Characterization of involuntary spontaneous focal muscle activity by means of motion-sensitive magnetic resonance imaging and automated post-processing of data

通过运动敏感磁共振成像和数据自动后处理来表征非自愿自发局灶性肌肉活动

基本信息

项目摘要

In single images of series of diffusion-sensitive single-shot magnetic resonance images of resting skeletal muscles, distinct regionally limited signal voids often occur even in healthy subjects. These signal voids show different geometry and localization in the course of a series of measurements, with some muscle groups being affected more frequently than others. The signal voids show a high correlation to weak electrical activities in the simultaneously derived surface electromyography (sEMG). Short involuntary focal contractions, which microscopically do not affect all muscle fibers equally and thus lead to incoherent movement patterns, are assumed to be the cause of the signal voids. The relative movements on the microscopic scale induce a dephasing of the signal components of the pixels (like real diffusion movements) and lead to the observed signal voids in diffusion-sensitive images. The pattern of signal voids indicates spontaneous activities with individual activations of motor neurons. This research project aims to further characterize the phenomenon of spontaneous muscle activity, based on the findings of the funded initial DFG proposal, in different age and gender groups of healthy volunteers and in specific patient groups. A parallel application of surface electromyographic (sEMG) methods and sEMG triggering of the acquisition of MRI images will be used to characterize more precisely the course of the mechanical reaction, which is delayed compared to the electrical activity. Furthermore, the value of the new method will be investigated by comparing it with clinically established diagnostic procedures. In neurological diagnostics for the investigation of spontaneous muscular movements (fasciculations), sonographic methods, which are sometimes difficult to detect deeper muscle layers, as well as electromyographic examinations with needle electrodes are available. Although the latter method is somewhat invasive, it can reveal specific changes in motor neuron diseases. In the first phase of the project, MRI sequences and evaluation procedures will be adapted and optimized for applications in muscle areas that are relevant for neuromuscular diseases. A further development of the combined sEMG-MRI investigation with regard to the robustness of the detection algorithms for prospective images will provide a detailed insight into the interrelationships of electrical and mechanical activities. In the second phase of the project, systematic investigations with different clinically established methods (muscle sonography and needle electromyography) will be performed on healthy volunteers and specific patient groups. This will allow a better classification of the results of the MRI method by evaluation of its strengths and weaknesses compared to established procedures.
在静息骨骼肌的一系列扩散敏感单次磁共振图像的单幅图像中,即使在健康受试者中也经常出现明显的区域有限信号空洞。这些信号空洞在一系列测量过程中显示出不同的几何形状和定位,一些肌肉群比其他肌肉群更容易受到影响。信号空洞与同时导出的表面肌电图 (sEMG) 中的弱电活动显示出高度相关性。短暂的不自主局灶收缩在微观上不会平等地影响所有肌纤维,从而导致不连贯的运动模式,被认为是信号空白的原因。微观尺度上的相对运动会引起像素信号分量的相移(如真实的扩散运动),并导致在扩散敏感图像中观察到信号空白。信号空白的模式表明运动神经元个体激活的自发活动。该研究项目旨在根据资助的最初 DFG 提案的研究结果,进一步描述不同年龄和性别的健康志愿者以及特定患者群体的自发肌肉活动现象。表面肌电图 (sEMG) 方法和 MRI 图像采集的 sEMG 触发的并行应用将用于更精确地表征机械反应的过程,与电活动相比,机械反应是延迟的。此外,将通过与临床建立的诊断程序进行比较来研究新方法的价值。在用于研究自发肌肉运动(肌束颤动)的神经学诊断中,可以使用有时难以检测更深肌肉层的超声检查方法以及使用针电极的肌电图检查。虽然后一种方法具有一定的侵入性,但它可以揭示运动神经元疾病的具体变化。在该项目的第一阶段,将调整和优化 MRI 序列和评估程序,以适应与神经肌肉疾病相关的肌肉区域的应用。在前瞻性图像检测算法的鲁棒性方面,sEMG-MRI 联合研究的进一步发展将提供对电气和机械活动相互关系的详细了解。在该项目的第二阶段,将使用不同的临床既定方法(肌肉超声检查和针肌电图)对健康志愿者和特定患者群体进行系统研究。与既定程序相比,这将通过评估 MRI 方法的优缺点来更好地对 MRI 方法的结果进行分类。

项目成果

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Professor Dr. Fritz Schick其他文献

Professor Dr. Fritz Schick的其他文献

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{{ truncateString('Professor Dr. Fritz Schick', 18)}}的其他基金

Precise volumetry of human adipose tissue compartments by combining automatic post-processing algorithms and optimized MRI acquisition techniques
通过结合自动后处理算法和优化的 MRI 采集技术,对人体脂肪组织区室进行精确体积测定
  • 批准号:
    192749169
  • 财政年份:
    2011
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Strategien zur selektiven Darstellung magnetisch markierter Zellen mittels MRT in verschiedenen Geweben.
使用 MRI 对各种组织中的磁性标记细胞进行选择性成像的策略。
  • 批准号:
    45994738
  • 财政年份:
    2007
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Körperfettkompartimente und assoziierte Stoffwechselaktivitäten - Verlauf während diätetischer und sportlicher Therapie - Erfassung von prädiktiven Fettverteilungsmustern
身体脂肪室和相关代谢活动 - 饮食和运动治疗期间的进展 - 记录预测性脂肪分布模式
  • 批准号:
    5400305
  • 财政年份:
    2003
  • 资助金额:
    --
  • 项目类别:
    Clinical Research Units

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低剂量氯胺酮治疗帕金森病的机制 [Raveena Parmar 的多样性补充]
  • 批准号:
    10740600
  • 财政年份:
    2023
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    --
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Threat assessment of the involuntary celibate (incel) online community: developing a structured professional judgement tool to identify incels at risk
非自愿独身者 (incel) 在线社区的威胁评估:开发结构化专业判断工具来识别面临风险的 incels
  • 批准号:
    2884204
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    2023
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    Studentship
Understanding the Role of a Novel Cell Type in Triggering Voluntary Saccades
了解新型细胞类型在触发自愿眼跳中的作用
  • 批准号:
    10832719
  • 财政年份:
    2023
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    --
  • 项目类别:
Improving pregnancy outcomes for women with intellectual and developmental disabilities in Medicaid
通过医疗补助改善智力和发育障碍女性的妊娠结局
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    10657110
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    2023
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    --
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Watching the mind travel: Understanding internal distraction from our own involuntary thoughts
观察心灵的旅行:了解我们自己不自觉的想法造成的内部干扰
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    ES/W007320/1
  • 财政年份:
    2023
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    --
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    Research Grant
Striatal Microcircuit Mechanisms of Tardive Dyskinesia
迟发性运动障碍的纹状体微电路机制
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    10634474
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    2023
  • 资助金额:
    --
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Multi-level factors affecting postpartum sterilization
影响产后绝育的多层次因素
  • 批准号:
    10792263
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    2023
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Examining racial disparities in fatal overdose, self-harm, and perpetrating assaults following law enforcement-mediated involuntary commitment
检查执法介导的非自愿承诺后致死过量、自残和实施攻击的种族差异
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    10638446
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Health equity in fertility specialty care among cancer survivors
癌症幸存者生育专科护理的健康公平
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    10561780
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    2023
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    --
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Molecular mechanisms of dystonia and spastic paraplegia associated with mutations in ATP5G3
与 ATP5G3 突变相关的肌张力障碍和痉挛性截瘫的分子机制
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