AI Article Synopsis

  • - The study focuses on using IgG N-glycans from human plasma as biomarkers for screening and diagnosing chronic diseases and cancer, particularly their adaptability to various influences.
  • - An ML-based framework was developed to analyze these biomarkers and stratify patients by their risk of colorectal cancer (CRC), utilizing data from the SOCCS cohort to enhance the precision of predictions.
  • - The most effective ML pipeline, an XGBoost model, demonstrated promising performance in distinguishing between healthy individuals and CRC patients, suggesting the potential of glycan biomarkers in clinical settings with an emphasis on supporting open-source tools for further research.

Article Abstract

Effective management of chronic diseases and cancer can greatly benefit from disease-specific biomarkers that enable informative screening and timely diagnosis. IgG N-glycans found in human plasma have the potential to be minimally invasive disease-specific biomarkers for all stages of disease development due to their plasticity in response to various genetic and environmental stimuli. Data analysis and machine learning (ML) approaches can assist in harnessing the potential of IgG glycomics towards biomarker discovery and the development of reliable predictive tools for disease screening. This study proposes an ML-based N-glycomic analysis framework that can be employed to build, optimise, and evaluate multiple ML pipelines to stratify patients based on disease risk in an interpretable manner. To design and test this framework, a published colorectal cancer (CRC) dataset from the Study of Colorectal Cancer in Scotland (SOCCS) cohort (1999-2006) was used. In particular, among the different pipelines tested, an XGBoost-based ML pipeline, which was tuned using multi-objective optimisation, calibrated using an inductive Venn-Abers predictor (IVAP), and evaluated via a nested cross-validation (NCV) scheme, achieved a mean area under the Receiver Operating Characteristic Curve (AUC-ROC) of 0.771 when classifying between age-, and sex-matched healthy controls and CRC patients. This performance suggests the potential of using the relative abundance of IgG N-glycans to define populations at elevated CRC risk who merit investigation or surveillance. Finally, the IgG N-glycans that highly impact CRC classification decisions were identified using a global model-agnostic interpretability technique, namely Accumulated Local Effects (ALE). We envision that open-source computational frameworks, such as the one presented herein, will be useful in supporting the translation of glycan-based biomarkers into clinical applications.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10973724PMC
http://dx.doi.org/10.1016/j.csbj.2024.03.008DOI Listing

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