The pattern of amyloid accumulation in the brains of adults with Down syndrome

被引:111
作者
Annus, Tiina [1 ]
Wilson, Liam R. [1 ]
Hong, Young T. [2 ]
Acosta-Cabronero, Julio [3 ]
Fryer, Tim D. [2 ]
Cardenas-Blanco, Arturo [3 ]
Smith, Robert [2 ]
Boros, Istvan [2 ]
Coles, Jonathan P. [4 ]
Aigbirhio, Franklin I. [2 ]
Menon, David K. [4 ]
Zaman, Shahid H. [1 ,5 ]
Nestor, Peter J. [3 ]
Holland, Anthony J. [1 ,5 ]
机构
[1] Univ Cambridge, Dept Psychiat, Cambridge Intellectual & Dev Disabil Res Grp, Cambridge, England
[2] Univ Cambridge, Dept Clin Neurosci, Wolfson Brain Imaging Ctr, Cambridge Biomed Campus, Cambridge, England
[3] German Ctr Neurodegenerat Dis DZNE, Magdeburg, Germany
[4] Univ Cambridge, Dept Med, Div Anaesthesia, Cambridge Biomed Campus, Cambridge CB2 2QQ, England
[5] Cambridgeshire & Peterborough NHS Fdn Trust, Fulbourn Hosp, Cambridge, England
基金
英国医学研究理事会;
关键词
Alzheimer's disease; Down syndrome; Amyloid; PIB; PET; Dementia; Striatum; Preclinical; POSITRON-EMISSION-TOMOGRAPHY; PITTSBURGH-COMPOUND-B; ALZHEIMERS-DISEASE; CORPUS STRIATUM; BETA PROTEIN; DEMENTIA; DEPOSITION; AGE; ASSOCIATION; PLAQUES;
D O I
10.1016/j.jalz.2015.07.490
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Adults with Down syndrome (DS) invariably develop Alzheimer's disease (AD) neuropathology. Understanding amyloid deposition in DS can yield crucial information about disease pathogenesis. Methods: Forty-nine adults with DS aged 25-65 underwent positron emission tomography with Pittsburgh compound-B (PIB). Regional PIB binding was assessed with respect to age, clinical, and cognitive status. Results: Abnormal PIB binding became evident from 39 years, first in striatum followed by rostral prefrontal-cingulo-parietal regions, then caudal frontal, rostral temporal, primary sensorimotor and occipital, and finally parahippocampal cortex, thalamus, and amygdala. PM binding was related to age, diagnostic status, and cognitive function. Discussion: PIB binding in DS, first appearing in striatum, began around age 40 and was strongly associated with dementia and cognitive decline. The absence of a substantial time lag between amyloid accumulation and cognitive decline contrasts to sporadic/familial AD and suggests this population's suitability for an amyloid primary prevention trial. (C) 2015 The Authors. Published by Elsevier Inc. on behalf of Alzheimer's Association.
引用
收藏
页码:538 / 545
页数:8
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