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步行和力量的定量测量有助于深入了解多发性硬化症患者的脑皮质脊髓束病变情况。

Quantitative measures of walking and strength provide insight into brain corticospinal tract pathology in multiple sclerosis.

作者信息

Fritz Nora E, Keller Jennifer, Calabresi Peter A, Zackowski Kathleen M

机构信息

Motion Analysis Laboratory, Kennedy Krieger Institute, Baltimore, MD, USA; Johns Hopkins School of Medicine, Department of Physical Medicine and Rehabilitation, Baltimore, MD, USA; Wayne State University, Program in Physical Therapy, Department of Neurology, Detroit, MI, USA.

Motion Analysis Laboratory, Kennedy Krieger Institute, Baltimore, MD, USA.

出版信息

Neuroimage Clin. 2017 Feb 20;14:490-498. doi: 10.1016/j.nicl.2017.02.006. eCollection 2017.

DOI:10.1016/j.nicl.2017.02.006
PMID:28289599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5338912/
Abstract

At least 85% of individuals with multiple sclerosis report walking dysfunction as their primary complaint. Walking and strength measures are common clinical measures to mark increasing disability or improvement with rehabilitation. Previous studies have shown an association between strength or walking ability and spinal cord MRI measures, and strength measures with brainstem corticospinal tract magnetization transfer ratio. However, the relationship between walking performance and brain corticospinal tract magnetization transfer imaging measures and the contribution of clinical measurements of walking and strength to the underlying integrity of the corticospinal tract has not been explored in multiple sclerosis. The objectives of this study were explore the relationship of quantitative measures of walking and strength to whole-brain corticospinal tract-specific MRI measures and to determine the contribution of quantitative measures of function in addition to basic clinical measures (age, gender, symptom duration and Expanded Disability Status Scale) to structural imaging measures of the corticospinal tract. We hypothesized that quantitative walking and strength measures would be related to brain corticospinal tract-specific measures, and would provide insight into the heterogeneity of brain pathology. Twenty-nine individuals with relapsing-remitting multiple sclerosis (mean(SD) age 48.7 (11.5) years; symptom duration 11.9(8.7); 17 females; median[range] Expanded Disability Status Scale 4.0 [1.0-6.5]) and 29 age and gender-matched healthy controls (age 50.8(11.6) years; 20 females) participated in clinical tests of strength and walking (Timed Up and Go, Timed 25 Foot Walk, Two Minute Walk Test ) as well as 3 T imaging including diffusion tensor imaging and magnetization transfer imaging. Individuals with multiple sclerosis were weaker (p = 0.0024) and walked slower (p = 0.0013) compared to controls. Quantitative measures of walking and strength were significantly related to corticospinal tract fractional anisotropy (r > 0.26; p < 0.04) and magnetization transfer ratio (r > 0.29; p < 0.03) measures. Although the Expanded Disability Status Scale was highly correlated with walking measures, it was not significantly related to either corticospinal tract fractional anisotropy or magnetization transfer ratio (p > 0.05). Walk velocity was a significant contributor to magnetization transfer ratio (p = 0.006) and fractional anisotropy (p = 0.011) in regression modeling that included both quantitative measures of function and basic clinical information. Quantitative measures of strength and walking are associated with brain corticospinal tract pathology. The addition of these quantitative measures to basic clinical information explains more of the variance in corticospinal tract fractional anisotropy and magnetization transfer ratio than the basic clinical information alone. Outcome measurement for multiple sclerosis clinical trials has been notoriously challenging; the use of quantitative measures of strength and walking along with tract-specific imaging methods may improve our ability to monitor disease change over time, with intervention, and provide needed guidelines for developing more effective targeted rehabilitation strategies.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/3aeee5720ff7/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/ddae9145e187/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/34ad37c7ce9d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/4539dfbf17e6/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/be525ad5f089/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/3aeee5720ff7/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/ddae9145e187/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/34ad37c7ce9d/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/4539dfbf17e6/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/be525ad5f089/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b648/5338912/3aeee5720ff7/gr5.jpg
摘要

至少85%的多发性硬化症患者报告称行走功能障碍是他们的主要诉求。行走和力量测量是用于标记残疾程度加重或康复后改善情况的常见临床测量方法。先前的研究表明,力量或行走能力与脊髓磁共振成像测量结果之间存在关联,且力量测量与脑干皮质脊髓束磁化传递率之间也存在关联。然而,在多发性硬化症中,行走表现与脑皮质脊髓束磁化传递成像测量结果之间的关系,以及行走和力量的临床测量对皮质脊髓束潜在完整性的贡献尚未得到探索。本研究的目的是探讨行走和力量的定量测量与全脑皮质脊髓束特异性磁共振成像测量结果之间的关系,并确定除基本临床测量(年龄、性别、症状持续时间和扩展残疾状态量表)外,功能定量测量对皮质脊髓束结构成像测量结果的贡献。我们假设行走和力量的定量测量将与脑皮质脊髓束特异性测量结果相关,并能深入了解脑病理学的异质性。29例复发缓解型多发性硬化症患者(平均[标准差]年龄48.7(11.5)岁;症状持续时间11.9(8.7);17名女性;扩展残疾状态量表中位数[范围]为4.0 [1.0 - 6.5])和29名年龄及性别匹配的健康对照者(年龄50.8(11.6)岁;20名女性)参与了力量和行走的临床测试(起立行走计时测试、25英尺步行计时测试、两分钟步行测试)以及3T成像,包括扩散张量成像和磁化传递成像。与对照组相比,多发性硬化症患者力量较弱(p = 0.0024)且行走较慢(p = 0.0013)。行走和力量的定量测量与皮质脊髓束分数各向异性(r > 0.26;p < 0.04)和磁化传递率(r > 0.29;p < 0.03)测量结果显著相关。尽管扩展残疾状态量表与行走测量高度相关,但它与皮质脊髓束分数各向异性或磁化传递率均无显著相关性(p > 0.05)。在包含功能定量测量和基本临床信息的回归模型中,行走速度是磁化传递率(p = 0.006)和分数各向异性(p = 0.011)的重要贡献因素。力量和行走的定量测量与脑皮质脊髓束病理学相关。将这些定量测量添加到基本临床信息中,比单独的基本临床信息能解释更多皮质脊髓束分数各向异性和磁化传递率的方差。多发性硬化症临床试验的结果测量一直极具挑战性;使用力量和行走的定量测量以及束特异性成像方法可能会提高我们监测疾病随时间、干预变化的能力,并为制定更有效的靶向康复策略提供所需的指导方针。

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Diffusion tensor imaging of the corticospinal tract and walking performance in multiple sclerosis.多发性硬化症中皮质脊髓束的扩散张量成像与步行功能
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