Cortical activation associated with asterixis in manifest hepatic encephalopathy

Authors

  • M. Butz,

    Corresponding author
    1. Medical Faculty, Institute of Clinical Neuroscience and Medical Psychology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
    2. Sobell Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, London, UK
    3. Centre for Cognitive Neuroimaging (CCNi), Institute of Neuroscience and Psychology, University of Glasgow, Glasgow, UK
    • M. Butz, Medical Faculty, Institute of Clinical Neuroscience and Medical Psychology, Heinrich Heine University Düsseldorf, Universitätsstrasse 1, D-40225 Düsseldorf, Germany

      Tel.: +49 211 81 18415

      Fax: +49 212 211 81 13015

      e-mail: markus.butz@hhu.de

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  • L. Timmermann,

    1. Department of Neurology, University of Cologne, Cologne, Germany
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  • J. Gross,

    1. Centre for Cognitive Neuroimaging (CCNi), Institute of Neuroscience and Psychology, University of Glasgow, Glasgow, UK
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  • B. Pollok,

    1. Medical Faculty, Institute of Clinical Neuroscience and Medical Psychology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
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  • M. Südmeyer,

    1. Medical Faculty, Institute of Clinical Neuroscience and Medical Psychology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
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  • G. Kircheis,

    1. Medical Faculty, Department of Gastroenterology, Hepatology and Infectiology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
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  • D. Häussinger,

    1. Medical Faculty, Department of Gastroenterology, Hepatology and Infectiology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
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  • A. Schnitzler

    1. Medical Faculty, Institute of Clinical Neuroscience and Medical Psychology, Heinrich Heine University Düsseldorf, Düsseldorf, Germany
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Abstract

Objectives

Severe hepatic encephalopathy gives rise to asterixis, a striking motor symptom also called flapping tremor, which is characterized by a sudden ceasing of muscle tone in all muscles of a limb. In this study, we aimed at scrutinizing the cortical activation associated with asterixis and unraveling the underlying pathophysiological mechanisms.

Material and methods

We recorded simultaneously neural activity with magnetoencephalography (MEG) and muscle activity with surface EMG in nine patients with manifest hepatic encephalopathy showing asterixis. Asterixis events were detected semiautomatically and served as triggers for averaging MEG signals. Evoked responses averaged time-locked to asterixis events were subjected to equivalent current dipole (ECD) modeling. Additionally, we localized the strongest cortico-muscular coherence in the frequency of the co-occurring tremulousness.

Results

Evoked fields averaged time-locked to asterixis events were best explained by a single dipolar source in the contralateral primary motor cortex (M1, Talairach coordinates of mean localization: −40, −20, and 64; Brodmann area 4). This dipole showed a twofold field reversal, that is biphasic wave, with frontal dipole orientation at 49 ms before flap onset and 99 ms after flap onset. Conversely, two maxima with occipital dipole orientation were observed 2 ms and 160 ms after flap onset. Cortico-muscular coherence for the tremulousness was likewise localized in the contralateral M1 confirming earlier findings in the present patient cohort.

Conclusions

Our results reveal an involvement of M1 in the generation of asterixis. As also tremulousness, also called mini-asterixis, was shown to originate in M1, asterixis and mini-asterixis may share common pathophysiological mechanisms.

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