Repetitive TMS temporarily alters brain diffusion

The authors investigated whether repetitive transcranial magnetic stimulation (rTMS) at 1 Hz (12 minutes; 90% of motor threshold) to the primary motor cortex (M1) leads to changes in diffusion-weighted imaging (DWI). After the rTMS train, there was a temporary small restriction in diffusion within the targeted left M1 that disappeared after 5 minutes. These findings provide a physiologic correlate to the reported behavioral consequences of off-line 1-Hz rTMS and reveal the transitory nature of the effects.

[1]  J. Gore,et al.  Changes in water diffusion and relaxation properties of rat cerebrum during status epilepticus , 1993, Magnetic resonance in medicine.

[2]  J. Sanes,et al.  ε-Sarcoglycan, a Broadly Expressed Homologue of the Gene Mutated in Limb-Girdle Muscular Dystrophy 2D* , 1997, The Journal of Biological Chemistry.

[3]  Mark Hallett,et al.  Locating the Motor Cortex on the MRI with Transcranial Magnetic Stimulation and PET , 1996, NeuroImage.

[4]  N. Copeland,et al.  Zac1 (Lot1), a Potential Tumor Suppressor Gene, and the Gene for ɛ-Sarcoglycan Are Maternally Imprinted Genes: Identification by a Subtractive Screen of Novel Uniparental Fibroblast Lines , 2000, Molecular and Cellular Biology.

[5]  L. Cohen,et al.  Reduction of human visual cortex excitability using 1-Hz transcranial magnetic stimulation , 2000, Neurology.

[6]  R R Edelman,et al.  Time course of the apparent diffusion coefficient (ADC) abnormality in human stroke , 1997, Neurology.

[7]  M. Hallett,et al.  Transcranial magnetic stimulation techniques in clinical investigation , 2002, Neurology.

[8]  R R Edelman,et al.  Clinical experience with diffusion-weighted MR in patients with acute stroke. , 1998, AJNR. American journal of neuroradiology.

[9]  J. Takamatsu,et al.  McCune-Albright Syndrome Associated with Non-Autoimmune Type of Hyperthyroidism with Development of Thyrotoxic Crisis , 2000, Hormone Research in Paediatrics.

[10]  M Gangitano,et al.  Segregation of areas related to visual working memory in the prefrontal cortex revealed by rTMS. , 2002, Cerebral cortex.

[11]  T. Gasser Inherited myoclonus-dystonia syndrome. , 1998, Advances in neurology.

[12]  K. Hossmann Viability thresholds and the penumbra of focal ischemia , 1994, Annals of neurology.

[13]  G. Schlaug,et al.  The ischemic penumbra: operationally defined by diffusion and perfusion MRI. , 1999, Neurology.

[14]  S Fahn,et al.  Association of a missense change in the D2 dopamine receptor with myoclonus dystonia. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[15]  Y. Samson,et al.  False-negative diffusion-weighted MR findings in acute ischemic stroke. , 2000, AJNR. American journal of neuroradiology.

[16]  Mark Hallett,et al.  Mechanisms of Deafferentation-Induced Plasticity in Human Motor Cortex , 1998, The Journal of Neuroscience.

[17]  Xingbao Li,et al.  Prefrontal Cortex Transcranial Magnetic Stimulation Does not Change Local Diffusion: A Magnetic Resonance Imaging Study in Patients With Depression , 2003, Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology.

[18]  Ziad Nahas,et al.  Handbook of Transcranial Magnetic Stimulation , 2003 .

[19]  B. Meyer,et al.  MRI study of human brain exposed to high-dose repetitive magnetic stimulation of visual cortex , 2000, Neurology.

[20]  M. Hallett,et al.  Depression of motor cortex excitability by low‐frequency transcranial magnetic stimulation , 1997, Neurology.

[21]  G. Deuschl,et al.  Linkage studies in alcohol‐responsive myoclonic dystonia , 1996, Movement disorders : official journal of the Movement Disorder Society.

[22]  Á. Pascual-Leone,et al.  Transcranial magnetic stimulation in neurology , 2003, The Lancet Neurology.

[23]  A. Lang Essential myoclonus and myoclonic dystonia. , 1997, Movement disorders : official journal of the Movement Disorder Society.

[24]  D. Jennings,et al.  Localization of a gene for myoclonus‐dystonia to chromosome 7q21‐q31 , 1999, Annals of neurology.

[25]  J. Daube,et al.  Hereditary essential myoclonus. , 1966, Archives of neurology.

[26]  T. Meitinger,et al.  Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome , 2001, Nature Genetics.