MRI and CSF biomarkers in normal, MCI, and AD subjects Diagnostic discrimination and cognitive correlations

被引:195
作者
Vemuri, P. [1 ]
Wiste, H. J. [2 ]
Weigand, S. D. [2 ]
Shaw, L. M. [4 ]
Trojanowski, J. Q. [4 ]
Weiner, M. W. [5 ,6 ]
Knopman, D. S. [3 ]
Petersen, R. C. [3 ]
Jack, C. R., Jr. [1 ]
机构
[1] Mayo Clin & Mayo Fdn, Dept Radiol, Aging & Dementia Imaging Res Lab, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Hlth Sci Res, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
[4] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[5] Univ Calif San Francisco, San Francisco, CA 94143 USA
[6] Ctr Imaging Neurodegenerat Dis, Dept Vet Affairs Med Ctr, San Francisco, CA USA
关键词
INCIPIENT ALZHEIMERS-DISEASE; CEREBROSPINAL-FLUID TAU; TEMPORAL-LOBE ATROPHY; HIPPOCAMPAL VOLUME; VASCULAR DEMENTIA; NEURON NUMBER; IMPAIRMENT; MARKERS; NEUROPATHOLOGY; ASSOCIATION;
D O I
10.1212/WNL.0b013e3181af79e5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To assess the correlations of both MRI and CSF biomarkers with clinical diagnosis and with cognitive performance in cognitively normal (CN) subjects and patients with amnestic mild cognitive impairment (aMCI) and Alzheimer disease (AD). Methods: This is a cross-sectional study with data from the Alzheimer's Disease Neuroimaging Initiative, which consists of CN subjects, subjects with aMCI, and subjects with AD with both CSF and MRI. Baseline CSF (t-tau, A beta(1-42), and p-tau(181P)) and MRI scans were obtained in 399 subjects (109 CN, 192 aMCI, 98 AD). Structural Abnormality Index (STAND) scores, which reflect the degree of AD-like anatomic features on MRI, were computed for each subject. Results: We found no significant correlation between CSF biomarkers and cognitive scores in any of the 3 clinical groups individually. Conversely, STAND scores correlated with both Clinical Dementia Rating-sum of boxes and Mini-Mental State Examination in aMCI and AD (p <= 0.01). While STAND and all CSF biomarkers were predictors of clinical group membership (CN, aMCI, or AD) univariately (p < 0.001), STAND was more predictive than CSF both univariately and in combined models. Conclusions: CSF and MRI biomarkers independently contribute to intergroup diagnostic discrimination and the combination of CSF and MRI provides better prediction than either source of data alone. However, MRI provides greater power to effect cross-sectional groupwise discrimination and better correlation with general cognition and functional status cross-sectionally. We therefore conclude that although MRI and CSF provide complementary information, MRI reflects clinically defined disease stage better than the CSF biomarkers tested. Neurology (R) 2009; 73: 287-293
引用
收藏
页码:287 / 293
页数:7
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