权益分类	功能权益	普通用户	{{item.name}}会员
{{category.name}}	{{benefitItem.name}}

Electrical impedance myography and quantitative ultrasound in Duchenne muscular d

电阻抗肌电图和定量超声在杜兴肌病中的应用

基本信息

批准号：
8718768
负责人：
BASIL T DARRAS
金额：
$ 40.4万
依托单位：
BETH ISRAEL DEACONESS MEDICAL CENTER
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：
2011-09-17 至 2016-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8718768
关键词：
12 year old Acoustics Address Affect Age Back Binding Biological Markers Birth Calibration Cessation of life Child Childhood Clinical Trials Data Data Set Deterioration Development Devices Disease Disease Progression Duchenne muscular dystrophy Electrodes Enrollment Evaluation Fibrosis Foundations Frequencies Future Goals Gray unit of radiation dose Health Hour Human Resources Image Analysis Individual Infiltration Lead Left Life Lower Extremity Magnetic Resonance Imaging Measurement Measures Methodology Methods Modality Moods Muscle Muscle Weakness Muscular Dystrophies Myography Myopathy Neuromuscular Diseases Outcome Outcome Measure Painless Pathogenesis Pathology Patients Pattern Pharmaceutical Preparations Phase Phase II Clinical Trials Phase III Clinical Trials Physiological Process Role Severity of illness Speed Staging Surface Surrogate Markers Techniques Testing Therapeutic Time Training Ultrasonography Upper Extremity Variant Visit Walking Wheelchairs Work age group aged base boys clinically significant cost effective disability effective therapy electric impedance exon skipping functional status improved innovation male neuromuscular novel quantitative ultrasound standard measure stem cell therapy time interval treatment effect treatment strategy voltage

项目摘要

DESCRIPTION (provided by applicant): Duchenne muscular dystrophy (DMD) is one of the most common neuromuscular diseases of children affecting approximately 1 in 3500 live male births, producing progressive muscle weakness and leaving affected individuals wheelchair bound by approximately 12 years of age with death occurring by the third decade of life. Over the past 20 years great inroads have been made into understanding the basic mechanisms underlying disease pathogenesis and many new potential therapeutic strategies have been developed, ranging from exon-skipping methodologies to stem cell therapies. This expanding range of disease treatment options has also greatly increased the need for improved methods to speed the assessment of promising drugs in Phase II and Phase III clinical trials. The current biomarkers that are employed, such as the 6-minute walk test, are relatively insensitive to change and require clinical trials to enroll large numbers of subjects while still being powered to detect an often overly optimistic treatment effect. Two highly innovative, easily applied, office-based, painless methodologies that offer great promise in serving as novel, sensitive markers of disease progression, are electrical impedance myography (EIM) and quantitative ultrasound (QUS). In EIM, a weak, high-frequency electrical current is applied via surface electrodes and alterations in the consequent surface voltage pattern are measured. In QUS, ultrasound images obtained using standard devices are distilled down to numerical data that can be used to quantify disease severity. This can be accomplished either via post-processing image analysis with use of a phantom for calibration or via a reduction of the raw backscattered acoustic data. In this proposed work, we will study both EIM and QUS independently to assess their potential use in DMD trials. Specifically we will do this by studying a group of 35 normal subjects and 35 boys with DMD aged 5 to 12 years followed for a 2-year period of time. In Specific Aim 1, we will establish the repeatability of both techniques both immediately and over several days time. In Specific Aim 2, we will assess the clinical significance of alterations in both EIM and QUS over time by comparing their rate of progression to that seen with functional measures out to two years. In Specific Aim 3, we will assess the ability of both measures to detect disease progression over very short periods of time-1 to 2 months-and how well that rate of progression predicts long-term functional change. As part of our planned exploratory analyses, we will also assess approaches for fusing EIM and QUS data sets into single composite biomarkers and the potential value of following contraction-induced alterations in the EIM data over time. With the successful completion of this work, we will have set the stage for the use of one or both of these techniques as the preferred biomarkers in Phase II clinical trials in DMD.

