• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肌萎缩侧索硬化症肌肉的磁共振成像

Magnetic resonance imaging of muscle in amyotrophic lateral sclerosis.

作者信息

Bryan W W, Reisch J S, McDonald G, Herbelin L L, Barohn R J, Fleckenstein J L

机构信息

Department of Neurology, The University of Texas Southwestern Medical Center at Dallas, 75235-8897, USA.

出版信息

Neurology. 1998 Jul;51(1):110-3. doi: 10.1212/wnl.51.1.110.

DOI:10.1212/wnl.51.1.110
PMID:9674787
Abstract

OBJECTIVE

To characterize leg muscle abnormalities in patients with ALS using MRI, and to correlate MRI with standard neurologic measures of motor neuron dysfunction.

METHODS

Eleven ALS patients were studied twice (once at baseline and again after 4 months) and compared with eight normal control subjects. MRI data of the lower extremities were compared with tibialis anterior compound muscle action potential amplitude (CMAPa) and foot dorsiflexion maximal voluntary isometric contraction (MVIC).

RESULTS

Muscle MRI was abnormal by visual inspection in six of 11 patients. The mean muscle T1 time and muscle volume were not different in patients compared with normal control subjects (p > 0.1). However, the mean T2 times were increased in the patients compared with normal control subjects (p = 0.009). T1 times did not correlate with CMAPa or MVIC. Muscle volume correlated with MVIC (r = 0.73 to 0.78, p < 0.02) but not with CMAPa (p > 0.05). There was a strong negative correlation (r < -0.8, p < or = 0.01) between muscle T2 time and MVIC and CMAPa. Also, the change in T2 relaxation time correlated with the change in CMAPa as the disease progressed (r = -0.63, p = 0.037).

CONCLUSION

Of the MRI characteristics studied, T2 relaxation time was the best indicator of motor neuron dysfunction and may have a role in objective evaluation of motor neuron dysfunction.

摘要

目的

利用磁共振成像(MRI)对肌萎缩侧索硬化症(ALS)患者的腿部肌肉异常进行特征描述,并将MRI与运动神经元功能障碍的标准神经学测量指标相关联。

方法

对11例ALS患者进行了两次研究(一次在基线时,另一次在4个月后),并与8名正常对照受试者进行比较。将下肢的MRI数据与胫前肌复合肌肉动作电位幅度(CMAPa)和足背屈最大自主等长收缩(MVIC)进行比较。

结果

11例患者中有6例经肉眼观察肌肉MRI异常。与正常对照受试者相比,患者的平均肌肉T1时间和肌肉体积无差异(p>0.1)。然而,与正常对照受试者相比,患者的平均T2时间增加(p = 0.009)。T1时间与CMAPa或MVIC无相关性。肌肉体积与MVIC相关(r = 0.73至0.78,p < 0.02),但与CMAPa无关(p>0.05)。肌肉T2时间与MVIC和CMAPa之间存在强烈的负相关(r < -0.8,p≤0.01)。此外,随着疾病进展,T2弛豫时间的变化与CMAPa的变化相关(r = -0.63,p = 0.037)。

