Literature DB >> 23606523

A model-based approach to predict longitudinal HbA1c, using early phase glucose data from type 2 diabetes mellitus patients after anti-diabetic treatment.

Maria C Kjellsson1, Valérie F Cosson, Norman A Mazer, Nicolas Frey, Mats O Karlsson.   

Abstract

Predicting late phase outcomes from early-phase findings can help inform decisions in drug development. If the measurements in early-phase differ from those in late phase, forecasting is more challenging. In this paper, we present a model-based approach for predicting glycosylated hemoglobin (HbA1c) in late phase using glucose and insulin concentrations from an early-phase study, investigating an anti-diabetic treatment. Two previously published models were used; an integrated glucose and insulin (IGI) model for meal tolerance tests and an integrated glucose-red blood cell-HbA1c (IGRH) model predicting the formation of HbA1c from the average glucose concentration (Cg,av ). Output from the IGI model was used as input to the IGRH model. Parameters of the IGI model and drug effects were estimated using data from a phase1 study in 59 diabetic patients receiving various doses of a glucokinase activator. Cg,av values were simulated according to a Phase 2 study design and used in the IGRH model for predictions of HbA1c. The performance of the model-based approach was assessed by comparing the predicted to the actual outcome of the Phase 2 study. We have shown that this approach well predicts the longitudinal HbA1c response in a 12-week study using only information from a 1-week study where glucose and insulin concentrations were measured.
© The Author(s) 2013.

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Year:  2013        PMID: 23606523     DOI: 10.1002/jcph.86

Source DB:  PubMed          Journal:  J Clin Pharmacol        ISSN: 0091-2700            Impact factor:   3.126


  8 in total

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Review 2.  Requirements for multi-level systems pharmacology models to reach end-usage: the case of type 2 diabetes.

Authors:  Elin Nyman; Yvonne J W Rozendaal; Gabriel Helmlinger; Bengt Hamrén; Maria C Kjellsson; Peter Strålfors; Natal A W van Riel; Peter Gennemark; Gunnar Cedersund
Journal:  Interface Focus       Date:  2016-04-06       Impact factor: 3.906

3.  Application of the integrated glucose-insulin model for cross-study characterization of T2DM patients on metformin background treatment.

Authors:  Joanna Parkinson; Bengt Hamrén; Maria C Kjellsson; Stanko Skrtic
Journal:  Br J Clin Pharmacol       Date:  2016-08-16       Impact factor: 4.335

4.  Comparison of Power, Prognosis, and Extrapolation Properties of Four Population Pharmacodynamic Models of HbA1c for Type 2 Diabetes.

Authors:  Gustaf J Wellhagen; Mats O Karlsson; Maria C Kjellsson
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2018-03-25

5.  Study Design Selection in Early Clinical Anti-Hyperglycemic Drug Development: A Simulation Study of Glucose Tolerance Tests.

Authors:  Moustafa M A Ibrahim; Siti M S Ghadzi; Maria C Kjellsson; Mats O Karlsson
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2018-05-06

6.  An Updated Organ-Based Multi-Level Model for Glucose Homeostasis: Organ Distributions, Timing, and Impact of Blood Flow.

Authors:  Tilda Herrgårdh; Hao Li; Elin Nyman; Gunnar Cedersund
Journal:  Front Physiol       Date:  2021-06-01       Impact factor: 4.566

7.  Model-Based Interspecies Scaling of Glucose Homeostasis.

Authors:  Oskar Alskär; Mats O Karlsson; Maria C Kjellsson
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2017-09-28

8.  Urinary glucose excretion after dapagliflozin treatment: An exposure-response modelling comparison between Japanese and non-Japanese patients diagnosed with type 1 diabetes mellitus.

Authors:  Victor Sokolov; Tatiana Yakovleva; Shinya Ueda; Joanna Parkinson; David W Boulton; Robert C Penland; Weifeng Tang
Journal:  Diabetes Obes Metab       Date:  2018-12-16       Impact factor: 6.577

  8 in total

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