Structural white matter abnormalities in patients with idiopathic dystonia

We investigated whether structural white matter abnormalities, in the form of disruption of axonal coherence and integrity as measured with diffusion tensor imaging (DTI), constitute an underlying pathological mechanism of idiopathic dystonia (ID), independent of genotype status. We studied seven subjects with ID: all had cervical dystonia as their main symptom (one patient also had spasmodic dysphonia and two patients had concurrent generalized dystonia, both DYT1‐negative). We compared DTI MR images of patients with 10 controls, evaluating differences in mean diffusivity (MD) and fractional anisotropy (FA). ID was associated with increased FA values in the thalamus and adjacent white matter, and in the white matter underlying the middle frontal gyrus. ID was also associated with increase in MD in adjacent white matter to the pallidum and putamen bilaterally, left caudate, and in subcortical hemispheric regions, including the postcentral gyrus. Abnormal FA and MD in patients with ID indicate that abnormal axonal coherence and integrity contribute to the pathophysiology of dystonia. These findings suggest that ID is not only a functional disorder, but also associated with structural brain changes. Impaired connectivity and disrupted flow of information may contribute to the impairment of motor planning and regulation in dystonia. © 2006 Movement Disorder Society

[1]  C. Rorden,et al.  Stereotaxic display of brain lesions. , 2000, Behavioural neurology.

[2]  C. Beaulieu,et al.  The basis of anisotropic water diffusion in the nervous system – a technical review , 2002, NMR in biomedicine.

[3]  Derek K. Jones,et al.  The effect of gradient sampling schemes on measures derived from diffusion tensor MRI: A Monte Carlo study † , 2004, Magnetic resonance in medicine.

[4]  D. Perani,et al.  Basal ganglia and thalamo‐cortical hypermetabolism in patients with spasmodic torticollis , 1996, Acta neurologica Scandinavica.

[5]  David Eidelberg,et al.  Microstructural white matter changes in carriers of the DYT1 gene mutation , 2004 .

[6]  M. Ghilardi,et al.  Impaired sequence learning in carriers of the DYT1 dystonia mutation , 2003, Annals of neurology.

[7]  Kevin J. Black,et al.  Putamen volume in idiopathic focal dystonia , 1998, Neurology.

[8]  D. Eidelberg Brain networks and clinical penetrance: lessons from hyperkinetic movement disorders , 2003, Current Opinion in Neurology.

[9]  P. Basser,et al.  Diffusion tensor MR imaging of the human brain. , 1996, Radiology.

[10]  O. Devinsky,et al.  Cognitive functioning after pallidotomy for refractory Parkinson’s disease , 1998, Journal of neurology, neurosurgery, and psychiatry.

[11]  Bogdan Draganski,et al.  “Motor circuit” gray matter changes in idiopathic cervical dystonia , 2003, Neurology.

[12]  V. Dhawan,et al.  The metabolic topography of essential blepharospasm , 2000, Neurology.

[13]  V. Dhawan,et al.  Functional brain networks in DYT1 dystonia , 1998, Annals of neurology.

[14]  David Eidelberg,et al.  Abnormal brain networks in primary torsion dystonia. , 2004, Advances in neurology.

[15]  A Berardelli,et al.  Diffusion tensor imaging in primary cervical dystonia , 2005, Journal of Neurology, Neurosurgery & Psychiatry.

[16]  D. Eidelberg,et al.  Primary dystonia: Is abnormal functional brain architecture linked to genotype? , 2002, Annals of neurology.