首页> 外文期刊>Frontiers in Human Neuroscience >Mapping the “What” and “Where” Visual Cortices and Their Atrophy in Alzheimer's Disease: Combined Activation Likelihood Estimation with Voxel-Based Morphometry
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Mapping the “What” and “Where” Visual Cortices and Their Atrophy in Alzheimer's Disease: Combined Activation Likelihood Estimation with Voxel-Based Morphometry

机译:映射阿尔茨海默氏病中“什么”和“何处”的视觉皮层及其萎缩:结合激活似然估计和基于体素的形态计量学

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The human cortical regions for processing high-level visual (HLV) functions of different categories remain ambiguous, especially in terms of their conjunctions and specifications. Moreover, the neurobiology of declined HLV functions in patients with Alzheimer's disease (AD) has not been fully investigated. This study provides a functionally sorted overview of HLV cortices for processing “what” and “where” visual perceptions and it investigates their atrophy in AD and MCI patients. Based upon activation likelihood estimation (ALE), brain regions responsible for processing five categories of visual perceptions included in “what” and “where” visions (i.e., object, face, word, motion, and spatial visions) were analyzed, and subsequent contrast analyses were performed to show regions with conjunctive and specific activations for processing these visual functions. Next, based on the resulting ALE maps, the atrophy of HLV cortices in AD and MCI patients was evaluated using voxel-based morphometry. Our ALE results showed brain regions for processing visual perception across the five categories, as well as areas of conjunction and specification. Our comparisons of gray matter (GM) volume demonstrated atrophy of three “where” visual cortices in late MCI group and extensive atrophy of HLV cortices (25 regions in both “what” and “where” visual cortices) in AD group. In addition, the GM volume of atrophied visual cortices in AD and MCI subjects was found to be correlated to the deterioration of overall cognitive status and to the cognitive performances related to memory, execution, and object recognition functions. In summary, these findings may add to our understanding of HLV network organization and of the evolution of visual perceptual dysfunction in AD as the disease progresses.
机译:用于处理不同类别的高级视觉(HLV)功能的人类皮层区域仍然模棱两可,尤其是在它们的结合和规格方面。此外,阿尔茨海默氏病(AD)患者HLV功能下降的神经生物学尚未得到充分研究。这项研究从功能上分类了HLV皮质,用于处理“什么”和“何处”的视觉感知,并调查了AD和MCI患者的萎缩。基于激活可能性估计(ALE),分析了负责处理“什么”和“何处”视觉(即物体,面部,单词,运动和空间视觉)中的五类视觉感知的大脑区域,并进行了后续对比进行分析以显示具有联合和特定激活作用的区域,以处理这些视觉功能。接下来,基于生成的ALE图,使用基于体素的形态计量学评估AD和MCI患者中HLV皮质的萎缩。我们的ALE结果显示出大脑区域可用于处理五个类别以及连接和规范区域中的视觉感知。我们对灰质(GM)体积的比较显示,晚期MCI组的三个“何处”视皮层萎缩,AD组的HLV皮质(“何处”和“何处”皮层25个区域)广泛萎缩。此外,发现AD和MCI受试者萎缩性视皮质的GM量与整体认知状态的恶化以及与记忆,执行和物体识别功能有关的认知表现有关。总而言之,这些发现可能会增加我们对HLV网络组织以及随着疾病进展AD中视觉知觉功能障碍演变的了解。

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