结论

在所研究的MRI特征中,T2弛豫时间是运动神经元功能障碍的最佳指标,可能在运动神经元功能障碍的客观评估中发挥作用。

相似文献

1
Magnetic resonance imaging of muscle in amyotrophic lateral sclerosis.肌萎缩侧索硬化症肌肉的磁共振成像
Neurology. 1998 Jul;51(1):110-3. doi: 10.1212/wnl.51.1.110.
2
Use of electrophysiologic tests to measure disease progression in ALS therapeutic trials.在肌萎缩侧索硬化症治疗试验中使用电生理测试来测量疾病进展。
Muscle Nerve. 1990 Jun;13(6):471-9. doi: 10.1002/mus.880130602.
3
Relationships between motor-unit number estimates and isometric strength in distal muscles in ALS/MND.肌萎缩侧索硬化症/运动神经元病中远端肌肉运动单位数量估计值与等长肌力之间的关系。
J Neurol Sci. 1996 Aug;139 Suppl:38-42. doi: 10.1016/0022-510x(96)00074-3.
4
Functional significance of upper and lower motor neuron impairment in amyotrophic lateral sclerosis.肌萎缩侧索硬化症中上、下运动神经元损伤的功能意义
Muscle Nerve. 1998 Jun;21(6):762-8. doi: 10.1002/(sici)1097-4598(199806)21:6<762::aid-mus8>3.0.co;2-5.
5
Quantitating progression in ALS.量化肌萎缩侧索硬化症的病情进展。
Neurology. 2005 May 24;64(10):1783-5. doi: 10.1212/01.WNL.0000162036.76024.AB.
6
[An analysis of characteristics of nerve conduction in 154 cases of amyotrophic lateral sclerosis].154例肌萎缩侧索硬化症患者神经传导特征分析
Zhonghua Nei Ke Za Zhi. 2016 Oct 1;55(10):755-758. doi: 10.3760/cma.j.issn.0578-1426.2016.10.006.
7
Clinical utility of trapezius muscle studies in the evaluation of amyotrophic lateral sclerosis.斜方肌研究在肌萎缩侧索硬化症评估中的临床应用
J Clin Neurosci. 2006 Nov;13(9):908-12. doi: 10.1016/j.jocn.2006.01.044. Epub 2006 Oct 16.
8
Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS.区分进行性延髓麻痹(PLS)、上运动神经元为主型肌萎缩侧索硬化症(ALS)和典型ALS的临床特征。
Neurology. 2009 Jun 2;72(22):1948-52. doi: 10.1212/WNL.0b013e3181a8269b.
9
Rapidly progressive amyotrophic lateral sclerosis initially masquerading as a demyelinating neuropathy.快速进展性肌萎缩侧索硬化症最初表现为脱髓鞘性神经病。
Neurophysiol Clin. 2013 Jun;43(3):181-7. doi: 10.1016/j.neucli.2013.05.001. Epub 2013 May 18.
10
Motor unit number estimation as a complementary test to routine electromyography in the diagnosis of amyotrophic lateral sclerosis.运动单位数量估计作为肌萎缩侧索硬化症诊断中常规肌电图的补充检查。
J Electromyogr Kinesiol. 2016 Feb;26:60-5. doi: 10.1016/j.jelekin.2015.11.001. Epub 2015 Nov 11.

引用本文的文献

1
Longitudinal Quantitative MRI Evaluation of Muscle Involvement in Amyotrophic Lateral Sclerosis.肌萎缩侧索硬化症肌肉受累的纵向定量MRI评估
Front Neurol. 2021 Nov 24;12:749736. doi: 10.3389/fneur.2021.749736. eCollection 2021.
2
Longitudinal multi-modal muscle-based biomarker assessment in motor neuron disease.运动神经元病中基于肌肉的纵向多模态生物标志物评估。
J Neurol. 2020 Jan;267(1):244-256. doi: 10.1007/s00415-019-09580-x. Epub 2019 Oct 17.
3
Skeletal muscle MRI differentiates SBMA and ALS and correlates with disease severity.
骨骼肌 MRI 可区分 SBMA 和 ALS,并与疾病严重程度相关。
Neurology. 2019 Aug 27;93(9):e895-e907. doi: 10.1212/WNL.0000000000008009. Epub 2019 Aug 7.
4
Biomarkers in Motor Neuron Disease: A State of the Art Review.运动神经元病中的生物标志物:最新综述
Front Neurol. 2019 Apr 3;10:291. doi: 10.3389/fneur.2019.00291. eCollection 2019.
5
A pilot study assessing T1-weighted muscle MRI in amyotrophic lateral sclerosis (ALS).一项评估肌萎缩侧索硬化症(ALS)中T1加权肌肉磁共振成像的初步研究。
Skeletal Radiol. 2019 Apr;48(4):569-575. doi: 10.1007/s00256-018-3073-7. Epub 2018 Sep 17.
6
Imaging muscle as a potential biomarker of denervation in motor neuron disease.将肌肉成像作为运动神经元疾病去神经支配的潜在生物标志物。
J Neurol Neurosurg Psychiatry. 2018 Mar;89(3):248-255. doi: 10.1136/jnnp-2017-316744. Epub 2017 Oct 31.
7
Skeletal Muscle Quantitative Nuclear Magnetic Resonance Imaging and Spectroscopy as an Outcome Measure for Clinical Trials.骨骼肌定量磁共振成像和波谱分析作为临床试验的结局指标。
J Neuromuscul Dis. 2016 Mar 3;3(1):1-28. doi: 10.3233/JND-160145.
8
Reproducibility, and age, body-weight and gender dependency of candidate skeletal muscle MRI outcome measures in healthy volunteers.健康志愿者中候选骨骼肌MRI结果测量指标的可重复性以及年龄、体重和性别依赖性
Eur Radiol. 2014 Jul;24(7):1610-20. doi: 10.1007/s00330-014-3145-6. Epub 2014 Apr 20.
9
Lessons of ALS imaging: Pitfalls and future directions - A critical review.肌萎缩侧索硬化症成像的经验教训:陷阱与未来方向——一项批判性综述
Neuroimage Clin. 2014 Feb 27;4:436-43. doi: 10.1016/j.nicl.2014.02.011. eCollection 2014.
10
Quantitative MRI can detect subclinical disease progression in muscular dystrophy.定量 MRI 可检测出肌肉萎缩症的亚临床疾病进展。
J Neurol. 2012 Aug;259(8):1648-54. doi: 10.1007/s00415-011-6393-2.