White matter integrity changes in mild cognitive impairment associated with Aspirin use

Objectives: Alzheimer's disease (AD) represents a significant public health challenge, particularly as its prevalence is projected to rise sharply. Aspirin, known for its anti-inflammatory and antiplatelet properties, has been hypothesized to affect AD progression, although findings from observ...

Full description

Saved in:
Bibliographic Details
Published in:Neurology letters Vol. 3; no. 2; pp. 13 - 18
Main Authors: Atefeh Kashanizadeh, Mona Zamanpour, Sahar Oftadeh Balani, Atiyeh Janbozorgi, Negin Noruozi
Format: Journal Article
Language:English
Published: Iran University of Medical Sciences 01-08-2024
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Objectives: Alzheimer's disease (AD) represents a significant public health challenge, particularly as its prevalence is projected to rise sharply. Aspirin, known for its anti-inflammatory and antiplatelet properties, has been hypothesized to affect AD progression, although findings from observational studies and clinical trials remain inconsistent.Methods: This study utilized data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) to investigate the potential association between aspirin use and white matter (WM) microstructural changes in a cohort of 148 mild cognitive impairment (MCI) subjects. Diffusion tensor imaging (DTI) was employed to assess WM integrity, with fractional anisotropy (FA) and diffusivity metrics serving as primary outcomes. Statistical analyses were conducted using ANCOVA, adjusting for age, sex, APOE ε4 genotype, and MMSE score.Results: Aspirin users exhibited significantly higher FA values in the anterior corona radiata and left external capsule, alongside lower axial and radial diffusivity values in the right cingulum, indicating better-preserved WM microstructure compared to non-users.Conclusion: These findings suggest that aspirin may confer neuroprotective effects on WM in early AD, potentially delaying cognitive decline. Further research is warranted to confirm these results and explore the underlying mechanisms. Aspirin is widely prescribed to millions of adults, yet its impact on WM regions in the brain remains largely unclear. Further research is necessary to replicate these findings and to assess whether the effects of aspirin on WM structure could contribute to delaying or preventing cognitive decline.
ISSN:2821-1723
DOI:10.61186/nl.3.3.13