Evidence map›Paper›PMID 37455284›Full record

ArticleScientific reports2023

Stratification of diabetes in the context of comorbidities, using representation learning and topological data analysis.

Malgorzata Wamil, Abdelaali Hassaine, Shishir Rao, Yikuan Li, Mohammad Mamouei, Dexter Canoy, Milad Nazarzadeh, Zeinab Bidel, Emma Copland, Kazem Rahimi and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. 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
1.8field-weighted citation impact, top 13% 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, 9 citations in OpenAlex.

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  3. How can we predict mortality in acute stroke?Revista da Associacao Medica Brasileira (1992) · 2025
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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

11 authors at 1 institution in 1 country.

Malgorzata Wamil *Deep Medicine, Oxford Martin School, University of Oxford, Oxford, UK. malgorzata.wamil@gtc.ox.ac.uk.
Abdelaali Hassaine *Deep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Shishir RaoDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Yikuan LiDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Mohammad MamoueiDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Dexter CanoyDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Milad NazarzadehDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Zeinab BidelDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Emma CoplandDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Kazem RahimiDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
Gholamreza Salimi-KhorshidiDeep Medicine, Oxford Martin School, University of Oxford, Oxford, UK.
University of Oxford · GB

Funding

British Heart Foundation FS/19/36/34346British Heart Foundation FS/PHD/21/29110British Heart Foundation PG/18/65/33872Department of Health
6 · The paper itself

Abstract

Diabetes is a heterogenous, multimorbid disorder with a large variation in manifestations, trajectories, and outcomes. The aim of this study is to validate a novel machine learning method for the phenotyping of diabetes in the context of comorbidities. Data from 9967 multimorbid patients with a new diagnosis of diabetes were extracted from Clinical Practice Research Datalink. First, using BEHRT (a transformer-based deep learning architecture), the embeddings corresponding to diabetes were learned. Next, topological data analysis (TDA) was carried out to test how different areas in high-dimensional manifold correspond to different risk profiles. The following endpoints were considered when profiling risk trajectories: major adverse cardiovascular events (MACE), coronary artery disease (CAD), stroke (CVA), heart failure (HF), renal failure (RF), diabetic neuropathy, peripheral arterial disease, reduced visual acuity and all-cause mortality. Kaplan Meier curves were plotted for each derived phenotype. Finally, we tested the performance of an established risk prediction model (QRISK) by adding TDA-derived features. We identified four subgroups of patients with diabetes and divergent comorbidity patterns differing in their risk of future cardiovascular, renal, and other microvascular outcomes. Phenotype 1 (young with chronic inflammatory conditions) and phenotype 2 (young with CAD) included relatively younger patients with diabetes compared to phenotypes 3 (older with hypertension and renal disease) and 4 (older with previous CVA), and those subgroups had a higher frequency of pre-existing cardio-renal diseases. Within ten years of follow-up, 2592 patients (26%) experienced MACE, 2515 patients (25%) died, and 2020 patients (20%) suffered RF. QRISK3 model's AUC was augmented from 67.26% (CI 67.25-67.28%) to 67.67% (CI 67.66-67.69%) by adding specific TDA-derived phenotype and the distances to both extremities of the TDA graph improving its performance in the prediction of CV outcomes. We confirmed the importance of accounting for multimorbidity when risk stratifying heterogenous cohort of patients with new diagnosis of diabetes. Our unsupervised machine learning method improved the prediction of clinical outcomes.

Indexed as

Diabetes MellitusUnsupervised Machine LearningAgedCardiovascular DiseasesComorbidityData AnalysisFemaleHumansKidney DiseasesMaleMiddle AgedPhenotypeRisk Assessment

Identifiers

PMID37455284
PMCPMC10350454
OpenAlexW4384454344

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.