Mapping Cortical Anatomical and Electrophysiological Abnormalities in Human MTLE

绘制人类 MTLE 的皮质解剖学和电生理学异常

基本信息

  • 批准号:
    8108991
  • 负责人:
  • 金额:
    $ 33.69万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2011
  • 资助国家:
    美国
  • 起止时间:
    2011-02-01 至 2016-01-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): The NINDS and several epilepsy organizations have established benchmarks that emphasize the need to develop new therapeutic strategies and optimize current approaches to treat and cure epilepsy. Mesial temporal lobe epilepsy (MTLE) with hippocampal sclerosis (HS) is the most common type of pharmacoresistant epilepsy. Patients with this type of epilepsy are often treated surgically, but surgical outcome studies indicate too many patients continue to have postoperative seizures. Surgical resection is based on determining the epileptogenic zone (EZ), i.e. the brain areas necessary and sufficient for generating spontaneous seizures, and surgical failure is believed to result from an incomplete resection of the EZ. The fundamental challenge in defining the EZ is that it can not be measured directly, but is inferred from diagnostic tests, most important of which is localization of sites of ictal onset and early propagation and the presence of an epileptogenic lesion. Our recent work using advanced structural imaging in patients with MTLE found specific spatial patterns and levels of hippocampal atrophy that were associated with different types of ictal onset. These data indicate there could be several types of MTLE with HS and each associated with specific anatomical abnormalities, ictal and interictal electrophysiological disturbances and clinical features. If this hypothesis is correct, then a combination of these measures of epileptogenicity could define the EZ and provide important information on prognosis for a seizure-free surgical outcome. The proposed studies will use structural imaging and functional measures in an attempt to accurately delineate the EZ in patients with MTLE. Specifically, first, we will quantitatively evaluate the spatial patterns and levels of hippocampal and neocortical gray matter atrophy in patients with different types of depth electrode-recorded ictal onsets and clinical features. Second, we will characterize pathological high frequency oscillations (pHFOs) and localize their sites of generation in hippocampal and neocortical networks that include areas of ictal onset and early propagation and remote areas. Studies by us and others suggest pHFOs represent fundamental neuronal disturbances responsible for spontaneous seizure genesis, and because these abnormal events occur during interictal as well as during ictal periods, recording pHFOs will allow us to identify areas of epileptogenicity more rapidly than capturing seizures. And third, we will determine whether a combination of these measures of epileptogenicity accurately defines the EZ by correlating their removal with seizure-free surgical outcomes. We anticipate completion of these specific aims will develop safer, more accurate and less expensive approaches to defining the EZ and increase the likelihood for postoperative seizure freedom. In addition, we expect that the results of the proposed studies will provide valuable insights into the fundamental neuronal basis of the EZ in MTLE. PUBLIC HEALTH RELEVANCE: Individuals with poorly controlled epilepsy, as well as their families and communities, sustain considerable physical, social and economic costs. This study is designed to identify specific anatomical and electrophysiological disturbances that define the brain areas capable of generating spontaneous seizures in order to more clearly understand mechanisms of seizure genesis, improve surgical treatment and develop new therapies to eliminate seizures and the burden of epilepsy.
描述(由申请人提供):NINDS和几个癫痫组织已经建立了基准,强调需要开发新的治疗策略,并优化目前治疗和治愈癫痫的方法。内侧颞叶癫痫(MTLE)伴海马硬化(HS)是最常见的耐药性癫痫类型。这种类型的癫痫患者通常通过手术治疗,但手术结果研究表明,太多的患者继续术后癫痫发作。手术切除是基于确定致痫区(EZ),即产生自发性癫痫发作所必需和足够的大脑区域,手术失败被认为是由于不完全切除EZ。定义EZ的根本挑战是它不能直接测量,而是从诊断测试中推断出来,其中最重要的是定位发作和早期传播的部位以及致痫性病变的存在。我们最近的工作使用先进的结构成像在MTLE患者中发现特定的空间模式和海马萎缩水平与不同类型的发作发作相关。这些数据表明,可能有几种类型的MTLE与HS,每一个与特定的解剖异常,发作和发作间期电生理紊乱和临床特征。如果这一假设是正确的,那么这些致痫性的措施的组合可以定义EZ,并提供重要的信息预后无癫痫的手术结果。拟议的研究将使用结构成像和功能测量,试图准确描绘MTLE患者的EZ。具体来说,首先,我们将定量评估不同类型的深度电极记录的发作和临床特征的患者海马和新皮质灰质萎缩的空间模式和水平。其次,我们将描述病理性高频振荡(pHFOs)和本地化的网站在海马和新皮层网络,包括发作和早期传播和偏远地区的发电。我们和其他人的研究表明,pHFO代表了自发性癫痫发作发生的基本神经元紊乱,因为这些异常事件发生在发作间期和发作期间,记录pHFO将使我们能够比捕获癫痫发作更快地识别致癫痫区域。第三,我们将确定这些致痫性指标的组合是否通过将其去除与无癫痫手术结果相关联来准确定义EZ。我们预计这些特定目标的完成将开发更安全,更准确,更便宜的方法来定义EZ,并增加术后癫痫发作的可能性。此外,我们预计,拟议的研究结果将提供有价值的见解的基本神经元基础的EZ在MTLE。 公共卫生相关性:癫痫控制不佳的个人及其家庭和社区承受着相当大的身体、社会和经济成本。本研究旨在确定能够产生自发性癫痫发作的脑区的特定解剖学和电生理学紊乱,以便更清楚地了解癫痫发作的发生机制,改善手术治疗并开发新的治疗方法以消除癫痫发作和癫痫负担。

项目成果

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Richard Staba其他文献

Richard Staba的其他文献

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{{ truncateString('Richard Staba', 18)}}的其他基金

Defining the Epileptogenic Network and Identifying which Components Generate Seizures
定义癫痫发作网络并确定哪些成分会导致癫痫发作
  • 批准号:
    10201767
  • 财政年份:
    2018
  • 资助金额:
    $ 33.69万
  • 项目类别:
Defining the Epileptogenic Network and Identifying which Components Generate Seizures
定义癫痫发作网络并确定哪些成分会导致癫痫发作
  • 批准号:
    9792287
  • 财政年份:
    2018
  • 资助金额:
    $ 33.69万
  • 项目类别:
Defining the Epileptogenic Network and Identifying which Components Generate Seizures
定义癫痫发作网络并确定哪些成分会导致癫痫发作
  • 批准号:
    10401487
  • 财政年份:
    2018
  • 资助金额:
    $ 33.69万
  • 项目类别:
Mapping Cortical Anatomical and Electrophysiological Abnormalities in Human MTLE
绘制人类 MTLE 的皮质解剖学和电生理学异常
  • 批准号:
    8417846
  • 财政年份:
    2011
  • 资助金额:
    $ 33.69万
  • 项目类别:
Mapping Cortical Anatomical and Electrophysiological Abnormalities in Human MTLE
绘制人类 MTLE 的皮质解剖学和电生理学异常
  • 批准号:
    8217082
  • 财政年份:
    2011
  • 资助金额:
    $ 33.69万
  • 项目类别:
Mapping Cortical Anatomical and Electrophysiological Abnormalities in Human MTLE
绘制人类 MTLE 的皮质解剖学和电生理学异常
  • 批准号:
    8606662
  • 财政年份:
    2011
  • 资助金额:
    $ 33.69万
  • 项目类别:

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