4.7 Article

Importance of Treatment Status in Links Between Type 2 Diabetes and Alzheimer's Disease

Journal

DIABETES CARE
Volume 42, Issue 5, Pages 972-979

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/dc18-1399

Keywords

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Funding

  1. National Institutes of Health [R21-AG-055034, P01-AG-052350, P50-AG-005142]
  2. Alzheimer's Association [AA-008369]
  3. ADNI (National Institutes of Health) [U01-AG-024904]
  4. Department of Defense (DOD) ADNI (U.S. Department of Defense) [W81XWH-12-2-0012]
  5. National Institute on Aging
  6. National Institute of Biomedical Imaging and Bioengineering
  7. AbbVie
  8. Alzheimer's Drug Discovery Foundation
  9. Araclon Biotech
  10. Bioclinica, Inc.
  11. Biogen
  12. Bristol-Myers Squibb
  13. CereSpir Inc.
  14. Cogstate
  15. Eisai Inc.
  16. Elan Pharmaceuticals
  17. Eli Lilly and Company
  18. EURO-IMMUN
  19. F. Hoffmann-La Roche Ltd. and its affiliated company Genentech, Inc.
  20. Fujirebio
  21. GE Healthcare
  22. IXICO Ltd.
  23. Janssen Alzheimer Immunotherapy Research & Development LLC
  24. Johnson & Johnson Pharmaceutical Research and Development
  25. Lumosity
  26. Lundbeck
  27. Merck Co., Inc.
  28. Meso Scale Diagnostics, LLC
  29. NeuroRx Research
  30. Neurotrack Technologies
  31. Novartis Pharmaceuticals Corporation
  32. Pfizer Inc.
  33. Piramal Imaging
  34. Servier
  35. Takeda Pharmaceuticals
  36. Transition Therapeutics Inc.
  37. Canadian Institutes of Health Research

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OBJECTIVE To investigate relationships among type 2 diabetes treatment, Alzheimer's disease(AD) biomarkers, and risk for dementia. RESEARCH DESIGN AND METHODS Participants were from the Alzheimer's Disease Neuroimaging Initiative (N = 1,289) and were dementia-free at baseline and underwent health assessment, cognitive testing, and MRI. A subset (n = 900) obtained a lumbar puncture to determine cerebrospinal fluid (CSF) phosphorylated tau (p-tau), total tau (t-tau), and beta-amyloid 1-42 (A beta 1-42). Participants were grouped by fasting blood glucose and medication history: euglycemia (EU), prediabetes (PD), untreated diabetes (UD), and treated diabetes (TD). Relationships were investigated between treatment status and CSF biomarkers and risk for dementia. RESULTS The UD group displayed greater p-tau, t-tau, and p-tau/A beta 1-42 levels than the EU, PD, and TD groups (P values <0.05) and higher t-tau/A beta 1-42 than the EU and PD groups (P values <0.05). The UD group progressed to dementia at higher rates than the EU group (hazard ratio 1.602 [95% CI 1.057-2.429]; P = 0.026). CONCLUSIONS Treatment status may alter the relationship between type 2 diabetes and both AD biomarker profile and risk for dementia. UD is associated with elevated tau pathology and risk for dementia, whereas TD is not. Although this study is observational and therefore causality cannot be inferred, findings support the potential importance of treatment status in AD risk associated with type 2 diabetes.

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