Noh Young, Jeon Seun, Lee Jong Min, Seo Sang Won, Kim Geon Ha, Cho Hanna, Ye Byoung Seok, Yoon Cindy W, Kim Hee Jin, Chin Juhee, Park Kee Hyung, Heilman Kenneth M, Na Duk L
From the Department of Neurology (Y.N., K.H.P.), Gachon University Gil Medical Center, Incheon; Department of Biomedical Engineering (S.J., J.M.L.), Hanyang University, Seoul; Department of Neurology (S.W.S., H.J.K., J.C., D.L.N.), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul; Department of Neurology (G.H.K.), Ewha Womans University Mokdong Hospital, Ewha Womans University School of Medicine, Seoul; Department of Neurology (H.C.), Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul; Department of Neurology (B.S.Y.), Yonsei University College of Medicine, Seoul; Department of Neurology (C.W.Y.), Inha University Hospital, Inha University School of Medicine, Incheon, Korea; and Department of Neurology (K.M.H.), University of Florida and Veterans Affairs Medical Center, Gainesville.
Neurology. 2014 Nov 18;83(21):1936-44. doi: 10.1212/WNL.0000000000001003. Epub 2014 Oct 24.
Because the signs associated with dementia due to Alzheimer disease (AD) can be heterogeneous, the goal of this study was to use 3-dimensional MRI to examine the various patterns of cortical atrophy that can be associated with dementia of AD type, and to investigate whether AD dementia can be categorized into anatomical subtypes.
High-resolution T1-weighted volumetric MRIs were taken of 152 patients in their earlier stages of AD dementia. The images were processed to measure cortical thickness, and hierarchical agglomerative cluster analysis was performed using Ward's clustering linkage. The identified clusters of patients were compared with an age- and sex-matched control group using a general linear model.
There were several distinct patterns of cortical atrophy and the number of patterns varied according to the level of cluster analyses. At the 3-cluster level, patients were divided into (1) bilateral medial temporal-dominant atrophy subtype (n = 52, ∼ 34.2%), (2) parietal-dominant subtype (n = 28, ∼ 18.4%) in which the bilateral parietal lobes, the precuneus, along with bilateral dorsolateral frontal lobes, were atrophic, and (3) diffuse atrophy subtype (n = 72, ∼ 47.4%) in which nearly all association cortices revealed atrophy. These 3 subtypes also differed in their demographic and clinical features.
This cluster analysis of cortical thickness of the entire brain showed that AD dementia in the earlier stages can be categorized into various anatomical subtypes, with distinct clinical features.
由于阿尔茨海默病(AD)所致痴呆的体征可能具有异质性,本研究的目的是使用三维磁共振成像(MRI)检查与AD型痴呆相关的各种皮质萎缩模式,并研究AD痴呆是否可分为解剖学亚型。
对152例处于AD痴呆早期阶段的患者进行高分辨率T1加权容积MRI检查。对图像进行处理以测量皮质厚度,并使用沃德聚类连接法进行层次凝聚聚类分析。使用一般线性模型将确定的患者聚类与年龄和性别匹配的对照组进行比较。
存在几种不同的皮质萎缩模式,模式数量根据聚类分析水平而有所不同。在三聚类水平上,患者被分为:(1)双侧内侧颞叶为主的萎缩亚型(n = 52,约34.2%);(2)顶叶为主的亚型(n = 28,约18.4%),其中双侧顶叶、楔前叶以及双侧背外侧额叶萎缩;(3)弥漫性萎缩亚型(n = 72,约47.4%),其中几乎所有联合皮质均显示萎缩。这三种亚型在人口统计学和临床特征方面也存在差异。
对全脑皮质厚度进行的聚类分析表明,早期AD痴呆可分为具有不同临床特征的各种解剖学亚型。