4.7 Article

Amyloid-related imaging abnormalities in amyloid-modifying therapeutic trials: Recommendations from the Alzheimer's Association Research Roundtable Workgroup

Journal

ALZHEIMERS & DEMENTIA
Volume 7, Issue 4, Pages 367-385

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jalz.2011.05.2351

Keywords

MRI; Amyloid; Therapeutic trials; Vasogenic edema; Microhemorrhage

Funding

  1. Pfizer
  2. Allon
  3. Baxter, Inc.
  4. Roche
  5. GlaxoSmithKline
  6. Novartis Pharmaceuticals
  7. Myriad Pharmaceuticals
  8. Sanofi-Aventis
  9. Boehringer Ingelheim
  10. Novo Nordisk
  11. AstraZeneca

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Amyloid imaging related abnormalities (ARIA) have now been reported in clinical trials with multiple therapeutic avenues to lower amyloid-beta burden in Alzheimer's disease (AD). In response to concerns raised by the Food and Drug Administration, the Alzheimer's Association Research Roundtable convened a working group to review the publicly available trial data, attempts at developing animal models, and the literature on the natural history and pathology of related conditions. The spectrum of ARIA includes signal hyperintensities on fluid attenuation inversion recoverysequences thought to represent vasogenic edema and/or sulcal effusion (ARIA-E), as well as signal hypointensities on GRE/T2* thought to represent hemosiderin deposits (ARIA-H), including microhemorrhage and superficial siderosis. The etiology of ARIA remains unclear but the prevailing data support vascular amyloid as a common pathophysiological mechanism leading to increased vascular permeability. The workgroup proposes recommendations for the detection and monitoring of ARIA in ongoing AD clinical trials, as well as directions for future research. (C) 2011 The Alzheimer's Association. All rights reserved.

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