PMID- 33354917 OWN - NLM STAT- MEDLINE DCOM- 20211015 LR - 20220531 IS - 1467-789X (Electronic) IS - 1467-7881 (Linking) VI - 22 IP - 6 DP - 2021 Jun TI - GLP-1 agonists for obesity and type 2 diabetes in children: Systematic review and meta-analysis. PG - e13177 LID - 10.1111/obr.13177 [doi] AB - Pharmacological options for management of obesity and type 2 diabetes mellitus (T2DM) in children are limited. We aimed to synthesize published randomized controlled trial (RCT) evidence on the efficacy of glucagon-like peptide-1 (GLP-1) agonists in T2DM, pre-diabetes, and obesity in children aged <18 years. Inclusion criteria were RCTs of any GLP-1 agonist, solely or in conjunction with other drugs, for the treatment of obesity, pre-diabetes, and/or T2DM in children aged <18 years old. Nine studies met the inclusion criteria (two for T2DM, one for pre-diabetes, and six for obesity without diabetes). In total, 286 children were allocated to GLP-1 agonist therapy. Compared with controls, GLP-1 agonist therapy reduced HbA1c by -0.30% (95% confidence interval [CI] -0.57, -0.04) with a larger effect in children with (pre-)diabetes (-0.72%; 95% CI -1.17, -0.28; three studies) than in children with obesity (-0.08%; 95% CI -0.13, -0.02; four studies). Conversely, GLP-1 agonist therapy reduced body weight more in children with obesity (-2.74 kg; 95% CI -3.77, -1.70; six studies) than in children with T2DM (-0.97 kg; 95% CI -2.01, 0.08; two studies). Adverse effects included gastrointestinal symptoms and minor hypoglycemic episodes, but not severe hypoglycemia. GLP-1 agonists are efficacious in treating children with obesity and/or T2DM. Effect sizes are comparable with those reported in adults. CI - (c) 2020 World Obesity Federation. FAU - Chadda, Karan R AU - Chadda KR AUID- ORCID: 0000-0002-8060-8408 AD - Department of Paediatrics, University of Cambridge, Cambridge, UK. FAU - Cheng, Tuck Seng AU - Cheng TS AUID- ORCID: 0000-0003-4442-7332 AD - MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge, UK. FAU - Ong, Ken K AU - Ong KK AD - Department of Paediatrics, University of Cambridge, Cambridge, UK. AD - MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge, UK. LA - eng GR - MC_UU_00006/2/MRC_/Medical Research Council/United Kingdom GR - MC_UU_12015/2/MRC_/Medical Research Council/United Kingdom PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Review PT - Systematic Review DEP - 20201222 PL - England TA - Obes Rev JT - Obesity reviews : an official journal of the International Association for the Study of Obesity JID - 100897395 RN - 0 (Glucagon-Like Peptide-1 Receptor) RN - 0 (Hypoglycemic Agents) RN - 89750-14-1 (Glucagon-Like Peptide 1) SB - IM MH - Adolescent MH - Child MH - *Diabetes Mellitus, Type 2/drug therapy MH - *Glucagon-Like Peptide 1/antagonists & inhibitors MH - Glucagon-Like Peptide-1 Receptor MH - Humans MH - Hypoglycemic Agents/therapeutic use MH - *Pediatric Obesity/drug therapy MH - Randomized Controlled Trials as Topic OTO - NOTNLM OT - glucagon-like peptide-1 OT - obesity OT - pediatric OT - type 2 diabetes EDAT- 2020/12/24 06:00 MHDA- 2021/10/16 06:00 CRDT- 2020/12/23 05:54 PHST- 2020/11/05 00:00 [revised] PHST- 2020/09/12 00:00 [received] PHST- 2020/11/12 00:00 [accepted] PHST- 2020/12/24 06:00 [pubmed] PHST- 2021/10/16 06:00 [medline] PHST- 2020/12/23 05:54 [entrez] AID - 10.1111/obr.13177 [doi] PST - ppublish SO - Obes Rev. 2021 Jun;22(6):e13177. doi: 10.1111/obr.13177. Epub 2020 Dec 22.