The future of amyloid-beta imaging: a tale of radionuclides and tracer proliferation

被引:68
作者
Klunk, William E. [1 ,2 ]
Mathis, Chester A. [3 ,4 ,5 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Sch Med, Dept Radiol, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Sch Med, Dept Pharmacol, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Sch Med, Dept Pharmaceut Sci, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; carbon-11; fluorine-18; mild cognitive impairment; Pittsburgh compound-B; positron emission tomography;
D O I
10.1097/WCO.0b013e3283168e1a
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose of review This review will focus on the coming proliferation of amyloid-beta imaging tracers and give an opinion on how the Alzheimer's disease field can develop a systematic means of evaluating which tracers are useful and how the useful tracers compare to each other. Recent findings Several new tracers have been reported to be useful for human amyloid-beta imaging. The most recent of these are labeled with fluorine-18. Compared with the 20 min half-life of carbon-11 used in the most widely used tracer, Pittsburgh Compound-B, the 110 min half-life of fluorine-18 allows for wider utilization in research and clinical settings. Summary It is likely that more than one fluorine-18-labeled tracer will come into common use. The use of preclinical and clinical 'bridging studies' to [C-11]Pittsburgh Compound-B could be a means to determine whether the sizable body of knowledge already gained in [C-11]Pittsburgh Compound-B studies can be applied to the understanding of these new tracers and to form a basis for the comparison among them. This approach could save resources and help sort out a potentially bewildering onslaught of new amyloid-beta imaging tracers.
引用
收藏
页码:683 / 687
页数:5
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