Suppr超能文献

原发性颈肌张力障碍患者的磁共振成像基于体素的形态计量学的横断和纵向研究。

A transverse and longitudinal MR imaging voxel-based morphometry study in patients with primary cervical dystonia.

机构信息

Department of Neurological Sciences, Sapienza University of Rome, Rome, Italy.

出版信息

AJNR Am J Neuroradiol. 2011 Jan;32(1):81-4. doi: 10.3174/ajnr.A2242. Epub 2010 Oct 14.

Abstract

BACKGROUND AND PURPOSE

Findings of standard MR imaging examinations are usually normal in primary CD. These findings are now increasingly challenged by studies using advanced neuroimaging techniques detecting abnormalities in brain areas that may be functionally involved in the pathophysiology of CD. Our purpose was to evaluate GM volumes in patients with CD at baseline and 5 years later.

MATERIALS AND METHODS

We enrolled 19 patients (F/M = 15:4, mean age = 53.2 + 11.2 years), 12 of whom were studied at baseline and again approximately 5 years later. Twenty-eight healthy volunteers acted as controls (F/M = 17:11, mean age = 47.5 + 15.6 years). The subjects were imaged with a 1.5T scanner by using a 3D T1-weighted sequence on 150 contiguous axial 1-mm-thick sections to apply VBM.

RESULTS

At entry, VBM analysis disclosed significantly lower GM volumes in the left caudate head and putamen and in the premotor and primary sensorimotor cortices bilaterally in patients than in controls. No correlation was found between decreased GM volumes and patient age, severity of dystonia, or disease duration. At the 5-year follow-up, GM volumes in the left primary sensorimotor cortex in patients had decreased significantly from baseline.

CONCLUSIONS

The findings obtained at entry and after a 5-year follow-up consistently showed decreased caudate, putamen, and sensorimotor cortex GM volumes in patients with CD, and they probably play a pathophysiologic role in CD.

摘要

背景与目的

原发性 CD 的标准磁共振成像检查结果通常正常。现在,越来越多的研究使用先进的神经影像学技术发现大脑区域的异常,这些异常可能与 CD 的病理生理学有关,这些发现对标准磁共振成像检查结果提出了挑战。我们的目的是评估 CD 患者在基线时和 5 年后的 GM 体积。

材料与方法

我们纳入了 19 名患者(F/M=15:4,平均年龄=53.2+11.2 岁),其中 12 名患者在基线时和大约 5 年后再次接受了研究。28 名健康志愿者作为对照组(F/M=17:11,平均年龄=47.5+15.6 岁)。使用 1.5T 扫描仪对受试者进行成像,采用 3D T1 加权序列对 150 个连续的轴向 1mm 厚切片进行 VBM。

结果

在入组时,VBM 分析显示患者的左侧尾状核头部和壳核以及双侧运动前皮质和初级感觉运动皮质的 GM 体积明显低于对照组。GM 体积减少与患者年龄、肌张力障碍严重程度或疾病持续时间之间无相关性。在 5 年随访时,患者左侧初级感觉运动皮质的 GM 体积与基线相比明显减少。

结论

在入组时和 5 年随访时获得的结果一致显示,CD 患者的尾状核、壳核和感觉运动皮质的 GM 体积减少,它们可能在 CD 中发挥病理生理作用。

相似文献

引用本文的文献

1
No reliable gray matter alterations in idiopathic dystonia.原发性肌张力障碍中无可靠的灰质改变。
Front Neurol. 2025 Mar 3;16:1510115. doi: 10.3389/fneur.2025.1510115. eCollection 2025.
6
DYT- dystonia: an update on pathogenesis and treatment.DYT - 肌张力障碍:发病机制与治疗的最新进展
Front Neurosci. 2023 Aug 10;17:1216929. doi: 10.3389/fnins.2023.1216929. eCollection 2023.

本文引用的文献

9
Writer's cramp: questions of causation.书写痉挛:病因问题。
Neurology. 2007 Jul 24;69(4):331-2. doi: 10.1212/01.wnl.0000269330.95232.7c.

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