Melanie A Morrison, Jingwen Yao, Radhika Bhalerao, Angela Jakary, Julia Glueck, Theresa Driscoll, Michael D Geschwind, Alexandra B Nelson, Katherine L Possin, Christopher P Hess, Janine M Lupo
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引用次数: 0
Abstract
Background: There are no disease modifying therapies for Huntington's disease (HD), a rare but fatal genetic neurodegenerative condition. To develop and test new management strategies, a better understanding of the mechanisms underlying HD progression is needed. Aberrant changes in thalamo-cortical and striato-cerebellar circuitry have been observed in asymptomatic HD, along with transient enlargement of the dentate nucleus.
Purpose: To evaluate the relationship between thalamo-cerebellar connectivity and HD progression.
Study type: Prospective and retrospective.
Population: Patients with HD and healthy controls from a single-center dataset (n=34), and patients from the public TRACK-HD dataset (n=91).
Field strength/sequence: 3T and 7T.
Assessment: Thalamo-cerebellar connectivity was compared across patients and controls and related to motor scores and predicted years to symptom onset. Cross-sectional findings were validated within-patient by mapping changes in individual connectivity over time. HD effects on cognitive performance were also explored and related to connectivity.
Statistical tests: Kruskal-Wallis with post hoc Dunn's tests and Pearson correlations (p significant <0.05).
Results: In the 7T cohort, significant premanifest and control group differences in thalamo-dentate connectivity were observed (p Dunn <0.05, η 2 =.19-.22), with manifest HD connectivity approaching normative values. Thalamic connectivity with the dentate nucleus and anterior cerebellum also correlated with years to onset (p Den =0.06, r=0.42, p Ant <0.05, r=-0.45), together indicating potential transient functional alterations in premanifest HD. Similar patterns were observed between connectivity (thalamus to dentate nucleus and anterior lobe) and cognitive performance scores across all subjects (p<0.05, r Den =-0.17, r Ant =-0.18). In the premanifest TRACK-HD cohort, connectivity of multiple thalamo-cerebellar connections correlated with years to onset, revealing distinct patterns for patients with low versus high motor scores, again indicative of potential transient alterations. Exploratory non-parametric regression of serial imaging data further supported these findings.
Data conclusion: Transient changes in thalamo-cerebellar connectivity are seen in premanifest HD with increasing progression. More studies are needed to validate this potentially useful biomarker.
背景:亨廷顿舞蹈病(HD)是一种罕见但致命的遗传性神经退行性疾病,目前尚无疾病改善疗法。为了开发和测试新的管理策略,需要更好地了解HD进展的机制。在无症状HD患者中,丘脑-皮质和纹状体-小脑回路发生了异常变化,并伴有齿状核的短暂增大。目的:探讨丘脑-小脑连通性与HD进展的关系。研究类型:前瞻性和回顾性。人群:来自单中心数据集的HD患者和健康对照者(n=34),以及来自公共TRACK-HD数据集的患者(n=91)。场强/序列:3T和7T。评估:比较了患者和对照组的丘脑-小脑连通性,并与运动评分和预测症状发作的年份相关。通过绘制个体连通性随时间的变化,在患者内部验证了横断面研究结果。HD对认知表现的影响也被探讨并与连通性有关。统计检验:Kruskal-Wallis与post - hoc Dunn检验和Pearson相关性(p显著)结果:在7T队列中,观察到显前组和对照组在丘脑-齿状体连通性方面的显著差异(p Dunn 2 = 0.19 - 0.22),显前HD连通性接近正常值。丘脑与齿状核和小脑前部的连通性也与发病年龄相关(p Den =0.06, r=0.42, p Ant Den =-0.17, r Ant =-0.18)。在前期TRACK-HD队列中,多个丘脑-小脑连接的连通性与发病年龄相关,揭示了运动得分低与高的患者的不同模式,再次表明潜在的短暂改变。序列影像数据的探索性非参数回归进一步支持了这些发现。数据结论:丘脑-小脑连通性的短暂性改变在先期HD中随着进展的增加而出现。需要更多的研究来验证这种潜在有用的生物标志物。