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经尸检证实的阿尔茨海默病和额颞叶痴呆的不同MRI萎缩模式。

Distinct MRI atrophy patterns in autopsy-proven Alzheimer's disease and frontotemporal lobar degeneration.

作者信息

Rabinovici G D, Seeley W W, Kim E J, Gorno-Tempini M L, Rascovsky K, Pagliaro T A, Allison S C, Halabi C, Kramer J H, Johnson J K, Weiner M W, Forman M S, Trojanowski J Q, Dearmond S J, Miller B L, Rosen H J

机构信息

Memory and Aging Center, University of California, San Francisco, California 94143, USA.

出版信息

Am J Alzheimers Dis Other Demen. 2007;22(6):474-88. doi: 10.1177/1533317507308779.

Abstract

To better define the anatomic distinctions between Alzheimer's disease (AD) and frontotemporal lobar degeneration (FTLD), we retrospectively applied voxel-based morphometry to the earliest magnetic resonance imaging scans of autopsy-proven AD (N = 11), FTLD (N = 18), and controls (N = 40). Compared with controls, AD patients showed gray matter reductions in posterior temporoparietal and occipital cortex; FTLD patients showed atrophy in medial prefrontal and medial temporal cortex, insula, hippocampus, and amygdala; and patients with both disorders showed atrophy in dorsolateral and orbital prefrontal cortex and lateral temporal cortex (P(FWE-corr) < .05). Compared with FTLD, AD patients had decreased gray matter in posterior parietal and occipital cortex, whereas FTLD patients had selective atrophy in anterior cingulate, frontal insula, subcallosal gyrus, and striatum (P < .001, uncorrected). These findings suggest that AD and FTLD are anatomically distinct, with degeneration of a posterior parietal network in AD and degeneration of a paralimbic fronto-insular-striatal network in FTLD.

摘要

为了更好地界定阿尔茨海默病(AD)与额颞叶变性(FTLD)之间的解剖学差异,我们对经尸检证实的AD患者(N = 11)、FTLD患者(N = 18)和对照组(N = 40)的最早磁共振成像扫描结果进行了回顾性体素形态学分析。与对照组相比,AD患者在颞顶叶后部和枕叶皮质出现灰质减少;FTLD患者在内侧前额叶、内侧颞叶皮质、脑岛、海马体和杏仁核出现萎缩;两种疾病的患者在背外侧和眶额皮质以及颞叶外侧皮质均出现萎缩(P(FWE校正) < 0.05)。与FTLD相比,AD患者顶叶后部和枕叶皮质的灰质减少,而FTLD患者在前扣带回、额叶脑岛、胼胝体下回和纹状体出现选择性萎缩(P < 0.001,未校正)。这些发现表明,AD和FTLD在解剖学上是不同的,AD表现为顶叶后部网络的退化,而FTLD表现为边缘旁额-岛-纹状体网络的退化。

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