Pathophysiology of Spasmodic Dysphonia: a TMS study

痉挛性发声障碍的病理生理学:一项 TMS 研究

基本信息

  • 批准号:
    8443814
  • 负责人:
  • 金额:
    $ 17.56万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2012
  • 资助国家:
    美国
  • 起止时间:
    2012-04-01 至 2016-03-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): One of the most meaningful aspects to human life is communication. The primary method of communication in humans is voice, thus impairment of the voice can have a devastating consequences in one's ability to fully participate in society. Adductor spasmodic Dysphonia (AdSD) is a type of focal dystonia that affects the muscles of the vocal cords and can severely impair the ability to speak. There is no diagnostic marker for this neurologic-based movement disorder and it is frequently confused with other voice disorders. Often people go years before being correctly diagnosed, only to learn that there are no long-term efficacious treatments available. Misdiagnosis of AdSD leads to provision of ineffective treatment such as voice therapy prolonging this debilitating communication disorder and resulting in unnecessary health care expenses. There is growing evidence that people with other types of focal dystonia have reduced cortical inhibition, leading to excessive excitation, which may contribute to the resultant abnormal motor control. Transcranial magnetic stimulation (TMS) is a safe, non-invasive tool that can provide extensive information about the neurophysiologic underpinnings in a disorder. This has been used extensively to investigate focal hand dystonia, greatly enhancing the understanding of that disorder, but has not been used in spasmodic dysphonia. This R21 proposal in response to PA 10-156 will use fine wire EMG electrodes in the muscle primarily affected by SD, the thyroarytenoid, and TMS to measure the central conduction latency and intracortical excitation and inhibition associated with the corticobulbar control of the larynx in healthy people and people with SD. It will also use well established techniques to collect the same data in the unaffected corticospinal control of the hand. Design: Two group comparison (healthy vs. AdSD) of the cortical excitability of the thyroarytenoid muscle and first dorsal interosseous muscle will be performed. Expected outcomes: It will refine techniques described in the preliminary data section to optimize procedures for TMS measurement in the larynx; begin to establish norms for the excitability measures in healthy people; determine the relationship of measures in the hand to the larynex; and compare data in subjects with SD to healthy. Impact: The results of this study will: (1) advance the knowledge regarding the central nervous system pathophysiology in AdDS, (2) elucidate potential neurophysiologic underpinnings of the disorder such as which intracortical mechanism differs from healthy and if it is localized to the affected musculature or pervasive. (3) It will refine techniques for other investigations of excitability in the larynx. Long term objecties: Future work may lead to a more definitive differential diagnosis between AdSD and other disorders and the development of innovative evidence-based interventions directly advancing the mission of NIDCD.
描述(由申请人提供):人类生活中最有意义的方面之一就是沟通。人类交流的主要方法是声音,因此,声音损害会对一个人充分参与社会的能力产生毁灭性的后果。加入器痉挛性吞咽困难(ADSD)是一种局灶性肌张力障碍,会影响声带的肌肉,并可能严重损害说话能力。这种基于神经系统的运动障碍没有诊断标记,并且经常与其他语音疾病混淆。人们经常在正确诊断之前去几年,只是得知没有长期有效的治疗方法。 ADSD的误诊导致提供无效的治疗方法,例如语音疗法延长这种使人衰弱的通信障碍,并导致不必要的医疗保健费用。越来越多的证据表明,患有其他类型的局灶性肌张力障碍的人会降低皮质抑制,从而导致过度兴奋,这可能导致导致的异常运动控制。经颅磁刺激(TMS)是一种安全的,无创的工具,可以提供有关疾病中神经生理基础的广泛信息。这已被广泛用于研究局灶性手部肌张力障碍,大大增强了对该疾病的理解,但尚未用于痉挛性吞咽困难。对PA 10-156响应的R21提案将在主要受SD,甲状腺毒素和TMS影响的肌肉中使用细线EMG电极,以测量与健康人员和SD患者的larynx的Corticobulbar对照相关的中心传导潜伏期和心脏内抑制和抑制作用。它也会很好 建立的技术在手的未受影响的皮质脊髓控制中收集相同的数据。设计:将进行两组比较(健康与ADSD)的甲状腺素肌肉和第一背侧骨间肌的皮质兴奋性。预期结果:它将完善在初步数据部分中描述的技术,以优化喉中的TMS测量程序;开始建立健康人的兴奋性措施的规范;确定手中的措施与喉部的关系;并将SD受试者的数据与健康的受试者进行比较。影响:这项研究的结果将:(1)促进有关中枢神经系统病理生理学的知识,(2)阐明该疾病的潜在神经生理基础,例如这种内部机制与健康的机制不同,并且如果将其定位于受影响的肌肉或普遍性或普遍性。 (3) 它将完善喉中的其他兴奋性研究的技术。长期对象:未来的工作可能会导致ADSD和其他疾病之间的更确定的差异诊断,并发展创新的基于证据的干预措施,直接推进了NIDCD的使命。

