MRI measures of temporoparietal regions show differential rates of atrophy during prodromal AD

被引:74
作者
Desikan, R. S.
Fischl, B. [2 ,5 ]
Cabral, H. J. [6 ]
Kemper, T. L.
Guttmann, C. R. G. [8 ]
Blacker, D. [3 ]
Hyman, B. T. [4 ]
Albert, M. S. [9 ]
Killiany, R. J. [1 ,3 ,7 ,8 ]
机构
[1] Boston Univ, Sch Med, Dept Anat & Neurobiol, Ctr Biomed Imaging, Boston, MA 02118 USA
[2] Massachusetts Gen Hosp, Dept Radiol, Athinoula A Martinos Ctr Biomed Imaging, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
[5] MIT, Comp Sci & Artificial Intelligence Lab, Boston, MA USA
[6] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USA
[7] Boston Univ, Sch Publ Hlth, Dept Environm Hlth, Boston, MA 02118 USA
[8] Brigham & Womens Hosp, Dept Radiol, Boston, MA 02115 USA
[9] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
关键词
D O I
10.1212/01.wnl.0000320055.57329.34
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: MRI studies have demonstrated differential rates of atrophy in the entorhinal cortex and hippocampus during the prodromal phase of Alzheimer disease (AD). The current study was designed to determine whether a broader set of temporoparietal regions show differential rates of atrophy during the evolution of AD. Methods: Sixteen regions of interest ( ROIs) were analyzed on MRI scans obtained at baseline and follow-up in 66 subjects comprising three groups: controls = individuals who were cognitively normal at both baseline and follow-up; nonconverters = subjects with mild cognitive impairment (MCI) at both baseline and follow-up; converters had MCI at baseline but had progressed to AD at follow-up. Results: Annualized percent change was analyzed with multivariate analysis of variance (MANOVA), covaried for age. The MANOVA demonstrated an effect of group (p = 0.004). Post hoc comparisons demonstrated greater rates of atrophy for converters vs nonconverters for six ROIs: hippocampus, entorhinal cortex, temporal pole, middle temporal gyrus, fusiform gyrus, and inferior temporal gyrus. Converters showed differentially greater rates of atrophy than controls in five of the same ROIs (and inferior parietal lobule). Rates of change in clinical status were correlated with the atrophy rates in these regions. Comparisons between controls and nonconverters demonstrated no differences. Conclusion: These results demonstrate that temporoparietal regions show differential rates of atrophy on MRI during prodromal Alzheimer disease (AD). MRI data correlate with measures of clinical severity and cognitive decline, suggesting the potential of these regions of interest as antemortem markers of prodromal AD.
引用
收藏
页码:819 / 825
页数:7
相关论文
共 37 条
[1]   Preclinical prediction of AD using neuropsychological tests [J].
Albert, MS ;
Moss, MB ;
Tanzi, R ;
Jones, K .
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY, 2001, 7 (05) :631-639
[2]  
Anderson Valerie C, 2005, Top Magn Reson Imaging, V16, P439, DOI 10.1097/01.rmr.0000245458.05654.d0
[3]   NEUROFIBRILLARY TANGLES BUT NOT SENILE PLAQUES PARALLEL DURATION AND SEVERITY OF ALZHEIMERS-DISEASE [J].
ARRIAGADA, PV ;
GROWDON, JH ;
HEDLEYWHYTE, ET ;
HYMAN, BT .
NEUROLOGY, 1992, 42 (03) :631-639
[4]  
BLACKER D, 2008, ARCH NEUROL IN PRESS
[5]   ASSOCIATION BETWEEN QUANTITATIVE MEASURES OF DEMENTIA AND OF SENILE CHANGE IN CEREBRAL GREY MATTER OF ELDERLY SUBJECTS [J].
BLESSED, G ;
TOMLINSON, BE ;
ROTH, M .
BRITISH JOURNAL OF PSYCHIATRY, 1968, 114 (512) :797-+
[6]  
Braak H, 1998, J NEURAL TRANSM-SUPP, P127
[7]   NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[8]   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
[9]   ESTIMATING SAMPLE SIZES FOR BINARY, ORDERED CATEGORICAL, AND CONTINUOUS OUTCOMES IN 2 GROUP COMPARISONS [J].
CAMPBELL, MJ ;
JULIOUS, SA ;
ALTMAN, DG .
BRITISH MEDICAL JOURNAL, 1995, 311 (7013) :1145-1148
[10]   Comparison of methods for measuring longitudinal brain change in cognitive impairment and dementia [J].
Cardenas, VA ;
Du, AT ;
Hardin, D ;
Ezekiel, F ;
Weber, P ;
Jagust, WJ ;
Chui, HC ;
Schuff, N ;
Weiner, MW .
NEUROBIOLOGY OF AGING, 2003, 24 (04) :537-544