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行为变异型额颞叶痴呆患者早期衰弱的神经影像学相关性研究:一项MRI和FDG-PET研究

Investigating Neuroimaging Correlates of Early Frailty in Patients With Behavioral Variant Frontotemporal Dementia: A MRI and FDG-PET Study.

作者信息

Amanzio Martina, Palermo Sara, Stanziano Mario, D'Agata Federico, Galati Antonello, Gentile Salvatore, Castellano Giancarlo, Bartoli Massimo, Cipriani Giuseppina Elena, Rubino Elisa, Fonio Paolo, Rainero Innocenzo

机构信息

Department of Psychology, University of Turin, Turin, Italy.

European Innovation Partnership on Active and Healthy Ageing (EIP-AHA), Brussels, Belgium.

出版信息

Front Aging Neurosci. 2021 Apr 14;13:637796. doi: 10.3389/fnagi.2021.637796. eCollection 2021.

DOI:10.3389/fnagi.2021.637796
PMID:33935684
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8079404/
Abstract

Frailty is a dynamic clinical condition characterized by the reduction of interconnections among different psychobiological domains, which leads to a homeostatic vulnerability. The association between physical frailty and cognitive dysfunctions is a possible predictor of poor prognosis in patients with neurodegenerative disorders. However, this construct has not been fully analyzed by a multidimensional neuropsychogeriatric assessment matched with multimodal neuroimaging methods in patients with behavioral variant frontotemporal dementia (bvFTD). We have investigated cognitive dysfunctions and frailty status, assessed by both a neuropsychological evaluation and the Multidimensional Prognostic Index (MPI), in a sample of 18 bvFTD patients and compared to matched healthy controls. Gray matter (GM) volume (as assessed by voxel-based morphometry) and metabolism (on fluorodeoxyglucose positron emission tomography) were first separately compared between groups, then voxelwise compared and correlated to each other within patients. Linear regression of the MPI was performed on those voxels presenting a significant correlation between altered GM volume and metabolism. The neuropsychological assessment reflected the diagnoses and the functional-anatomical alterations documented by neuroimaging analyses. In particular, the majority of patients presented significant executive dysfunction and mood changes in terms of apathy, depression, and anxiety. In the overall MPI score, the patients fell in the lower range (indicating an early frailty status). On imaging, they exhibited a bilateral decrease of GM density and hypometabolism involving the frontal pole, the anterior opercular region, and the anterior cingulate cortex. Greater atrophy than hypometabolism was observed in the bilateral orbitofrontal cortex, the triangular part of the inferior frontal gyrus, and the ventral striatum, whereas the contrary was detected in the bilateral dorsal anterior cingulate cortex and pre-supplementary motor area. MPI scores significantly correlated only with the co-occurrence of a decrease of GM density and hypometabolism in the right anterior insular cortex, but not with the separate pathological phenomena. Our results show a correlation between a specific pattern of co-occurring GM atrophy and hypometabolism with early frailty in bvFTD patients. These aspects, combined with executive dysfunction and mood changes, may lead to an increased risk of poor prognosis, highlighting a potentially critical and precocious role of the insula in the pathogenesis of frailty.

摘要

衰弱是一种动态临床状况,其特征是不同心理生物学领域之间的联系减少,这会导致内稳态脆弱性。身体衰弱与认知功能障碍之间的关联可能是神经退行性疾病患者预后不良的一个预测指标。然而,行为变异型额颞叶痴呆(bvFTD)患者的这种结构尚未通过与多模态神经影像学方法相匹配的多维神经心理老年病学评估进行全面分析。我们对18例bvFTD患者样本进行了研究,通过神经心理学评估和多维预后指数(MPI)评估认知功能障碍和衰弱状态,并与匹配的健康对照进行比较。首先分别比较两组之间的灰质(GM)体积(通过基于体素的形态计量学评估)和代谢(在氟脱氧葡萄糖正电子发射断层扫描上),然后在患者内部进行体素级比较并相互关联。对那些GM体积改变与代谢之间存在显著相关性的体素进行MPI的线性回归分析。神经心理学评估反映了神经影像学分析所记录的诊断结果和功能 - 解剖学改变。特别是,大多数患者在冷漠、抑郁和焦虑方面表现出显著的执行功能障碍和情绪变化。在总体MPI评分中,患者处于较低范围(表明早期衰弱状态)。在影像学上,他们表现出双侧GM密度降低和代谢减退,累及额极、前岛叶区域和前扣带回皮质。在双侧眶额皮质、额下回三角部和腹侧纹状体观察到萎缩大于代谢减退,而在双侧背侧前扣带回皮质和前辅助运动区则相反。MPI评分仅与右侧前岛叶皮质GM密度降低和代谢减退同时出现显著相关,而与单独的病理现象无关。我们的结果表明,bvFTD患者中GM萎缩和代谢减退同时出现的特定模式与早期衰弱之间存在相关性。这些方面,再加上执行功能障碍和情绪变化,可能导致预后不良风险增加,突出了岛叶在衰弱发病机制中潜在的关键和早熟作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce07/8079404/42a51a09c12f/fnagi-13-637796-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce07/8079404/7178b388d1a7/fnagi-13-637796-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce07/8079404/d7ef3aca1d60/fnagi-13-637796-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce07/8079404/42a51a09c12f/fnagi-13-637796-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce07/8079404/7178b388d1a7/fnagi-13-637796-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce07/8079404/d7ef3aca1d60/fnagi-13-637796-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce07/8079404/42a51a09c12f/fnagi-13-637796-g0003.jpg

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