The association of insulin responses and insulin sensitivity with cognition in adults with pre-diabetes: The Diabetes Prevention Program Outcomes Study.

Cognitive function Insulin response Pre-diabetes

Journal

Journal of diabetes and its complications
ISSN: 1873-460X
Titre abrégé: J Diabetes Complications
Pays: United States
ID NLM: 9204583

Informations de publication

Date de publication:
01 May 2024
Historique:
received: 14 02 2024
revised: 06 04 2024
accepted: 29 04 2024
medline: 4 5 2024
pubmed: 4 5 2024
entrez: 3 5 2024
Statut: aheadofprint

Résumé

Dysglycemia is a significant risk factor for cognitive impairment. However, which pathophysiologic determinant(s) of dysglycemia, impaired insulin sensitivity (ISens) or the islet β-cell's response (IResp), contribute to poorer cognitive function, independent of dysglycemia is not established. Among 1052 adults with pre-diabetes from the Diabetes Prevention Program Outcomes Study (DPPOS), we investigated the relationship between IResp, ISens and cognitive function. IResp was estimated by the insulinogenic index (IGI; pmol/mmol) and ISens as 1/fasting insulin from repeated annual oral glucose tolerance tests. The mean IResp and mean ISens were calculated over approximately 12 years of follow-up. Verbal learning (Spanish-English Verbal Learning Test [SEVLT]) and executive function (Digital Symbol Substitution Test [DSST]) were assessed at the end of the follow-up period. Linear regression models were run for each cognitive outcome and were adjusted for dysglycemia and other factors. Higher IResp was associated with poorer performance on the DSST (-0.69 points per 100 unit increase in IGI, 95 % CI: -1.37, -0.01). ISens was not associated with DSST, nor were IResp or ISens associated with performance on the SEVLT. These results suggest that a greater β-cell response in people at high risk for type 2 diabetes is associated with poorer executive function, independent of dysglycemia and ISens.

Identifiants

pubmed: 38701667
pii: S1056-8727(24)00090-4
doi: 10.1016/j.jdiacomp.2024.108764
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108764

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest None.

Auteurs

Allison L B Shapiro (ALB)

Lifecourse Epidemiology of Adiposity and Diabetes (LEAD) Center, University of Colorado at Anschutz (CU-Anschutz), USA; Section of Endocrinology, Department of Pediatrics, School of Medicine, CU-Anschutz, USA. Electronic address: dppmail@bsc.gwu.edu.

Ashley H Tjaden (AH)

Biostatistics Center, Milken Institute School of Public Health, George Washington University, Rockville, MD, USA.

Sharon L Edelstein (SL)

Biostatistics Center, Milken Institute School of Public Health, George Washington University, Rockville, MD, USA.

Steven E Kahn (SE)

Division of Metabolism, Endocrinology and Nutrition, Department of Medicine, VA Puget Sound Health Care System and University of Washington, Seattle, WA, USA.

Preethi Srikanthan (P)

Division of Endocrinology, UCLA Health System, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.

William C Knowler (WC)

Consultant: Biostatistics Center, Milken Institute School of Public Health, George Washington University, Rockville, MD, USA.

Elizabeth M Venditti (EM)

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.

Sherita H Golden (SH)

Division of Endocrinology, Diabetes, and Metabolism, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Owen Carmichael (O)

Pennington Biomedical Research Center, Baton Rouge, LA, USA.

José A Luchsinger (JA)

Departments of Medicine and Epidemiology, Columbia University Irving Medical Center, New York, NY, USA.

Classifications MeSH