Evaluation of postprandial total triglycerides within the TIGG model for characterizing postprandial response of glucose, insulin, and GLP‐1

Abstract The TIGG model is the first model to integrate glucose and insulin regulation, incretin effect, and triglyceride (TG) response in the lipoprotein subclasses of chylomicrons and VLDL‐V6. This model described the response following a high‐fat meal in individuals who are lean, obese, and very...

Full description

Bibliographic Details
Main Authors: Jennifer Leohr, Maria C. Kjellsson
Format: Article
Language:English
Published: Wiley 2023-10-01
Series:CPT: Pharmacometrics & Systems Pharmacology
Online Access:https://doi.org/10.1002/psp4.13030
_version_ 1797657203860045824
author Jennifer Leohr
Maria C. Kjellsson
author_facet Jennifer Leohr
Maria C. Kjellsson
author_sort Jennifer Leohr
collection DOAJ
description Abstract The TIGG model is the first model to integrate glucose and insulin regulation, incretin effect, and triglyceride (TG) response in the lipoprotein subclasses of chylomicrons and VLDL‐V6. This model described the response following a high‐fat meal in individuals who are lean, obese, and very obese and provided insights into the possible regulation of glucose homeostasis in the extended period following a meal. Often, total TGs are analyzed within clinical studies, instead of lipoprotein subclasses. We extended the existing TIGG model to capture the observed total TGs and determined if this model could be used to predict the postprandial TG response of chylomicron and VLDL‐V6 when only total TGs are available. To assess if the lipoprotein distinction was important for the model, a second model (tTIGG) was developed using only the postprandial response in total TGs, instead of postprandial TG response in chylomicrons and VLDL‐V6. The two models were compared on their predictability to characterize the postprandial response of glucose, insulin, and active GLP‐1. Both models were able to characterize the postprandial TG response in individuals who are lean, obese, or very obese following a high‐fat meal. The extended TIGG model resulted in a better model fit of the glucose data compared to the tTIGG model, indicating that chylomicron and VLDL‐V6 provided additional information compared to total TGs. Furthermore, the expanded TIGG model was able to predict the postprandial TG response of chylomicrons and VLDL‐V6 using the total TGs and could therefore be used in studies where only total TGs were collected.
first_indexed 2024-03-11T17:41:03Z
format Article
id doaj.art-a840e8429e754b49abbd787a0d074e29
institution Directory Open Access Journal
issn 2163-8306
language English
last_indexed 2024-03-11T17:41:03Z
publishDate 2023-10-01
publisher Wiley
record_format Article
series CPT: Pharmacometrics & Systems Pharmacology
spelling doaj.art-a840e8429e754b49abbd787a0d074e292023-10-18T10:22:39ZengWileyCPT: Pharmacometrics & Systems Pharmacology2163-83062023-10-0112101529154010.1002/psp4.13030Evaluation of postprandial total triglycerides within the TIGG model for characterizing postprandial response of glucose, insulin, and GLP‐1Jennifer Leohr0Maria C. Kjellsson1Department of Pharmacokinetics/Pharmacodynamics, Lilly Research Laboratories Lilly Corporate Center Indianapolis Indiana USAPharmacometrics Research Group, Department of Pharmacy Uppsala University Uppsala SwedenAbstract The TIGG model is the first model to integrate glucose and insulin regulation, incretin effect, and triglyceride (TG) response in the lipoprotein subclasses of chylomicrons and VLDL‐V6. This model described the response following a high‐fat meal in individuals who are lean, obese, and very obese and provided insights into the possible regulation of glucose homeostasis in the extended period following a meal. Often, total TGs are analyzed within clinical studies, instead of lipoprotein subclasses. We extended the existing TIGG model to capture the observed total TGs and determined if this model could be used to predict the postprandial TG response of chylomicron and VLDL‐V6 when only total TGs are available. To assess if the lipoprotein distinction was important for the model, a second model (tTIGG) was developed using only the postprandial response in total TGs, instead of postprandial TG response in chylomicrons and VLDL‐V6. The two models were compared on their predictability to characterize the postprandial response of glucose, insulin, and active GLP‐1. Both models were able to characterize the postprandial TG response in individuals who are lean, obese, or very obese following a high‐fat meal. The extended TIGG model resulted in a better model fit of the glucose data compared to the tTIGG model, indicating that chylomicron and VLDL‐V6 provided additional information compared to total TGs. Furthermore, the expanded TIGG model was able to predict the postprandial TG response of chylomicrons and VLDL‐V6 using the total TGs and could therefore be used in studies where only total TGs were collected.https://doi.org/10.1002/psp4.13030
spellingShingle Jennifer Leohr
Maria C. Kjellsson
Evaluation of postprandial total triglycerides within the TIGG model for characterizing postprandial response of glucose, insulin, and GLP‐1
CPT: Pharmacometrics & Systems Pharmacology
title Evaluation of postprandial total triglycerides within the TIGG model for characterizing postprandial response of glucose, insulin, and GLP‐1
title_full Evaluation of postprandial total triglycerides within the TIGG model for characterizing postprandial response of glucose, insulin, and GLP‐1
title_fullStr Evaluation of postprandial total triglycerides within the TIGG model for characterizing postprandial response of glucose, insulin, and GLP‐1
title_full_unstemmed Evaluation of postprandial total triglycerides within the TIGG model for characterizing postprandial response of glucose, insulin, and GLP‐1
title_short Evaluation of postprandial total triglycerides within the TIGG model for characterizing postprandial response of glucose, insulin, and GLP‐1
title_sort evaluation of postprandial total triglycerides within the tigg model for characterizing postprandial response of glucose insulin and glp 1
url https://doi.org/10.1002/psp4.13030
work_keys_str_mv AT jenniferleohr evaluationofpostprandialtotaltriglycerideswithinthetiggmodelforcharacterizingpostprandialresponseofglucoseinsulinandglp1
AT mariackjellsson evaluationofpostprandialtotaltriglycerideswithinthetiggmodelforcharacterizingpostprandialresponseofglucoseinsulinandglp1