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A model for glucose, insulin, and beta-cell dynamics in subjects with insulin resistance and patients with type 2 diabetes.

Ribbing, Jakob (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Hamrén, Bengt (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Svensson, M.K, 1965 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine
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Karlsson, Mats O. (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
visa färre...
 (creator_code:org_t)
2013-03-07
2010
Engelska.
Ingår i: Journal of clinical pharmacology. - : Wiley. - 1552-4604 .- 0091-2700. ; 50:8, s. 861-72
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Type 2 diabetes mellitus (T2DM) is a progressive, metabolic disorder characterized by reduced insulin sensitivity and loss of beta-cell mass (BCM), resulting in hyperglycemia. Population pharmacokinetic-pharmacodynamic (PKPD) modeling is a valuable method to gain insight into disease and drug action. A semi-mechanistic PKPD model incorporating fasting plasma glucose (FPG), fasting insulin, insulin sensitivity, and BCM in patients at various disease stages was developed. Data from 3 clinical trials (phase II/III) with a peroxisome proliferator-activated receptor agonist, tesaglitazar, were used to develop the model. In this, a modeling framework proposed by Topp et al was expanded to incorporate the effects of treatment and impact of disease, as well as variability between subjects. The model accurately described FPG and fasting insulin data over time. The model included a strong relation between insulin clearance and insulin sensitivity, predicted 40% to 60% lower BCM in T2DM patients, and realistic improvements of BCM and insulin sensitivity with treatment. The treatment response on insulin sensitivity occurs within the first weeks, whereas the positive effects on BCM arise over several months. The semi-mechanistic PKPD model well described the heterogeneous populations, ranging from nondiabetic, insulin-resistant subjects to long-term treated T2DM patients. This model also allows incorporation of clinical-experimental studies and actual observations of BCM.

Nyckelord

Alkanesulfonates
pharmacology
Blood Glucose
metabolism
Clinical Trials
Phase II as Topic
Clinical Trials
Phase III as Topic
Diabetes Mellitus
Type 2
physiopathology
Fasting
blood
Humans
Hypoglycemic Agents
pharmacology
Insulin
metabolism
Insulin Resistance
physiology
Insulin-Secreting Cells
drug effects
metabolism
Models
Biological
Peroxisome Proliferator-Activated Receptors
agonists
Phenylpropionates
pharmacology
Predictive Value of Tests
Time Factors
type-2 diabetes
PHARMACY

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