Evidence map›Paper›PMID 42812060›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University

[Plasma metabolomics combined with machine learning for classifying ischemic stroke subtypes and predicting the etiology of cryptogenic stroke].

Yinyu Zi, Zimiao Liu, Zhen Deng

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Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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3 authors.

Yinyu ZiDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Zimiao LiuDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Zhen DengDepartment of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

Funding

National Natural Science Foundation of China 82271305
6 · The paper itself

Abstract

objectivesTo analyze plasma metabolic profiles of different ischemic stroke subtypes and construct machine learning (ML)-based models to identify these subtypes for accurate diagnosis of cryptogenic stroke.

methodsA total of 277 patients with acute ischemic stroke (AIS) from 3 hospitals were prospectively enrolled and stratified according to the TOAST classification criteria. Venous blood samples were collected for ¹H-NMR metabolomics detection, resulting in the identification of 46 metabolites. Metabolomics and Mendelian randomization analyses were employed to identify the potential biomarkers, and PyCaret was used to develop and optimize the ML models. A Plasma Metabolite Machine Learning (PMML) model was developed to differentiate the ischemic stroke subtypes, and the efficacy of the model was validated using a cryptogenic stroke (SUE) cohort.

resultsSignificantly different metabolite profiles were observed among patients with large artery atherosclerosis (LAA), small vessel occlusion (SVO), and cardioembolism (CE). Mendelian randomization analysis indicated that glucose and proline may serve as potential biomarkers for SVO and LAA. The PMML model developed based on the metabolic profiles of LAA, SVO, and CE demonstrated a high predictive accuracy for distinguishing these ischemic stroke subtypes with an accuracy of 0.8630 and an area under the ROC curve of 0.9586. In the SUE patients (the validation cohort), 23.9% of the patients predicted to have LAA exhibited vulnerable plaques, as compared with a rate of 10.9% in those predicted to have SVO or CE. Five patients predicted to have CE were diagnosed with paroxysmal atrial fibrillation via long-term electrocardiographic monitoring.

conclusionsDifferent ischemic stroke subtypes have distinct plasma metabolic profiles. The PMML model developed based on plasma metabolic features of the 3 well-diagnosed stroke subtypes demonstrates a high accuracy in identifying these subtypes with a great potential for predicting the etiology of cryptogenic stroke.

Indexed as

Ischemic StrokeMachine LearningMetabolomicsStrokeAgedBiomarkersBrain IschemiaFemaleHumansMaleMiddle AgedPredictive Learning ModelsProspective StudiesBiomarkersacute ischemic strokecryptogenic strokemachine learningMendelian randomizationplasma metabolites

Identifiers

PMID42812060
PMCPMC13624998

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