视神经脊髓炎
光谱紊乱
多路复用
髓鞘少突胶质细胞糖蛋白
多发性硬化
医学
质谱法
鉴别诊断
免疫学
病理
化学
生物信息学
实验性自身免疫性脑脊髓炎
生物
色谱法
精神科
作者
Wei Chen,Haojun Yu,Yong Hao,Wanshan Liu,Ruimin Wang,Yida Huang,Jiao Wu,Lei Feng,Yangtai Guan,Lin Huang,Kun Qian
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-10-11
卷期号:17 (20): 19779-19792
被引量:16
标识
DOI:10.1021/acsnano.3c03765
摘要
Timely screening of neuromyelitis optica spectrum disorder (NMOSD) and differential diagnosis from myelin oligodendrocyte glycoprotein associated disorder (MOGAD) are the keys to improving the quality of life of patients. Metabolic disturbance occurs with the development of NMOSD. Still, advanced tools are required to probe the metabolic phenotype of NMOSD. Here, we developed a fast nanoparticle-enhanced laser desorption/ionization mass spectrometry assay for multiplexing metabolic fingerprints (MFs) from trace plasma and cerebrospinal fluid (CSF) samples in 30 s. Machine learning of the plasma MFs achieved the timely screening of NMOSD from healthy donors with an area under receiver operator characteristic curve (AUROC) of 0.998, and it comprehensively revealed the dysregulated neurotransmitter and energy metabolisms. Combining comprehensive MFs from both plasma and CSF, we constructed an integrated panel for differential diagnosis of NMOSD versus MOGAD with an AUROC of 0.923. This approach demonstrated performance superior to that of human experts in classifying two diseases, especially in antibody assay-limited regions. Together, this approach provides an advanced nanomaterial-based tool for identifying vulnerable populations below the antibody threshold of aquaporin-4 positivity.
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