Domain-specific brain regions are associated with cognitive impairment in progressive supranuclear palsy

Q4 Neuroscience
N. Schröter , M. Rijntjes , J.A. Hosp , M. Reisert , H. Mast , C. Weiller , P. Oikonomou , L. Frings , H. Urbach , W.H. Jost , A. Rau
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Abstract

Background

Cognitive impairment significantly contributes to the disease burden of progressive supranuclear palsy (PSP), however, the underlying pathophysiologiy is not well understood.

Objectives

To gain a better understanding of the pathophysiology, we identified the brain regions associated with individual domains of impaired cognition.

Methods

We analyzed MRI data from a cohort of 31 patients with PSP (age 71.0 +-7.0 years, range 58–87; 15 females; disease duration 2.9 +- 1.8 years). Cerebral microstructure was approximated with Diffusion Microstructure Imaging and cognitive performance was measured using the Frontal Assessment Battery (FAB) and Montreal Cognitive Assessment (MoCA). To reveal the underlying affected brain regions, whole-brain voxel-wise associations were employed to test the microstructural metrics regarding their correlation with the FAB as well as the individual cognitive domains ‚Attention‘, ‚Execution‘, ‚Language‘, ‚Memory‘, ‚Orientation‘, and ‚Visuoconstruction‘ derived from MoCA.

Results

MoCA performance was impaired in 87.5% of patients (20.2 +- 5.4 points, range 8–28; cut-off value: <26/30). In the voxel-wise analyses, we noted significant associations of cerebral microstructure and FAB in the right-sided frontal and temporopolar white matter, deficits in ‚Memory‘ with hippocampal and temporomesial regions, in reduced ‚Orientation‘ with wide spread white-matter areas with a parietal accentuation, whereas deficits in ‚Attention‘ correlated with frontal and prefrontal structures.

Conclusions

Diffusion Microstructure Imaging revealed domain-specific regions of neurodegenerative alterations in PSP. The regions identified in this approach integrate well in existing disease concepts. They might therefore be a possible biomarker for cognitive impairment, as well as amonitoring parameter for future disease modifying therapeutics.
脑区域特异性与进行性核上性麻痹的认知障碍有关
认知障碍是进行性核上性麻痹(PSP)的疾病负担的重要因素,然而,其潜在的病理生理机制尚不清楚。目的为了更好地理解病理生理学,我们确定了与个体认知障碍相关的大脑区域。方法分析31例PSP患者的MRI数据(年龄71.0 +-7.0岁,范围58-87;15个女性;病程2.9 +- 1.8年)。采用扩散微结构成像(Diffusion microstructimaging,简称弥散微结构成像)模拟大脑微结构,采用前额叶评估电池(FAB)和蒙特利尔认知评估(MoCA)测试认知能力。为了揭示潜在的受影响的大脑区域,采用全脑体素关联来测试微观结构指标与FAB以及来自MoCA的个体认知领域(注意力、执行、语言、记忆、方向和视觉构建)的相关性。结果87.5%的患者smoca功能受损(20.2 + ~ 5.4分,范围8 ~ 28分;截止值:26/30)。在体素分析中,我们注意到大脑微观结构和FAB在右侧额叶和颞叶白质中的显著关联,“记忆”缺陷与海马和颞叶区域有关,“定向”缺陷与广泛的白质区域有关,顶叶突出,而“注意力”缺陷与额叶和前额叶结构有关。结论弥散显微成像显示了PSP神经退行性改变的特定区域。这种方法确定的区域与现有的疾病概念很好地结合在一起。因此,它们可能是认知障碍的可能生物标志物,以及未来疾病修饰治疗的监测参数。
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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来源期刊
Neuroimage. Reports
Neuroimage. Reports Neuroscience (General)
CiteScore
1.90
自引率
0.00%
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0
审稿时长
87 days
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