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肌张力障碍中的网络结构和功能紊乱:病理性连接与适应性反应。

Disordered network structure and function in dystonia: pathological connectivity vs. adaptive responses.

机构信息

Center for Neurosciences, The Feinstein Institutes for Medical Research, Manhasset, NY 11030, USA.

Department of Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Cereb Cortex. 2023 May 24;33(11):6943-6958. doi: 10.1093/cercor/bhad012.

Abstract

Primary dystonia is thought to emerge through abnormal functional relationships between basal ganglia and cerebellar motor circuits. These interactions may differ across disease subtypes and provide a novel biomarker for diagnosis and treatment. Using a network mapping algorithm based on resting-state functional MRI (rs-fMRI), a method that is readily implemented on conventional MRI scanners, we identified similar disease topographies in hereditary dystonia associated with the DYT1 or DYT6 mutations and in sporadic patients lacking these mutations. Both networks were characterized by contributions from the basal ganglia, cerebellum, thalamus, sensorimotor areas, as well as cortical association regions. Expression levels for the two networks were elevated in hereditary and sporadic dystonia, and in non-manifesting carriers of dystonia mutations. Nonetheless, the distribution of abnormal functional connections differed across groups, as did metrics of network organization and efficiency in key modules. Despite these differences, network expression correlated with dystonia motor ratings, significantly improving the accuracy of predictions based on thalamocortical tract integrity obtained with diffusion tensor MRI (DTI). Thus, in addition to providing unique information regarding the anatomy of abnormal brain circuits, rs-fMRI functional networks may provide a widely accessible method to help in the objective evaluation of new treatments for this disorder.

摘要

原发性肌张力障碍被认为是通过基底神经节和小脑运动回路之间的异常功能关系而出现的。这些相互作用可能因疾病亚型而异,并为诊断和治疗提供了一种新的生物标志物。我们使用基于静息状态功能磁共振成像(rs-fMRI)的网络映射算法,一种在常规 MRI 扫描仪上易于实现的方法,在与 DYT1 或 DYT6 突变相关的遗传性肌张力障碍和缺乏这些突变的散发性患者中,识别出了相似的疾病拓扑结构。这两个网络的特征是基底神经节、小脑、丘脑、感觉运动区以及皮质联合区的贡献。遗传性和散发性肌张力障碍以及肌张力障碍突变的非表现携带者中,两个网络的表达水平均升高。尽管存在这些差异,但异常功能连接的分布在不同组之间存在差异,关键模块的网络组织和效率指标也存在差异。尽管存在这些差异,但网络表达与肌张力障碍运动评分相关,显著提高了基于弥散张量 MRI(DTI)获得的丘脑皮质束完整性的预测准确性。因此,除了提供关于异常大脑回路解剖结构的独特信息外,rs-fMRI 功能网络还可能提供一种广泛可用的方法,有助于客观评估这种疾病的新治疗方法。

相似文献

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Abnormal structure-function relationships in hereditary dystonia.遗传性肌张力障碍中的结构-功能关系异常。
Neuroscience. 2009 Nov 24;164(1):220-9. doi: 10.1016/j.neuroscience.2008.12.041. Epub 2009 Jan 1.

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