The early-onset Alzheimer's disease MRI signature: a replication and extension analysis in early-stage AD.

IF 2.9 2区 医学 Q2 NEUROSCIENCES Cerebral cortex Pub Date : 2024-12-03 DOI:10.1093/cercor/bhae475
Rashi I Mehta, Cierra M Keith, Camila Vieira Ligo Teixeira, Patrick D Worhunsky, Holly E Phelps, Melanie Ward, Mark Miller, R Osvaldo Navia, Stephanie Pockl, Nafiisah Rajabalee, Michelle M Coleman, Pierre-François D'Haese, Ali R Rezai, Kirk C Wilhelmsen, Marc W Haut
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Abstract

Early-onset Alzheimer's disease (EOAD) is less investigated than the more common late-onset Alzheimer's disease (LOAD) despite its more aggressive course. A cortical signature of EOAD was recently proposed and may facilitate EOAD investigation. Here, we aimed to validate this proposed MRI biomarker of EOAD neurodegeneration in an Appalachian clinical cohort. We also compared differences in EOAD signature atrophy in participants with biomarker-positive EOAD, LOAD, early-onset non-AD pathologies, and cognitively normal individuals. Cortical thinning was reliably detected in eight of nine signature areas of persons with EOAD relative to cognitively normal individuals despite very early disease stage. Additionally, individuals with EOAD showed thinner cortex in most signature regions relative to those with early-onset non-AD pathologies. EOAD and LOAD showed similar cortical atrophy within most EOAD signature regions. Whole-brain vertex-wise cortical analyses supported these findings. Furthermore, signature cortical atrophy showed expected relationships with measures of global and specific cognitive and functional status. This investigation further validates and expands upon the recently defined EOAD signature and suggests its robustness within a rural population, even at early disease stage. Larger scale and longitudinal studies employing this marker of EOAD neurodegeneration are needed to further understand clinical effects and appropriate management of persons with EOAD.

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早发性阿尔茨海默病的MRI特征:早期AD的复制和扩展分析。
早发性阿尔茨海默病(EOAD)的研究少于更常见的晚发性阿尔茨海默病(LOAD),尽管其病程更具侵袭性。最近提出了EOAD的皮质特征,这可能有助于EOAD的研究。在这里,我们的目的是在阿巴拉契亚临床队列中验证这种提出的EOAD神经退行性变的MRI生物标志物。我们还比较了生物标志物阳性EOAD、LOAD、早发性非ad病理和认知正常个体在EOAD特征萎缩方面的差异。尽管疾病处于非常早期的阶段,但相对于认知正常的个体,在EOAD患者的9个特征区域中,有8个区域可靠地检测到皮质变薄。此外,与早发性非阿尔茨海默病患者相比,EOAD患者在大多数特征区域的皮层更薄。在大多数EOAD特征区域,EOAD和LOAD表现出相似的皮质萎缩。全脑皮层顶点分析支持这些发现。此外,特征皮质萎缩与整体和特定认知和功能状态的测量显示出预期的关系。这项研究进一步验证和扩展了最近定义的EOAD特征,并表明其在农村人口中的稳健性,即使在早期疾病阶段。为了进一步了解EOAD患者的临床效果和适当的管理,需要采用这种神经退行性变标志物进行更大规模的纵向研究。
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来源期刊
Cerebral cortex
Cerebral cortex 医学-神经科学
CiteScore
6.30
自引率
8.10%
发文量
510
审稿时长
2 months
期刊介绍: Cerebral Cortex publishes papers on the development, organization, plasticity, and function of the cerebral cortex, including the hippocampus. Studies with clear relevance to the cerebral cortex, such as the thalamocortical relationship or cortico-subcortical interactions, are also included. The journal is multidisciplinary and covers the large variety of modern neurobiological and neuropsychological techniques, including anatomy, biochemistry, molecular neurobiology, electrophysiology, behavior, artificial intelligence, and theoretical modeling. In addition to research articles, special features such as brief reviews, book reviews, and commentaries are included.
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