Cognitive performance declines in older adults with type 1 diabetes: results from 32 years of follow-up in the DCCT and EDIC Study.


Journal

The lancet. Diabetes & endocrinology
ISSN: 2213-8595
Titre abrégé: Lancet Diabetes Endocrinol
Pays: England
ID NLM: 101618821

Informations de publication

Date de publication:
07 2021
Historique:
received: 26 01 2021
revised: 23 03 2021
accepted: 23 03 2021
pubmed: 31 5 2021
medline: 18 8 2021
entrez: 30 5 2021
Statut: ppublish

Résumé

With improved treatment, individuals with type 1 diabetes are living longer but there is limited information on the effects of type 1 diabetes on cognitive ability as they become older adults. We followed up individuals with type 1 diabetes to identify independent risk factors for cognitive decline as people age. 1051 participants with type 1 diabetes enrolled in the Diabetes Control and Complications Trial (DCCT) and its follow-up Epidemiology of Diabetes Interventions and Complications (EDIC) study. Participants completed cognitive assessments at baseline (median age 27 years) and 2, 5, 18, and 32 years later (median age 59). HbA Over 32 years of follow-up, we found substantive declines in memory and psychomotor and mental efficiency. Between 18 and 32 years of follow-up, the decline in psychomotor and mental efficiency was five times larger than the change from baseline to year 18. Independent of the other risk factors and comorbidities, exposure to higher HbA Cognitive function declines with ageing in type 1 diabetes. The association of glycaemia and blood pressure levels with cognitive decline suggests that better management might preserve cognitive function. United States National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Disease.

Sections du résumé

BACKGROUND
With improved treatment, individuals with type 1 diabetes are living longer but there is limited information on the effects of type 1 diabetes on cognitive ability as they become older adults. We followed up individuals with type 1 diabetes to identify independent risk factors for cognitive decline as people age.
METHODS
1051 participants with type 1 diabetes enrolled in the Diabetes Control and Complications Trial (DCCT) and its follow-up Epidemiology of Diabetes Interventions and Complications (EDIC) study. Participants completed cognitive assessments at baseline (median age 27 years) and 2, 5, 18, and 32 years later (median age 59). HbA
FINDINGS
Over 32 years of follow-up, we found substantive declines in memory and psychomotor and mental efficiency. Between 18 and 32 years of follow-up, the decline in psychomotor and mental efficiency was five times larger than the change from baseline to year 18. Independent of the other risk factors and comorbidities, exposure to higher HbA
INTERPRETATION
Cognitive function declines with ageing in type 1 diabetes. The association of glycaemia and blood pressure levels with cognitive decline suggests that better management might preserve cognitive function.
FUNDING
United States National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Disease.

Identifiants

pubmed: 34051936
pii: S2213-8587(21)00086-3
doi: 10.1016/S2213-8587(21)00086-3
pmc: PMC8583716
mid: NIHMS1711529
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT00360893', 'NCT00360815']

Types de publication

Clinical Trial Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

436-445

Subventions

Organisme : NIDDK NIH HHS
ID : DP3 DK114812
Pays : United States
Organisme : NIA NIH HHS
ID : K24 AG045334
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK094157
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK094176
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests JAL discloses being funded by K24AG045334; consulting for vTv therapeutics; receiving royalties from Springer; and receiving a stipend from Wolters Kluwer. NC discloses personal fees and non-financial support from Eli Lilly, outside the submitted work. All other authors declare no competing interests.

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Auteurs

Alan M Jacobson (AM)

NYU Long Island School of Medicine, NYU Langone Hospital-Long Island, Mineola, NY, USA. Electronic address: alan.jacobson@nyulangone.org.

Christopher M Ryan (CM)

University of Pittsburgh, Pittsburgh, PA, USA.

Barbara H Braffett (BH)

George Washington University, Biostatistics Center, Rockville, MD, USA.

Rose A Gubitosi-Klug (RA)

Case Western Reserve University, Rainbow Babies and Children's Hospital, Cleveland, OH, USA.

Gayle M Lorenzi (GM)

University of California San Diego, La Jolla, CA, USA.

José A Luchsinger (JA)

Columbia University Irving Medical Center, New York, NY, USA.

Victoria R Trapani (VR)

George Washington University, Biostatistics Center, Rockville, MD, USA.

Ionut Bebu (I)

George Washington University, Biostatistics Center, Rockville, MD, USA.

Naomi Chaytor (N)

Elson S Floyd College of Medicine, Washington State University, Spokane, WA, USA.

Susan M Hitt (SM)

Columbia School of Medicine, University of Missouri, Columbia, MO, USA.

Kaleigh Farrell (K)

Case Western Reserve University, Rainbow Babies and Children's Hospital, Cleveland, OH, USA.

John M Lachin (JM)

George Washington University, Biostatistics Center, Rockville, MD, USA.

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