Distinguishing Prodromal Dementia With Lewy Bodies From Prodromal Alzheimer Disease: A Longitudinal Study.

IF 2.3 Q3 CLINICAL NEUROLOGY Neurology. Clinical practice Pub Date : 2025-02-01 Epub Date: 2024-10-08 DOI:10.1212/CPJ.0000000000200380
Kathryn A Wyman-Chick, Tanis J Ferman, Daniel Weintraub, Melissa J Armstrong, Bradley F Boeve, Ece Bayram, Ella Chrenka, Matthew J Barrett
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Abstract

Background and objectives: It can be clinically challenging to differentiate dementia with Lewy bodies (DLB) and Alzheimer disease (AD). As potential therapies emerge with the goal of slowing or halting misfolded protein aggregation, it is imperative to be able to identify individuals before the disease becomes disabling. Differentiating between DLB and AD in the preclinical or prodromal phase of DLB and AD becomes more important. Studies are needed to validate the proposed criteria for prodromal DLB.

Methods: Longitudinal data were obtained from the Uniform Data Set of the National Alzheimer's Coordinating Center. Included participants had a baseline diagnosis of normal or mild cognitive impairment and a consecutive 2-year follow-up diagnosis of DLB or AD. We examined whether core DLB clinical features, supportive neuropsychiatric features, and neuropsychological data in the 2 years preceding the dementia diagnosis distinguished DLB from AD.

Results: We identified 143 participants with DLB and 429 age-matched/sex-matched participants with AD. The presence of 2 or more core DLB features in the year before dementia diagnosis yielded the greatest AUC (0.793; 95% CI 0.748-0.839) in distinguishing prodromal DLB from prodromal AD. Sleep disturbances, hallucinations, and a cognitive profile of worse processing speed, attention, and visuoconstruction performance were evident at least 2 years before the dementia diagnosis in DLB compared with AD.

Discussion: Data from this multisite, longitudinal, well-characterized research North American cohort support the validity of the recently published criteria for prodromal DLB. In the prodromal stage, patients who subsequently develop DLB are more likely to have core DLB clinical features and worse attention, processing speed, and visuospatial performance than those who go on to develop AD. Differentiation of DLB and AD before dementia emerges provides an opportunity for early, disease-specific intervention and overall management.

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区分前驱型路易体痴呆与前驱型阿尔茨海默病:一项纵向研究
背景和目的:区分路易体痴呆(DLB)和阿尔茨海默病(AD)在临床上具有挑战性。随着以减缓或阻止错误折叠蛋白聚集为目标的潜在疗法的出现,必须能够在疾病致残之前识别出患者。在 DLB 和 AD 的临床前或前驱阶段区分 DLB 和 AD 变得更加重要。需要进行研究来验证所提出的DLB前驱期标准:纵向数据来自国家阿尔茨海默氏症协调中心的统一数据集。纳入的参与者基线诊断为正常或轻度认知障碍,并连续两年随访诊断为DLB或AD。我们研究了核心 DLB 临床特征、支持性神经精神特征以及痴呆诊断前 2 年的神经心理学数据是否将 DLB 与 AD 区分开来:我们发现了 143 名 DLB 患者和 429 名年龄/性别匹配的 AD 患者。在痴呆诊断前一年出现 2 个或 2 个以上 DLB 核心特征的 AUC(0.793;95% CI 0.748-0.839)最高,可将前驱 DLB 与前驱 AD 区分开来。与AD相比,DLB患者在确诊痴呆症至少2年前就出现了明显的睡眠障碍、幻觉以及处理速度、注意力和视觉建构能力下降等认知特征:这个多地点、纵向、特征明确的北美研究队列的数据支持了最近公布的前驱DLB标准的有效性。在前驱阶段,后来发展为DLB的患者更有可能具有DLB的核心临床特征,其注意力、处理速度和视觉空间表现也比后来发展为AD的患者差。在痴呆症出现之前区分 DLB 和 AD,为早期进行疾病特异性干预和整体管理提供了机会。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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