Advances in therapy

Combined Use of Two Diabetes Drugs in People with Type 2 Diabetes and Heart Disease

Updated

Abstract

Real-world data on the combined use of GLP-1 receptor agonists and SGLT2 inhibitors in type 2 diabetes patients is limited.

  • GLP-1 receptor agonists and SGLT2 inhibitors may provide complementary metabolic benefits.
  • Both therapies have independently shown cardiovascular advantages in individuals with type 2 diabetes and existing cardiovascular disease.
  • There is a growing interest in the potential additive benefits of using these treatments together in high-risk populations.
  • The study aimed to identify clinical factors related to the use of combined GLP-1RA and SGLT2i therapy in everyday clinical practice.

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Full Text

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Funding

Competing interests

Declarations. Conflict of Interest: Theocharis Koufakis has received honoraria for lectures/advisory boards and research support from AstraZeneca, Boehringer Ingelheim, Pharmaserve Lilly, Sanofi, Roche Diagnostics, ELPEN, Krka, Menarini, and Novo Nordisk. Theocharis Koufakis is an Editorial Board member of Advances in Therapy. Theocharis Koufakis was not involved in the selection of peer reviewers for the manuscript nor any of the subsequent editorial decisions. Evangelos N. Liberopoulos has participated in educational, research, and advisory activities sponsored by AstraZeneca, MSD, Lilly, Bayer, Amgen, Sanofi, Boehringer Ingelheim, Novartis, Novo Nordisk, and Servier. Kalliopi Kotsa has received honoraria for lectures/advisory boards and research support from AstraZeneca, Boehringer Ingelheim, Pharmaserve Lilly, Sanofi-Aventis, ELPEN, MSD, and Novo Nordisk. Georgios Vournas has nothing to disclose. Anastasia Sarvani has nothing to disclose. Maria Mavridou has nothing to disclose. Anastasios Tentolouris has nothing to disclose. Michael Doumas has nothing to disclose. Ethical Approval: The study was performed in accordance with the principles of the Declaration of Helsinki. Ethics approval for retrospective data collection and analysis was obtained from the Bioethics Committee of the Aristotle University of Thessaloniki (approval code: 26; approval date: 11 November 2025). Patient data were anonymized prior to analysis, with removal of all direct patient identifiers and replacement by non-traceable study codes accessible only to the investigators involved in data collection. In accordance with local institutional requirements and national practice in Greece for retrospective clinical data analyses, all patients provided written informed consent at the time of hospital discharge for the use of their anonymized data for research purposes. No interventions or treatment decisions were influenced by study participation. As this was a retrospective observational study based exclusively on anonymized routinely collected clinical data without prospective intervention or protocol-driven treatment allocation, formal registration on a clinical trial platform was not required.
PubMed

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