Study record

β-Amyloid and mitochondrial-derived peptide-c are additive predictors of adverse outcome to high-on-treatment platelet reactivity in type 2 diabetics with revascularized coronary artery disease

Ikonomidis I, Katogiannis K, Kyriakou E et al. · J Thromb Thrombolysis · 2020

Human obs.Endogenous MOTS-c measuredEvidence tier B

What this study reported

In adults with type 2 diabetes and coronary artery disease, low MOTS-c, high β-amyloid and high on-clopidogrel platelet reactivity were each predictors of cardiac death and acute coronary syndromes over 2 years of follow-up after adjustment. Patients with high platelet reactivity and low MOTS-c had about fourfold higher risk; results were reported as confirmed in an external validation cohort.

Limitations

Observational design with a modest number of events; MOTS-c threshold derived within the study.

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 studiedPatients with type 2 diabetes and revascularized coronary artery disease on clopidogrel and aspirin
Populationadults with type 2 diabetes and recently revascularized coronary artery disease
DesignProspective cohort with external validation cohort
Sample size as reported121 patients (93 males) plus an external validation cohort of 90
Control groupNot reported
Route (data field only)Not reported
Endpoints measuredplatelet reactivity (LTAmax); blood MOTS-c; β-amyloid; malondialdehyde; MACE over 2 years of follow-up
Pathways measuredOxidative stress
Research areasCardiovascular · Metabolic
Evidence tierB — Other human study
Publication typesClinical Trial, Journal Article, Multicenter Study

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
Adequate
Controls
n/a
Outcome validity
Clinical outcome
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.