Platelet Metabolites as Candidate Biomarkers in Sepsis Diagnosis and Management Using the Proposed Explainable Artificial Intelligence Approach

被引:4
作者
Yagin, Fatma Hilal [1 ]
Aygun, Umran [2 ]
Algarni, Abdulmohsen [3 ]
Colak, Cemil [1 ]
Al-Hashem, Fahaid [4 ]
Ardigo, Luca Paolo [5 ]
机构
[1] Inonu Univ, Fac Med, Dept Biostat & Med Informat, TR-44280 Malatya, Turkiye
[2] Malatya Yesilyurt Hasan Calik State Hosp, Dept Anesthesiol & Reanimat, TR-44929 Malatya, Turkiye
[3] King Khalid Univ, Cent Labs, POB 960, Abha, Saudi Arabia
[4] King Khalid Univ, Coll Med, Dept Physiol, Abha 61421, Saudi Arabia
[5] NLA Univ Coll, Dept Teacher Educ, N-0166 Oslo, Norway
关键词
sepsis; platelet metabolomics; biomarkers; machine learning; explainable artificial intelligence; L-CARNITINE INFUSION; SEPTIC SHOCK; GLUTAMATE EXCITOTOXICITY; ACID-METABOLISM; ORGAN FAILURE; METABOLOMICS; MACHINE; NMR; DEFINITIONS; PREDICTION;
D O I
10.3390/jcm13175002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Sepsis is characterized by an atypical immune response to infection and is a dangerous health problem leading to significant mortality. Current diagnostic methods exhibit insufficient sensitivity and specificity and require the discovery of precise biomarkers for the early diagnosis and treatment of sepsis. Platelets, known for their hemostatic abilities, also play an important role in immunological responses. This study aims to develop a model integrating machine learning and explainable artificial intelligence (XAI) to identify novel platelet metabolomics markers of sepsis. Methods: A total of 39 participants, 25 diagnosed with sepsis and 14 control subjects, were included in the study. The profiles of platelet metabolites were analyzed using quantitative 1H-nuclear magnetic resonance (NMR) technology. Data were processed using the synthetic minority oversampling method (SMOTE)-Tomek to address the issue of class imbalance. In addition, missing data were filled using a technique based on random forests. Three machine learning models, namely extreme gradient boosting (XGBoost), light gradient boosting machine (LightGBM), and kernel tree boosting (KTBoost), were used for sepsis prediction. The models were validated using cross-validation. Clinical annotations of the optimal sepsis prediction model were analyzed using SHapley Additive exPlanations (SHAP), an XAI technique. Results: The results showed that the KTBoost model (0.900 accuracy and 0.943 AUC) achieved better performance than the other models in sepsis diagnosis. SHAP results revealed that metabolites such as carnitine, glutamate, and myo-inositol are important biomarkers in sepsis prediction and intuitively explained the prediction decisions of the model. Conclusion: Platelet metabolites identified by the KTBoost model and XAI have significant potential for the early diagnosis and monitoring of sepsis and improving patient outcomes.
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页数:19
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共 82 条
[1]   XGBoost framework with feature selection for the prediction of RNA N5-methylcytosine sites [J].
Abbas, Zeeshan ;
Rehman, Mobeen ur ;
Tayara, Hilal ;
Zou, Quan ;
Chong, Kil To .
MOLECULAR THERAPY, 2023, 31 (08) :2543-2551
[2]   Prospective, multi-site study of patient outcomes after implementation of the TREWS machine learning-based early warning system for sepsis [J].
Adams, Roy ;
Henry, Katharine E. ;
Sridharan, Anirudh ;
Soleimani, Hossein ;
Zhan, Andong ;
Rawat, Nishi ;
Johnson, Lauren ;
Hager, David N. ;
Cosgrove, Sara E. ;
Markowski, Andrew ;
Klein, Eili Y. ;
Chen, Edward S. ;
Saheed, Mustapha O. ;
Henley, Maureen ;
Miranda, Sheila ;
Houston, Katrina ;
Linton, Robert C. ;
Ahluwalia, Anushree R. ;
Wu, Albert W. ;
Saria, Suchi .
NATURE MEDICINE, 2022, 28 (07) :1455-+
[3]   Explainable artificial intelligence: an analytical review [J].
Angelov, Plamen P. ;
Soares, Eduardo A. ;
Jiang, Richard ;
Arnold, Nicholas I. ;
Atkinson, Peter M. .
WILEY INTERDISCIPLINARY REVIEWS-DATA MINING AND KNOWLEDGE DISCOVERY, 2021, 11 (05)
[4]   Severe Sepsis and Septic Shock REPLY [J].
Angus, Derek C. ;
van der Poll, Tom .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 369 (21) :2063-2063
[5]   Transcriptomic Signatures in Sepsis and a Differential Response to Steroids From the VANISH Randomized Trial [J].
Antcliffe, David B. ;
Burnham, Katie L. ;
Al-Beidh, Farah ;
Santhakumaran, Shalini ;
Brett, Stephen J. ;
Hinds, Charles J. ;
Ashby, Deborah ;
Knight, Julian C. ;
Gordon, Anthony C. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2019, 199 (08) :980-986
[6]  
Basoglu A., 2014, Metabolomics, V4, P1
[7]   Metabolomic findings in sepsis as a damage of host-microbial metabolism integration [J].
Beloborodova, Natalia V. ;
Olenin, Andrei Yu. ;
Pautova, Alisa K. .
JOURNAL OF CRITICAL CARE, 2018, 43 :246-255
[8]   Metabolic response to injury and sepsis: Changes in protein metabolism [J].
Biolo, G ;
Toigo, G ;
Ciocchi, B ;
Situlin, R ;
Iscra, F ;
Gullo, A ;
Guarnieri, G .
NUTRITION, 1997, 13 (09) :S52-S57
[9]   Effect of organochlorine pesticides exposure on the maize root metabolome assessed using high-resolution magic-angle spinning 1H NMR spectroscopy [J].
Blondel, Claire ;
Khelalfa, Farid ;
Reynaud, Stephane ;
Fauvelle, Florence ;
Raveton, Muriel .
ENVIRONMENTAL POLLUTION, 2016, 214 :539-548
[10]   DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ .
CHEST, 1992, 101 (06) :1644-1655