Cargando…

Liraglutide pharmacokinetics and exposure‐response in adolescents with obesity

BACKGROUND: Obesity in adolescence presents a major public health challenge, often leading to obesity in adulthood with associated chronic disease. OBJECTIVES: This study aimed to perform a population pharmacokinetic and exposure‐response analysis of liraglutide by meta‐analysis of data from trials...

Descripción completa

Detalles Bibliográficos
Autores principales: Carlsson Petri, Kristin C., Hale, Paula M., Hesse, Dan, Rathor, Naveen, Mastrandrea, Lucy D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519033/
https://www.ncbi.nlm.nih.gov/pubmed/33963681
http://dx.doi.org/10.1111/ijpo.12799
_version_ 1784584364381700096
author Carlsson Petri, Kristin C.
Hale, Paula M.
Hesse, Dan
Rathor, Naveen
Mastrandrea, Lucy D.
author_facet Carlsson Petri, Kristin C.
Hale, Paula M.
Hesse, Dan
Rathor, Naveen
Mastrandrea, Lucy D.
author_sort Carlsson Petri, Kristin C.
collection PubMed
description BACKGROUND: Obesity in adolescence presents a major public health challenge, often leading to obesity in adulthood with associated chronic disease. OBJECTIVES: This study aimed to perform a population pharmacokinetic and exposure‐response analysis of liraglutide by meta‐analysis of data from trials conducted in children, adolescents and adults with obesity. METHODS: The population pharmacokinetic analysis investigated the effect of covariates body weight, age group (children, adolescents and adults) and sex on liraglutide exposure in adolescents compared with previous results in adults. The exposure‐response relationship of liraglutide for the change from baseline in body mass index standard deviation score (BMI SDS) was evaluated in adolescents and compared to that in adults. RESULTS: Body weight was the main covariate affecting liraglutide exposure, with lower exposures at higher body weights, whereas age group was of no importance and sex was of little importance. An exposure‐response relationship was demonstrated for liraglutide in both adolescents and adults as the decrease in BMI SDS from baseline increased in an exposure‐dependent manner with increasing liraglutide exposure. CONCLUSIONS: The population pharmacokinetic analysis supported similar liraglutide exposures in adolescents and adults; body weight was the most important covariate affecting exposure. An exposure‐response relationship was established for liraglutide.
format Online
Article
Text
id pubmed-8519033
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-85190332021-10-21 Liraglutide pharmacokinetics and exposure‐response in adolescents with obesity Carlsson Petri, Kristin C. Hale, Paula M. Hesse, Dan Rathor, Naveen Mastrandrea, Lucy D. Pediatr Obes Original Research BACKGROUND: Obesity in adolescence presents a major public health challenge, often leading to obesity in adulthood with associated chronic disease. OBJECTIVES: This study aimed to perform a population pharmacokinetic and exposure‐response analysis of liraglutide by meta‐analysis of data from trials conducted in children, adolescents and adults with obesity. METHODS: The population pharmacokinetic analysis investigated the effect of covariates body weight, age group (children, adolescents and adults) and sex on liraglutide exposure in adolescents compared with previous results in adults. The exposure‐response relationship of liraglutide for the change from baseline in body mass index standard deviation score (BMI SDS) was evaluated in adolescents and compared to that in adults. RESULTS: Body weight was the main covariate affecting liraglutide exposure, with lower exposures at higher body weights, whereas age group was of no importance and sex was of little importance. An exposure‐response relationship was demonstrated for liraglutide in both adolescents and adults as the decrease in BMI SDS from baseline increased in an exposure‐dependent manner with increasing liraglutide exposure. CONCLUSIONS: The population pharmacokinetic analysis supported similar liraglutide exposures in adolescents and adults; body weight was the most important covariate affecting exposure. An exposure‐response relationship was established for liraglutide. John Wiley & Sons, Inc. 2021-05-07 2021-10 /pmc/articles/PMC8519033/ /pubmed/33963681 http://dx.doi.org/10.1111/ijpo.12799 Text en © 2021 The Authors. Pediatric Obesity published by John Wiley & Sons Ltd on behalf of World Obesity Federation. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Carlsson Petri, Kristin C.
Hale, Paula M.
Hesse, Dan
Rathor, Naveen
Mastrandrea, Lucy D.
Liraglutide pharmacokinetics and exposure‐response in adolescents with obesity
title Liraglutide pharmacokinetics and exposure‐response in adolescents with obesity
title_full Liraglutide pharmacokinetics and exposure‐response in adolescents with obesity
title_fullStr Liraglutide pharmacokinetics and exposure‐response in adolescents with obesity
title_full_unstemmed Liraglutide pharmacokinetics and exposure‐response in adolescents with obesity
title_short Liraglutide pharmacokinetics and exposure‐response in adolescents with obesity
title_sort liraglutide pharmacokinetics and exposure‐response in adolescents with obesity
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519033/
https://www.ncbi.nlm.nih.gov/pubmed/33963681
http://dx.doi.org/10.1111/ijpo.12799
work_keys_str_mv AT carlssonpetrikristinc liraglutidepharmacokineticsandexposureresponseinadolescentswithobesity
AT halepaulam liraglutidepharmacokineticsandexposureresponseinadolescentswithobesity
AT hessedan liraglutidepharmacokineticsandexposureresponseinadolescentswithobesity
AT rathornaveen liraglutidepharmacokineticsandexposureresponseinadolescentswithobesity
AT mastrandrealucyd liraglutidepharmacokineticsandexposureresponseinadolescentswithobesity