Key result
Higher amyloid burden and white matter hyperintensities link to worse cognitive function in type-2 diabetes.
Why the study?
Diabetes is associated with cognitive decline, but the underlying mechanisms are complex and their relationship with Alzheimer's Disease biomarkers is not fully understood.
Cross-Sectional (n=47)
No
Effect estimate: β -1.30
p-value: p=0.01
In older adults with type 2 diabetes, both amyloid deposition and cerebral small vessel disease independently correlate with worse cognitive function, suggesting multiple distinct pathways contribute to cognitive decline in this population.
Hypothesis-generating for dual amyloid-SVD pathways in T2D cognition; should not yet change practice.
Diabetes is associated with cognitive decline, but the underlying mechanisms are complex and their relationship with Alzheimer's Disease biomarkers is not fully understood. We assessed the association of small vessel disease (SVD) and amyloid burden with cognitive functioning in 47 non-demented older adults with type-2 diabetes from the Israel Diabetes and Cognitive Decline Study (mean age 78Y, 64% females). FLAIR-MRI, Vizamyl amyloid-PET, and T1W-MRI quantified white matter hyperintensities as a measure of SVD, amyloid burden, and gray matter (GM) volume, respectively. Mean hemoglobin A1c levels and duration of type-2 diabetes were used as measures of diabetic control. Cholesterol level and blood pressure were used as measures of cardiovascular risk. A broad neuropsychological battery assessed cognition. Linear regression models revealed that both higher SVD and amyloid burden were associated with lower cognitive functioning. Additional adjustments for type-2 diabetes-related characteristics, GM volume, and cardiovascular risk did not alter the results. The association of amyloid with cognition remained unchanged after further adjustment for SVD, and the association of SVD with cognition remained unchanged after further adjustment for amyloid burden. Our findings suggest that SVD and amyloid pathology may independently contribute to lower cognitive functioning in non-demented older adults with type-2 diabetes, supporting a multimodal approach for diagnosing, preventing, and treating cognitive decline in this population.
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Lesman‐Segev et al. (2024) conducted a cross-sectional in Type 2 diabetes (n=47). Amyloid burden (Aβ-SUVR) and White matter hyperintensities (WMH) was evaluated on Global cognitive functioning (β -1.30, p=0.01). Higher amyloid burden (β = -1.30) and white matter hyperintensity volume (β = -0.02) were independently associated with lower global cognitive functioning in older adults with type-2 diabetes.
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