Amyloid burden and neural function in people at risk for Alzheimer's Disease

作者：Johnson Sterling C^*; Christian Bradley T; Okonkwo Ozioma C; Oh Jennifer M; Harding Sandra; Xu Guofan; Hillmer Ansel T; Wooten Dustin W; Murali Dhanabalan; Barnhart Todd E; Hall Lance T; Racine Annie M; Klunk William E; Mathis Chester A; Bendlin Barbara B; Gallagher Catherine L; Carlsson Cynthia M; Rowley Howard A; Hermann Bruce P; Dowling N Maritza; Asthana Sanjay; Sager Mark A

来源：Neurobiology of Aging, 2014, 35(3): 576-584.

DOI：10.1016/j.neurobiolaging.2013.09.028

• Alzheimer's disease
• Amyloid imaging
• Cognitive function
• Glucose metabolism
• AD risk

To determine the relationship between amyloid burden and neural function in healthy adults at risk for Alzheimer's Disease (AD), we used multimodal imaging with [C-11]Pittsburgh compound B positron emission tomography, [F-18]fluorodeoxyglucose, positron emission tomography, and magnetic resonance imaging, together with cognitive measurement in 201 subjects (mean age, 60.1 years; range, 46 -73 years) from the Wisconsin Registry for Alzheimer's Prevention. Using a qualitative rating, 18% of the samples were strongly positive Beta-amyloid (A beta+), 41% indeterminate (A beta i), and 41% negative (A beta-). A beta+ was associated with older age, female sex, and showed trends for maternal family history of AD and APOE4. Relative to the A beta group, A beta(vertical bar) and A beta i participants had increased glucose metabolism in the bilateral thalamus; A beta+ participants also had increased metabolism in the bilateral superior temporal gyrus. A beta+ participants exhibited increased gray matter in the lateral parietal lobe bilaterally relative to the A beta- group, and no areas of significant atrophy. Cognitive performance and self report cognitive and affective symptoms did not differ between groups. Amyloid burden can be identified in adults at a mean age of 60 years and is accompanied by glucometabolic increases in specific areas, but not atrophy or cognitive loss. This asymptomatic stage may be an opportune window for intervention to prevent progression to symptomatic AD. Published by Elsevier Inc.

• 出版日期2014-3