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DOI 10.1523/jneurosci.0770-12.2012

Медицинская библиотека · The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012

A pathway in the brainstem for roll-tilt of the subjective visual vertical: evidence from a lesion-behavior mapping study.

Baier Bernhard, Thömke Frank, Wilting Janine, Heinze Caroline, Geber Christian, Dieterich Marianne

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The perceived subjective visual vertical (SVV) is an important sign of a vestibular otolith tone imbalance in the roll plane. Previous studies suggested that unilateral pontomedullary brainstem lesions cause ipsiversive roll-tilt of SVV, whereas pontomesencephalic lesions cause contraversive roll-tilts of SVV. However, previous data were of limited quality and lacked a statistical approach. We therefore tested roll-tilt of the SVV in 79 human patients with acute unilateral brainstem lesions due to stroke by applying modern statistical lesion-behavior mapping analysis. Roll-tilt of the SVV was verified to be a brainstem sign, and for the first time it was confirmed statistically that lesions of the medial longitudinal fasciculus (MLF) and the medial vestibular nucleus are associated with ipsiversive tilt of the SVV, whereas contraversive tilts are associated with lesions affecting the rostral interstitial nucleus of the MLF, the superior cerebellar peduncle, the oculomotor nucleus, and the interstitial nucleus of Cajal. Thus, these structures constitute the anatomical pathway in the brainstem for verticality perception. Present data indicate that graviceptive otolith signals present a predominant role in the multisensory system of verticality perception.

Для цитирования: Baier Bernhard, Thömke Frank, Wilting Janine, Heinze Caroline, Geber Christian, Dieterich Marianne. A pathway in the brainstem for roll-tilt of the subjective visual vertical: evidence from a lesion-behavior mapping study.. The Journal of neuroscience : the official journal of the Society for Neuroscience. 2012. DOI: 10.1523/jneurosci.0770-12.2012.

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