The Alzheimer's Disease Neuroimaging Initiative positron emission tomography core.
The Alzheimer's Disease Neuroimaging Initiative positron emission tomography core.
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DOI:
10.1016/j.jalz.2010.03.003
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发表时间:
2010-05
期刊:
影响因子:
--
通讯作者:
Alzheimer's Disease Neuroimaging Initiative
中科院分区:
文献类型:
--
作者:
Jagust WJ;Bandy D;Chen K;Foster NL;Landau SM;Mathis CA;Price JC;Reiman EM;Skovronsky D;Koeppe RA;Alzheimer's Disease Neuroimaging Initiative
This is a progress report of the Alzheimer's Disease Neuroimaging Initiative (ADNI) PET Core. The Core has supervised the acquisition, quality control, and analysis of longitudinal [18F]fluorodeoxyglucose PET (FDG-PET) data in approximately half of the ADNI cohort. In an “add on” study, approximately 100 subjects also underwent scanning with [11C]PIB-PET for amyloid imaging. The Core developed quality control procedures and standardized image acquisition by developing an imaging protocol that has been widely adopted in academic and pharmaceutical industry studies. Data processing provides users with scans that have identical orientation and resolution characteristics despite acquisition on multiple scanner models. The Core labs have used a number of different approaches to characterize differences between subject groups (AD, MCI, controls), to examine longitudinal change over time in glucose metabolism and amyloid deposition, and to assess the use of FDG-PET as a potential outcome measure in clinical trials. ADNI data indicate that FDG-PET increases statistical power over traditional cognitive measures, might aid subject selection, and could substantially reduce the sample size in a clinical trial. PIB-PET data showed expected group differences, and identified subjects with significant annual increases in amyloid load across the subject groups. The next activities of the PET core in ADNI will entail developing standardized protocols for amyloid imaging using the [18F]-labeled amyloid imaging agent AV45, which can be delivered to virtually all ADNI sites. ADNI has demonstrated the feasibility and utility of multicenter PET studies and is helping to clarify the role of biomarkers in the study of aging and dementia.
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影响因子:
158.5
作者:
Reiman, EM;Caselli, RJ;Osborne, D
通讯作者:
Osborne, D
影响因子:
5.9
作者:
JACOBSON, NS;TRUAX, P
通讯作者:
TRUAX, P
影响因子:
9.9
作者:
Jagust, W. J.;Landau, S. M.;Mathis, C. A.
通讯作者:
Mathis, C. A.
影响因子:
5.7
作者:
Langbaum JB;Chen K;Lee W;Reschke C;Bandy D;Fleisher AS;Alexander GE;Foster NL;Weiner MW;Koeppe RA;Jagust WJ;Reiman EM;Alzheimer's Disease Neuroimaging Initiative
通讯作者:
Alzheimer's Disease Neuroimaging Initiative
影响因子:
--
作者:
Aizenstein, Howard Jay;Nebes, Robert D.;Saxton, Judith A.;Price, Julie C.;Mathis, Chester A.;Tsopelas, Nicholas D.;Ziolko, Scott K.;James, Jeffrey A.;Snitz, Beth E.;Houck, Patricia R.;Bi, Wenzhu;Cohen, Ann D.;Lopresti, Brian J.;DeKosky, Steven T.;Halligan, Edythe M.;Klunk, William E.
通讯作者:
Klunk, William E.