Personalized computational model quantifies heterogeneity in postprandial responses to oral glucose challenge.

Plasma glucose and insulin responses following an oral glucose challenge are representative of glucose tolerance and insulin resistance, key indicators of type 2 diabetes mellitus pathophysiology. A large heterogeneity in individuals' challenge test responses has been shown to underlie the effe...

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Main Authors: Balázs Erdős, Bart van Sloun, Michiel E Adriaens, Shauna D O'Donovan, Dominique Langin, Arne Astrup, Ellen E Blaak, Ilja C W Arts, Natal A W van Riel
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-03-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1008852
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spelling doaj-85352599a5ff40cbafd7a1b72f6e5ee72021-08-01T04:30:53ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582021-03-01173e100885210.1371/journal.pcbi.1008852Personalized computational model quantifies heterogeneity in postprandial responses to oral glucose challenge.Balázs ErdősBart van SlounMichiel E AdriaensShauna D O'DonovanDominique LanginArne AstrupEllen E BlaakIlja C W ArtsNatal A W van RielPlasma glucose and insulin responses following an oral glucose challenge are representative of glucose tolerance and insulin resistance, key indicators of type 2 diabetes mellitus pathophysiology. A large heterogeneity in individuals' challenge test responses has been shown to underlie the effectiveness of lifestyle intervention. Currently, this heterogeneity is overlooked due to a lack of methods to quantify the interconnected dynamics in the glucose and insulin time-courses. Here, a physiology-based mathematical model of the human glucose-insulin system is personalized to elucidate the heterogeneity in individuals' responses using a large population of overweight/obese individuals (n = 738) from the DIOGenes study. The personalized models are derived from population level models through a systematic parameter selection pipeline that may be generalized to other biological systems. The resulting personalized models showed a 4-5 fold decrease in discrepancy between measurements and model simulation compared to population level. The estimated model parameters capture relevant features of individuals' metabolic health such as gastric emptying, endogenous insulin secretion and insulin dependent glucose disposal into tissues, with the latter also showing a significant association with the Insulinogenic index and the Matsuda insulin sensitivity index, respectively.https://doi.org/10.1371/journal.pcbi.1008852
collection DOAJ
language English
format Article
sources DOAJ
author Balázs Erdős
Bart van Sloun
Michiel E Adriaens
Shauna D O'Donovan
Dominique Langin
Arne Astrup
Ellen E Blaak
Ilja C W Arts
Natal A W van Riel
spellingShingle Balázs Erdős
Bart van Sloun
Michiel E Adriaens
Shauna D O'Donovan
Dominique Langin
Arne Astrup
Ellen E Blaak
Ilja C W Arts
Natal A W van Riel
Personalized computational model quantifies heterogeneity in postprandial responses to oral glucose challenge.
PLoS Computational Biology
author_facet Balázs Erdős
Bart van Sloun
Michiel E Adriaens
Shauna D O'Donovan
Dominique Langin
Arne Astrup
Ellen E Blaak
Ilja C W Arts
Natal A W van Riel
author_sort Balázs Erdős
title Personalized computational model quantifies heterogeneity in postprandial responses to oral glucose challenge.
title_short Personalized computational model quantifies heterogeneity in postprandial responses to oral glucose challenge.
title_full Personalized computational model quantifies heterogeneity in postprandial responses to oral glucose challenge.
title_fullStr Personalized computational model quantifies heterogeneity in postprandial responses to oral glucose challenge.
title_full_unstemmed Personalized computational model quantifies heterogeneity in postprandial responses to oral glucose challenge.
title_sort personalized computational model quantifies heterogeneity in postprandial responses to oral glucose challenge.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2021-03-01
description Plasma glucose and insulin responses following an oral glucose challenge are representative of glucose tolerance and insulin resistance, key indicators of type 2 diabetes mellitus pathophysiology. A large heterogeneity in individuals' challenge test responses has been shown to underlie the effectiveness of lifestyle intervention. Currently, this heterogeneity is overlooked due to a lack of methods to quantify the interconnected dynamics in the glucose and insulin time-courses. Here, a physiology-based mathematical model of the human glucose-insulin system is personalized to elucidate the heterogeneity in individuals' responses using a large population of overweight/obese individuals (n = 738) from the DIOGenes study. The personalized models are derived from population level models through a systematic parameter selection pipeline that may be generalized to other biological systems. The resulting personalized models showed a 4-5 fold decrease in discrepancy between measurements and model simulation compared to population level. The estimated model parameters capture relevant features of individuals' metabolic health such as gastric emptying, endogenous insulin secretion and insulin dependent glucose disposal into tissues, with the latter also showing a significant association with the Insulinogenic index and the Matsuda insulin sensitivity index, respectively.
url https://doi.org/10.1371/journal.pcbi.1008852
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