4.7 Article

Biphasic cortical macro- and microstructural changes in autosomal dominant Alzheimer's disease

Journal

ALZHEIMERS & DEMENTIA
Volume 17, Issue 4, Pages 618-628

Publisher

WILEY
DOI: 10.1002/alz.12224

Keywords

Alzheimer' s disease; autosomal‐ dominant Alzheimer' s disease; biphasic cortical changes; cortical diffusivity; magnetic resonance imaging; preclinical Alzheimer' s disease

Funding

  1. NCATS NIH HHS [UL1 TR002345] Funding Source: Medline
  2. NIA NIH HHS [R01 AG052550, U01 AG059798, R21 AG056974, P30 AG066462, U19 AG032438, RF1 AG056850, P50 AG008702, P01 AG003991, RF1 AG061566, UF1 AG032438] Funding Source: Medline
  3. NIBIB NIH HHS [R01 EB009352] Funding Source: Medline

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The study suggests a biphasic trajectory for brain structural changes in early preclinical Alzheimer's disease, with increases in cortical thickness and decreases in cortical diffusivity followed by cortical thinning and cortical diffusivity increases in later stages. The timing of these changes aligns with the start of tau biomarker alterations.
INTRODUCTION A biphasic model for brain structural changes in preclinical Alzheimer's disease (AD) could reconcile some conflicting and paradoxical findings in observational studies and anti-amyloid clinical trials. METHODS In this study we tested this model fitting linear versus quadratic trajectories and computed the timing of the inflection points vertexwise of cortical thickness and cortical diffusivity-a novel marker of cortical microstructure-changes in 389 participants from the Dominantly Inherited Alzheimer Network. RESULTS In early preclinical AD, between 20 and 15 years before estimated symptom onset, we found increases in cortical thickness and decreases in cortical diffusivity followed by cortical thinning and cortical diffusivity increases in later preclinical and symptomatic stages. The inflection points 16 to 19 years before estimated symptom onset are in agreement with the start of tau biomarker alterations. DISCUSSION These findings confirm a biphasic trajectory for brain structural changes and have direct implications when interpreting magnetic resonance imaging measures in preventive AD clinical trials.

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