Relationship of fMR1 activation to clinical trial memory measures in Alzheimer disease

被引:28
作者
Diamond, E. L.
Miller, S.
Dickerson, B. C.
Atri, A.
DePeau, K.
Fenstermacher, E.
Pihlajamaeki, M.
Celone, K.
Salisbury, S.
Gregas, M.
Rentz, D.
Sperling, R. A.
机构
[1] Brigham & Womens Hosp, Dept Neurol, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Athinoula A Martinos Ctr Biomed Imaging, Boston, MA 02114 USA
[5] Harvard Univ, Sch Med, Boston, MA USA
[6] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[7] Univ Kuopio, Dept Neurosci & Neurol, FIN-70211 Kuopio, Finland
[8] Albert Einstein Coll Med, Bronx, NY 10467 USA
关键词
D O I
10.1212/01.wnl.0000277292.37292.69
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Functional MRI fMRI) has shown promise as a tool to characterize altered brain function in Alzheimer disease (AD) and for use in proof of concept clinical trials. FMRI studies of subjects with AD have demonstrated altered hippocampal and neocortical activation while encoding novel stimuli compared to older controls. However, the relationship between (fMRI) activation and performance on standardized clinical trial memory measures has not been fully investigated. Objective: To determine whether patterns of activation during an associative-memory fMRI paradigm correlate with performance on memory measures used in AD clinical trials. Methods: Twenty-nine subjects with AD underwent neuropsychological testing, including the AD Assessment Scale (ADAS-Cog), and an associative-encoding fMRI paradigm. Scores were entered as regressors in SPM2 analyses of the differential fMRI activation to novel-vs-repeated (NvR) stimuli. To account for cerebral atrophy, native-space structure-function analyses were performed with subjects' high-resolution structural images. Results: Performance on the ADAS-Cog verbal m emery component, and the ADAS-Cog total correlated with NvR activation in left superior temporal (p = 0.0003; r = -0.51) and left score, prefrontal (p = 0.00001; r = -0.63) cortices. In a subgroup with more extensive neuropsychological testing (n = 14), performance on the Free and Cued Selective Reminding Test was correlated activation remained correlated with with activation in these same regions. performance even when accounting for atrophy. Conclusions: The relationship between functional MRI (fMRI) activation and standardized memory measures supports the potential use of fMRI to investigate regional mechanisms of treatment response in clinical trials of novel therapies for Alzheimer disease.
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页码:1331 / 1341
页数:11
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