伴淀粉样蛋白和tau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个诊断步骤吗?

IF 1.8 Q3 CLINICAL NEUROLOGY
Augustin Moreau , Elisabeth Ruppert , Frédéric Blanc , Olivier BOUSIGES , Benjamin Cretin
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引用次数: 0

摘要

病因不明的迟发性癫痫(LOEU)与痴呆风险增加有关。目前的生物标志物,包括脑脊液(CSF)和正电子发射断层扫描(PET)评估淀粉样蛋白和tau蛋白,往往不能预测相当一部分LOEU患者的认知能力下降。本病例报告报告了一位67岁男性路易体痴呆患者,后来发展为路易体痴呆(DLB)。随着认知能力下降的进展,出现的轻度临床特征引起了对DLB的怀疑。值得注意的是,这一阶段的脑脊液分析显示淀粉样蛋白和tau生物标志物呈阴性,但α -突触核蛋白种子扩增试验(CSF asyna - saa)显示病理性α -突触核蛋白阳性。这一发现强调了CSF asyna - saa在实现早期和更准确的DLB诊断方面的潜在临床应用。对于表现出突触核蛋白病早期体征的LOEU患者,将CSF asyna - saa纳入诊断组可以显著提高诊断的确定性、预后分层和靶向治疗干预的机会。在LOEU和进行性认知症状患者的脑脊液痴呆面板中添加asyna - saa的效果有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Late-onset unexplained epilepsy with dual amyloid and tau negativity: are alpha-synuclein seed amplification assays the next diagnostic step?
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.
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来源期刊
Epilepsy and Behavior Reports
Epilepsy and Behavior Reports Medicine-Neurology (clinical)
CiteScore
2.70
自引率
13.30%
发文量
54
审稿时长
50 days
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