prevalence of prediabetic conditions. Non-diabetic individuals (n = 2201) were stratified into quartiles of insulin sensitivity based on eGDR index. Individuals in the upper quartiles of eGDR were defined as having metabolically healthy normal weight (MHNW), metabolically healthy overweight (MHOW) or metabolically healthy obesity (MHO) according to their body mass index, while those in the lower quartiles were classified as having metabolically unhealthy normal weight (MUNW), metabolically unhealthy overweight (MUOW) and metabolically unhealthy obesity (MUO), respectively. The frequency of impaired fasting glucose (IFG), impaired glucose tolerance (IGT), and IFG + IGT status was comparable among the MHNW, MHOW and MHO groups, while it increased from those with MUNW status towards those with MUOW and MUO status. As compared with participants with MHNW, the odds ratio of having IFG, IGT, or IFG + IGT was significantly higher in participants with MUOW and MUO but not in those with MUNW, MHOW and MHO, respectively. A metabolically healthy phenotype is associated with lower frequency of IFG, IGT, and IFG + IGT status across all body weight categories.

Identifiants

pubmed: 38720197
doi: 10.1111/dom.15646
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Sapienza Università di Roma
ID : RM1201728887461F
Organisme : European Foundation for the Study of Diabetes
ID : EFSD/Lilly Young Investigator Research Award
Organisme : Ministero dell'Università e della Ricerca
ID : 2020N5WK98_005
Organisme : Società Italiana di Medicina Interna Mario Condorelli award

Informations de copyright

© 2024 John Wiley & Sons Ltd.

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Auteurs

Chiara M A Cefalo (CMA)

Department of Clinical and Molecular Medicine, University of Rome-Sapienza, Rome, Italy.

Alessia Riccio (A)

Department of Clinical and Molecular Medicine, University of Rome-Sapienza, Rome, Italy.

Elena Succurro (E)

Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.

Maria Adelaide Marini (MA)

Department of Systems Medicine, University of Rome-Tor Vergata, Rome, Italy.

Teresa Vanessa Fiorentino (TV)

Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.

Mariangela Rubino (M)

Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.

Maria Perticone (M)

Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.

Angela Sciacqua (A)

Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.

Francesco Andreozzi (F)

Department of Medical and Surgical Sciences, University Magna Graecia of Catanzaro, Catanzaro, Italy.

Giorgio Sesti (G)

Department of Clinical and Molecular Medicine, University of Rome-Sapienza, Rome, Italy.

Classifications MeSH