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Diagnosis of epilepsy by machine learning of high-performance plasma metabolic fingerprinting.
Chen, Xiaonan; Yu, Wendi; Zhao, Yinbing; Ji, Yuxi; Qi, Ziheng; Guan, Yangtai; Wan, Jingjing; Hao, Yong.
Affiliation
  • Chen X; School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, PR China.
  • Yu W; Department of Neurology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, PR China.
  • Zhao Y; School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, PR China.
  • Ji Y; School of Medicine, Shanghai Jiao Tong University, Shanghai, 200025, PR China.
  • Qi Z; School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, PR China.
  • Guan Y; Department of Neurology, Punan Branch of Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200125, PR China. Electronic address: yangtaiguan@sina.com.
  • Wan J; School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200241, PR China. Electronic address: jjwan@chem.ecnu.edu.cn.
  • Hao Y; Department of Neurology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, 200127, PR China. Electronic address: haoyong@renji.com.
Talanta ; 277: 126328, 2024 Sep 01.
Article in En | MEDLINE | ID: mdl-38824860
ABSTRACT
Epilepsy is a chronic neurological disorder that causes a major threat to public health and the burden of disease worldwide. High-performance diagnostic tools for epilepsy need to be developed to improve diagnostic accuracy and efficiency while still missing. Herein, we utilized nanoparticle-enhanced laser desorption/ionization mass spectrometry (NELDI MS) to acquire plasma metabolic fingerprints (PMFs) from epileptic and healthy individuals for timely and accurate screening of epilepsy. The NELDI MS enabled high detection speed (∼30 s per sample), high throughput (up to 384 samples per run), and favorable reproducibility (coefficients of variation <15 %), acquiring high-performed PMFs. We next constructed an epilepsy diagnostic model by machine learning of PMFs, achieving desirable diagnostic capability with the area under the curve (AUC) value of 0.941 for the validation set. Furthermore, four metabolites were identified as a diagnostic biomarker panel for epilepsy, with an AUC value of 0.812-0.860. Our approach provides a high-performed and high-throughput platform for epileptic diagnostics, promoting the development of metabolic diagnostic tools in precision medicine.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Machine Learning Limits: Adult / Female / Humans / Male Language: En Journal: Talanta Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Machine Learning Limits: Adult / Female / Humans / Male Language: En Journal: Talanta Year: 2024 Document type: Article Country of publication: