4.5 Article

Longitudinal White and Gray Matter Response to Precision Medicine-Guided Intervention for Alzheimer's Disease

Journal

JOURNAL OF ALZHEIMERS DISEASE
Volume 96, Issue 3, Pages 1051-1058

Publisher

IOS PRESS
DOI: 10.3233/JAD-230481

Keywords

Alzheimer's disease; gray matter; neuroimaging; precision medicine; white matter

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This study investigated regional morphological responses to precision medicine-guided intervention in AD and MCI patients. The results suggest that precision medicine may help slow down WM and GM atrophy, although the observed changes were not statistically significant after multiple comparison correction. Improvements in cognitive scores were statistically significant, but may not necessarily have clinical significance.
Background: Alzheimer's disease (AD) is a debilitating condition that is widely known to adversely affect gray matter (GM) and white matter (WM) tracts within the brain. Recently, precision medicine has shown promise in alleviating the clinical and gross morphological trajectories of patients with AD. However, regional morphological changes have not yet been adequately characterized. Objective: Investigate regional morphological responses to a precision medicine-guided intervention with regards to white and gray matter in AD and mild cognitive impairment (MCI). Methods: Clinical and neuroimaging data were compiled over a 9-month period from 25 individuals who were diagnosed with AD or MCI receiving individualized treatment plans. Structural T1-weighted MRI scans underwent segmentation and volumetric quantifications via Neuroreader. Longitudinal changes were calculated via annualized percent change of WM or GM ratios. Results: Montreal Cognitive Assessment scores (p < 0.001) and various domains of the Computerized Neurocognitive Screening Vital Signs significantly improved from baseline to 9-month follow-up. There was regional variability in WM and GM atrophy or hypertrophy, but none of these observed changes were statistically significant after correction for multiple comparisons. Conclusions: A precision-medicine guided approach to intervention may carry potential in curtailing both WM and GM atrophy, as rates of morphological change aligned more closely with normal aging than AD across all studied regions. Improvements in cognitive scores were statistically significant but may not necessarily represent clinical significance. Further studies should be pursued to further delineate cognitive trends as well as the mechanisms behind subtle regional differences in response to precision medicine-guided intervention.

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