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Real-World Effectiveness Analysis of Switching From Liraglutide or Dulaglutide to Semaglutide in Patients With Type 2 Diabetes Mellitus: The Retrospective REALISE-DM Study.
Jain, Akshay B; Kanters, Steve; Khurana, Reena; Kissock, Jagoda; Severin, Naomi; Stafford, Sara G.
Afiliação
  • Jain AB; Fraser River Endocrinology, Surrey, BC, Canada. oxyjain@gmail.com.
  • Kanters S; Department of Medicine, Division of Endocrinology at University of British Columbia, Vancouver, BC, Canada. oxyjain@gmail.com.
  • Khurana R; School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.
  • Kissock J; Fraser River Endocrinology, Surrey, BC, Canada.
  • Severin N; Department of Medicine, Division of Endocrinology at University of British Columbia, Vancouver, BC, Canada.
  • Stafford SG; Fraser River Endocrinology, Surrey, BC, Canada.
Diabetes Ther ; 12(2): 527-536, 2021 Feb.
Article em En | MEDLINE | ID: mdl-33367981
ABSTRACT

INTRODUCTION:

Injectable semaglutide is a glucagon-like peptide-1 receptor agonist (GLP-1 RA) that was previously shown to be superior to liraglutide and dulaglutide in head-to-head comparisons in GLP-1 RA-naïve individuals. It is hypothesized that semaglutide will cause further reductions in glycated hemoglobin A1c (HbA1c) and weight in type 2 diabetes mellitus (T2DM) patients previously treated with liraglutide or dulaglutide. The REALISE-DM study provides the first real-world evidence of the effectiveness and tolerability of semaglutide in patients switching from another GLP-1 RA.

METHODS:

This retrospective real-world effectiveness analysis included T2DM adults who were on a stable dose of liraglutide or dulaglutide prior to switching to semaglutide. The primary outcome was change in HbA1c. Secondary outcomes were the changes in weight and body mass index (BMI), the occurrence of gastrointestinal side effects (GSEs), and discontinuations. Linear mixed models were used to estimate changes in HbA1c, weight, and BMI, and logistic regression was employed to analyze GSEs and discontinuations.

RESULTS:

Six months after the 164 patients in this study had switched to semaglutide, their mean HbA1c had decreased by 0.65% (7.1 mmol/mol) (95% prediction interval [PI] 0.48, 0.81% [5.2, 8.9 mmol/mol]) from a baseline of 7.9% (interquartile range [IQR] 7.3, 8.8) (62.8 mmol/mol [IQR 56.3, 72.7]), while their weight and BMI had reduced by 1.69 kg (95% PI 1.01, 2.37) and 0.59 kg/m2 (95% PI 0.34, 0.84), respectively. Nineteen patients (11.6%) developed GSEs after switching.

CONCLUSIONS:

This study supports switching T2DM patients on liraglutide or dulaglutide to injectable semaglutide to achieve further reductions in HbA1c and weight. Although a small number of GSEs occurred, semaglutide was well tolerated by the majority of the patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Diabetes Ther Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Diabetes Ther Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Canadá