The Body weight Reducing Effects of Tirzepatide in People with and without Type 2 Diabetes: A Review on Efficacy and Adverse Effects

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

The Body weight Reducing Effects of Tirzepatide in People with and without Type 2 Diabetes : A Review on Efficacy and Adverse Effects. / Jensen, Thomas Leth; Brønden, Andreas; Karstoft, Kristian; Sonne, David Peick; Christensen, Mikkel Bring.

I: Patient Preference and Adherence, Bind 18, 2024, s. 373-382.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Jensen, TL, Brønden, A, Karstoft, K, Sonne, DP & Christensen, MB 2024, 'The Body weight Reducing Effects of Tirzepatide in People with and without Type 2 Diabetes: A Review on Efficacy and Adverse Effects', Patient Preference and Adherence, bind 18, s. 373-382. https://doi.org/10.2147/PPA.S419304

APA

Jensen, T. L., Brønden, A., Karstoft, K., Sonne, D. P., & Christensen, M. B. (2024). The Body weight Reducing Effects of Tirzepatide in People with and without Type 2 Diabetes: A Review on Efficacy and Adverse Effects. Patient Preference and Adherence, 18, 373-382. https://doi.org/10.2147/PPA.S419304

Vancouver

Jensen TL, Brønden A, Karstoft K, Sonne DP, Christensen MB. The Body weight Reducing Effects of Tirzepatide in People with and without Type 2 Diabetes: A Review on Efficacy and Adverse Effects. Patient Preference and Adherence. 2024;18:373-382. https://doi.org/10.2147/PPA.S419304

Author

Jensen, Thomas Leth ; Brønden, Andreas ; Karstoft, Kristian ; Sonne, David Peick ; Christensen, Mikkel Bring. / The Body weight Reducing Effects of Tirzepatide in People with and without Type 2 Diabetes : A Review on Efficacy and Adverse Effects. I: Patient Preference and Adherence. 2024 ; Bind 18. s. 373-382.

Bibtex

@article{afa95078ee9e4993a06c6dc75dd37fb5,
title = "The Body weight Reducing Effects of Tirzepatide in People with and without Type 2 Diabetes: A Review on Efficacy and Adverse Effects",
abstract = "Obesity is becoming more frequent and has several negative health impacts. Recent advances in weight management strategies have primarily resided in pharmaceutical treatments, and the glucagon-like peptide-1 (GLP-1) receptor agonists have shown great potential in terms of body weight reduction in addition to improving glycemic control in patients with type 2 diabetes (T2D). Recently, the dual GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) receptor agonist tirzepatide has been developed. Tirzepatide has shown strong effects on glycated hemoglobin (HbA1C) levels in several clinical trials including participants with T2D (SURPASS program). In addition to its lowering effect on HbA1C, tirzepatide leads to substantial reductions in body weight, and a series of clinical trials (SURMOUNT program) have investigated the effects on body weight as the primary outcome. In these two trial programs, tirzepatide in doses of 5 mg to 15 mg administered subcutaneously once weekly resulted in body weight reduction of up to 15% in participants with T2D and up to 21% in participants without T2D, despite comparable baseline bodyweight. Across the two trial programs, adverse effects were mainly gastrointestinal (nausea, diarrhea, and vomiting) occurring with similar incidences of vomiting and lower incidences of diarrhea and nausea in trial participants with T2D compared to trials participants without T2D. Overall, discontinuation due to adverse events occurred in 3–7% of participants with no major differences between individuals with and without T2D. The higher weight-reducing efficacy of tirzepatide in trial participants without T2D is currently unexplained and may be partly reflected in dissimilarities in frequencies of gastrointestinal adverse events. The weight reducing effects of tirzepatide hold great promise for weight management in obese patients regardless of the presence of T2D.",
keywords = "dual agonists, GIP, GLP-1, safety, tirzepatide, type 2 diabetes, weight loss",
author = "Jensen, {Thomas Leth} and Andreas Br{\o}nden and Kristian Karstoft and Sonne, {David Peick} and Christensen, {Mikkel Bring}",
note = "Publisher Copyright: {\textcopyright} 2024 Jensen et al.",
year = "2024",
doi = "10.2147/PPA.S419304",
language = "English",
volume = "18",
pages = "373--382",
journal = "Patient Preference and Adherence",
issn = "1177-889X",
publisher = "Dove Medical Press Ltd",

}

RIS

TY - JOUR

T1 - The Body weight Reducing Effects of Tirzepatide in People with and without Type 2 Diabetes

T2 - A Review on Efficacy and Adverse Effects

AU - Jensen, Thomas Leth

AU - Brønden, Andreas

AU - Karstoft, Kristian

AU - Sonne, David Peick

AU - Christensen, Mikkel Bring

N1 - Publisher Copyright: © 2024 Jensen et al.

