Prevalence and clinical impact of alpha-synuclein pathology in idiopathic normal pressure hydrocephalus: Insights from RT-QuIC assay

IF 3.1 3区 医学 Q2 CLINICAL NEUROLOGY
Je kook Yu , Hye Joung Choi , Dongwoo Kim , Pham Hong Ngoc , In Hee Kwak , Huu Dat Nguyen , Trung Nguyen Thanh , Suk Jun Song , Jeongjae Lee , Hyeo-il Ma , Young Eun Kim
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Abstract

Background

The relationship between idiopathic normal pressure hydrocephalus (iNPH) and synucleinopathy remains unclear. This study aimed to explore the prevalence of α-synuclein pathology in iNPH patients and its impact on clinical outcomes.

Methods

We enrolled 33 iNPH patients without evidence of nigrostriatal degeneration. Cerebrospinal fluid (CSF) was analyzed using the real-time quaking-induced conversion (RT-QuIC) assay to detect α-synuclein aggregates. Clinical assessments included the Timed Up and Go (TUG) test and Mini-Mental State Examination (MMSE), performed before and after a CSF tap test.

Results

Among the 33 patients, 11 (33.3 %) tested positive for α-synuclein pathology. Baseline demographic and clinical characteristics were similar between α-synuclein positive and negative groups (p > 0.05). The MMSE and TUG tests showed no significant differences between the groups before or after the tap test. However, the RT-QuIC negative group showed significant improvement in TUG times and steps post-tap test (p < 0.05), while the positive group showed a non-significant trend towards improvement (p = 0.06). Clinical global impression improved in 26 patients after CSF drainage, with similar rates in both groups (p = 0.88). Eleven patients (5 α-synuclein RT-QuIC positive and 6 negative) underwent shunt surgery, all of whom reported improvement over a median follow-up of 1.29 years.

Conclusion

α-synuclein pathology is present in a significant proportion of iNPH patients. Although gait improvement during the tap test was evident in α-synuclein negative group, both groups showed improvement. These findings underscore the need for further longitudinal studies to elucidate the long-term clinical impact of α-synuclein pathology in iNPH.
特发性常压脑积水中α -突触核蛋白病理学的患病率和临床影响:来自RT-QuIC分析的见解
特发性正常压力脑积水(iNPH)与突触核蛋白病之间的关系尚不清楚。本研究旨在探讨α-突触核蛋白病理在iNPH患者中的患病率及其对临床预后的影响。方法33例无黑质纹状体变性的iNPH患者。采用实时地震诱导转化(RT-QuIC)法检测脑脊液α-突触核蛋白聚集体。临床评估包括在脑脊液抽头测试前后进行的Timed Up and Go (TUG)测试和迷你精神状态检查(MMSE)。结果33例患者中α-突触核蛋白病理阳性11例(33.3%)。α-突触核蛋白阳性组和阴性组的基线人口学和临床特征相似(p >;0.05)。MMSE和TUG测试结果显示,两组在抽头测试前后无显著差异。然而,RT-QuIC阴性组在TUG次数和步数上有显著改善(p <;0.05),阳性组无显著改善趋势(p = 0.06)。26例患者经脑脊液引流后临床整体印象改善,两组的改善率相似(p = 0.88)。11例患者(5例α-突触核蛋白RT-QuIC阳性,6例阴性)接受分流手术,所有患者均报告在中位随访1.29年期间改善。结论α-突触核蛋白病理在iNPH患者中占有显著比例。虽然α-synuclein阴性组在踢腿试验中步态改善明显,但两组均有改善。这些发现强调需要进一步的纵向研究来阐明α-突触核蛋白病理在iNPH中的长期临床影响。
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来源期刊
Parkinsonism & related disorders
Parkinsonism & related disorders 医学-临床神经学
CiteScore
6.20
自引率
4.90%
发文量
292
审稿时长
39 days
期刊介绍: Parkinsonism & Related Disorders publishes the results of basic and clinical research contributing to the understanding, diagnosis and treatment of all neurodegenerative syndromes in which Parkinsonism, Essential Tremor or related movement disorders may be a feature. Regular features will include: Review Articles, Point of View articles, Full-length Articles, Short Communications, Case Reports and Letter to the Editor.
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