Atrophy of the putamen at time of clinical motor onset in Huntington's disease: a 6-year follow-up study.

Journal of Clinical Movement Disorders Pub Date : 2018-03-23 eCollection Date: 2018-01-01 DOI:10.1186/s40734-018-0069-3
Emma M Coppen, Jeroen van der Grond, Raymund A C Roos
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引用次数: 8

Abstract

Background: Striatal atrophy is detectable many years before the predicted onset of motor symptoms in premanifest Huntington's disease (HD). However, the extent of these neurodegenerative changes at the actual time of conversion from premanifest to a motor manifest disease stage is not known. With this study, we aimed to assess differences in degree and rate of atrophy between converters, i.e. premanifest individuals who develop clinically manifest HD over the course of the study, and non-converters.

Methods: Structural T1-weighted Magnetic Resonance Imaging (MRI) scans were used to measure volumes of seven subcortical structures. Images were acquired yearly over a maximum follow-up period of 6 years (mean 4.8 ± 1.8 years) in 57 participants (healthy controls n = 28, premanifest HD gene carriers n = 29). Of the premanifest HD gene carriers, 20 individuals clinically developed manifest HD over the course of the study, i.e. converters, whereas 9 individuals did not show any clinical signs. Differences between controls, converters and non-converters in volumetric decline over time were assessed using a one-way ANCOVA with age, gender and intracranial volume as covariates. All data were adjusted for multiple comparisons using Bonferonni correction.

Results: The putamen showed a significant difference in volume at the time of conversion in the converters group compared to the non-converters group (adjusted p = 0.04). Although, volumes of all other subcortical structures were smaller at time of conversion compared to non-converters and controls, these differences were not statistically significant. Over time, rate of volumetric decline in all subcortical structures in converters did not significantly differ from non-converters.

Conclusions: Putamen volume is smaller at the time of manifestation of motor symptoms compared with premanifest HD that not showed any clinical disease progression during the course of this 6-year follow-up study.

Abstract Image

亨廷顿舞蹈病临床运动发病时壳核萎缩:一项6年随访研究
背景:在表现前亨廷顿舞蹈病(HD)中,纹状体萎缩在预测的运动症状发作前很多年就可以检测到。然而,这些神经退行性改变的程度,在实际时间从前期转化为运动显性疾病阶段尚不清楚。在这项研究中,我们旨在评估转化者(即在研究过程中出现临床表现的HD的预显个体)与非转化者之间萎缩程度和速度的差异。方法:采用结构t1加权磁共振成像(MRI)扫描测量7个皮质下结构的体积。在最长6年(平均4.8±1.8年)的随访期内,57名参与者(健康对照组n = 28,先兆HD基因携带者n = 29)每年获得图像。在未表现出HD基因的携带者中,20人在研究过程中临床表现出HD,即转化者,而9人没有表现出任何临床症状。使用以年龄、性别和颅内容积为协变量的单向ANCOVA评估对照组、转换者和非转换者随时间体积下降的差异。所有数据采用Bonferonni校正进行多重比较校正。结果:转换器组与非转换器组在转换时壳核体积差异有统计学意义(p = 0.04)。虽然与非转换者和对照组相比,转换时所有其他皮质下结构的体积都较小,但这些差异没有统计学意义。随着时间的推移,转换者与非转换者的所有皮质下结构的体积下降率没有显著差异。结论:在这项为期6年的随访研究中,与未出现任何临床疾病进展的HD前期相比,运动症状出现时的壳核体积更小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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