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Imaging outcomes for neuroprotection and repair in multiple sclerosis trials.多发性硬化症试验中神经保护和修复的影像学结果。
Nat Rev Neurol. 2009 May;5(5):256-66. doi: 10.1038/nrneurol.2009.41.
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Mitochondrial changes within axons in multiple sclerosis.多发性硬化症中轴突内的线粒体变化。
Brain. 2009 May;132(Pt 5):1161-74. doi: 10.1093/brain/awp046. Epub 2009 Mar 17.
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Review: Mitochondria and disease progression in multiple sclerosis.综述:线粒体与多发性硬化症的疾病进展
Neuropathol Appl Neurobiol. 2008 Dec;34(6):577-89. doi: 10.1111/j.1365-2990.2008.00987.x.
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MRI in multiple sclerosis: current status and future prospects.多发性硬化症的磁共振成像:现状与未来展望。
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Optical coherence tomography and disease subtype in multiple sclerosis.光学相干断层扫描与多发性硬化症的疾病亚型
Neurology. 2007 Nov 27;69(22):2085-92. doi: 10.1212/01.wnl.0000294876.49861.dc.
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Axonal damage in the spinal cord of multiple sclerosis patients detected by magnetic resonance spectroscopy.通过磁共振波谱检测多发性硬化症患者脊髓中的轴突损伤。
Magn Reson Med. 2007 Nov;58(5):880-5. doi: 10.1002/mrm.21382.
7
Spinal cord spectroscopy and diffusion-based tractography to assess acute disability in multiple sclerosis.脊髓光谱分析和基于扩散的纤维束成像用于评估多发性硬化症的急性残疾情况。
Brain. 2007 Aug;130(Pt 8):2220-31. doi: 10.1093/brain/awm152.
8
Discordant white matter N-acetylasparate and diffusion MRI measures suggest that chronic metabolic dysfunction contributes to axonal pathology in multiple sclerosis.不一致的白质N-乙酰天门冬氨酸和扩散磁共振成像测量结果表明,慢性代谢功能障碍导致多发性硬化症中的轴突病变。
Neuroimage. 2007 May 15;36(1):19-27. doi: 10.1016/j.neuroimage.2007.02.036. Epub 2007 Mar 3.
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N-Acetylaspartate in the CNS: from neurodiagnostics to neurobiology.中枢神经系统中的N-乙酰天门冬氨酸:从神经诊断学走向神经生物学。
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10
Increased axonal mitochondrial activity as an adaptation to myelin deficiency in the Shiverer mouse.轴突线粒体活性增加作为对颤抖小鼠髓鞘缺乏的一种适应性反应。
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多发性硬化症中的脊髓修复:线粒体代谢是否起作用?

Spinal cord repair in MS: does mitochondrial metabolism play a role?

机构信息

Department of Brain Repair and Rehabilitation, Institute of Neurology, University College London, Queen Square, London WC1N 3BG, UK.

出版信息

Neurology. 2010 Mar 2;74(9):721-7. doi: 10.1212/WNL.0b013e3181d26968. Epub 2010 Jan 27.

DOI:10.1212/WNL.0b013e3181d26968
PMID:20107138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2939018/
Abstract

OBJECTIVE

To investigate the mechanisms of spinal cord repair and their relative contribution to clinical recovery in patients with multiple sclerosis (MS) after a cervical cord relapse, using spinal cord (1)H-magnetic resonance spectroscopy (MRS) and volumetric imaging.

METHODS

Fourteen patients with MS and 13 controls underwent spinal cord imaging at baseline and at 1, 3, and 6 months. N-acetyl-aspartate (NAA) concentration, which reflects axonal count and metabolism in mitochondria, and the cord cross-sectional area, which indicates axonal count, were measured in the affected cervical region. Mixed effect linear regression models investigated the temporal evolution of these measures and their association with clinical changes. Ordinal logistic regressions identified predictors of recovery.

RESULTS

Patients who recovered showed a sustained increase in NAA after 1 month. In the whole patient group, a greater increase of NAA after 1 month was associated with greater recovery. Patients showed a significant decline in cord area during follow-up, which did not correlate with clinical changes. A worse recovery was predicted by a longer disease duration at study entry.

CONCLUSIONS

The partial recovery of N-acetyl-aspartate levels after the acute event, which is concurrent with a decline in cord cross-sectional area, may be driven by increased axonal mitochondrial metabolism. This possible repair mechanism is associated with clinical recovery, and is less efficient in patients with longer disease duration. These insights into the mechanisms of spinal cord repair highlight the need to extend spinal cord magnetic resonance spectroscopy to other spinal cord disorders, and explore therapies that enhance recovery by modulating mitochondrial activity.

摘要

目的

利用脊髓(1)H 磁共振波谱(MRS)和容积成像,研究多发性硬化症(MS)患者颈髓复发后脊髓修复的机制及其对临床恢复的相对贡献。

方法

14 例 MS 患者和 13 名对照者在基线及 1、3 和 6 个月时进行脊髓成像。在受累的颈段测量反映轴突计数和线粒体代谢的 N-乙酰天冬氨酸(NAA)浓度和脊髓横截面积,反映轴突计数。混合效应线性回归模型研究了这些指标的时间演变及其与临床变化的关系。有序逻辑回归确定了恢复的预测因素。

结果

恢复的患者在 1 个月后 NAA 持续增加。在整个患者组中,1 个月后 NAA 增加更多与恢复更大相关。患者在随访期间脊髓面积显著下降,但与临床变化无关。研究开始时疾病持续时间较长预测恢复较差。

结论

急性事件后 N-乙酰天冬氨酸水平的部分恢复,同时伴有脊髓横截面积下降,可能是由于轴突线粒体代谢增加所致。这种可能的修复机制与临床恢复相关,在疾病持续时间较长的患者中效率较低。这些对脊髓修复机制的深入了解,突出了将脊髓磁共振波谱扩展到其他脊髓疾病的必要性,并探索通过调节线粒体活性来增强恢复的治疗方法。