An evaluation of traditional and novel tools for lesion behavior mapping.
An evaluation of traditional and novel tools for lesion behavior mapping.
复制标题
DOI:
10.1016/j.neuroimage.2008.09.031
复制
发表时间:
2009-02-15
期刊:
影响因子:
5.7
通讯作者:
Karnath HO
中科院分区:
文献类型:
--
作者:
Rorden C;Fridriksson J;Karnath HO
Kinkingnéhun and colleagues (NeuroImage 37 [2007] 1237–1249) have recently described a novel approach for lesion-behavior mapping (LBM), referred to as Anatomo-Clinical Overlapping Maps (AnaCOM). Conventional voxelwise LBM tools apply statistics to contrast behavioral performance of patients with lesions that encompass given voxels to control patients where these voxels are spared. In contrast, AnaCOM contrasts performance of patients with injury involving given voxels to the performance of neurologically healthy participants. The authors correctly note that their procedure can offer substantially more statistical power than conventional LBM methods. We compared AnaCOM to conventional LBM techniques by examining hemiparesis (a common consequence of stroke) as the behavior of interest. We found that AnaCOM detected many regions of the middle cerebral artery territory not associated with the motor system. We suggest that conventional LBM techniques detect regions that are damaged in patients with a deficit while spared in those without a deficit, while AnaCOM detects regions that are associated with a deficit. Therefore, this new measure may offer poor specificity. Furthermore, on theoretical grounds we suggest that permutation-based thresholding will be a more sensitive method for controlling familywise error than the method of counting lesion-overlap clusters used by AnaCOM. Finally, we note that the within group variability tends to be smaller for neurologically healthy controls than in neurological patients, due to ceiling effects. Therefore, we suggest that nonparametric measures or the Welch’s t-test are more appropriate than the conventional pooled variance t-test used by AnaCOM.
登录
查看更多内容
影响因子:
19.7
作者:
Herskovits, EH;Megalooikonomou, V;Gerring, JP
通讯作者:
Gerring, JP
影响因子:
2.4
作者:
Ruxton, GD
通讯作者:
Ruxton, GD
影响因子:
3.2
作者:
Kimberg, Daniel Y.;Coslett, H. Branch;Schwartz, Myrna F.
通讯作者:
Schwartz, Myrna F.
影响因子:
3.7
作者:
Karnath, HO;Berger, MF;Rorden, C
通讯作者:
Rorden, C
影响因子:
5.7
作者:
Kinkingnehun, Serge;Volle, Emmanuelle;Dubois, Bruno
通讯作者:
Dubois, Bruno