Scintigraphy with 123I-serum amyloid P component in Alzheimer disease

被引:26
作者
Lovat, LB
O'Brien, AAJ
Armstrong, SF
Madhoo, S
Bulpitt, CJ
Rossor, MN
Pepys, MB
Hawkins, PN
机构
[1] Hammersmith Hosp, Royal Postgrad Med Sch, Dept Med, Immunol Med Unit, London W12 0NN, England
[2] Hammersmith Hosp, Royal Postgrad Med Sch, Dept Med, Div Med Elderly, London W12 0NN, England
[3] UCL Natl Hosp Neurol & Neurosurg, Dementia Res Grp, London WC1N 3BG, England
关键词
Alzheimer disease (AD); amyloid; serum amyloid P component (SAP); A beta protein;
D O I
10.1097/00002093-199809000-00014
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The neuropathology of Alzheimer disease (AD) includes cerebral and cerebrovascular amyloid deposits composed of A beta protein. Extracerebral deposits of A beta, identified immunohistochemically, have also been reported but without evidence for the presence of amyloid fibrils. Serum amyloid P component (SAP) is a normal plasma glycoprotein that binds to the fibrils in all types of amyloid deposit, and radiolabeled SAP is a specific, sensitive, quantitative diagnostic tracer for systemic amyloid deposits in vivo. However, we report that in 11 patients with probable or definite AD, conventional whole body planar scintigraphy after injection of I-123-SAP revealed no detectable localization of tracer within the brain or elsewhere. Significant amounts of systemic extracerebral A beta amyloid are thus probably not a feature of AD. Also, although plasma-derived SAP is always present in the cerebral and cerebrovascular amyloid lesions of AD, there was insufficient accumulation of injected labeled SAP to be detected by the present routine methodology.
引用
收藏
页码:208 / 210
页数:3
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