嗅觉作为肌张力障碍的标志物:背景、现状与方向

Olfaction as a Marker for Dystonia: Background, Current State and Directions.

作者信息

Herr Thorsten, Gamain Julie, Fleischmann Robert, Lehnert Bernhard, Vollmer Marcus, Willert Carsten, Veit Birgitt, Stenner Andrea, Mueller Jan-Uwe, Caspers Barbara, Kronenbuerger Martin

机构信息

Department of Neurology, University Medicine Greifswald, Fleischmannstraße 8, 17475 Greifswald, Germany.

Department of Otorhinolaryngology, University Medicine Greifswald, Fleischmannstraße 8, 17475 Greifswald, Germany.

出版信息

Brain Sci. 2020 Oct 13;10(10):727. doi: 10.3390/brainsci10100727.

Abstract

Dystonia is a heterogeneous group of hyperkinetic movement disorders. The unifying descriptor of dystonia is the motor manifestation, characterized by continuous or intermittent contractions of muscles that cause abnormal movements and postures. Additionally, there are psychiatric, cognitive, and sensory alterations that are possible or putative non-motor manifestations of dystonia. The pathophysiology of dystonia is incompletely understood. A better understanding of dystonia pathophysiology is highly relevant in the amelioration of significant disability associated with motor and non-motor manifestations of dystonia. Recently, diminished olfaction was found to be a potential non-motor manifestation that may worsen the situation of subjects with dystonia. Yet, this finding may also shed light into dystonia pathophysiology and yield novel treatment options. This article aims to provide background information on dystonia and the current understanding of its pathophysiology, including the key structures involved, namely, the basal ganglia, cerebellum, and sensorimotor cortex. Additionally, involvement of these structures in the chemical senses are reviewed to provide an overview on how olfactory (and gustatory) deficits may occur in dystonia. Finally, we describe the present findings on altered chemical senses in dystonia and discuss directions of research on olfactory dysfunction as a marker in dystonia.

摘要

肌张力障碍是一组异质性的运动亢进性运动障碍。肌张力障碍的统一特征是运动表现,其特点是肌肉持续或间歇性收缩,导致异常运动和姿势。此外,还存在精神、认知和感觉改变,这些可能是肌张力障碍的潜在非运动表现。肌张力障碍的病理生理学尚未完全明确。更好地理解肌张力障碍的病理生理学对于改善与肌张力障碍的运动和非运动表现相关的严重残疾至关重要。最近,嗅觉减退被发现是一种潜在的非运动表现,可能会使肌张力障碍患者的情况恶化。然而,这一发现也可能为肌张力障碍的病理生理学提供线索,并产生新的治疗选择。本文旨在提供有关肌张力障碍的背景信息及其病理生理学的当前认识,包括涉及的关键结构,即基底神经节、小脑和感觉运动皮层。此外,还综述了这些结构在化学感觉中的参与情况,以概述肌张力障碍中嗅觉(和味觉)缺陷可能如何发生。最后,我们描述了肌张力障碍中化学感觉改变的当前发现,并讨论了将嗅觉功能障碍作为肌张力障碍标志物的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6462/7601998/2425b9147a10/brainsci-10-00727-g001.jpg

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