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特发性快速眼动睡眠行为障碍中皮质灰质的进展及其与认知衰退的关系。

Cortical gray matter progression in idiopathic REM sleep behavior disorder and its relation to cognitive decline.

作者信息

Campabadal A, Inguanzo A, Segura B, Serradell M, Abos A, Uribe C, Gaig C, Santamaria J, Compta Y, Bargallo N, Junque C, Iranzo A

机构信息

Medical Psychology Unit, Department of Medicine, Institute of Neuroscience, University of Barcelona, Barcelona, Catalonia, Spain; Institute of Biomedical Research August Pi i Sunyer (IDIBAPS), Barcelona, Catalonia, Spain.

Medical Psychology Unit, Department of Medicine, Institute of Neuroscience, University of Barcelona, Barcelona, Catalonia, Spain; Institute of Biomedical Research August Pi i Sunyer (IDIBAPS), Barcelona, Catalonia, Spain; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED:CB06/05/0018-ISCIII), Barcelona, Spain.

出版信息

Neuroimage Clin. 2020;28:102421. doi: 10.1016/j.nicl.2020.102421. Epub 2020 Sep 9.

Abstract

BACKGROUND

Idiopathic Rapid eye movement sleep behavior disorder (IRBD) is recognized as the prodromal stage of the alpha-Synucleinopathies. Although some studies have addressed the characterization of brain structure in IRBD, little is known about its progression.

OBJECTIVE

The present work aims at further characterizing gray matter progression throughout IRBD relative to normal aging and investigating how these changes are associated with cognitive decline.

METHODS

Fourteen patients with polysomnography-confirmed IRBD and 18 age-matched healthy controls (HC) underwent neuropsychological, olfactory, motor, and T1-weighted MRI evaluation at baseline and follow-up. We compared the evolution of cortical thickness (CTh), subcortical volumes, smell, motor and cognitive performance in IRBD and HC after a mean of 1.6 years. FreeSurfer was used for CTh and volumetry preprocessing and analyses. The symmetrized percent of change (SPC) of the CTh was correlated with the SPC of motor and neuropsychological performance.

RESULTS

IRBD and HC differed significantly in the cortical thinning progression in regions encompassing bilateral superior parietal and precuneus, the right cuneus, the left occipital pole and lateral orbitofrontal gyri (FWE corrected, p < 0.05). The Visual form discrimination test showed worse progression in the IRBD relative to HC, that was associated with gray matter loss in the right superior parietal and the left precuneus. Increasing motor signs in IRBD were related to cortical thinning mainly involving frontal regions, and late-onset IRBD was associated with cortical thinning involving posterior areas (FWE corrected, p < 0.05). Despite finding olfactory identification deficits in IRBD, results did not show decline over the disease course.

CONCLUSION

Progression in IRBD patients is characterized by parieto-occipital and orbitofrontal thinning and visuospatial loss. The cognitive decline in IRBD is associated with degeneration in parietal regions.

摘要

背景

特发性快速眼动睡眠行为障碍(IRBD)被认为是α-突触核蛋白病的前驱阶段。尽管一些研究已经探讨了IRBD患者脑结构的特征,但对其进展情况知之甚少。

目的

本研究旨在进一步明确IRBD患者相对于正常衰老过程中灰质的进展情况,并研究这些变化与认知功能下降之间的关系。

方法

14例经多导睡眠图确诊的IRBD患者和18例年龄匹配的健康对照者(HC)在基线和随访时接受了神经心理学、嗅觉、运动功能及T1加权磁共振成像评估。平均1.6年后,我们比较了IRBD患者和HC的皮质厚度(CTh)、皮质下体积、嗅觉、运动和认知功能的变化。使用FreeSurfer进行CTh和体积测量的预处理及分析。CTh的对称变化百分比(SPC)与运动和神经心理学表现的SPC进行相关性分析。

结果

IRBD患者和HC在双侧顶上小叶和楔前叶、右侧楔叶、左侧枕极和外侧眶额回区域的皮质变薄进展存在显著差异(FWE校正,p<0.05)。视觉形态辨别测试显示,IRBD患者相对于HC进展更差,这与右侧顶上小叶和左侧楔前叶的灰质丢失有关。IRBD患者运动症状的加重主要与额叶皮质变薄有关,而晚发型IRBD与后部区域的皮质变薄有关(FWE校正,p<0.05)。尽管在IRBD患者中发现嗅觉识别缺陷,但结果未显示在病程中有所下降。

结论

IRBD患者的病情进展以顶枕叶和眶额叶变薄以及视觉空间功能丧失为特征。IRBD患者的认知功能下降与顶叶区域的退变有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9ae/7509231/0b58f6bce653/gr1.jpg

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