Biomarkers of Neurodegeneration and Alzheimer’s Disease Neuropathology in Adolescents and Young Adults with Youth-Onset Type 1 or Type 2 Diabetes: A Proof-of-Concept Study

Author:

Shapiro Allison L. B.12ORCID,Coughlan Christina34ORCID,Bettcher Brianne M.4,Pauley Meghan E.5ORCID,Kim Jeongchul6,Bjornstad Petter27,Rajic Benjamin1,Truong Jennifer1ORCID,Bell Christopher1,Choi Ye Ji2ORCID,Walker Keenan A.8ORCID,Potter Huntington34ORCID,Liese Angela D.9,Dabelea Dana1,Whitlow Christopher T.6

Affiliation:

1. Lifecourse Epidemiology of Adiposity and Diabetes Center, University of Colorado at Anschutz (CU-Anschutz), Aurora, CO 80045, USA

2. Section of Endocrinology, Department of Pediatrics, School of Medicine (SOM), CU-Anschutz, Aurora, CO 80045, USA

3. University of Colorado Alzheimer’s and Cognition Center, CU-Anschutz, Aurora, CO 80045, USA

4. Department of Neurology, SOM, CU-Anschutz, Aurora, CO 80045, USA

5. Barbara Davis Center for Diabetes, CU-Anschutz, Aurora, CO 80045, USA

6. Radiology Informatics and Image Processing Laboratory, Department of Radiology, Wake Forest School of Medicine, Winston-Salem, NC 27101, USA

7. Division of Renal Diseases and Hypertension, Department of Medicine, SOM, CU-Anschutz, Aurora, CO 80045, USA

8. Laboratory of Behavioral Neuroscience, National Institute on Aging, Intramural Research Program, Baltimore, MD 20814, USA

9. Department of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina, Columbia, SC 29208, USA

Abstract

Adult-onset diabetes increases one’s risk of neurodegenerative disease including Alzheimer’s disease (AD); however, the risk associated with youth-onset diabetes (Y-DM) remains underexplored. We quantified plasma biomarkers of neurodegeneration and AD in participants with Y-DM from the SEARCH cohort at adolescence and young adulthood (Type 1, n = 25; Type 2, n = 25; 59% female; adolescence, age = 15 y/o [2.6]; adulthood, age = 27.4 y/o [2.2]), comparing them with controls (adolescence, n = 25, age = 14.8 y/o [2.7]; adulthood, n = 21, age = 24.9 y/o [2.8]). Plasma biomarkers, including glial fibrillary acidic protein (GFAP), neurofilament light chain protein (NfL), phosphorylated tau-181 (pTau181), and amyloid beta (Aβ40, Aβ42), were measured via Simoa. A subset of participants (n = 7; age = 27.5 y/o [5.7]) and six controls (age = 25.1 y/o [4.5]) underwent PET scans to quantify brain amyloid and tau densities in AD sensitive brain regions. Y-DM adolescents exhibited lower plasma levels of Aβ40, Aβ42, and GFAP, and higher pTau181 compared to controls (p < 0.05), a pattern persisting into adulthood (p < 0.001). All biomarkers showed significant increases from adolescence to adulthood in Y-DM (p < 0.01), though no significant differences in brain amyloid or tau were noted between Y-DM and controls in adulthood. Preliminary evidence suggests that preclinical AD neuropathology is present in young people with Y-DM, indicating a potential increased risk of neurodegenerative diseases.

Funder

American College of Radiology (ACR) Fund

Centers for Disease Control and Prevention

National Institute of Diabetes and Digestive and Kidney Diseases

National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases

Juvenile Diabetes Research Foundation

National Institute on Aging’s Intramural Research Program

Publisher

MDPI AG

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