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PMID: 19636048 Published · ppublish English Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

MRI and CSF biomarkers in normal, MCI, and AD subjects: diagnostic discrimination and cognitive correlations.

Neurology ·Vol. 73 ·No. 4 ·2009-07-28 ·Pages 287-93

Vemuri P, Wiste HJ, Weigand SD, Shaw LM, Trojanowski JQ, Weiner MW, Knopman DS, Petersen RC, Jack CR, Alzheimer's Disease Neuroimaging Initiative

Abstract

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). 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, Abeta(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. 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 < or = 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. 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.

MeSH Terms
Aged Aged, 80 and over Alzheimer Disease/cerebrospinal fluid,pathology,physiopathology Amyloid beta-Peptides/analysis,cerebrospinal fluid Biomarkers/analysis,cerebrospinal fluid Brain/metabolism,pathology,physiopathology Cognition/physiology Cognition Disorders/cerebrospinal fluid,pathology,physiopathology Cohort Studies Cross-Sectional Studies Diagnosis, Differential Female Humans Longitudinal Studies Magnetic Resonance Imaging Male Middle Aged Nerve Tissue Proteins/analysis,cerebrospinal fluid Neuropsychological Tests Predictive Value of Tests Reference Values Severity of Illness Index tau Proteins/analysis,cerebrospinal fluid
Chemicals
Amyloid beta-Peptides Biomarkers Nerve Tissue Proteins tau Proteins
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Vemuri P
Aging and Dementia Imaging Research Laboratory, Department of Radiology, Mayo Clinic and Foundation, Rochester, MN 55905, USA.
Wiste H J
Weigand S D
Shaw L M
Trojanowski J Q
Weiner M W
Knopman D S
Petersen R C
Jack C R
Alzheimer's Disease Neuroimaging Initiative
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Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
1526-632X
Published
2009-07-28
Pages
287-93
Language
English
Region
United States
NLM ID
0401060
PMCID
PMC2715210
Subset
IM
Grants
NIA NIH HHS · R01 AG10897 · United States
NIA NIH HHS · U01-AG024904 · United States
NCRR NIH HHS · P41 RR023953-02 · United States
NIA NIH HHS · R01 AG010897 · United States
NIA NIH HHS · R01-AG11378 · United States
NIA NIH HHS · P01-AG19724 · United States
NIA NIH HHS · U01 AG024904-05 · United States
NIA NIH HHS · U01-AG06786 · United States
NIA NIH HHS · U01 AG024904 · United States
NIA NIH HHS · U19 AG010483 · United States
NIA NIH HHS · R01 AG010897-22 · United States
NIA NIH HHS · P01 AG019724 · United States
NIA NIH HHS · P50-AG16574 · United States
NIA NIH HHS · P01 AG019724-050002 · United States
NCRR NIH HHS · P41 RR023953 · United States
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