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Pharmacometrics Modelling in Type 2 Diabetes Mellitus : Implications on Study Design and Diabetes Disease Progression

Ghadzi, Siti Maisharah Sheikh (author)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Pharmacometrics
Kjellsson, Maria C., Associate Professor (thesis advisor)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Karlsson, Mats O., Professor (thesis advisor)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
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Visser, Sandra, PhD (opponent)
Early Stage Quantitative Pharmacology & Pharmacometrics, Merck, USA
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 (creator_code:org_t)
ISBN 9789155498443
Uppsala : Acta Universitatis Upsaliensis, 2017
English 93 s.
Series: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Pharmacy, 1651-6192 ; 226
  • Doctoral thesis (other academic/artistic)
Abstract Subject headings
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  • Pharmacometric modelling is widely used in many aspects related to type 2 diabetes mellitus (T2DM), for instance in the anti-diabetes drug development, and in quantifying the disease progression of T2DM.The aim of this thesis were to improve the design of early phase anti-diabetes drug development studies with the focus on the power to identify mechanism of drug action (MoA), and to characterize and quantify the progression from prediabetes to overt diabetes, both the natural progression and the progression with diet and exercise interventions, using pharmacometrics modelling.The appropriateness of a study design depends on the MoAs of the anti-hyperglycaemic drug. Depending on if the focus is power to identify drug effect or accuracy and precision of drug effect, the best design will be different. Using insulin measurements on top of glucose has increase the power to identify a correct drug effect, distinguish a correct MoA from the incorrect, and to identify a secondary MoA in most cases. The accuracy and precision of drug parameter estimates, however, was not affected by insulin. A natural diabetes disease progression model was successfully added in a previously developed model to describe parameter changes of glucose and insulin regulation among impaired glucose tolerance (IGT) subjects, with the quantification of the lifestyle intervention. In this model, the assessment of multiple short-term provocations was combined to predict the long-term disease progression, and offers apart from the assessment of the onset of T2DM also the framework for how to perform similar analysis. Another previously published model was further developed to characterize the weight change in driving the changes in glucose homeostasis in subjects with IGT. This model includes the complex relationship between dropout from study and weight and glucose changes.This thesis has provided a first written guidance in designing a study for pharmacometrics analysis when characterizing drug effects, for early phase anti-diabetes drug development. The characterisation of the progression from prediabetes to overt diabetes using pharmacometrics modelling was successfully performed. Both the natural progression and the progression with diet and exercise interventions were quantified in this thesis.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Keyword

Pharmacometric
type 2 diabetes mellitus
impaired glucose tolerance
prediabetes
anti-diabetes drug development
insulin
glucose
natural diabetes disease progression
lifestyle intervention
short-term provocation
long-term effect
glucose homeostasis
glucose and insulin regulation
weight
dropout
Pharmaceutical Science
Farmaceutisk vetenskap
Endokrinologi och Diabetologi
Endocrinology and Diabetology

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