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轻度认知障碍中基底前脑萎缩及相关皮质低代谢的认知关联

Cognitive Correlates of Basal Forebrain Atrophy and Associated Cortical Hypometabolism in Mild Cognitive Impairment.

作者信息

Grothe Michel J, Heinsen Helmut, Amaro Edson, Grinberg Lea T, Teipel Stefan J

机构信息

German Center for Neurodegenerative Diseases (DZNE), Rostock, Germany.

Laboratory of Morphological Brain Research, Department of Psychiatry, University of Würzburg, Würzburg, Germany.

出版信息

Cereb Cortex. 2016 Jun;26(6):2411-2426. doi: 10.1093/cercor/bhv062. Epub 2015 Apr 2.

Abstract

Degeneration of basal forebrain (BF) cholinergic nuclei is associated with cognitive decline, and this effect is believed to be mediated by neuronal dysfunction in the denervated cortical areas. MRI-based measurements of BF atrophy are increasingly being used as in vivo surrogate markers for cholinergic degeneration, but the functional implications of reductions in BF volume are not well understood. We used high-resolution MRI, fluorodeoxyglucose-positron emission tomography (PET), and neuropsychological test data of 132 subjects with mild cognitive impairment (MCI) and 177 cognitively normal controls to determine associations between BF atrophy, cortical hypometabolism, and cognitive deficits. BF atrophy in MCI correlated with both impaired memory function and attentional control deficits, whereas hippocampus volume was more specifically associated with memory deficits. BF atrophy was also associated with widespread cortical hypometabolism, and path analytic models indicated that hypometabolism in domain-specific cortical networks mediated the association between BF volume and cognitive dysfunction. The presence of cortical amyloid pathology, as assessed using AV45-PET, did not significantly interact with the observed associations. These data underline the potential of multimodal imaging markers to study structure-function-cognition relationships in the living human brain and provide important in vivo evidence for an involvement of the human BF in cortical activity and cognitive function.

摘要

基底前脑(BF)胆碱能核团的退化与认知功能下降有关,并且这种效应被认为是由去神经支配的皮质区域的神经元功能障碍介导的。基于MRI的BF萎缩测量越来越多地被用作胆碱能退化的体内替代标志物,但BF体积减少的功能意义尚未得到很好的理解。我们使用了132名轻度认知障碍(MCI)受试者和177名认知正常对照的高分辨率MRI、氟脱氧葡萄糖正电子发射断层扫描(PET)和神经心理学测试数据,以确定BF萎缩、皮质代谢减退和认知缺陷之间的关联。MCI中的BF萎缩与记忆功能受损和注意力控制缺陷均相关,而海马体积更具体地与记忆缺陷相关。BF萎缩还与广泛的皮质代谢减退相关,路径分析模型表明,特定领域皮质网络中的代谢减退介导了BF体积与认知功能障碍之间的关联。使用AV45-PET评估的皮质淀粉样蛋白病理学的存在与观察到的关联没有显著相互作用。这些数据强调了多模态成像标志物在研究活体人类大脑结构-功能-认知关系方面的潜力,并为人类BF参与皮质活动和认知功能提供了重要的体内证据。

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