ArticleACS infectious diseases2025
A New Approach for Chagas Disease Screening Using Serum Infrared Spectroscopy and Machine Learning Algorithms.
Article in ACS infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Double-antigen sandwich ELISA based on chimeric antigens for detection of antibodies to Trypanosoma cruzi in human sera - A phase II study.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026Article
- A Rapid, Antigen-Independent Diagnostic Strategy for Chronic Chagas Disease Based on Serum ATR-FTIR Spectroscopy and Machine Learning.ACS omega · 2026Article
- Diagnostic performance of the TR Chagas Bio-Manguinhos rapid test for detecting anti-Trypanosoma cruzi IgG in human samples from three Southern Cone countries.PLoS neglected tropical diseases · 2026Article
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Chagas disease (CD) affects an estimated 6-7 million people worldwide, predominantly in Latin America. However, migration has expanded its geographic reach. Diagnosing chronic CD is challenging due to low parasitemia and the limitations of existing serological assays. This study evaluates the diagnostic potential of attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectroscopy combined with machine learning (ML). A total of 100 serum samples (49 CD-positive, 51 negative controls) were analyzed using ATR-FTIR spectroscopy under two conditions: (i) dry analysis (air-dried samples) and (ii) wet analysis (direct serum analysis). Spectral data were processed using ML algorithms, including logistic regression (LR), partial least-squares discriminant analysis (PLS-DA), random forest (RF), and extreme gradient boosting (XGBoost) for sample classification. The best-performing models were LR for dry data set (accuracy and F1-score: 93%) and XGBoost for the wet data set (accuracy and F1-score: 87%). The area under the receiver operating characteristic (ROC) curve (AUC) was 0.99 and 0.92 for the dry and wet data sets, respectively. The robustness and reliability of the model were confirmed through permutation tests. These results demonstrate that ATR-FTIR spectroscopy combined with ML is a promising diagnostic tool for CD. Despite the study's limited sample size, results suggest this approach could serve as a cost-effective alternative to conventional serological assays, particularly in resource- constrained settings. Further validation with larger data sets and diverse control groups is essential to assess its specificity and clinical applicability. If successful, this method could significantly enhance early diagnosis and improve disease managements strategies for CD.
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