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.
Allison L B ShapiroChristina CoughlanBrianne M BettcherMeghan E PauleyJeongchul KimPetter BjornstadBenjamin RajicJennifer TruongChristopher BellYe Ji ChoiKeenan A WalkerHuntington PotterAngela D LieseDana DabeleaChristopher T WhitlowPublished in: Endocrines (2024)
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.
Keyphrases
- depressive symptoms
- type diabetes
- glycemic control
- young adults
- physical activity
- early life
- cerebrospinal fluid
- cardiovascular disease
- mental health
- computed tomography
- white matter
- adipose tissue
- cognitive decline
- stem cells
- risk assessment
- multiple sclerosis
- insulin resistance
- cerebral ischemia
- binding protein
- metabolic syndrome
- ionic liquid
- small molecule
- spinal cord
- mesenchymal stem cells
- positron emission tomography
- neuropathic pain
- subarachnoid hemorrhage
- human health