Type 2 & other diabetes

Effect of Empagliflozin on the plasma lipidome in patients with type 2 diabetes mellitus: results from the EmDia clinical trial

Cardiovasc DiabetolPublished Secondary analysis of the EmDia randomised trial

Authors' conclusion

This study identified distinct lipid signatures associated with Empagliflozin treatment after both one and twelve weeks, respectively, with five lipids overlapping between signatures and three with consistent directions, revealing that some of the beneficial effects of Empagliflozin could be through lipid modulation. Notably, Empagliflozin-modulated lipids associated with changes in clinical traits and lipid-specific profiles among clinical subgroups were observed. However, challenges remain in establishing direct associations between individual lipids and clinical outcomes. Future research integrating lipidomics data with other omics datasets could provide a more comprehensive understanding of the identified lipid signatures and their potential roles in health and diseases.

Study context

Population
Patients with T2D and heart failure (HF) from the EmDia trial, University Medical Center of Mainz
Participants
144 patients
Comparison
Empagliflozin treatment, lipid signatures after 1 and 12 weeks
Methodological detailsdouble-blind, single-centre
  • Double-blind
  • Single-centre

Primary result

As reported in the abstract

Plasma lipid signatures (4D-LC-TIMS/IMS lipidomics; sparse group LASSO)

Lipid signature after 1 week: lipids from lysophosphatidylcholine (LPC), phosphatidylcholine (PC), phosphatidylethanolamine (PE), sphingomyelin (SM) and triacylglycerol (TG) groups

37 lipids

Lipid signature after 12 weeks: lipids from the same five groups plus ceramides

24 lipids

Lipids altered at both time points with consistent directional trends

3 of 5

Original publication

Effect of Empagliflozin on the plasma lipidome in patients with type 2 diabetes mellitus: results from the EmDia clinical trial. Cardiovasc Diabetol. Published 8 September 2025. doi:10.1186/s12933-025-02916-0

Composed by AI from the published abstract and checked against it. How Briefs are made →

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