Evidence map›Paper›PMID 38550971›Full record

ArticleComputational and structural biotechnology journal2024

Machine learning framework to extract the biomarker potential of plasma IgG N-glycans towards disease risk stratification.

Konstantinos Flevaris, Joseph Davies, Shoh Nakai, Frano Vučković, Gordan Lauc, Malcolm G Dunlop, Cleo Kontoravdi

Open access · goldAbstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Konstantinos FlevarisDepartment of Chemical Engineering, Imperial College London, London SW7 2AZ, United Kingdom.
Joseph DaviesDepartment of Chemical Engineering, Imperial College London, London SW7 2AZ, United Kingdom.
Shoh NakaiDepartment of Chemical Engineering, Imperial College London, London SW7 2AZ, United Kingdom.
Frano VučkovićGenos Glycoscience Research Laboratory, Zagreb 10000, Croatia.
Gordan LaucGenos Glycoscience Research Laboratory, Zagreb 10000, Croatia.
Malcolm G DunlopColon Cancer Genetics Group, Institute of Genetics and Cancer, Cancer Research UK Scotland Centre, University of Edinburgh and Medical Research Council Human Genetics Unit, Edinburgh, United Kingdom.
Cleo KontoravdiDepartment of Chemical Engineering, Imperial College London, London SW7 2AZ, United Kingdom.
Imperial College London · GBEdinburgh Cancer Research · GBGenos (Croatia) · HRUniversity of Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

CancerGlycosylationInterpretable machine learningMulti-objective optimizationProbability calibration

Identifiers

PMID38550971
PMCPMC10973724
OpenAlexW4392648312

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.