Comparison of different methodological implementations of voxel-based morphometry in neurodegenerative disease

被引:160
作者
Senjem, ML [1 ]
Gunter, JL [1 ]
Shiung, MM [1 ]
Petersen, RC [1 ]
Jack, CR [1 ]
机构
[1] Mayo Clin & Mayo Fdn, Dept Radiol, Rochester, MN 55905 USA
关键词
voxel-based morphometry; neurodegenerative disease; inter-group differences;
D O I
10.1016/j.neuroimage.2005.02.005
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Voxel-based morphometry (VBM) is a popular method for probing inter-group differences in brain morphology. Variation in the detailed implementation of the algorithm, however, will affect the apparent results of VBM analyses and in turn the inferences drawn about the anatomic expression of specific disease states. We qualitatively assessed group comparisons of 43 normal elderly control subjects and 51 patients with probable Alzheimer's disease, using five different VBM variations. Based on the known pathologic expression of the disease, we evaluated the biological plausibility of each. The use of a custom template and custom tissue class prior probability images (priors) produced inter-group comparison maps with greater biological plausibility than the use of the Montreal Neurological Institute (MNI) template and priors. We present a method for initializing the normalization to a custom template, and conclude that, when incorporated into the VBM processing chain, it yields the most biologically plausible inter-group differences of the five methods presented. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:600 / 608
页数:9
相关论文
共 25 条
[1]
[Anonymous], 2003, HUMAN BRAIN FUNCTION
[2]
Voxel-based morphometry - The methods [J].
Ashburner, J ;
Friston, KJ .
NEUROIMAGE, 2000, 11 (06) :805-821
[3]
Why voxel-based morphometry should be used [J].
Ashburner, J ;
Friston, KJ .
NEUROIMAGE, 2001, 14 (06) :1238-1243
[4]
Ashburner J, 1999, HUM BRAIN MAPP, V7, P254, DOI 10.1002/(SICI)1097-0193(1999)7:4<254::AID-HBM4>3.0.CO
[5]
2-G
[6]
In vivo mapping of gray matter loss with voxel-based morphometry in mild Alzheimer's disease [J].
Baron, JC ;
Chételat, G ;
Desgranges, B ;
Perchey, G ;
Landeau, B ;
de la Sayette, V ;
Eustache, F .
NEUROIMAGE, 2001, 14 (02) :298-309
[7]
Voxel-based morphometry should not be used with imperfectly registered images [J].
Bookstein, FL .
NEUROIMAGE, 2001, 14 (06) :1454-1462
[8]
NEUROPATHOLOGICAL STAGING OF ALZHEIMER-RELATED CHANGES [J].
BRAAK, H ;
BRAAK, E .
ACTA NEUROPATHOLOGICA, 1991, 82 (04) :239-259
[9]
Why voxel-based morphometric analysis should be used with great caution when characterizing group differences [J].
Davatzikos, C .
NEUROIMAGE, 2004, 23 (01) :17-20
[10]
Davis B, 2004, 2004 2ND IEEE INTERNATIONAL SYMPOSIUM ON BIOMEDICAL IMAGING: MACRO TO NANO, VOLS 1 AND 2, P173