MRI-guided SPECT perfusion measures and volumetric MRI in prodromal Alzheimer disease

被引:59
作者
El Fakhri, G
Kijewski, MF
Johnson, KA
Syrkin, G
Killiany, RJ
Becker, JA
Zimmerman, RE
Albert, MS
机构
[1] Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Massachusetts Gen Hosp, Dept Radiol, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[6] Boston Univ, Med Ctr, Dept Anat, Boston, MA USA
[7] Boston Univ, Med Ctr, Dept Neurobiol, Boston, MA USA
关键词
D O I
10.1001/archneur.60.8.1066
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To identify group differences in the prodromal phase of Alzheimer disease (AD) using quantitative single-photon emission computed tomography (SPECT) perfusion and magnetic resonance imaging (MRI) volume measures within specific volumes of interest. Setting: Gerontology research unit. Participants: There were 17 healthy controls, 56 non-demented patients with memory problems who did not develop AD during 3 to 5 years of follow-up (questionables), and 27 non-demented patients with memory problems who developed AD during follow-up (converters). Methods: A Tc 99m hexamethylpropyleneamine oxime SPECT study and an MRI were performed in each participant at baseline. Mean SPECT activity concentration and MRI volume were estimated within 9 structures: rostral anterior cingulate, caudal anterior cingulate, posterior cingulate, hippocampus, entorhinal cortex, basal forebrain, temporal horn, amygdala, and the banks of the superior temporal sulcus. Data were analyzed using overall and pairwise discriminant analysis, and performance in pairwise group discrimination was measured using correlated receiver operating characteristic curve analysis. Results: The overall (3-group) discriminant function was significant for SPECT (F test, P < .001) and MRI (F test, P < .0001). For the SPECT analysis, the ranking of structures for discriminating among the 3 groups was, in order of decreasing discriminating power, caudal anterior cingulate, temporal horn, superior temporal sulcus, entorhinal cortex, hippocampus, rostral anterior cingulate, amygdala, basal forebrain, and posterior cingulate. For the MRI analysis, this ranking was entorhinal cortex, superior temporal sulcus, temporal horn, hippocampus, amygdala, caudal anterior cingulate, rostral anterior cingulate, basal forebrain, and posterior cingulate. Combining the 2 modalities yielded significantly better discrimination performance than did either alone. Furthermore, the correlation between SPECT and MRI measures was low. Conclusion: Measures of structure activity concentration and volume carry independent information; both reveal group differences in prodromal AD.
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页码:1066 / 1072
页数:7
相关论文
共 33 条
  • [1] Preclinical prediction of AD using neuropsychological tests
    Albert, MS
    Moss, MB
    Tanzi, R
    Jones, K
    [J]. JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY, 2001, 7 (05) : 631 - 639
  • [2] ALBERT MS, 2002, NEUROPSYCHOLOGY MEMO, P248
  • [3] Consensus recommendations for the postmortem diagnosis of Alzheimer's disease
    Ball, M
    Braak, H
    Coleman, P
    Dickson, D
    Duyckaerts, C
    Gambetti, P
    Hansen, L
    Hyman, B
    Jellinger, K
    Markesbery, W
    Perl, D
    Powers, J
    Price, J
    Trojanowski, JQ
    Wisniewski, H
    Phelps, C
    Khachaturian, Z
    [J]. NEUROBIOLOGY OF AGING, 1997, 18 (04) : S1 - S2
  • [4] Specific hippocampal volume reductions in individuals at risk for Alzheimer's disease
    Convit, A
    DeLeon, MJ
    Tarshish, C
    DeSanti, S
    Tsui, W
    Rusinek, H
    George, A
    [J]. NEUROBIOLOGY OF AGING, 1997, 18 (02) : 131 - 138
  • [5] Predicting conversion to Alzheimer disease using standardized clinical information
    Daly, E
    Zaitchik, D
    Copeland, M
    Schmahmann, J
    Gunther, J
    Albert, M
    [J]. ARCHIVES OF NEUROLOGY, 2000, 57 (05) : 675 - 680
  • [6] From healthy aging to early Alzheimer's disease:: In vivo detection of entorhinal cortex atrophy
    De Toledo-Morrell, L
    Goncharova, I
    Dickerson, B
    Wilson, RS
    Bennett, DA
    [J]. PARAHIPPOCAMPAL REGION: IMPLICATIONS FOR NEUROLOGICAL AND PSYCHIATRIC DISEASES, 2000, 911 : 240 - 253
  • [7] DEKOSKY S T, 1990, Alzheimer Disease and Associated Disorders, V4, P14, DOI 10.1097/00002093-199040100-00002
  • [8] Magnetic resonance imaging of the entorhinal cortex and hippocampus in mild cognitive impairment and Alzheimer's disease
    Du, AT
    Schuff, N
    Amend, D
    Laakso, MP
    Hsu, YY
    Jagust, WJ
    Yaffe, K
    Kramer, JH
    Reed, B
    Norman, D
    Chui, HC
    Weiner, MW
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2001, 71 (04) : 441 - 447
  • [9] El Fakhri G, 2000, J NUCL MED, V41, P1400
  • [10] Absolute activity quantitation from projections using an analytical approach: Comparison with iterative methods in Tc-99m and I-123 brain SPECT
    El Fakhri, G
    Kijewski, MF
    Moore, SC
    [J]. IEEE TRANSACTIONS ON NUCLEAR SCIENCE, 2001, 48 (03) : 768 - 773