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Increased cortical hyperexcitability and exaggerated myoclonus with aging in benign adult familial myoclonus epilepsy

The clinical implications of enlarged early cortical components of somatosensory evoked potentials in benign adult familial myoclonus epilepsy remain unknown. Somatosensory evoked potentials following electrical stimulation of the median nerve at the wrist were studied in 16 patients with a clinical...

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Published in:Movement disorders 2011-07, Vol.26 (8), p.1509-1514
Main Authors: Hitomi, Takefumi, Ikeda, Akio, Kondo, Takayuki, Imamura, Hisaji, Inouchi, Morito, Matsumoto, Riki, Terada, Kiyohito, Kanda, Masutaro, Matsuhashi, Masao, Nagamine, Takashi, Shibasaki, Hiroshi, Takahashi, Ryosuke
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creator Hitomi, Takefumi
Ikeda, Akio
Kondo, Takayuki
Imamura, Hisaji
Inouchi, Morito
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Matsuhashi, Masao
Nagamine, Takashi
Shibasaki, Hiroshi
Takahashi, Ryosuke
description The clinical implications of enlarged early cortical components of somatosensory evoked potentials in benign adult familial myoclonus epilepsy remain unknown. Somatosensory evoked potentials following electrical stimulation of the median nerve at the wrist were studied in 16 patients with a clinical diagnosis of benign adult familial myoclonus epilepsy (7 men and 9 women; mean age, 51 ± 18 years) and 19 age‐matched apparently healthy control subjects (11 men and 8 women; mean age, 49 ± 18 years). Giant somatosensory evoked potentials were observed in 13 of the 16 patients. P25 and N35 amplitudes in the patient group were 11.4 ± 6.1 and 19.2 ± 11.5 μV, respectively, and both were significantly larger compared with those in control subjects (P = 0.008 for P25 and P < 0.0001 for N35). There was a significant positive relationship between age at somatosensory evoked potential examination and N20, P25, and N35 amplitudes, both in the patient and in the control groups (P < 0.05). The linear regression gradient of the N35 amplitude with respect to age was significantly larger in the patient group than in the control group (P = 0.04). Furthermore, regression analysis showed a significant positive relationship between the myoclonus rating scale and age at time of somatosensory evoked potential examination (R = 0.645, P = 0.007). Somatosensory evoked potential amplitude increased with age in patients with benign adult familial myoclonus epilepsy to a greater extent than in the control subjects, which suggests a progressive increase in cortical excitability based on progressive pathophysiology in benign adult familial myoclonus epilepsy. © 2011 Movement Disorder Society
doi_str_mv 10.1002/mds.23653
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Somatosensory evoked potentials following electrical stimulation of the median nerve at the wrist were studied in 16 patients with a clinical diagnosis of benign adult familial myoclonus epilepsy (7 men and 9 women; mean age, 51 ± 18 years) and 19 age‐matched apparently healthy control subjects (11 men and 8 women; mean age, 49 ± 18 years). Giant somatosensory evoked potentials were observed in 13 of the 16 patients. P25 and N35 amplitudes in the patient group were 11.4 ± 6.1 and 19.2 ± 11.5 μV, respectively, and both were significantly larger compared with those in control subjects (P = 0.008 for P25 and P &lt; 0.0001 for N35). There was a significant positive relationship between age at somatosensory evoked potential examination and N20, P25, and N35 amplitudes, both in the patient and in the control groups (P &lt; 0.05). The linear regression gradient of the N35 amplitude with respect to age was significantly larger in the patient group than in the control group (P = 0.04). 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Disord</addtitle><date>2011-07</date><risdate>2011</risdate><volume>26</volume><issue>8</issue><spage>1509</spage><epage>1514</epage><pages>1509-1514</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>The clinical implications of enlarged early cortical components of somatosensory evoked potentials in benign adult familial myoclonus epilepsy remain unknown. Somatosensory evoked potentials following electrical stimulation of the median nerve at the wrist were studied in 16 patients with a clinical diagnosis of benign adult familial myoclonus epilepsy (7 men and 9 women; mean age, 51 ± 18 years) and 19 age‐matched apparently healthy control subjects (11 men and 8 women; mean age, 49 ± 18 years). Giant somatosensory evoked potentials were observed in 13 of the 16 patients. 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Somatosensory evoked potential amplitude increased with age in patients with benign adult familial myoclonus epilepsy to a greater extent than in the control subjects, which suggests a progressive increase in cortical excitability based on progressive pathophysiology in benign adult familial myoclonus epilepsy. © 2011 Movement Disorder Society</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21506164</pmid><doi>10.1002/mds.23653</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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ispartof Movement disorders, 2011-07, Vol.26 (8), p.1509-1514
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subjects Adult
Aged
Aging
benign adult familial myoclonus epilepsy
Biological and medical sciences
cortical myoclonic tremor
Electroencephalography
Epilepsies, Myoclonic - pathology
Epilepsies, Myoclonic - physiopathology
Evoked Potentials, Somatosensory - physiology
Female
giant somatosensory evoked potential
Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
Humans
Male
Medical sciences
Middle Aged
Myoclonus - physiopathology
Nervous system (semeiology, syndromes)
Neurology
Reaction Time
Severity of Illness Index
Somatosensory Cortex - physiopathology
title Increased cortical hyperexcitability and exaggerated myoclonus with aging in benign adult familial myoclonus epilepsy
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