双相情感障碍躁狂和抑郁期的前庭生物标志物

A. Soza, S. Barroilhet, P. Vohringer
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引用次数: 1

摘要

背景和目的:双相情感障碍(BD)是一种以情绪在低活跃、悲观(抑郁期)和多活跃、乐观(躁狂/轻躁期)之间循环变化为特征的神经精神障碍。先前对重度抑郁症患者的研究表明,与左侧相比,右侧前庭系统(内耳平衡系统)的活跃程度较低。这表明情绪与前庭活动异常侧化之间存在关系。本探索性研究分析了双相障碍患者和健康对照者在不同情绪期的左右前庭活动。设计:横断面研究。方法:我们将研究和比较符合抑郁、躁狂/轻躁狂、心境愉悦和健康对照(每组6例)不同情绪期选择标准的BD I或II患者前庭活动的偏侧性。结果测量:对于前庭评估,我们将使用旋转椅技术和眼震电图。主要的结果测量是旋转前后的不对称性。次要观察指标是眼球震颤的慢相速度、眼球震颤的节律性和眼球慢追踪的类型。讨论:本研究探讨了情绪状态与双相障碍患者前庭活动左右侧偏异常之间的关系。伦理与传播:本研究方案于2016年6月21日在智利圣地亚哥获得了东方大都会医疗服务中心伦理委员会的批准。受试者在参加试验前应提供书面知情同意书。试验注册:ClinicalTrials.gov识别码:NCT02827045,于2016年7月6日注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A vestibular biomarker of manic and depressive phase in bipolar disorder
Background and objectives: Bipolar disorder (BD) is a neuropsychiatric disorder characterized by cyclic changes in mood between hypoactive, pessimistic (depressive phase) and hyperactive, optimistic (manic/hypomanic phase). Prior studies in major depression patients show that the right side of the vestibular system (inner ear's equilibrium system) is less active compared to the left. It suggests a relationship between mood and abnormal lateralization of the vestibular activity. This exploratory investigation analyzes the right and left vestibular activity in different mood phases of BD and healthy controls. Design: A transversal cross-sectional study. Methods: We will study and compare the lateralization of the vestibular activity of BD I or II patients, who match the selection criteria for different mood phases: depression, mania/hypomania, euthymia and healthy controls (6 patients each group). Outcome measures: For vestibular evaluation, we will use rotary chair technique and electronystagmography. The primary outcome measure is the per- and post-rotatory asymmetry. The secondary outcome measures are the slow phase velocity of the nystagmus, the rhythmicity of nystagmus, and the type of slow ocular tracking. Discussion: This study addresses the relationship between mood states and abnormal right-left side lateralization of the vestibular activity in BD patients. Ethics and dissemination: The study protocol was approved by the ethics committee of Servicio de Salud Metropolitano Oriente, in Santiago, Chile on June 21st, 2016. Participants will provide written informed consent prior to participation in the trial. Trial registration: ClinicalTrials.gov identifier: NCT02827045 on July 6th, 2016.
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