TY - JOUR
T1 - Diffusion tensor tractography analysis of the corpus callosum fibers in amyotrophic lateral sclerosis
AU - Kim, Jee Eun
AU - Oh, Jungsu S.
AU - Sung, Jung Joon
AU - Lee, Kwang Woo
AU - Song, In Chan
AU - Hong, Yoon Ho
PY - 2014/7
Y1 - 2014/7
N2 - Background and Purposezz Involvement of the corpus callosum (CC)is reported to be a consistent feature of amyotrophic lateral sclerosis (ALS). We examined the CC pathology using diffusion tensor tractography analysis to identify precisely which fiber bundles are involved in ALS. Methodszz Diffusion tensor imaging was performed in 14 sporadic ALS patients and 16 agematched healthy controls. Whole brain tractography was performed using the multiple-region of interest (ROI)approach, and CC fiber bundles were extracted in two ways based on functional and structural relevance: (i)cortical ROI selection based on Brodmann areas (BAs), and (ii)the sulcal-gyral pattern of cortical gray matter using Free NSurfer software, respectively. Resultszz The mean fractional anisotropy (FA)values of the CC fibers interconnecting the primary motor (BA4), supplementary motor (BA6), and dorsolateral prefrontal cortex (BA9/46) were significantly lower in ALS patients than in controls, whereas those of the primary sensory cortex (BA1, BA2, BA3), Broca's area (BA44/45), and the orbitofrontal cortex (BA11/47)did not differ significantly between the two groups. The Free Surfer ROI approach revealed a very similar pattern of abnormalities. In addition, a significant correlation was found between the mean FA value of the CC fibers interconnecting the primary motor area and disease severity, as assessed using the revised Amyotrophic Lateral Sclerosis Functional Rating Scale, and the clinical extent of upper motor neuron signs. Conclusionszz Our findings suggest that there is some degree of selectivity or a gradient in the CC pathology in ALS. The CC fibers interconnecting the primary motor and dorsolateral prefrontal cortices may be preferentially involved in ALS.
AB - Background and Purposezz Involvement of the corpus callosum (CC)is reported to be a consistent feature of amyotrophic lateral sclerosis (ALS). We examined the CC pathology using diffusion tensor tractography analysis to identify precisely which fiber bundles are involved in ALS. Methodszz Diffusion tensor imaging was performed in 14 sporadic ALS patients and 16 agematched healthy controls. Whole brain tractography was performed using the multiple-region of interest (ROI)approach, and CC fiber bundles were extracted in two ways based on functional and structural relevance: (i)cortical ROI selection based on Brodmann areas (BAs), and (ii)the sulcal-gyral pattern of cortical gray matter using Free NSurfer software, respectively. Resultszz The mean fractional anisotropy (FA)values of the CC fibers interconnecting the primary motor (BA4), supplementary motor (BA6), and dorsolateral prefrontal cortex (BA9/46) were significantly lower in ALS patients than in controls, whereas those of the primary sensory cortex (BA1, BA2, BA3), Broca's area (BA44/45), and the orbitofrontal cortex (BA11/47)did not differ significantly between the two groups. The Free Surfer ROI approach revealed a very similar pattern of abnormalities. In addition, a significant correlation was found between the mean FA value of the CC fibers interconnecting the primary motor area and disease severity, as assessed using the revised Amyotrophic Lateral Sclerosis Functional Rating Scale, and the clinical extent of upper motor neuron signs. Conclusionszz Our findings suggest that there is some degree of selectivity or a gradient in the CC pathology in ALS. The CC fibers interconnecting the primary motor and dorsolateral prefrontal cortices may be preferentially involved in ALS.
KW - Amyotrophic lateral sclerosis
KW - Corpus callosum
KW - Cortical parcellation
KW - Diffusion tensor imaging
KW - Motor neuron disease
KW - Tractography
UR - http://www.scopus.com/inward/record.url?scp=84904334786&partnerID=8YFLogxK
U2 - 10.3988/jcn.2014.10.3.249
DO - 10.3988/jcn.2014.10.3.249
M3 - Article
AN - SCOPUS:84904334786
SN - 1738-6586
VL - 10
SP - 249
EP - 256
JO - Journal of Clinical Neurology (Korea)
JF - Journal of Clinical Neurology (Korea)
IS - 3
ER -