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Alterations of motor cortical excitability and anatomy in Unverricht‐Lundborg disease
Author(s) -
Danner Nils,
Julkunen Petro,
Hyppönen Jelena,
Niskanen Eini,
Säisänen Laura,
Könönen Mervi,
Koskenkorva Päivi,
Vanninen Ritva,
Kälviäinen Reetta,
Mervaala Esa
Publication year - 2013
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.25615
Subject(s) - myoclonus , progressive myoclonus epilepsy , motor cortex , transcranial magnetic stimulation , primary motor cortex , scalp , neuroscience , silent period , cortex (anatomy) , inhibitory postsynaptic potential , stimulation , psychology , degenerative disease , medicine , central nervous system disease , anatomy
Unverricht‐Lundborg disease is the most common form of progressive myoclonus epilepsies. In addition to generalized seizures, it is characterized by myoclonus, which usually is the most disabling feature of the disease. Classically, the myoclonus has been attributed to increased excitability of the primary motor cortex. However, inhibitory cortical phenomena have also been described along with anatomical alterations. We aimed to characterize the relationship between the excitability and anatomy of the motor cortex and their association with the severity of the clinical symptoms. Seventy genetically verified patients were compared with forty healthy controls. The symptoms were evaluated with the Unified Myoclonus Rating Scale. Navigated transcranial magnetic stimulation was applied to characterize the excitability of the primary motor cortex by determining the motor thresholds and cortical silent periods. In addition, the induced cortical electric fields were estimated using individual scalp‐to‐cortex distances measured from MRIs. A cortical thickness analysis was performed to elucidate possible disease‐related anatomical alterations. The motor thresholds, cortical electric fields, and silent periods were significantly increased in the patients ( P < 0.01). The silent periods correlated with the myoclonus scores ( r = 0.48 to r = 0.49, P < 0.001). The scalp‐to‐cortex distance increased significantly with disease duration ( r = 0.56, P < 0.001) and correlated inversely with cortical thickness. The results may reflect the refractory nature of the myoclonus and indicate a possible reactive cortical inhibitory mechanism to the underlying disease process. This is the largest clinical series on Unverricht‐Lundborg disease and the first study describing parallel pathophysiological and structural alterations associated with the severity of the symptoms. © 2013 International Parkinson and Movement Disorder Society