Use of oral diabetes medications and the risk of incident dementia in US veterans aged ≥60 years with type 2 diabetes
Author
Tang, X.Brinton, R.D.
Chen, Z.
Farland, L.V.
Klimentidis, Y.
Migrino, R.
Reaven, P.
Rodgers, K.
Zhou, J.J.
Affiliation
Epidemiology and Biostatistics, University of Arizona Mel and Enid Zuckerman College of Public HealthUA Center for Innovation in Brain Science, University of Arizona Health Sciences
Division of Cardiology, University of Arizona College of Medicine Phoenix
Division of Endocrinology, University of Arizona College of Medicine Phoenix
Department of Pharmacology and Toxicology, University of Arizona
Issue Date
2022
Metadata
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BMJCitation
Tang, X., Brinton, R. D., Chen, Z., Farland, L. V., Klimentidis, Y., Migrino, R., Reaven, P., Rodgers, K., & Zhou, J. J. (2022). Use of oral diabetes medications and the risk of incident dementia in US veterans aged ≥60 years with type 2 diabetes. BMJ Open Diabetes Research & Care, 10(5).Rights
Copyright © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
INTRODUCTION: Studies have reported that antidiabetic medications (ADMs) were associated with lower risk of dementia, but current findings are inconsistent. This study compared the risk of dementia onset in patients with type 2 diabetes (T2D) treated with sulfonylurea (SU) or thiazolidinedione (TZD) to patients with T2D treated with metformin (MET). RESEARCH DESIGN AND METHODS: This is a prospective observational study within a T2D population using electronic medical records from all sites of the Veterans Affairs Healthcare System. Patients with T2D who initiated ADM from January 1, 2001, to December 31, 2017, were aged ≥60 years at the initiation, and were dementia-free were identified. A SU monotherapy group, a TZD monotherapy group, and a control group (MET monotherapy) were assembled based on prescription records. Participants were required to take the assigned treatment for at least 1 year. The primary outcome was all-cause dementia, and the two secondary outcomes were Alzheimer's disease and vascular dementia, defined by International Classification of Diseases (ICD), 9th Revision, or ICD, 10th Revision, codes. The risks of developing outcomes were compared using propensity score weighted Cox proportional hazard models. RESULTS: Among 559 106 eligible veterans (mean age 65.7 (SD 8.7) years), the all-cause dementia rate was 8.2 cases per 1000 person-years (95% CI 6.0 to 13.7). After at least 1 year of treatment, TZD monotherapy was associated with a 22% lower risk of all-cause dementia onset (HR 0.78, 95% CI 0.75 to 0.81), compared with MET monotherapy, and 11% lower for MET and TZD dual therapy (HR 0.89, 95% CI 0.86 to 0.93), whereas the risk was 12% higher for SU monotherapy (HR 1.12 95% CI 1.09 to 1.15). CONCLUSIONS: Among patients with T2D, TZD use was associated with a lower risk of dementia, and SU use was associated with a higher risk compared with MET use. Supplementing SU with either MET or TZD may partially offset its prodementia effects. These findings may help inform medication selection for elderly patients with T2D at high risk of dementia. © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.Note
Open access journalISSN
2052-4897PubMed ID
36220195Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1136/bmjdrc-2022-002894
Scopus Count
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Except where otherwise noted, this item's license is described as Copyright © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC.
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