Evidence map›Paper›PMID 37498860›Full record

ArticlePloS one2023

Quantifying postprandial glucose responses using a hybrid modeling approach: Combining mechanistic and data-driven models in The Maastricht Study.

Balázs Erdős, Bart van Sloun, Gijs H Goossens, Shauna D O'Donovan, Bastiaan E de Galan, Marleen M J van Greevenbroek, Coen D A Stehouwer, Miranda T Schram, Ellen E Blaak, Michiel E Adriaens and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. 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
0.8field-weighted citation impact, top 25% 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, 4 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
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

12 authors at 2 institutions in 1 country.

Balázs ErdősTiFN, Wageningen, Netherlands.ORCID 0000-0001-8643-4915
Bart van SlounTiFN, Wageningen, Netherlands.ORCID 0000-0002-2827-9889
Gijs H GoossensTiFN, Wageningen, Netherlands.
Shauna D O'DonovanDivision of Human Nutrition and Health, Wageningen University, Wageningen, Netherlands.
Bastiaan E de GalanCARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, Netherlands.
Marleen M J van GreevenbroekCARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, Netherlands.
Coen D A StehouwerCARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, Netherlands.
Miranda T SchramCARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, Netherlands.
Ellen E BlaakTiFN, Wageningen, Netherlands.ORCID 0000-0002-2496-3464
Michiel E AdriaensTiFN, Wageningen, Netherlands.
Natal A W van RielDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, Netherlands.ORCID 0000-0001-9375-4730
Ilja C W ArtsMaCSBio Maastricht Centre for Systems Biology, Maastricht University, Maastricht, Netherlands.
Maastricht University · NLEindhoven University of Technology · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Computational models of human glucose homeostasis can provide insight into the physiological processes underlying the observed inter-individual variability in glucose regulation. Modelling approaches ranging from "bottom-up" mechanistic models to "top-down" data-driven techniques have been applied to untangle the complex interactions underlying progressive disturbances in glucose homeostasis. While both approaches offer distinct benefits, a combined approach taking the best of both worlds has yet to be explored. Here, we propose a sequential combination of a mechanistic and a data-driven modeling approach to quantify individuals' glucose and insulin responses to an oral glucose tolerance test, using cross sectional data from 2968 individuals from a large observational prospective population-based cohort, the Maastricht Study. The best predictive performance, measured by R2 and mean squared error of prediction, was achieved with personalized mechanistic models alone. The addition of a data-driven model did not improve predictive performance. The personalized mechanistic models consistently outperformed the data-driven and the combined model approaches, demonstrating the strength and suitability of bottom-up mechanistic models in describing the dynamic glucose and insulin response to oral glucose tolerance tests.

Indexed as

Blood GlucoseGlucoseCross-Sectional StudiesHumansInsulinProspective StudiesBlood GlucoseGlucoseInsulin

Identifiers

PMID37498860
PMCPMC10374070
OpenAlexW4385327021

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.