血浆和脑脊液神经丝蛋白轻链在临床中区分神经退行性疾病和原发性精神疾病

D. Eratne, M. Kang, C. Lewis, C. Dang, C. Malpas, M. Keem, J. Grewal, Vladimir Marinov, A. Coe, Cath Kaylor-Hughes, Thomas Borchard, Chhoa Keng-Hong, Alexandra Waxmann, Burcu Saglam, Tomáš Kalinčík, Richard Kanaan, W. Kelso, Andrew Evans, S. Farrand, S. Loi, M. Walterfang, C. Stehmann, Qiao-Xin Li, Steven Collins, C. L. Masters, A. Santillo, Henrik Zetterberg, K. Blennow, S. Berkovic, Dennis Velakoulis, Terence J. O’Brien, Patrick Kwan, O. Hansson, Christopher Fowler, Jane Gunn
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摘要

简介:许多神经退行性疾病(ND)患者面临诊断延误和误诊。我们研究了血液和脑脊液(CSF)中的神经丝蛋白轻链(NfL),以区分神经退行性疾病和原发性精神障碍(ND),这在临床上是一个常见的难题。方法:测量血浆和脑脊液中的神经丝蛋白轻链水平,并与年龄、性别和体重进行比较。结果:包括 337 名参与者:136 名 ND,77 名 PPD,124 名对照组。与 PPD 相比,ND 患者的血浆 NfL 高出 2.5 倍,诊断性能很强(曲线下面积,AUC 0.86,81%/85% 特异性/敏感性),与 CSF NfL(高出 2 倍,AUC 0.89,95%/71% 特异性/敏感性)相当。诊断性能在年轻人(40-<60 岁)中尤为突出。研究还发现了灵敏度和特异性的最佳临界值,以及对未来临床应用具有重要意义的问题:这项研究为一种基于血液的简单生物标志物提供了重要证据,有助于在临床环境中筛查神经变性并与 PPD 区分开来。
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Plasma and CSF neurofilament light chain distinguish neurodegenerative from primary psychiatric conditions in a clinical setting
INTRODUCTION: Many patients with neurodegenerative disorders (ND) face diagnostic delay and misdiagnosis. We investigated blood and cerebrospinal fluid (CSF) neurofilament light chain (NfL) to distinguish ND from primary psychiatric disorders (ND), a common challenge in clinical settings. METHODS: Plasma and CSF NfL levels were measured and compared between groups, adjusting for age, sex, weight. RESULTS: 337 participants included: 136 ND, 77 PPD, 124 Controls. Plasma NfL was 2.5 fold elevated in ND compared to PPD and had strong diagnostic performance (area under the curve, AUC 0.86, 81%/85% specificity/sensitivity) that was comparable to CSF NfL (2 fold elevated, AUC 0.89, 95%/71% specificity/sensitivity). Diagnostic performance was especially strong in younger people (40-<60years). Additional findings were cut-offs optimised for sensitivity and specificity, and issues important for future clinical translation CONCLUSIONS: This study adds important evidence for a simple blood-based biomarker to assist as a screening test for neurodegeneration and distinction from PPD, in clinical settings.
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