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The variability in beta‐cell function in placebo‐treated subjects with type 2 diabetes: application of the weight‐HbA1c‐insulin‐glucose (WHIG) model
Author(s) -
Duong Janna K.,
Winter Willem,
Choy Steve,
Plock Nele,
Naik Himanshu,
Krauwinkel Walter,
Visser Sandra A.G.,
Verhamme Katia M.,
Sturkenboom Miriam C.,
Stricker B.H.,
Danhof Meindert
Publication year - 2017
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/bcp.13144
Subject(s) - nonmem , diabetes mellitus , medicine , insulin , endocrinology , type 2 diabetes , placebo , population , pharmacokinetics , pathology , alternative medicine , environmental health
Aim The weight‐glycosylated haemoglobin (HbA1C)‐insulin‐glucose (WHIG) model describes the effects of changes in weight on insulin sensitivity (IS) in newly diagnosed, obese subjects receiving placebo treatment. This model was applied to a wider population of placebo‐treated subjects, to investigate factors influencing the variability in IS and β‐cell function. Methods The WHIG model was applied to the WHIG dataset (Study 1) and two other placebo datasets (Studies 2 and 3). Studies 2 and 3 consisted of nonobese subjects and subjects with advanced type 2 diabetes mellitus (T2DM). Body weight, fasting serum insulin (FSI), fasting plasma glucose (FPG) and HbA1c were used for nonlinear mixed‐effects modelling (using NONMEM v7.2 software). Sources of interstudy variability (ISV) and potential covariates (age, gender, diabetes duration, ethnicity, compliance) were investigated. Results An ISV for baseline parameters (body weight and β‐cell function) was required. The baseline β‐cell function was significantly lower in subjects with advanced T2DM (median difference: Study 2: 15.6%, P < 0.001; Study 3: 22.7%, P < 0.001) than in subjects with newly diagnosed T2DM (Study 1). A reduction in the estimated insulin secretory response in subjects with advanced T2DM was observed but diabetes duration was not a significant covariate. Conclusion The WHIG model can be used to describe the changes in weight, IS and β‐cell function in the diabetic population. IS remained relatively stable between subjects but a large ISV in β‐cell function was observed. There was a trend towards decreasing β‐cell responsiveness with diabetes duration, and further studies, incorporating subjects with a longer history of diabetes, are required.