Evidence map›Paper›PMID 42690529›Full record

ArticleMedical & biological engineering & computing2026

Hierarchical contrastive learning from GP-recorded and eGFR labels for CKD staging.

Ali Guran, Avishek Siris, Gary K L Tam, James Chess, Xianghua Xie

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Article in Medical & biological engineering & computing, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Ali GuranDepartment of Computer Science, Swansea University, Swansea, SA1 8EN, UK. 935538@swansea.ac.uk.ORCID http://orcid.org/0009-0009-4064-5552
Avishek SirisDepartment of Computer Science, Swansea University, Swansea, SA1 8EN, UK.ORCID http://orcid.org/0000-0002-3064-2202
Gary K L TamDepartment of Computer Science, Swansea University, Swansea, SA1 8EN, UK.ORCID http://orcid.org/0000-0001-7387-5180
James ChessRenal Unit, Morriston Hospital, Swansea Bay University Health Board, Swansea, SA6 6NL, UK.ORCID http://orcid.org/0000-0001-8805-6962
Xianghua XieDepartment of Computer Science, Swansea University, Swansea, SA1 8EN, UK.ORCID http://orcid.org/0000-0002-2701-8660

Funding

CHERISH- DE Centre via the International Mobility Award EP/M022722/1Engineering and Physical Sciences Research Council EP/Y007697/1
6 · The paper itself

Abstract

Chronic kidney disease staging from longitudinal clinical records is challenging because routinely recorded GP stage labels are scarce, whereas rule-based eGFR labels are more abundant but may not capture the broader clinical context reflected in primary-care coding. This study proposes a hierarchical contrastive learning framework for CKD staging under heterogeneous supervision, designed to maximise the use of available data by leveraging both scarce GP annotations and abundant rule-based labels, which provide complementary but partially inconsistent information. Rather than treating these supervision sources as fully consistent or conflicting, the proposed approach models graded levels of agreement and incorporates this structure into a contrastive objective. This encourages clinically concordant cases to form compact representations while progressively separating increasingly discordant cases, yielding a structured and clinically meaningful embedding space. The framework is extensively evaluated across multiple neural architectures for longitudinal CKD modelling, including recurrent, convolutional, temporal convolutional, Transformer-based, and hybrid models. Results show consistent improvements over classification-only and binary contrastive baselines, with the best performance achieved using a TCN+Transformer backbone. These findings show that structured contrastive supervision can effectively exploit complementary information from clinician-annotated and rule-based labels and provide a practical framework for longitudinal disease modelling, with potential applicability beyond CKD.

Indexed as

Chronic kidney diseaseClassificationContrastive learningMachine learning

Identifiers

PMID42690529

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Registered trials

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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.