描述（由申请人提供）：杜氏肌营养不良症（DMD）是儿童最常见的神经肌肉疾病之一，影响约1/3500活产男婴，产生进行性肌无力，并使受影响的个体在约12岁时轮椅受限，在30岁时死亡。在过去的20年里，人们对疾病发病机制的理解取得了很大的进展，并开发了许多新的潜在治疗策略，从外显子跳跃方法到干细胞治疗。疾病治疗选择范围的扩大也大大增加了对改进方法的需求，以加快II期和III期临床试验中有前途药物的评估。目前使用的生物标志物，如6分钟步行试验，对变化相对不敏感，需要临床试验招募大量受试者，同时仍有能力检测通常过于乐观的治疗效果。两种高度创新，易于应用，基于办公室的无痛方法，提供了很大的希望，作为新的，敏感的疾病进展的标志物，是电阻抗肌电图（EIM）和定量超声（QUS）。在EIM中，通过表面电极施加微弱的高频电流，并测量随之产生的表面电压模式的变化。在QUS中，使用标准设备获得的超声图像被提炼为可用于量化疾病严重程度的数字数据。这可以通过使用用于校准的体模的后处理图像分析或通过减少原始后向散射声学数据来实现。在这项拟议的工作中，我们将独立研究EIM和QUS，以评估它们在DMD试验中的潜在用途。具体来说，我们将通过研究一组35名正常受试者和35名年龄在5至12岁的DMD男孩进行为期2年的研究。在具体目标1中，我们将立即和几天内确定两种技术的重复性。在特定目标2中，我们将通过比较EIM和QUS随时间变化的进展率与功能指标在2年内观察到的进展率，评估EIM和QUS随时间变化的临床意义。在具体目标3中，我们将评估这两种方法在非常短的时间内（1至2个月）检测疾病进展的能力，以及进展速度预测长期功能变化的能力。作为我们计划的探索性分析的一部分，我们还将评估将EIM和QUS数据集融合为单一复合生物标志物的方法，以及EIM数据随时间推移发生收缩诱导变化的潜在价值。随着这项工作的成功完成，我们将为使用这些技术中的一种或两种作为DMD II期临床试验的首选生物标志物奠定基础。

项目成果

期刊论文数量（7）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Electrical impedance myography for assessment of Duchenne muscular dystrophy.

DOI：
10.1002/ana.24874
发表时间：
2017-05
期刊：
Annals of neurology
影响因子：
11.2
作者：
Rutkove SB;Kapur K;Zaidman CM;Wu JS;Pasternak A;Madabusi L;Yim S;Pacheck A;Szelag H;Harrington T;Darras BT
通讯作者：
Darras BT

Minimal training is required to reliably perform quantitative ultrasound of muscle.

DOI：
10.1002/mus.24117
发表时间：
2014-07
期刊：
MUSCLE & NERVE
影响因子：
3.4
作者：
Zaidman, Craig M.;Wu, Jim S.;Wilder, Sarah;Darras, Basil T.;Rutkove, Seward B.
通讯作者：
Rutkove, Seward B.

Inter-session reliability of electrical impedance myography in children in a clinical trial setting.

DOI：
10.1016/j.clinph.2014.11.017
发表时间：
2015-09
期刊：
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
影响因子：
0
作者：
Geisbush TR;Visyak N;Madabusi L;Rutkove SB;Darras BT
通讯作者：
Darras BT

Quantitative muscle ultrasound detects disease progression in Duchenne muscular dystrophy.

DOI：
10.1002/ana.24904
发表时间：
2017-05
期刊：
Annals of neurology
影响因子：
11.2
作者：
Zaidman CM;Wu JS;Kapur K;Pasternak A;Madabusi L;Yim S;Pacheck A;Szelag H;Harrington T;Darras BT;Rutkove SB
通讯作者：
Rutkove SB

Force-controlled ultrasound to measure passive mechanical properties of muscle in Duchenne muscular dystrophy.

力控超声测量杜氏肌营养不良症患者肌肉的被动机械特性。