Human study PLS-00054
Circulating mitochondrial biomarkers in acute coronary syndrome.
Version 1 · published November 7, 2026 · evidence through November 7, 2026 · research snapshot 2026.1.1 · methodology ev-1 · Automated assessment by AI (claude-opus-5-5 and claude-sonnet-5-5), not reviewed by a person.
Only the abstract was available. Essential methods may be missing, which limits what can be judged.
Reports of this study
Every publication, registration and abstract describing this one study. Participants are counted once.
- Circulating mitochondrial biomarkers in acute coronary syndrome.primary · Frontiers in medicine · 2025-05-15 · PMID 40443515 · DOI
Design and participants
- Design
- Case-control study
- Population
- Patients with acute coronary syndrome (8 women, 10 men) and controls (8 women, 12 men)
- Conditions
- Acute coronary syndrome
- Planned enrollment (registry)
- Not reported
- Enrolled
- 38
- Randomized
- Not reported
- Completed follow-up
- Not reported
Intervention and comparator
What each group received. Related peptides, analogs and combinations are never treated as the compound itself.
What the authors reported
As stated in the sources. This is the authors’ account, not Peptide Library’s assessment.
Adverse events
None reported. That is not evidence of safety, and how safety was monitored isn’t described.
The authors concluded (paraphrased): Mitochondrial markers MOTS-c and PGC-1α are altered in ACS patients, with no sex differences. The authors see this as an initial step toward personalized ACS management and say further studies are needed.
Peptide Library’s assessment
An automated assessment, made by AI separately from the authors’ conclusions and not reviewed by a person. How risk of bias is assessed.
Limitations
- other: MOTS-c was not administered; only endogenous plasma levels were measured, so the study gives no evidence about MOTS-c as an intervention.
- small or imprecise: Only 18 ACS patients and 20 controls were included, which limits precision.
- confounding: The abstract describes no adjustment for differences between ACS patients and controls.
- abstract only: Only the abstract is available; methods, numbers and statistics are not reported.
- inappropriate endpoint: Outcomes are plasma biomarker levels and correlations, not clinical outcomes.
No risk-of-bias assessment has been published for this study’s results.
Claims this study informs
- Improves metabolic health: not eligible (not primary study) for “Insulin sensitivity, glucose control or body weight”
- Is safe for human administration: not eligible (not primary study) for “Adverse events, serious adverse events and discontinuations”
Where each value comes from
- arms: PMID 40443515, abstract (Methods, sentences 1-3) · extracted by AI (automated, not verified by a person) · abstract only
- author_conclusion: PMID 40443515, abstract (Conclusion, sentences 1-3) · extracted by AI (automated, not verified by a person) · abstract only
- design: PMID 40443515, abstract (Methods, sentence 1) · extracted by AI (automated, not verified by a person) · abstract only
- limitations: PMID 40443515, abstract (Methods and Conclusion) · extracted by AI (automated, not verified by a person) · abstract only
- outcomes: PMID 40443515, abstract (Methods, sentence 3) · extracted by AI (automated, not verified by a person) · abstract only
- participants: PMID 40443515, abstract (Methods, sentence 1) · extracted by AI (automated, not verified by a person) · abstract only
- population: PMID 40443515, abstract (Methods, sentence 1) · extracted by AI (automated, not verified by a person) · abstract only
- results: PMID 40443515, abstract (Results, sentences 1-3) · extracted by AI (automated, not verified by a person) · abstract only
Version 1 · published November 7, 2026 · evidence through November 7, 2026 · research snapshot 2026.1.1 · methodology ev-1 · Automated assessment by AI (claude-opus-5-5 and claude-sonnet-5-5), not reviewed by a person.
These assessments describe published research. Records marked automated were produced by AI under the published methodology and have not been reviewed by a person; they can contain errors. None of this is medical advice, not a statement about any product’s safety for human use, and not a regulatory approval. Peptide Library’s vendor and partner relationships play no part in them (editorial independence).