Safety and efficacy of glucagon-like peptide-1 receptor agonists in children and adolescents with obesity: A meta-analysis

dc.contributor.authorRyan, Paul M.
dc.contributor.authorSeltzer, Sean
dc.contributor.authorHayward, Nathaniel E.
dc.contributor.authorAvelar Rodriguez, David
dc.contributor.authorSless, Ryan T.
dc.contributor.authorHawkes, Colin P.
dc.date.accessioned2021-11-29T13:53:26Z
dc.date.available2021-11-29T13:53:26Z
dc.date.issued2021-05-11
dc.date.updated2021-11-29T13:39:59Z
dc.description.abstractTo determine the weight, body mass index (BMI), cardiometabolic, and gastrointestinal effects of glucagon-like peptide-1 (GLP-1) receptor agonists in children with obesity. Study design: Web of Science, PubMed/MEDLINE, and Scopus databases from 01/01/1994-01/01/2021 for randomized control trials examining the weight, BMI, cardiometabolic, or gastrointestinal effects of GLP-1 receptor agonists in children and adolescents with obesity. Data were extracted by 2 independent surveyors and a random effects model was applied to meta-analyze generic inverse variance outcomes. Primary outcomes were related to weight and cardiometabolic profile, and secondary outcomes of interest were gastrointestinal-related treatment-emergent adverse events. Results: Nine studies involving 574 participants were identified, of which 3 involved exenatide and 6 involved liraglutide. GLP-1 receptor agonists use caused a modest reduction in body weight (mean difference [MD] -1.50 [-2.50,-0.50] kg, I2 64%), BMI (MD -1.24 [-1.71,-0.77] kg/m2, I2 0%), and BMI z score (MD -0.14 [-0.23,-0.06], I2 43%). Glycemic control was improved in children with proven insulin resistance (glycated hemoglobin A1c MD -1.05 [-1.93,-0.18] %, I2 76%). Although no lipid profile improvements were noted, a modest decrease in systolic blood pressure was detected (MD -2.30 [-4.11,-0.49] mm Hg; I2 0%). Finally, analysis of gastrointestinal-related treatment-emergent adverse events revealed an increased risk of nausea (risk ratio 2.11 [1.44, 3.09]; I2 0%), without significant increases in other gastrointestinal symptoms. Conclusions: This meta-analysis indicates that GLP-1 receptor agonists are safe and effective in modestly reducing weight, BMI, glycated hemoglobin A1c, and systolic blood pressure in children and adolescents with obesity in a clinical setting, albeit with increased rates of nausea.en
dc.description.statusPeer revieweden
dc.description.versionPublished Versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationRyan, P. M., Seltzer, S., Hayward, N. E., Avelar Rodriguez, D., Sless, R. T. and Hawkes, C. P. (2021) 'Safety and efficacy of glucagon-like peptide-1 receptor agonists in children and adolescents with obesity: A meta-analysis', Journal of Pediatrics, 236 , pp. 137-147. doi: 10.1016/j.jpeds.2021.05.009en
dc.identifier.doi10.1016/j.jpeds.2021.05.009en
dc.identifier.endpage147en
dc.identifier.issn1097-6833
dc.identifier.issn0022-3476
dc.identifier.journaltitleJournal of Pediatricsen
dc.identifier.startpage137en
dc.identifier.urihttps://hdl.handle.net/10468/12281
dc.identifier.volume236en
dc.language.isoenen
dc.publisherElsevier B. V.en
dc.rights© 2021, the Authors. Published by Elsevier inc. This is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en
dc.subjectPediatric obesityen
dc.subjectIncretinen
dc.subjectGLP-1en
dc.titleSafety and efficacy of glucagon-like peptide-1 receptor agonists in children and adolescents with obesity: A meta-analysisen
dc.typeArticle (peer-reviewed)en
Files
Original bundle
Now showing 1 - 2 of 2
Loading...
Thumbnail Image
Name:
1-s2.0-S0022347621004327-main.pdf
Size:
5.14 MB
Format:
Adobe Portable Document Format
Description:
Published Version
Loading...
Thumbnail Image
Name:
1-s2.0-S0022347621004327-mmc1.pdf
Size:
101.2 KB
Format:
Adobe Portable Document Format
Description:
Supplementary Data
License bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
2.71 KB
Format:
Item-specific license agreed upon to submission
Description: