Evidence map›Paper›PMID 37486667›Full record

ArticleChaos (Woodbury, N.Y.)2023

A simple modeling framework for prediction in the human glucose-insulin system.

Melike Sirlanci, Matthew E Levine, Cecilia C Low Wang, David J Albers, Andrew M Stuart

Open access · greenAbstract read
In one paragraph

Article in Chaos (Woodbury, N.Y.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Melike SirlanciDepartment of Computing and Mathematical Sciences, California Institute of Technology, Pasadena, California 91125, USA.ORCID 0000-0002-4749-4752
Matthew E LevineDepartment of Computing and Mathematical Sciences, California Institute of Technology, Pasadena, California 91125, USA.ORCID 0000-0002-5627-3169
Cecilia C Low WangDivision of Endocrinology, Metabolism and Diabetes, Department of Medicine, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, USA.ORCID 0000-0001-8557-5417
David J AlbersDepartment of Biomedical Informatics, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, USA.ORCID 0000-0002-5369-526X
Andrew M StuartDepartment of Computing and Mathematical Sciences, California Institute of Technology, Pasadena, California 91125, USA.ORCID 0000-0001-9091-7266
California Institute of Technology · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Mechanistic Machine LearningR01LM012734 · NLM · UNIVERSITY OF COLORADO DENVER · PI ALBERS, DAVID J., GLUCKMAN, BRUCE J · 2017 to 2019
$2.0M
NLM NIH HHS R01 LM012734
6 · The paper itself

Abstract

Forecasting blood glucose (BG) levels with routinely collected data is useful for glycemic management. BG dynamics are nonlinear, complex, and nonstationary, which can be represented by nonlinear models. However, the sparsity of routinely collected data creates parameter identifiability issues when high-fidelity complex models are used, thereby resulting in inaccurate forecasts. One can use models with reduced physiological fidelity for robust and accurate parameter estimation and forecasting with sparse data. For this purpose, we approximate the nonlinear dynamics of BG regulation by a linear stochastic differential equation: we develop a linear stochastic model, which can be specialized to different settings: type 2 diabetes mellitus (T2DM) and intensive care unit (ICU), with different choices of appropriate model functions. The model includes deterministic terms quantifying glucose removal from the bloodstream through the glycemic regulation system and representing the effect of nutrition and externally delivered insulin. The stochastic term encapsulates the BG oscillations. The model output is in the form of an expected value accompanied by a band around this value. The model parameters are estimated patient-specifically, leading to personalized models. The forecasts consist of values for BG mean and variation, quantifying possible high and low BG levels. Such predictions have potential use for glycemic management as part of control systems. We present experimental results on parameter estimation and forecasting in T2DM and ICU settings. We compare the model's predictive capability with two different nonlinear models built for T2DM and ICU contexts to have a sense of the level of prediction achieved by this model.

Indexed as

Diabetes Mellitus, Type 2GlucoseBlood GlucoseHumansInsulinNonlinear DynamicsBlood GlucoseGlucoseInsulin

Identifiers

PMID37486667
PMCPMC10368459
OpenAlexW4385186882

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.