Evidence map›Paper›PMID 40730832›Full record

ArticleScientific reports2025

A multimodal deep learning architecture for predicting interstitial glucose for effective type 2 diabetes management.

Muhammad Salman Haleem, Daphne Katsarou, Eleni I Georga, George E Dafoulas, Alexandra Bargiota, Laura Lopez-Perez, Miguel Rujas, Giuseppe Fico, Leandro Pecchia, Dimitrios Fotiadis and 1 more

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Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Muhammad Salman HaleemSchool of Engineering, University of Warwick, Coventry, CV4 7AL, UK. salman.haleem@warwick.ac.uk.
Daphne KatsarouDept. of Materials Science and Engineering, University of Ioannina, Ioannina, Greece.
Eleni I GeorgaDept. of Materials Science and Engineering, University of Ioannina, Ioannina, Greece.
George E DafoulasFaculty of Medicine, University of Thessaly, Volos, Greece.
Alexandra BargiotaDepartment of Endocrinology and Metabolic Diseases, University Hospital of Larisa, Larissa, Greece.
Laura Lopez-PerezUniversidad Politécnica de Madrid-Life Supporting Technologies Research Group, ETSIT, Madrid, Spain.
Miguel RujasUniversidad Politécnica de Madrid-Life Supporting Technologies Research Group, ETSIT, Madrid, Spain.
Giuseppe FicoUniversidad Politécnica de Madrid-Life Supporting Technologies Research Group, ETSIT, Madrid, Spain.
Leandro PecchiaUniversità Campus Bio-Medico, Via Álvaro del Portillo, 21, 00128, Roma, Italy.
Dimitrios FotiadisDept. of Materials Science and Engineering, University of Ioannina, Ioannina, Greece.
Gatekeeper Consortium

Funding

GATEKEEPER EU Horizon 2020 857223
6 · The paper itself

Abstract

The accurate prediction of blood glucose is critical for the effective management of diabetes. Modern continuous glucose monitoring (CGM) technology enables real-time acquisition of interstitial glucose concentrations, which can be calibrated against blood glucose measurements. However, a key challenge in the effective management of type 2 diabetes lies in forecasting critical events driven by glucose variability. While recent advances in deep learning enable modeling of temporal patterns in glucose fluctuations, most of the existing methods rely on unimodal inputs and fail to account for individual physiological differences that influence interstitial glucose dynamics. These limitations highlight the need for multimodal approaches that integrate additional personalized physiological information. One of the primary reasons for multimodal approaches not being widely studied in this field is the bottleneck associated with the availability of subjects' health records. In this paper, we propose a multimodal approach trained on sequences of CGM values and enriched with physiological context derived from health records of 40 individuals with type 2 diabetes. The CGM time series were processed using a stacked Convolutional Neural Network (CNN) and a Bidirectional Long Short-Term Memory (BiLSTM) network followed by an attention mechanism. The BiLSTM learned long-term temporal dependencies, while the CNN captured local sequential features. Physiological heterogeneity was incorporated through a separate pipeline of neural networks that processed baseline health records and was later fused with the CGM modeling stream. To validate our model, we utilized CGM values of 30 min sampled with a moving window of 5 min to predict the CGM values with a prediction horizon of (a) 15 min, (b) 30 min, and (c) 60 min. We achieved the multimodal architecture prediction results with Mean Absolute Point Error (MAPE) between 14 and 24 mg/dL, 19-22 mg/dL, 25-26 mg/dL in case of Menarini sensor and 6-11 mg/dL, 9-14 mg/dL, 12-18 mg/dL in case of Abbot sensor for 15, 30 and 60 min prediction horizon respectively. The results suggested that the proposed multimodal model achieved higher prediction accuracy compared to unimodal approaches; with upto 96.7% prediction accuracy; supporting its potential as a generalizable solution for interstitial glucose prediction and personalized management in the type 2 diabetes population.

Indexed as

Blood GlucoseDeep LearningDiabetes Mellitus, Type 2Blood Glucose Self-MonitoringFemaleHumansMaleMiddle AgedNeural Networks, ComputerBlood GlucoseDeep learningInterstitial glucose predictionMultimodal AI

Identifiers

PMID40730832
PMCPMC12307872

What Socratic holds

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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 Socratic graph.