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亨廷顿病基因携带者纹状体扩散率降低:何种解释?

Decreased diffusivity in the caudate nucleus of presymptomatic huntington disease gene carriers: which explanation?

机构信息

Neuroradiology Department, Fondazione Istituto Nazionale Neurologico "Carlo Besta," Milan, Italy.

出版信息

AJNR Am J Neuroradiol. 2010 Apr;31(4):706-10. doi: 10.3174/ajnr.A1891. Epub 2009 Nov 26.

Abstract

BACKGROUND AND PURPOSE

The neostriatum is known to be affected in HD. In this work, our aim was to determine whether microstructural and volumetric alterations occur in the neostriatum of presymptomatic HD gene carriers and in patients with early-stage HD.

MATERIALS AND METHODS

We studied a group of 15 presymptomatic gene carriers who were far from the estimated symptom onset (16% probability of developing the disease within 5 years), a group of 9 patients with early symptomatic HD, and 2 groups of age-matched controls. Volumetric MR imaging and DWIs were acquired, and statistical analyses were performed on the volumes of the caudate nucleus and putamen and on the corresponding MD measurements.

RESULTS

Neostriatal volumes were significantly smaller in both presymptomatic HD gene carriers and symptomatic patients with respect to controls. However, whereas the diffusivity in the caudate nucleus was increased in the symptomatic patients, it was decreased in the presymptomatic gene carriers.

CONCLUSIONS

Altered diffusivity and reduced volume of the caudate nucleus in presymptomatic HD gene carriers indicate that the neostriatum is affected well before the onset of symptoms. The observed initial decrease and subsequent increase of MD might be related to the combined effect of increased oligodendroglial population, putatively a developmental abnormality, and incipient neurodegeneration.

摘要

背景与目的

已知新纹状体在 HD 中受到影响。在这项工作中,我们的目的是确定在无症状的 HD 基因携带者和早期 HD 患者的新纹状体中是否存在微观结构和体积改变。

材料与方法

我们研究了一组 15 名远未达到预计发病时间的无症状基因携带者(5 年内发病概率为 16%),一组 9 名早期有症状的 HD 患者,以及两组年龄匹配的对照组。采集了体积磁共振成像和 DWI,并对尾状核和壳核的体积和相应的 MD 测量值进行了统计分析。

结果

与对照组相比,无症状 HD 基因携带者和有症状的患者的新纹状体体积明显较小。然而,在有症状的患者中,尾状核的扩散度增加,而在无症状的基因携带者中则减少。

结论

无症状 HD 基因携带者的尾状核扩散度改变和体积减小表明,新纹状体在症状出现之前就受到了影响。观察到的 MD 最初的减少和随后的增加可能与增加的少突胶质细胞群体的联合效应有关,推测这是一种发育异常,并且是神经退行性变的早期表现。

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