Automated MRI measures predict progression to Alzheimer's disease

被引:76
作者
Desikan, Rahul S. [1 ]
Cabral, Howard J. [2 ]
Settecase, Fabio [3 ]
Hess, Christopher P. [3 ]
Dillon, William P. [3 ]
Glastonbury, Christine M. [3 ]
Weiner, Michael W. [3 ,4 ]
Schmansky, Nicholas J. [1 ]
Salat, David H. [1 ]
Fischl, Bruce [1 ,5 ,6 ]
机构
[1] Massachusetts Gen Hosp, Athinoula A Martinos Ctr Biomed Imaging, Dept Radiol, Charlestown, MA 02129 USA
[2] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA USA
[3] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94143 USA
[4] Dept Vet Affairs, San Francisco, CA USA
[5] MIT, CSAIL, Cambridge, MA 02139 USA
[6] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
关键词
Computational MRI; AD; Mild cognitive impairment; Clinical biomarker; MILD COGNITIVE IMPAIRMENT; SURFACE-BASED ANALYSIS; HUMAN CEREBRAL-CORTEX; FUNCTIONAL CONNECTIVITY; CORTICAL THICKNESS; ATROPHY; AD; CONVERSION; HIPPOCAMPAL; BIOMARKERS;
D O I
10.1016/j.neurobiolaging.2010.04.023
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The prediction of individuals with mild cognitive impairment (MCI) destined to develop Alzheimer's disease (AD) is of increasing clinical importance. In this study, using baseline T1-weighted MRI scans of 324 MCI individuals from two cohorts and automated software tools, we employed factor analyses and Cox proportional hazards models to identify a set of neuroanatomic measures that best predicted the time to progress from MCI to AD. For comparison, cerebrospinal fluid (CSF) assessments of cellular pathology and positron emission tomography (PET) measures of metabolic activity were additionally examined. By 3 years follow-up, 60 MCI individuals from the first cohort and 58 MCI individuals from the second cohort had progressed to a diagnosis of AD. Cox models on the first cohort demonstrated significant effects for the medial temporal factor [Hazards Ratio (HR) = 0.43(95% confidence interval (CI), 0.32-0.55), p<0.0001], the fronto-parietoccipital factor [HR = 0.59[95% CI, 0.48-0.80), p<0.001], and the lateral temporal factor [HR = 0.67 (95% CI, 0.52-0.871, p<0.011. When applied to the second cohort, these Cox models showed significant effects for the medial temporal factor [HR = 0.44 (0.32-0.61), p<0.0011 and lateral temporal factor [HR = 0.49 (0.38-0.62), p<0.001]. In a combined Cox model, consisting of individual CSF, PET, and MRI measures that best predicted disease progression, only the medial temporal factor [HR = 0.53 195% CI, 0.34-0.811, p<0.001] demonstrated a significant effect. These findings illustrate that automated MRI measures of the medial temporal cortex accurately and reliably predict time to disease progression, outperform cellular and metabolic measures as predictors of clinical decline, and can potentially serve as a predictive marker for AD. (C) 2010 Elsevier Inc. All rights reserved.
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页码:1364 / 1374
页数:11
相关论文
共 47 条
[1]   Conversion of mild cognitive impairment to Alzheimer disease predicted by hippocampal atrophy maps [J].
Apostolova, Liana G. ;
Dutton, Rebecca A. ;
Dinov, Ivo D. ;
Hayashi, Kiralee M. ;
Toga, Arthur W. ;
Cummings, Jeffrey L. ;
Thompson, Paul M. .
ARCHIVES OF NEUROLOGY, 2006, 63 (05) :693-699
[2]   The Topographical and Neuroanatomical Distribution of Neurofibrillary Tangles and Neuritic Plaques in the Cerebral Cortex of Patients with Alzheimer's Disease [J].
Arnold, Steven E. ;
Hyman, Bradley T. ;
Flory, Jill ;
Damasio, Antonio R. ;
Van Hoesen, Gary W. .
CEREBRAL CORTEX, 1991, 1 (01) :103-116
[3]   An energy budget for signaling in the grey matter of the brain [J].
Attwell, D ;
Laughlin, SB .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2001, 21 (10) :1133-1145
[4]   The cortical signature of prodromal AD Regional thinning predicts mild AD dementia [J].
Bakkour, Akram ;
Morris, John C. ;
Dickerson, Bradford C. .
NEUROLOGY, 2009, 72 (12) :1048-1055
[5]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[6]   Cortical Hubs Revealed by Intrinsic Functional Connectivity: Mapping, Assessment of Stability, and Relation to Alzheimer's Disease [J].
Buckner, Randy L. ;
Sepulcre, Jorge ;
Talukdar, Tanveer ;
Krienen, Fenna M. ;
Liu, Hesheng ;
Hedden, Trey ;
Andrews-Hanna, Jessica R. ;
Sperling, Reisa A. ;
Johnson, Keith A. .
JOURNAL OF NEUROSCIENCE, 2009, 29 (06) :1860-1873
[7]   Molecular, structural, and functional characterization of Alzheimer's disease: Evidence for a relationship between default activity, amyloid, and memory [J].
Buckner, RL ;
Snyder, AZ ;
Shannon, BJ ;
LaRossa, G ;
Sachs, R ;
Fotenos, AF ;
Sheline, YI ;
Klunk, WE ;
Mathis, CA ;
Morris, JC ;
Mintun, MA .
JOURNAL OF NEUROSCIENCE, 2005, 25 (34) :7709-7717
[8]   A unified approach for morphometric and functional data analysis in young, old, and demented adults using automated atlas-based head size normalization: reliability and validation against manual measurement of total intracranial volume [J].
Buckner, RL ;
Head, D ;
Parker, J ;
Fotenos, AF ;
Marcus, D ;
Morris, JC ;
Snyder, AZ .
NEUROIMAGE, 2004, 23 (02) :724-738
[9]   Cortical surface-based analysis - I. Segmentation and surface reconstruction [J].
Dale, AM ;
Fischl, B ;
Sereno, MI .
NEUROIMAGE, 1999, 9 (02) :179-194
[10]   Longitudinal cerebrospinal fluid tau load increases in mild cognitive impairment [J].
de Leon, MJ ;
Segal, S ;
Tarshish, CY ;
DeSanti, S ;
Zinkowski, R ;
Mehta, PD ;
Convit, A ;
Caraos, C ;
Rusinek, H ;
Tsui, W ;
Saint Louis, LA ;
DeBernardis, J ;
Kerkman, D ;
Qadri, F ;
Gary, A ;
Lesbre, P ;
Wisniewski, T ;
Poirier, J ;
Davies, P .
NEUROSCIENCE LETTERS, 2002, 333 (03) :183-186