项目成果

期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Evaluation of the Cortical Silent Period of the Laryngeal Motor Cortex in Healthy Individuals.
  • DOI:
    10.3389/fnins.2017.00088
  • 发表时间:
    2017
  • 期刊:
  • 影响因子:
    4.3
  • 作者:
    Chen M;Summers RL;Goding GS;Samargia S;Ludlow CL;Prudente CN;Kimberley TJ
  • 通讯作者:
    Kimberley TJ
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Teresa Jacobson Kimberley其他文献

Teresa Jacobson Kimberley的其他文献

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{{ truncateString('Teresa Jacobson Kimberley', 18)}}的其他基金

The effects of neural modulation on phonatory function in laryngeal dystonia
神经调节对喉肌张力障碍发声功能的影响
  • 批准号:
    10578816
  • 财政年份:
    2021
  • 资助金额:
    $ 17.56万
  • 项目类别:
DYT1 Genotype- and Phenotype-Specific Brain Circuits in Dystonia
肌张力障碍中 DYT1 基因型和表型特异性脑回路
  • 批准号:
    10303426
  • 财政年份:
    2021
  • 资助金额:
    $ 17.56万
  • 项目类别:
The effects of neural modulation on phonatory function in laryngeal dystonia
神经调节对喉肌张力障碍发声功能的影响
  • 批准号:
    10347323
  • 财政年份:
    2021
  • 资助金额:
    $ 17.56万
  • 项目类别:
A Multimodal Assessment of Neurophysiology in Focal Dystonia
局灶性肌张力障碍神经生理学的多模式评估
  • 批准号:
    9239016
  • 财政年份:
    2017
  • 资助金额:
    $ 17.56万
  • 项目类别:
A Multimodal Assessment of Neurophysiology in Focal Dystonia
局灶性肌张力障碍神经生理学的多模式评估
  • 批准号:
    9564458
  • 财政年份:
    2017
  • 资助金额:
    $ 17.56万
  • 项目类别:
Pathophysiology of Spasmodic Dysphonia: a TMS study
痉挛性发声障碍的病理生理学:一项 TMS 研究
  • 批准号:
    8281729
  • 财政年份:
    2012
  • 资助金额:
    $ 17.56万
  • 项目类别:
INTEGRATION OF NEUROIMAGING AND BIOMECHANICS OF LOW BACK PAIN
腰痛的神经影像学和生物力学的整合
  • 批准号:
    8362836
  • 财政年份:
    2011
  • 资助金额:
    $ 17.56万
  • 项目类别:
INTEGRATION OF NEUROIMAGING AND BIOMECHANICS OF LOW BACK PAIN
腰痛的神经影像学和生物力学的整合
  • 批准号:
    8170441
  • 财政年份:
    2010
  • 资助金额:
    $ 17.56万
  • 项目类别:
EFFECT OF AEROBIC EXERCISE ON BRAIN ACTIVITY FOLLOWING TRAUMATIC BRAIN INJURY
有氧运动对脑外伤后大脑活动的影响
  • 批准号:
    7954954
  • 财政年份:
    2009
  • 资助金额:
    $ 17.56万
  • 项目类别:
INTEGRATION OF NEUROIMAGING AND BIOMECHANICS OF LOW BACK PAIN
腰痛的神经影像学和生物力学的整合
  • 批准号:
    7954975
  • 财政年份:
    2009
  • 资助金额:
    $ 17.56万
  • 项目类别:

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