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首页> 外文期刊>Neurobiology of Aging: Experimental and Clinical Research >CSF YKL-40 and pTau181 are related to different cerebral morphometric patterns in early AD
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CSF YKL-40 and pTau181 are related to different cerebral morphometric patterns in early AD

机译:CSF YKL-40和pTau181与AD早期不同的大脑形态计量模式有关

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摘要

Cerebrospinal fluid (CSF) concentrations of YKL-40 that serve as biomarker of neuroinflammation are known to be altered along the clinico-biological continuum of Alzheimer's disease (AD). The specific structural cerebral correlates of CSF YKL-40 were evaluated across the early stages of AD from normal to preclinical to mild dementia. Nonlinear gray matter (GM) volume associations with CSF YKL-40 levels were assessed in a total of 116 subjects, including normal controls and those with preclinical AD as defined by CSF Ab < 500 pg/mL, mild cognitive impairment (MCI) due to AD, or mild AD dementia. Agecorrected YKL-40 levels were increased in MCIs versus the rest of groups and showed an inverse u-shaped association with p-tau values. A similar nonlinear relationship was found between GM volume and YKL-40 in inferior and lateral temporal regions spreading to the supramarginal gyrus, insula, inferior frontal cortex, and cerebellum in MCI and AD. These findings for YKL-40 remained unchanged after adjusting for p-tau, which was found to be associated with GM volumes in distinct anatomic areas. CSF YKL-40, a biomarker of glial inflammation, is associated with a cerebral structural signature distinct from that related to p-tau neurodegeneration at the earliest stages of cognitive decline due to AD. (C) 2016 Elsevier Inc. All rights reserved.
机译:已知作为神经炎症生物标志物的YKL-40的脑脊液(CSF)浓度会随着阿尔茨海默氏病(AD)的临床生物学连续性而改变。在从正常,临床前到轻度痴呆的AD早期,评估了CSF YKL-40的特定结构脑相关性。总共评估了116名受试者的非线性灰质(GM)量与CSF YKL-40水平的关联,包括正常对照组和临床前AD定义为CSF Ab <500 pg / mL,轻度认知障碍(MCI)的受试者。 AD,或轻度AD痴呆。与其他组相比,年龄校正的YKL-40水平在MCI中升高,并显示出与p-tau值呈反U形关联。在MCI和AD中,颞下外侧区域的GM体积与YKL-40之间存在相似的非线性关系,并扩散到上颌回,岛突,额额皮层和小脑。调整了p-tau后,YKL-40的这些发现保持不变,这被发现与不同解剖区域的GM体积有关。脑脊液YKL-40是神经胶质炎症的生物标志物,在与AD相关的认知功能减退的最早阶段,其脑结构特征不同于与p-tau神经变性相关的脑结构特征。 (C)2016 Elsevier Inc.保留所有权利。

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