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认知障碍个体路易体病理的临床影响。

Clinical effects of Lewy body pathology in cognitively impaired individuals.

机构信息

IRCCS, Istituto delle Scienze Neurologiche di Bologna (ISNB), Bologna, Italy.

Clinical Memory Research Unit, Department of Clinical Sciences, Malmö, Lund University, Lund, Sweden.

出版信息

Nat Med. 2023 Aug;29(8):1964-1970. doi: 10.1038/s41591-023-02449-7. Epub 2023 Jul 18.

DOI:10.1038/s41591-023-02449-7
PMID:37464058
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10427416/
Abstract

There is poor knowledge about the clinical effects of Lewy body (LB) pathology in patients with cognitive impairment, especially when coexisting with Alzheimer's disease (AD) pathology (amyloid-β and tau). Using a seed amplification assay, we analyzed cerebrospinal fluid for misfolded LB-associated α-synuclein in 883 memory clinic patients with mild cognitive impairment or dementia from the BioFINDER study. Twenty-three percent had LB pathology, of which only 21% fulfilled clinical criteria of Parkinson's disease or dementia with Lewy bodies at baseline. Among these LB-positive patients, 48% had AD pathology. Fifty-four percent had AD pathology in the whole sample (17% of mild cognitive impairment and 24% of patients with dementia were also LB-positive). When examining independent cross-sectional effects, LB pathology but not amyloid-β or tau, was associated with hallucinations and worse attention/executive, visuospatial and motor function. LB pathology was also associated with faster longitudinal decline in all examined cognitive functions, independent of amyloid-β, tau, cognitive stage and a baseline diagnosis of dementia with Lewy bodies/Parkinson's disease. LB status provides a better precision-medicine approach to predict clinical trajectories independent of AD biomarkers and a clinical diagnosis, which could have implications for the clinical management of cognitive impairment and the design of AD and LB drug trials.

摘要

对于认知障碍患者,尤其是合并阿尔茨海默病(AD)病理(β淀粉样蛋白和 tau)的患者,路易体(LB)病理的临床影响知之甚少。本研究使用种子扩增检测法,分析了 BioFINDER 研究中 883 名记忆诊所轻度认知障碍或痴呆患者的脑脊液中错误折叠的 LB 相关 α-突触核蛋白。23%的患者存在 LB 病理,但只有 21%的患者在基线时符合帕金森病或路易体痴呆的临床标准。在这些 LB 阳性患者中,48%存在 AD 病理。在整个样本中,54%存在 AD 病理(轻度认知障碍患者中占 17%,痴呆患者中占 24%)。当检查独立的横断面影响时,LB 病理而非β淀粉样蛋白或 tau 与幻觉以及注意力/执行、视空间和运动功能更差相关。LB 病理也与所有检查的认知功能的纵向衰退更快相关,独立于β淀粉样蛋白、tau、认知阶段和路易体痴呆/帕金森病的基线诊断。LB 状态提供了一种更好的精准医学方法,可以预测独立于 AD 生物标志物和临床诊断的临床轨迹,这可能对认知障碍的临床管理以及 AD 和 LB 药物试验的设计具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/10427416/cb4f39c83338/41591_2023_2449_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/10427416/44cc740e86e9/41591_2023_2449_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/10427416/408051b080ca/41591_2023_2449_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/10427416/cb4f39c83338/41591_2023_2449_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/10427416/44cc740e86e9/41591_2023_2449_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/10427416/408051b080ca/41591_2023_2449_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/10427416/cb4f39c83338/41591_2023_2449_Fig3_HTML.jpg

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