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伴有淀粉样蛋白和tau蛋白双阴性的迟发性不明原因癫痫:α-突触核蛋白种子扩增检测是下一步的诊断手段吗?

Late-onset unexplained epilepsy with dual amyloid and tau negativity: are alpha-synuclein seed amplification assays the next diagnostic step?

作者信息

Moreau Augustin, Ruppert Elisabeth, Blanc Frédéric, Bousiges Olivier, Cretin Benjamin

机构信息

Centre Mémoire, de Ressources et de Recherche d'Alsace (Strasbourg-Colmar), France.

Unité de Neuropsychologie, Service de Neurologie et hôpital de jour de Gériatrie, pôle de Gériatrie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

出版信息

Epilepsy Behav Rep. 2025 Jun 13;31:100783. doi: 10.1016/j.ebr.2025.100783. eCollection 2025 Sep.

Abstract

Late-onset epilepsy of unknown etiology (LOEU) is associated with an increased risk of dementia. Current biomarkers, including cerebrospinal fluid (CSF) and positron emission tomography (PET) assessments for amyloid and tau, often fail to predict cognitive decline in a substantial proportion of LOEU patients. This case report presents a 67-year-old man with LOEU who later developed dementia with Lewy bodies (DLB). As cognitive decline progressed, emerging mild clinical features raised suspicion for DLB. Notably, cerebrospinal fluid analysis at this stage revealed negative amyloid and tau biomarkers but was positive for pathological alpha-synuclein using alpha-synuclein seed amplification assay (CSF ASyn-SAA). This finding highlights the potential clinical utility of CSF ASyn-SAA in achieving both earlier and more accurate DLB diagnosis. For LOEU patients exhibiting early signs of synucleinopathy, incorporating CSF ASyn-SAA into diagnostic panels could significantly improve diagnostic certainty, prognostic stratification, and opportunities for targeted therapeutic interventions. Further research is needed to investigate the yield of adding ASyn-SAA to CSF dementia panels in people with LOEU and progressive cognitive symptoms.

摘要

病因不明的迟发性癫痫(LOEU)与痴呆风险增加相关。目前的生物标志物,包括用于评估淀粉样蛋白和tau的脑脊液(CSF)及正电子发射断层扫描(PET)检查,在很大一部分LOEU患者中常常无法预测认知功能下降。本病例报告介绍了一名67岁患有LOEU的男性,其后来发展为路易体痴呆(DLB)。随着认知功能下降的进展,新出现的轻微临床特征引发了对DLB的怀疑。值得注意的是,在此阶段的脑脊液分析显示淀粉样蛋白和tau生物标志物为阴性,但使用α-突触核蛋白种子扩增检测(CSF ASyn-SAA)检测病理性α-突触核蛋白呈阳性。这一发现凸显了CSF ASyn-SAA在更早、更准确地诊断DLB方面的潜在临床应用价值。对于表现出突触核蛋白病早期迹象的LOEU患者,将CSF ASyn-SAA纳入诊断指标体系可显著提高诊断确定性、预后分层以及进行靶向治疗干预的机会。需要进一步研究来调查在患有LOEU和进行性认知症状的人群中,将ASyn-SAA添加到脑脊液痴呆指标体系中的诊断价值。

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