Evidence map›Paper›PMID 38493243›Full record

ArticleCommunications medicine2024

Generative deep learning for the development of a type 1 diabetes simulator.

Omer Mujahid, Ivan Contreras, Aleix Beneyto, Josep Vehi

Open access · goldAbstract read
In one paragraph

Article in Communications medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Generative AI models for type 2 diabetes mellitus risk prediction.Health systems (Basingstoke, England) · 2026
    Article
  3. Review
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

4 authors at 1 institution in 1 country.

Omer MujahidModelling, Identification and Control Engineering Laboratory, Institut d'Informatica i Aplicacions, Universitat de Girona, Girona, 17003, Girona, Spain.ORCID http://orcid.org/0000-0001-9694-9621
Ivan ContrerasModelling, Identification and Control Engineering Laboratory, Institut d'Informatica i Aplicacions, Universitat de Girona, Girona, 17003, Girona, Spain.ORCID http://orcid.org/0000-0001-6896-818X
Aleix BeneytoModelling, Identification and Control Engineering Laboratory, Institut d'Informatica i Aplicacions, Universitat de Girona, Girona, 17003, Girona, Spain.ORCID http://orcid.org/0000-0001-8207-2259
Josep VehiModelling, Identification and Control Engineering Laboratory, Institut d'Informatica i Aplicacions, Universitat de Girona, Girona, 17003, Girona, Spain. josep.vehi@udg.edu.ORCID http://orcid.org/0000-0001-6884-9789
Universitat de Girona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundType 1 diabetes (T1D) simulators, crucial for advancing diabetes treatments, often fall short of capturing the entire complexity of the glucose-insulin system due to the imprecise approximation of the physiological models. This study introduces a simulation approach employing a conditional deep generative model. The aim is to overcome the limitations of existing T1D simulators by synthesizing virtual patients that more accurately represent the entire glucose-insulin system physiology.

methodsOur methodology utilizes a sequence-to-sequence generative adversarial network to simulate virtual T1D patients causally. Causality is embedded in the model by introducing shifted input-output pairs during training, with a 90-min shift capturing the impact of input insulin and carbohydrates on blood glucose. To validate our approach, we train and evaluate the model using three distinct datasets, each consisting of 27, 12, and 10 T1D patients, respectively. In addition, we subject the trained model to further validation for closed-loop therapy, employing a state-of-the-art controller.

resultsThe generated patients display statistical similarity to real patients when evaluated on the time-in-range results for each of the standard blood glucose ranges in T1D management along with means and variability outcomes. When tested for causality, authentic causal links are identified between the insulin, carbohydrates, and blood glucose levels of the virtual patients. The trained generative model demonstrates behaviours that are closer to reality compared to conventional T1D simulators when subjected to closed-loop insulin therapy using a state-of-the-art controller.

conclusionsThese results highlight our approach's capability to accurately capture physiological dynamics and establish genuine causal relationships, holding promise for enhancing the development and evaluation of therapies in diabetes.

Identifiers

PMID38493243
PMCPMC10944502
OpenAlexW4392878112

What OpenQuestion holds

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LicenceCC BY
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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.