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      The Current and Future Role of Insulin Therapy in the Management of Type 2 Diabetes: A Narrative Review

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          Abstract

          Early initiation of intensive insulin therapy has been demonstrated to be effective in controlling glycemia and possibly preserving beta-cell function. Innovations in insulin formulations and delivery systems continue. However, we have seen an acceleration in the development of new classes of diabetes medications for individuals with type 2 diabetes and obesity, such as, for example, glucagon-like peptide-1 receptor agonists (GLP-1 RAs). These formulations have been shown to confer significant benefits in achieving good glycemic control with reduced hypoglycemia risk, weight loss, and cardiorenal protection. Therefore, it is reasonable to question whether there is still a role for insulin therapy in the management of type 2 diabetes. However, there are clear limitations inherent to GLP-1 RA therapy, including high rates of suboptimal adherence and treatment discontinuation due to high cost and side effects, which diminish long-term efficacy, and supply issues. In addition, newer formulations have shown improvements in convenience and tolerability, and have been shown to be even more effective when used in conjunction with basal insulin. In this narrative review, we discuss current evidence that supports GLP-1 RA use in combination with insulin therapy and the potential pitfalls of reliance on GLP-1 RAs as a substitute for insulin therapy.

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          Oral Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes

          Establishing cardiovascular safety of new therapies for type 2 diabetes is important. Safety data are available for the subcutaneous form of the glucagon-like peptide-1 receptor agonist semaglutide but are needed for oral semaglutide.
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            Tirzepatide Once Weekly for the Treatment of Obesity

            Obesity is a chronic disease that results in substantial global morbidity and mortality. The efficacy and safety of tirzepatide, a novel glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 receptor agonist, in people with obesity are not known.
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              Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes

              Tirzepatide is a dual glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 (GLP-1) receptor agonist that is under development for the treatment of type 2 diabetes. The efficacy and safety of once-weekly tirzepatide as compared with semaglutide, a selective GLP-1 receptor agonist, are unknown.
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                Author and article information

                Contributors
                chris@cgparkin.org
                Journal
                Diabetes Ther
                Diabetes Ther
                Diabetes Therapy
                Springer Healthcare (Cheshire )
                1869-6953
                1869-6961
                4 April 2024
                4 April 2024
                May 2024
                : 15
                : 5
                : 1085-1098
                Affiliations
                [1 ]GRID grid.4367.6, ISNI 0000 0001 2355 7002, Division of Endocrinology, Metabolism and Lipid Research, School of Medicine, , Washington University in St. Louis, ; 660 S. Euclid, Campus Box 8127, St. Louis, MO 63110 USA
                [2 ]GRID grid.34477.33, ISNI 0000000122986657, UW Medicine Diabetes Institute, , University of Washington School of Medicine, ; 750 Republican Street, Building F, Seattle, WA 98109 USA
                [3 ]CGParkin Communications, Inc., 2675 Windmill Pkwy, Ste. 2721, Henderson, NV 89074 USA
                [4 ]Division of Endocrinology, Metabolism and Molecular Medicine, Feinberg School of Medicine Northwestern University, ( https://ror.org/000e0be47) 675 N St Clair St Galter Pavilion, Ste 14-100, Chicago, IL 60611 USA
                [5 ]Division of Endocrinology, Diabetes, and Metabolism, Mount Sinai Diabetes Center and T1D Clinical Research, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) 5 E 98th St, New York, NY 10029 USA
                [6 ]GRID grid.189967.8, ISNI 0000 0001 0941 6502, Emory University School of Medicine, ; 100 Woodruff Circle, Atlanta, GA 30322 USA
                Author information
                http://orcid.org/0000-0001-6838-5355
                Article
                1569
                10.1007/s13300-024-01569-8
                11043311
                38573469
                12812ff4-4765-4f66-b467-a9aa97640e33
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 28 February 2024
                : 14 March 2024
                Funding
                Funded by: embecta
                Categories
                Review
                Custom metadata
                © Springer Healthcare Ltd., part of Springer Nature 2024

                Endocrinology & Diabetes
                type 2 diabetes,insulin,glucagon-like peptide-1 receptor agonists,glp-1 ra,adherence,discontinuation,hba1c

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