Corticomuscular coherence in asymptomatic first‐degree relatives of patients with essential tremor

  • Background Essential tremor (ET) follows an autosomal dominant type of inheritance in the majority of patients, yet its genetic basis has not been identified. Its exact origin is still elusive, but coherence measurements between electromyography tremor bursts and electroencephalography unequivocally demonstrate a correlation. Methods We tested these measurements in 37 healthy first-degree relatives (children) of patients with essential tremor (ET) and a group of 37 age-matched and sex-matched controls. Pooled coherence spectra of the maximally coherent electroencephalogram electrodes were computed for ET relatives and controls. Results The maximal coherence and its frequency were significantly higher in ET relatives than in controls during the pinch grip task and during slow hand movements. Electromyography amplitude (root-mean-square) was slightly but significantly greater in ET relatives, whereas 2-Hz to 40-Hz power and spectral peak frequency were notBackground Essential tremor (ET) follows an autosomal dominant type of inheritance in the majority of patients, yet its genetic basis has not been identified. Its exact origin is still elusive, but coherence measurements between electromyography tremor bursts and electroencephalography unequivocally demonstrate a correlation. Methods We tested these measurements in 37 healthy first-degree relatives (children) of patients with essential tremor (ET) and a group of 37 age-matched and sex-matched controls. Pooled coherence spectra of the maximally coherent electroencephalogram electrodes were computed for ET relatives and controls. Results The maximal coherence and its frequency were significantly higher in ET relatives than in controls during the pinch grip task and during slow hand movements. Electromyography amplitude (root-mean-square) was slightly but significantly greater in ET relatives, whereas 2-Hz to 40-Hz power and spectral peak frequency were not different. Conclusions The presymptomatic alteration in corticomuscular interaction may reflect a role of genetic factors.show moreshow less

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Metadaten
Author:Jan Raethjen, Muthuraman MuthuramanORCiDGND, Achim Kostka, Martin Nahrwold, Helge Hellriegel, Delia Lorenz, Günther Deuschl
URN:urn:nbn:de:bvb:384-opus4-1103413
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/110341
ISSN:0885-3185OPAC
ISSN:1531-8257OPAC
Parent Title (English):Movement Disorders
Publisher:Wiley
Place of publication:Weinheim
Type:Article
Language:English
Year of first Publication:2013
Publishing Institution:Universität Augsburg
Release Date:2023/12/20
Tag:Neurology (clinical); Neurology
Volume:28
Issue:5
First Page:679
Last Page:682
DOI:https://doi.org/10.1002/mds.25425
Institutes:Fakultät für Angewandte Informatik
Fakultät für Angewandte Informatik / Institut für Informatik
Fakultät für Angewandte Informatik / Institut für Informatik / Professur für Informatik in der Medizintechnik
Dewey Decimal Classification:0 Informatik, Informationswissenschaft, allgemeine Werke / 00 Informatik, Wissen, Systeme / 004 Datenverarbeitung; Informatik
Licence (German):Deutsches Urheberrecht