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Weight loss efficiency and safety of tirzepatide: A Systematic review

OBJECTIVE: Tirzeptide is a novel glucagon-like peptide-1 receptor (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) drug, which shows good efficiency for weight loss. Therefore, we aim to investigate the efficacy and safety of tirzepatide for weight loss in type 2 diabetes mellitus (T2D...

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Autores principales: Lin, Fei, Yu, Bin, Ling, Baodong, Lv, Guangyao, Shang, Huijun, Zhao, Xia, Jie, Xiaoling, Chen, Jing, Li, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159347/
https://www.ncbi.nlm.nih.gov/pubmed/37141329
http://dx.doi.org/10.1371/journal.pone.0285197
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author Lin, Fei
Yu, Bin
Ling, Baodong
Lv, Guangyao
Shang, Huijun
Zhao, Xia
Jie, Xiaoling
Chen, Jing
Li, Yan
author_facet Lin, Fei
Yu, Bin
Ling, Baodong
Lv, Guangyao
Shang, Huijun
Zhao, Xia
Jie, Xiaoling
Chen, Jing
Li, Yan
author_sort Lin, Fei
collection PubMed
description OBJECTIVE: Tirzeptide is a novel glucagon-like peptide-1 receptor (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) drug, which shows good efficiency for weight loss. Therefore, we aim to investigate the efficacy and safety of tirzepatide for weight loss in type 2 diabetes mellitus (T2DM) and obesity patients in this meta-analysis study. METHODS: Cochrane Library, PubMed, Embase, Clinical Trials, and Web of Science were searched from inception to October 5, 2022. All randomized controlled trials (RCTs) were included. The odds ratio (OR) was calculated using fixed-effects or random-effects models by Review Manager 5.3 software. RESULTS: In total, ten studies (12 reports) involving 9,873 patients were identified. A significant loss body weight in the tirzepatide group versus the placebo by -9.81 kg (95% CI (-12.09, -7.52), GLP-1 RAs by -1.05 kg (95% CI (-1.48, -0.63), and insulin by -1.93 kg (95% CI (-2.81, -1.05), respectively. In sub-analysis, the body weight of patients was significantly reduced in three tirzepatide doses (5 mg, 10 mg, and 15 mg) when compared with those of the placebo/GLP-1 RA/insulin. In terms of safety, the incidence of any adverse events and adverse events leading to study drug discontinuation was higher in the tirzepatide group, but the incidence of serious adverse events and hypoglycaemia was lower. Additionally, the gastrointestinal adverse events (including diarrhea, nausea, vomiting and decreased appetite) of tirzepatide were higher than those of placebo/basal insulin, but similar to GLP-1 RAs. CONCLUSION: In conclusion, tirzeptide can significantly reduce the weight of T2DM and patient with obesity, and it is a potential therapeutic regimen for weight-loss, but we need to be vigilant about its gastrointestinal reaction.
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spelling pubmed-101593472023-05-05 Weight loss efficiency and safety of tirzepatide: A Systematic review Lin, Fei Yu, Bin Ling, Baodong Lv, Guangyao Shang, Huijun Zhao, Xia Jie, Xiaoling Chen, Jing Li, Yan PLoS One Research Article OBJECTIVE: Tirzeptide is a novel glucagon-like peptide-1 receptor (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) drug, which shows good efficiency for weight loss. Therefore, we aim to investigate the efficacy and safety of tirzepatide for weight loss in type 2 diabetes mellitus (T2DM) and obesity patients in this meta-analysis study. METHODS: Cochrane Library, PubMed, Embase, Clinical Trials, and Web of Science were searched from inception to October 5, 2022. All randomized controlled trials (RCTs) were included. The odds ratio (OR) was calculated using fixed-effects or random-effects models by Review Manager 5.3 software. RESULTS: In total, ten studies (12 reports) involving 9,873 patients were identified. A significant loss body weight in the tirzepatide group versus the placebo by -9.81 kg (95% CI (-12.09, -7.52), GLP-1 RAs by -1.05 kg (95% CI (-1.48, -0.63), and insulin by -1.93 kg (95% CI (-2.81, -1.05), respectively. In sub-analysis, the body weight of patients was significantly reduced in three tirzepatide doses (5 mg, 10 mg, and 15 mg) when compared with those of the placebo/GLP-1 RA/insulin. In terms of safety, the incidence of any adverse events and adverse events leading to study drug discontinuation was higher in the tirzepatide group, but the incidence of serious adverse events and hypoglycaemia was lower. Additionally, the gastrointestinal adverse events (including diarrhea, nausea, vomiting and decreased appetite) of tirzepatide were higher than those of placebo/basal insulin, but similar to GLP-1 RAs. CONCLUSION: In conclusion, tirzeptide can significantly reduce the weight of T2DM and patient with obesity, and it is a potential therapeutic regimen for weight-loss, but we need to be vigilant about its gastrointestinal reaction. Public Library of Science 2023-05-04 /pmc/articles/PMC10159347/ /pubmed/37141329 http://dx.doi.org/10.1371/journal.pone.0285197 Text en © 2023 Lin et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lin, Fei
Yu, Bin
Ling, Baodong
Lv, Guangyao
Shang, Huijun
Zhao, Xia
Jie, Xiaoling
Chen, Jing
Li, Yan
Weight loss efficiency and safety of tirzepatide: A Systematic review
title Weight loss efficiency and safety of tirzepatide: A Systematic review
title_full Weight loss efficiency and safety of tirzepatide: A Systematic review
title_fullStr Weight loss efficiency and safety of tirzepatide: A Systematic review
title_full_unstemmed Weight loss efficiency and safety of tirzepatide: A Systematic review
title_short Weight loss efficiency and safety of tirzepatide: A Systematic review
title_sort weight loss efficiency and safety of tirzepatide: a systematic review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10159347/
https://www.ncbi.nlm.nih.gov/pubmed/37141329
http://dx.doi.org/10.1371/journal.pone.0285197
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