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阿尔茨海默病导致轻度认知障碍时偶然发现的突触核蛋白病的影响。

Impact of incidental synucleinopathy in mild cognitive impairment due to Alzheimer disease.

机构信息

University of Arizona College of Medicine, Phoenix, Arizona, USA.

Department of Biomedical Informatics, University of Arizona College of Medicine, Phoenix, Arizona, USA.

出版信息

J Neuropathol Exp Neurol. 2024 Mar 20;83(4):230-237. doi: 10.1093/jnen/nlae009.

Abstract

Recent evidence suggests that the presence of α-synuclein Lewy bodies (LBs) correlates with accelerated disease progression in patients with Alzheimer disease (AD) but it is unclear whether this effect is also exerted in the mild cognitive impairment (MCI) phase of AD. We sought to determine whether incidental LB pathology in patients with MCI due to AD is associated with a faster rate of cognitive decline compared to MCI controls without LB pathology. We identified patients within the National Alzheimer's Coordinating Center (NACC) database with MCI due to AD and stratified the cohort by the presence or absence of synucleinopathy. We utilized a repeated measures longitudinal analysis of Mini-Mental State Examination (MMSE) scores to determine whether the decline in performance occurred at a greater rate in the synucleinopathy patients. A total of 206 participants were studied; 80 had coincident synucleinopathy. The rate of decline in MMSE scores between the groups did not differ. This may suggest that a synergistic effect of LB and AD neuropathology is only appreciable in the later stages of disease progression. Further investigation into the effect of mixed LB and AD pathology in the early stages of cognitive impairment is warranted to highlight opportunities for targeted early intervention in patients.

摘要

最近的证据表明,α-突触核蛋白路易体(LB)的存在与阿尔茨海默病(AD)患者的疾病进展加速相关,但尚不清楚这种影响是否也存在于 AD 的轻度认知障碍(MCI)阶段。我们试图确定 AD 引起的 MCI 患者偶然存在的 LB 病理学是否与无 LB 病理学的 MCI 对照组相比,认知下降速度更快。我们在国家阿尔茨海默病协调中心(NACC)数据库中确定了由于 AD 而患有 MCI 的患者,并根据是否存在突触核蛋白病对队列进行分层。我们利用 Mini-Mental State Examination(MMSE)评分的重复测量纵向分析来确定在突触核蛋白病患者中,表现下降的速度是否更快。共有 206 名参与者接受了研究;80 人有同时发生的突触核蛋白病。两组之间 MMSE 评分的下降速度没有差异。这可能表明 LB 和 AD 神经病理学的协同作用仅在疾病进展的后期阶段才明显。进一步研究混合 LB 和 AD 病理学在认知障碍早期的影响,对于强调针对患者的早期干预机会是必要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdd4/10951969/8fadd19a588d/nlae009f1.jpg

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