4.3 Article Proceedings Paper

Impact of amyloid imaging on drug development in Alzheimer's disease

Journal

NUCLEAR MEDICINE AND BIOLOGY
Volume 34, Issue 7, Pages 809-822

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.nucmedbio.2007.06.015

Keywords

amyloid imaging; amyloid beta; a beta; PiB; Alzheimer's disease; anti-amyloid therapy

Funding

  1. NIA NIH HHS [R37 AG025516-05S1, P01 AG025204-06, P01 AG025204-08, RF1 AG025516, R37 AG025516-08, P50 AG005133, R37 AG025516, R37 AG025516-04, P01 AG025204-07, P01 AG025204-05, R37 AG025516-03, P01 AG025204-04S1, P01 AG025204, R37 AG025516-05, R01 AG020226, R37 AG025516-02, R37 AG025516-06, R37 AG025516-01, R01 AG018402, R01 AG018402-05, R37 AG025516-07, P01 AG025204-04] Funding Source: Medline
  2. NIMH NIH HHS [P30 MH052247, P30 MH052247-109005] Funding Source: Medline

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Imaging agents capable of assessing amyloid-beta (A) content in vivo in the brains of Alzheimer's disease (AD) subjects likely will be important as diagnostic agents to detect A plaques in the brain as well as to help test the amyloid cascade hypothesis of AD and as an aid to assess the efficacy of anti-amyloid therapeutics currently under development and in clinical trials. Positron emission tomography (PET) imaging studies of amyloid deposition in human subjects with several A imaging agents are currently underway. We reported the first PET studies of the carbon 11-labeled thioflavin-T derivative Pittsburgh Compound B in 2004, and this work has subsequently been extended to include a variety of subject groups, including AD patients, mild cognitive impairment patients and healthy controls. The ability to quantify regional A plaque load in the brains of living human subjects has provided a means to begin to apply this technology as a diagnostic agent to detect regional concentrations of A plaques and as a surrogate marker of therapeutic efficacy in anti-amyloid drug trials. (C) 2007 Elsevier Inc. All rights reserved.

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