Plasmonic alloys enhance metabolic fingerprints for rapid diagnosis and classification of myocardial infarction
Although cardiac troponin (cTn) is a recommended clinical biomarker of myocardial infarction (MI), it is inefficient for MI diagnosis requiring serial cTn measurements and is inaccurate for MI subtype identification. Advanced bioanalytical platforms commonly rely on materials with tailored structure...
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Published in | Nano today Vol. 62; p. 102702 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.06.2025
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Subjects | |
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Abstract | Although cardiac troponin (cTn) is a recommended clinical biomarker of myocardial infarction (MI), it is inefficient for MI diagnosis requiring serial cTn measurements and is inaccurate for MI subtype identification. Advanced bioanalytical platforms commonly rely on materials with tailored structure and composition. Here, we construct porous PtAu alloys to effectively extract serum metabolic fingerprints (SMFs) via laser desorption/ionization mass spectrometry (LDI-MS), achieving accurate diagnosis and classification of MI by machine learning of SMFs. The PtAu alloys demonstrate enhanced metabolite detection, superior to the monometallic nanoparticles and organic matrix. It is attributed to the porous structure, enhanced photocurrent response, electromagnetic field, and photothermal conversion. Machine learning of SMFs yields diagnostic models with the area under curves (AUCs) of 0.941–1 for 604 subjects from multiple centers in a serum test, overcoming the clinical inefficiency for serial cTn measurements. In particular, our platform achieves accurate discrimination among patients with type 1 MI, type 2 MI, and myocardial injury, with a maximum AUC of 0.905, outperforming the cTn biomarker. Notably, the diagnosis and classification for MI can be finished within ∼30 min. Our platform has the potential to reduce time spent in the emergency department and improve treatment for MI.
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•The mesoporous PtAu alloys achieved ultrasensitive detection of metabolites with the limit of detection of fmol.•The mechanism of enhanced LDI process by alloys was revealed by experimental results and theoretical simulation.•Machine learning of SMFs yielded accurate diagnostic models with the area under curves (AUCs) of 0.941–1 for 604 subjects.•Our platform achieved accurate discrimination of MI subtypes within ∼30 min, with a maximum AUC of 0.905. |
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AbstractList | Although cardiac troponin (cTn) is a recommended clinical biomarker of myocardial infarction (MI), it is inefficient for MI diagnosis requiring serial cTn measurements and is inaccurate for MI subtype identification. Advanced bioanalytical platforms commonly rely on materials with tailored structure and composition. Here, we construct porous PtAu alloys to effectively extract serum metabolic fingerprints (SMFs) via laser desorption/ionization mass spectrometry (LDI-MS), achieving accurate diagnosis and classification of MI by machine learning of SMFs. The PtAu alloys demonstrate enhanced metabolite detection, superior to the monometallic nanoparticles and organic matrix. It is attributed to the porous structure, enhanced photocurrent response, electromagnetic field, and photothermal conversion. Machine learning of SMFs yields diagnostic models with the area under curves (AUCs) of 0.941–1 for 604 subjects from multiple centers in a serum test, overcoming the clinical inefficiency for serial cTn measurements. In particular, our platform achieves accurate discrimination among patients with type 1 MI, type 2 MI, and myocardial injury, with a maximum AUC of 0.905, outperforming the cTn biomarker. Notably, the diagnosis and classification for MI can be finished within ∼30 min. Our platform has the potential to reduce time spent in the emergency department and improve treatment for MI.
[Display omitted]
•The mesoporous PtAu alloys achieved ultrasensitive detection of metabolites with the limit of detection of fmol.•The mechanism of enhanced LDI process by alloys was revealed by experimental results and theoretical simulation.•Machine learning of SMFs yielded accurate diagnostic models with the area under curves (AUCs) of 0.941–1 for 604 subjects.•Our platform achieved accurate discrimination of MI subtypes within ∼30 min, with a maximum AUC of 0.905. |
ArticleNumber | 102702 |
Author | Kong, Xiangqing Gu, Sai Qian, Kun Li, Jinshuang Li, Yong Wang, Ruimin Yang, Shouzhi Gu, Yang Yan, Xiaoxiang Li, Peng Meng, Kexin Su, Haiyang Zhang, Ziyue Zhao, Kun Pu, Jun |
Author_xml | – sequence: 1 givenname: Ziyue surname: Zhang fullname: Zhang, Ziyue organization: State Key Laboratory of Systems Medicine for Cancer, School of Biomedical Engineering, Institute of Medical Robotics and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai 200030, PR China – sequence: 2 givenname: Yong surname: Li fullname: Li, Yong email: liyongmydream@126.com organization: Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing 210029, PR China – sequence: 3 givenname: Ruimin surname: Wang fullname: Wang, Ruimin organization: State Key Laboratory of Systems Medicine for Cancer, School of Biomedical Engineering, Institute of Medical Robotics and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai 200030, PR China – sequence: 4 givenname: Shouzhi surname: Yang fullname: Yang, Shouzhi organization: State Key Laboratory of Systems Medicine for Cancer, School of Biomedical Engineering, Institute of Medical Robotics and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai 200030, PR China – sequence: 5 givenname: Peng surname: Li fullname: Li, Peng organization: Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing 210029, PR China – sequence: 6 givenname: Kun surname: Zhao fullname: Zhao, Kun organization: Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing 210029, PR China – sequence: 7 givenname: Yang surname: Gu fullname: Gu, Yang organization: Department of Cardiology, The Affiliated Huaian No.1 People’s Hospital of Nanjing Medical University, Huai’an, Jiangsu 223300, PR China – sequence: 8 givenname: Kexin surname: Meng fullname: Meng, Kexin organization: State Key Laboratory of Systems Medicine for Cancer, School of Biomedical Engineering, Institute of Medical Robotics and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai 200030, PR China – sequence: 9 givenname: Jinshuang surname: Li fullname: Li, Jinshuang organization: Department of Cardiology, Suqian Hospital Affiliated of Xuzhou Medical University, Suqian, Jiangsu 263800, PR China – sequence: 10 givenname: Jun surname: Pu fullname: Pu, Jun organization: Division of Cardiology, State Key Laboratory for Systems Medicine for Cancer, Shanghai Cancer Institute, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200001, PR China – sequence: 11 givenname: Xiaoxiang surname: Yan fullname: Yan, Xiaoxiang organization: Department of Cardiovascular Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200001, PR China – sequence: 12 givenname: Sai surname: Gu fullname: Gu, Sai organization: School of Engineering, University of Warwick, W Midlands, Coventry, England CV4 7AL, UK – sequence: 13 givenname: Haiyang surname: Su fullname: Su, Haiyang email: hy.su@sjtu.edu.cn organization: State Key Laboratory of Systems Medicine for Cancer, School of Biomedical Engineering, Institute of Medical Robotics and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai 200030, PR China – sequence: 14 givenname: Xiangqing surname: Kong fullname: Kong, Xiangqing email: kongxq@njmu.edu.cn organization: Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing 210029, PR China – sequence: 15 givenname: Kun orcidid: 0000-0003-1666-1965 surname: Qian fullname: Qian, Kun email: k.qian@sjtu.edu.cn organization: State Key Laboratory of Systems Medicine for Cancer, School of Biomedical Engineering, Institute of Medical Robotics and Med-X Research Institute, Shanghai Jiao Tong University, Shanghai 200030, PR China |
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