ReviewJMIR diabetes2026
Data, Process, and Data-Driven Representations of Digital Twins in Diabetes: Scoping Review.
Review in JMIR diabetes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Diabetes is a chronic metabolic condition characterized by impaired blood glucose regulation. It is often linked to serious health complications and comorbidities that significantly affect quality of life, requiring effective management, continuous monitoring, and advanced data analytics. Notably, tailored diabetes management can be enhanced by digital twins (DTs), which serve as adaptive digital representations of patients, using clinical, physiological, and lifestyle data. Objective: This review explores diabetes-related DTs by examining their patient representation levels. We aim to synthesize the current state of the art and outline the foundations of a holistic, multilevel, multifunctional personalized DT for diabetes management. Methods: We investigate requirements for a personalized holistic DT and classify existing approaches into three representation levels: (1) data representation, involving structured, context-aware, and AI-ready data architectures that support data analysis, enable semantic interoperability, relationship extraction, and real-time bidirectional data exchange between patient and virtual replica. (2) Process representation, primarily based on mechanistic models simulating glucose-insulin-meal and exercise-glucose dynamics. (3) Data-driven representation, focusing on individualization through predictive modeling of disease onset, adverse events, and the generation of explainable, personalized recommendations. The literature is synthesized to provide a holistic, multilevel perspective on DTs, and to identify research gaps. Results: DTs accompany patients throughout their lifecycle and span a wide range of use cases, from long-term disease prediction to timely prediction of severe events. However, personalized DTs remain at an early stage of development. Most existing systems primarily function as simulation tools and lack comprehensive integration of data, processes, and data-driven representations. Key gaps include limited use of standardized semantic data models and ontologies, insufficient real-time bidirectional architectures, and fragmented integration of mechanistic and machine learning models, which are often treated as independent rather than complementary components. Conclusions: Although DTs hold substantial potential to advance personalized diabetes care, current implementations remain fragmented and incomplete. Future research should prioritize the development of holistic, multilevel DTs that integrate interoperable data infrastructures, mechanistic simulations, and data-driven models into cohesive, personalized systems capable of supporting lifelong disease management.
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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.