Department of Neurology and Institute of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
Department of Laboratory Medicine, Fujian Medical University, Fuzhou, China.
Ann Clin Transl Neurol. 2020 Oct;7(10):2010-2018. doi: 10.1002/acn3.51194. Epub 2020 Sep 19.
Amyotrophic lateral sclerosis (ALS) is an adult-onset fatal neurodegenerative disease which lacks identified biological markers. A label-free plasma surface-enhanced Raman spectroscopy (SERS) method was developed to explore a simple and noninvasive test for ALS.
ALS patients were enrolled serially and plasma samples were collected at the time of diagnosis prior to the start of ALS treatment. SERS spectra were recorded using a Renishaw micro-Raman system.
To exclude the interference by varying disease severity, we enrolled three groups of ALS patients, including ALS-1 (n = 60; ALSFRS-R ≥ 42 and time interval ≤ 12 months), ALS-2 (n = 61; ALSFRS-R < 42 and time interval ≤ 12 months), and ALS-3 (n = 61; ALSFRS-R ≥ 38 and time interval> 12 months). The SERS spectra were analyzed using principal component analysis (PCA), which showed that ALS-1, ALS-2, ALS-3, and control groups were separated significantly. Then, decision tree (DT) models and receiver operating characteristic curves were employed and identified that bands at 722 and 739 cm , and ratios of 635-722 cm and 635-739 cm were able to distinguish ALS from controls significantly. Finally, we highlighted six metabolism pathways correlated with ALS, including phenylalanine-tyrosine-tryptophan biosynthesis, aminoacyl-tRNA biosynthesis, phenylalanine metabolism, pantothenate and CoA biosynthesis, porphyrin and chlorophyll metabolism, and pyrimidine metabolism.
Plasma SERS could be a promising tool for the detection of ALS. The bands at 722 and 739 cm , and the ratios of 635-722 cm and 635-739 cm could serve as potential indicator for ALS.
肌萎缩侧索硬化症(ALS)是一种成年起病的致命神经退行性疾病,目前缺乏明确的生物学标志物。本研究建立了一种无标记的血浆表面增强拉曼光谱(SERS)方法,旨在探索一种简单、无创的 ALS 检测方法。
连续纳入 ALS 患者,在开始 ALS 治疗前采集诊断时的血浆样本。使用 Renishaw 微拉曼系统记录 SERS 光谱。
为排除疾病严重程度的干扰,我们纳入了三组 ALS 患者,包括 ALS-1 组(n=60;ALSFRS-R≥42 且时间间隔≤12 个月)、ALS-2 组(n=61;ALSFRS-R<42 且时间间隔≤12 个月)和 ALS-3 组(n=61;ALSFRS-R≥38 且时间间隔>12 个月)。采用主成分分析(PCA)对 SERS 光谱进行分析,结果显示 ALS-1、ALS-2、ALS-3 和对照组之间存在显著差异。然后,我们采用决策树(DT)模型和受试者工作特征曲线来识别,发现 722 和 739cm处的波段以及 635-722cm 和 635-739cm 的比值能够显著区分 ALS 与对照组。最后,我们还重点分析了与 ALS 相关的 6 条代谢途径,包括苯丙氨酸-酪氨酸-色氨酸生物合成、氨酰-tRNA 生物合成、苯丙氨酸代谢、泛酸和 CoA 生物合成、卟啉和叶绿素代谢以及嘧啶代谢。
血浆 SERS 可能是 ALS 检测的一种很有前途的工具。722 和 739cm 处的波段以及 635-722cm 和 635-739cm 的比值可作为 ALS 的潜在标志物。