Study record

Effects of empagliflozin and dapagliflozin on serum humanin, MOTS-c levels, nitrosative stress, and ferroptosis parameters in diabetic patients with heart failure

Asil H, Demiryürek AT, Düzen IV et al. · Eur J Pharmacol · 2024

Human obs.Endogenous MOTS-c measuredEvidence tier B

What this study reported

Measured higher serum MOTS-c in diabetic patients with heart failure taking SGLT2 inhibitors than in controls, with no corresponding difference in humanin. Also reported higher GPX4 and lower ACSL4 in the SGLT2 inhibitor group, while TFRC was higher in patients and unchanged by SGLT2 inhibitor use.

Limitations

Non-randomised comparison of existing treatment groups, open to confounding by indication; single time point with modest group sizes and no adjustment described in the abstract.

Study record

Annotated fields for this study
Study modelHuman observational
Substance studiedEndogenous MOTS-c measuredNaturally occurring MOTS-c was measured; nothing was given.
Specieshuman
System studiedSerum MOTS-c, humanin, nitrosative stress and ferroptosis markers in diabetic patients with heart failure with reduced ejection fraction, with or without SGLT2 inhibitor use
Populationadults with type 2 diabetes and heart failure with reduced ejection fraction, with or without SGLT2 inhibitor treatment, and healthy controls
DesignProspective observational study
Sample size as reported111 participants (74 patients with diabetes and HFrEF, 37 healthy controls)
Control grouphealthy controls and patients not taking SGLT2 inhibitors
Route (data field only)Not reported
Endpoints measuredserum MOTS-c; serum humanin; nitric oxide and 3-nitrotyrosine; GPX4; ACSL4; TFRC
Pathways measuredOxidative stress · Other
Research areasCardiovascular · Metabolic
Evidence tierB — Other human study
Publication typesJournal Article

Appraisal

Each dimension is recorded separately and never combined into a single score. A study can be well controlled and still tell you little about people.

Relevance to MOTS-c
Direct
Model applicability
Human
Sample size
Small
Controls
Limited
Outcome validity
Surrogate
Support for its own conclusion
Moderate

Provenance

  • Bibliographic fields retrieved from PubMed E-utilities efetch (title, journal, date, authors, DOI) on 2026-11-11.
  • Annotated from the published abstract.
  • Editorial review: approved (2026-11-11).
  • Classification follows the site methodology; the record describes the study, not what MOTS-c does in people.