Efficacy and Safety of Tirzepatide in Type 2 Diabetes and Obesity Management

The combination of glucagon-like peptide-1 (GLP-1) with other gut hormones including the glucose-dependent insulinotropic polypeptide (GIP) has been explored to complement and enhance further the GLP-1 effects on glycemia and weight loss. Tirzepatide is the first dual GLP-1/GIP receptor co-agonist w...

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Main Authors: Rachel Sinha, Dimitris Papamargaritis, Jack A. Sargeant, Melanie J. Davies
Format: Article
Language:English
Published: Korean Society for the Study of Obesity 2023-03-01
Series:Journal of Obesity & Metabolic Syndrome
Subjects:
Online Access:http://www.jomes.org/journal/view.html?doi=10.7570/jomes22067
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author Rachel Sinha
Dimitris Papamargaritis
Jack A. Sargeant
Melanie J. Davies
author_facet Rachel Sinha
Dimitris Papamargaritis
Jack A. Sargeant
Melanie J. Davies
author_sort Rachel Sinha
collection DOAJ
description The combination of glucagon-like peptide-1 (GLP-1) with other gut hormones including the glucose-dependent insulinotropic polypeptide (GIP) has been explored to complement and enhance further the GLP-1 effects on glycemia and weight loss. Tirzepatide is the first dual GLP-1/GIP receptor co-agonist which has been approved for treatment of type 2 diabetes mellitus (T2DM) based on the findings from the SURPASS program. The SURPASS trials assessed the safety and efficacy of tirzepatide in people with T2DM, from monotherapy through to insulin add-on in global populations, with another two trials dedicated to Japanese population. Over periods of treatment up to 104 weeks, once weekly tirzepatide 5 to 15 mg reduced glycosylated hemoglobin (1.87% to 3.02%), body weight (5.4 to 12.9 kg) and improved multiple cardiometabolic risk factors (including reduction in liver fat, new-onset macroalbuminuria, blood pressure, and lipids) across the T2DM spectrum. Tirzepatide provided better efficacy than placebo and other commonly used glucose-lowering medications such as semaglutide 1 mg, dulaglutide, insulin degludec, and glargine. All tirzepatide doses were well tolerated with similar side-effect profile to the GLP-1 receptor analogues. In people without diabetes, tirzepatide 5 to 15 mg once weekly for the treatment for obesity (SURMOUNT-1) resulted in substantial reductions in body weight (16.5% to 22.4%) over 72 weeks. Overall, the SURPASS program and SURMOUNT-1 study suggest that tirzepatide is marking a new era in T2DM and/or obesity management through dual agonism of gut hormones.
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spelling doaj.art-4f2d536150df4bb98bb1d74acaeb188b2023-03-30T06:55:15ZengKorean Society for the Study of ObesityJournal of Obesity & Metabolic Syndrome2508-62352023-03-01321254510.7570/jomes22067jomes22067Efficacy and Safety of Tirzepatide in Type 2 Diabetes and Obesity ManagementRachel Sinha0Dimitris Papamargaritis1Jack A. Sargeant2Melanie J. Davies3Diabetes Research Centre, University of Leicester College of Life Sciences, Leicester, UKDiabetes Research Centre, University of Leicester College of Life Sciences, Leicester, UKDiabetes Research Centre, University of Leicester College of Life Sciences, Leicester, UKDiabetes Research Centre, University of Leicester College of Life Sciences, Leicester, UKThe combination of glucagon-like peptide-1 (GLP-1) with other gut hormones including the glucose-dependent insulinotropic polypeptide (GIP) has been explored to complement and enhance further the GLP-1 effects on glycemia and weight loss. Tirzepatide is the first dual GLP-1/GIP receptor co-agonist which has been approved for treatment of type 2 diabetes mellitus (T2DM) based on the findings from the SURPASS program. The SURPASS trials assessed the safety and efficacy of tirzepatide in people with T2DM, from monotherapy through to insulin add-on in global populations, with another two trials dedicated to Japanese population. Over periods of treatment up to 104 weeks, once weekly tirzepatide 5 to 15 mg reduced glycosylated hemoglobin (1.87% to 3.02%), body weight (5.4 to 12.9 kg) and improved multiple cardiometabolic risk factors (including reduction in liver fat, new-onset macroalbuminuria, blood pressure, and lipids) across the T2DM spectrum. Tirzepatide provided better efficacy than placebo and other commonly used glucose-lowering medications such as semaglutide 1 mg, dulaglutide, insulin degludec, and glargine. All tirzepatide doses were well tolerated with similar side-effect profile to the GLP-1 receptor analogues. In people without diabetes, tirzepatide 5 to 15 mg once weekly for the treatment for obesity (SURMOUNT-1) resulted in substantial reductions in body weight (16.5% to 22.4%) over 72 weeks. Overall, the SURPASS program and SURMOUNT-1 study suggest that tirzepatide is marking a new era in T2DM and/or obesity management through dual agonism of gut hormones.http://www.jomes.org/journal/view.html?doi=10.7570/jomes22067diabetes mellitustype 2obesitytirzepatideglucagon-like peptide 1gastric inhibitory polypeptide
spellingShingle Rachel Sinha
Dimitris Papamargaritis
Jack A. Sargeant
Melanie J. Davies
Efficacy and Safety of Tirzepatide in Type 2 Diabetes and Obesity Management
Journal of Obesity & Metabolic Syndrome
diabetes mellitus
type 2
obesity
tirzepatide
glucagon-like peptide 1
gastric inhibitory polypeptide
title Efficacy and Safety of Tirzepatide in Type 2 Diabetes and Obesity Management
title_full Efficacy and Safety of Tirzepatide in Type 2 Diabetes and Obesity Management
title_fullStr Efficacy and Safety of Tirzepatide in Type 2 Diabetes and Obesity Management
title_full_unstemmed Efficacy and Safety of Tirzepatide in Type 2 Diabetes and Obesity Management
title_short Efficacy and Safety of Tirzepatide in Type 2 Diabetes and Obesity Management
title_sort efficacy and safety of tirzepatide in type 2 diabetes and obesity management
topic diabetes mellitus
type 2
obesity
tirzepatide
glucagon-like peptide 1
gastric inhibitory polypeptide
url http://www.jomes.org/journal/view.html?doi=10.7570/jomes22067
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AT jackasargeant efficacyandsafetyoftirzepatideintype2diabetesandobesitymanagement
AT melaniejdavies efficacyandsafetyoftirzepatideintype2diabetesandobesitymanagement