Evidence map›Paper›PMID 42837410›Full record

ArticlePloS one2026

Empirical transition probability modeling of continuous glucose monitoring data.

Yuanzhi Yu, Margaret Banker, Jennifer Sherr, Denise M Scholtens

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Article in PloS one, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yuanzhi YuNorthwestern University Feinberg School of Medicine, Department of Preventive Medicine, Division of Biostatistics and Informatics, Chicago, Illinois, United States of America.ORCID https://orcid.org/0000-0002-8651-3856
Margaret BankerNorthwestern University Feinberg School of Medicine, Department of Preventive Medicine, Division of Biostatistics and Informatics, Chicago, Illinois, United States of America.
Jennifer SherrDepartment of Pediatrics, Yale School of Medicine, New Haven, Connecticut, United States of America.
Denise M ScholtensNorthwestern University Feinberg School of Medicine, Department of Preventive Medicine, Division of Biostatistics and Informatics, Chicago, Illinois, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionContinuous glucose monitoring (CGM) produces rich time series data. Standard metrics such as time-in-range summarize glycemia but miss the sequence of changes. We aimed to characterize glucose dynamics using empirical transition probability techniques. MATERIALS AND

methodsUsing publicly available data for 244 participants who enrolled in the Insulin-Only Bionic Pancreas (IOBP2) randomized clinical trial, we mapped each CGM reading to one of five states: < 54, 54-69, 70-180, 181-250, or >250 mg/dL. We counted state changes between consecutive readings collected every 5 minutes. For each participant, we built a 5 × 5 transition probability matrix and averaged matrices within comparator groups. Statistical inference using estimated transition probability matrices was compared to inferences based on standard metrics including mean glucose, standard deviation, coefficient of variation, time-in-range metrics, Glycemia Risk Index (GRI), Mean of Daily Differences (MODD), and Mean Amplitude of Glycemic Excursions (MAGE).

resultsTransition probability analysis showed more frequent moves from hyperglycemia (181-250 or >250 mg/dL) to the in-range (70-180 mg/dL) state for the bionic pancreas that was evaluated in the IOBP2 trial compared to control. This pattern appeared in both adults and in children and persisted through the trial. Conventional CGM metrics also showed treatment differences in mean glucose, GRI, and time in range; MODD, MAGE, and coefficient of variation showed less consistent differences between treatment groups.

conclusionTransition probability matrices provide an informative summary of glucose dynamics that complements established CGM metrics. In IOBP2, this approach highlighted improved patterns of recovery from hyperglycemia with the bionic pancreas compared with control. Future studies should determine whether transition-based summaries are associated with clinically meaningful outcomes.

Indexed as

Blood GlucoseContinuous Glucose MonitoringDiabetes Mellitus, Type 1HumansHyperglycemiaInsulinModels, StatisticalProbabilityBlood GlucoseInsulin

Identifiers

PMID42837410
PMCPMC13641706

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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.