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首页> 外文期刊>Human brain mapping >Longitudinal Resting State fMRI Analysis in Healthy Controls and Premanifest Huntington's Disease Gene Carriers: A Three-Year Follow-Up Study
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Longitudinal Resting State fMRI Analysis in Healthy Controls and Premanifest Huntington's Disease Gene Carriers: A Three-Year Follow-Up Study

机译:在健康对照组和预后亨廷顿氏病基因携带者中的纵向静止状态功能磁共振成像分析:一项为期三年的随访研究

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摘要

Background: We previously demonstrated that in the premanifest stage of Huntington's disease (preHD), a reduced functional connectivity exists compared to healthy controls. In the current study, we look at possible changes in functional connectivity occurring longitudinally over a period of 3 years, with the aim of assessing the potential usefulness of this technique as a biomarker for disease progression in preHD. Methods: Twenty-two preHD and 17 healthy control subjects completed resting state functional magnetic resonance imaging (fMRI) scans in two visits with 3 years in between. Differences in resting state connectivity were examined for eight networks of interest using FSL with three different analysis types: a dual regression method, region of interest approach, and an independent component analysis. To evaluate a possible combined effect of gray matter volume change and the change in blood oxygenation level dependent signal, the analysis was performed with and without voxel-wise correction for gray matter volume. To evaluate possible correlations between functional connectivity change and the predicted time to disease onset, the preHD group was classed as preHD-A if 10.9 years and preHD-B if <10.9 years from predicted disease onset. Possible correlations between burden of pathology score and functional connectivity change in preHD were also assessed. Finally, longitudinal change in whole brain and striatal volumetric measures was assessed in the studied cohort. Results: Longitudinal analysis of the resting state-fMRI (RS-fMRI) data revealed no differences in the degree of connectivity change between the groups over a period of 3 years, though a significantly higher rate of striatal atrophy was found in the preHD group compared to controls in the same period. Discussion: Based on the results found in this study, the provisional conclusion is that RS-fMRI lacks sensitivity in detecting changes in functional connectivity in HD gene carriers prior to disease manifestation over a 3-year follow-up period. Hum Brain Mapp, 36:110-119, 2015. (c) 2014 Wiley Periodicals, Inc.
机译:背景:我们先前证明,在亨廷顿舞蹈病(preHD)的预示阶段,与健康对照组相比,功能连接性降低。在当前的研究中,我们研究了在3年内纵向发生的功能连通性可能发生的变化,目的是评估该技术作为preHD中疾病进展的生物标志物的潜在用途。方法:22名preHD和17名健康对照受试者在3年之间的两次访问中完成了静息状态功能磁共振成像(fMRI)扫描。使用FSL通过三种不同的分析类型检查了八个感兴趣的网络的静止状态连通性差异:对偶回归方法,感兴趣区域方法和独立分量分析。为了评估灰质体积变化和血液氧合水平依赖性信号变化的可能组合影响,在有和无体素的情况下对灰质体积进行了校正。为了评估功能连通性变化与预计疾病发作时间之间的可能相关性,如果preHD组距预期疾病发作时间为10.9年,则将其分类为preHD-A,如果距疾病预测发病时间<10.9年,则将其分类为preHD-B。还评估了病理评分负担与preHD功能连接改变之间的可能相关性。最后,在研究的队列中评估了全脑和纹状体容积测量的纵向变化。结果:静息状态fMRI(RS-fMRI)数据的纵向分析显示,在3年的时间里,两组之间的连通性变化程度没有差异,尽管与preHD组相比,纹状体萎缩的发生率明显更高在同一时期进行控制。讨论:基于本研究的结果,初步结论是,在三年的随访期内,RS-fMRI缺乏在疾病表现之前检测HD基因携带者功能连通性变化的敏感性。嗡嗡的大脑Mapp,36:110-119,2015年。(c)2014 Wiley Periodicals,Inc.

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