PY - 2024

Y1 - 2024

N2 - Obesity is becoming more frequent and has several negative health impacts. Recent advances in weight management strategies have primarily resided in pharmaceutical treatments, and the glucagon-like peptide-1 (GLP-1) receptor agonists have shown great potential in terms of body weight reduction in addition to improving glycemic control in patients with type 2 diabetes (T2D). Recently, the dual GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) receptor agonist tirzepatide has been developed. Tirzepatide has shown strong effects on glycated hemoglobin (HbA1C) levels in several clinical trials including participants with T2D (SURPASS program). In addition to its lowering effect on HbA1C, tirzepatide leads to substantial reductions in body weight, and a series of clinical trials (SURMOUNT program) have investigated the effects on body weight as the primary outcome. In these two trial programs, tirzepatide in doses of 5 mg to 15 mg administered subcutaneously once weekly resulted in body weight reduction of up to 15% in participants with T2D and up to 21% in participants without T2D, despite comparable baseline bodyweight. Across the two trial programs, adverse effects were mainly gastrointestinal (nausea, diarrhea, and vomiting) occurring with similar incidences of vomiting and lower incidences of diarrhea and nausea in trial participants with T2D compared to trials participants without T2D. Overall, discontinuation due to adverse events occurred in 3–7% of participants with no major differences between individuals with and without T2D. The higher weight-reducing efficacy of tirzepatide in trial participants without T2D is currently unexplained and may be partly reflected in dissimilarities in frequencies of gastrointestinal adverse events. The weight reducing effects of tirzepatide hold great promise for weight management in obese patients regardless of the presence of T2D.

AB - Obesity is becoming more frequent and has several negative health impacts. Recent advances in weight management strategies have primarily resided in pharmaceutical treatments, and the glucagon-like peptide-1 (GLP-1) receptor agonists have shown great potential in terms of body weight reduction in addition to improving glycemic control in patients with type 2 diabetes (T2D). Recently, the dual GLP-1 and glucose-dependent insulinotropic polypeptide (GIP) receptor agonist tirzepatide has been developed. Tirzepatide has shown strong effects on glycated hemoglobin (HbA1C) levels in several clinical trials including participants with T2D (SURPASS program). In addition to its lowering effect on HbA1C, tirzepatide leads to substantial reductions in body weight, and a series of clinical trials (SURMOUNT program) have investigated the effects on body weight as the primary outcome. In these two trial programs, tirzepatide in doses of 5 mg to 15 mg administered subcutaneously once weekly resulted in body weight reduction of up to 15% in participants with T2D and up to 21% in participants without T2D, despite comparable baseline bodyweight. Across the two trial programs, adverse effects were mainly gastrointestinal (nausea, diarrhea, and vomiting) occurring with similar incidences of vomiting and lower incidences of diarrhea and nausea in trial participants with T2D compared to trials participants without T2D. Overall, discontinuation due to adverse events occurred in 3–7% of participants with no major differences between individuals with and without T2D. The higher weight-reducing efficacy of tirzepatide in trial participants without T2D is currently unexplained and may be partly reflected in dissimilarities in frequencies of gastrointestinal adverse events. The weight reducing effects of tirzepatide hold great promise for weight management in obese patients regardless of the presence of T2D.

KW - dual agonists

KW - GIP

KW - GLP-1

KW - safety

KW - tirzepatide

KW - type 2 diabetes

KW - weight loss

U2 - 10.2147/PPA.S419304

DO - 10.2147/PPA.S419304

M3 - Review

C2 - 38352159

AN - SCOPUS:85185122756

VL - 18

SP - 373

EP - 382

JO - Patient Preference and Adherence

JF - Patient Preference and Adherence

SN - 1177-889X

ER -

ID: 383883583