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Serum Irisin in Myocardial Infraction and Following Percutaneous Coronary Intevention

Serum Irisin Levels in Myocardial Infraction and Following Percutaneous Coronary Intevention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02498431
Acronym
IRICARDIO
Enrollment
116
Registered
2015-07-15
Start date
2015-06-30
Completion date
2015-12-31
Last updated
2017-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Myocardial Infarction

Keywords

irisin, myocardial infarction, coronary

Brief summary

The investigators aim to evaluate circulating irisin levels alterations in patients with acute myocardial infraction and in patients with coronary artery disease subjected to percutaneous coronary intervention.

Detailed description

Irisin is a newly discovered myokine induced in exercise. There is evidence that cardiac muscle produces more irisin than skeletal muscle in response to exercise. Furthermore, irisin has been associated with isoproterenol-induced myocardial infarction (MI) in rats while it has been reported to decrease after acute myocardial infarction in humans. The investigators aim 1) to investigate circulating irisin levels in patients at the time of acute myocardial infarction and after reprefusion \[primary percutaneous coronary intervention (PCI)\] 2) to compare irisin' s diagnostic and prognostic value and specificity value in myocardial infarction with known markers of cardiac injury such as creatine kinase-MB isoenzyme (CK-MB) and troponin 3) to evaluate irisin as an early necrosis biomarker 4) To evaluate irisin's sensitivity as a biomarker to detect minor myocardial necrosis after elective percutaneous coronary intervention

Interventions

PROCEDUREpercutaneous coronary intervention

a non-surgical procedure used to treat the stenotic (narrowed) coronary arteries of the heart found in coronary heart disease

PROCEDUREcoronary angiography

is a procedure performed along with cardiac catheterization that uses X-ray imaging to see your heart's blood vessels

DEVICEStent, Medronic Resolute Integrity

A stent is placed in an artery as part of a procedure called percutaneous coronary intervention (PCI) to restore blood flow through narrow or blocked arteries. A stent helps support the inner wall of the artery in the months or years after PCI.

Sponsors

424 General Military Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with acute myocardial infraction (MI) or with coronary artery disease without myocardial infraction who need percutaneous coronary intervention

Exclusion criteria

* age \< 20 years old * diseases or medications that could affect cardiac muscle or skeletal muscle metabolism * musculoskeletal injury of surgery 6 months prior to recruitment * severe liver or kidney disease (creatinine clearance \< 60ml/min/1.73m2) or liver or kidney transplantation

Design outcomes

Primary

MeasureTime frame
changes from baseline in serum irisin measured by ELISAbaseline and 6 hours or 24 hours

Secondary

MeasureTime frame
changes from baseline in troponinbaseline and 6 hours or 24 hours
changes from baseline in serum lactate dehydrogenasebaseline and 6 hours or 24 hours
changes from baseline in serum creatine kinasebaseline and 6 hours or 24 hours
changes from baseline in serum creatine kinase-MB isoenzymebaseline and 6 hours or 24 hours
changes from baseline in serum follistatinbaseline and 6 hours or 24 hours
changes from baseline in serum follistatin-like protein 3 (FSTL-3)baseline and 6 hours or 24 hours
changes from baseline in serum Activin Abaseline and 6 hours or 24 hours
changes from baseline in serum Activin Bbaseline and 6 hours or 24 hours
changes from baseline in serum insulin growth factor 1 (IGF1)baseline and 6 hours or 24 hours
changes from baseline in serum insulin growth factor binding protein 3 (IGFBP3)baseline and 6 hours or 24 hours
changes from baseline in serum insulin growth factor binding protein 4 (IGFBP4)baseline and 6 hours or 24 hours
changes from baseline in serum pico pregnancy-associated plasma protein A (PAPP-A)baseline and 6 hours or 24 hours

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026