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Diagnostic and prognostic value of H-ficolin for functionally relevant coronary artery disease
Ganna Isayeva1, Eliska Potlukova2, Klara Rumora1
1Cardiovascular Research Institute Basel (CRIB), University Heart Center, University Hospital Basel, University of Basel, Switzerland.
Insights
H-ficolin, a complement system protein, showed no diagnostic or prognostic value for functionally relevant coronary artery disease (fCAD). This study found no significant association between H-ficolin levels and fCAD diagnosis or cardiovascular outcomes.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Complement System
Background:
- H-ficolin initiates the lectin pathway of the complement system.
- Investigating H-ficolin's role in coronary artery disease (CAD) is crucial for understanding cardiovascular health.
- The diagnostic and prognostic capabilities of H-ficolin in functionally relevant CAD (fCAD) require further elucidation.
Purpose of the Study:
- To evaluate the diagnostic and prognostic utility of H-ficolin in patients with suspected fCAD.
- To explore potential determinants of H-ficolin levels in this patient cohort.
Main Methods:
- Utilized myocardial perfusion imaging and coronary angiography to diagnose fCAD in 1,571 patients.
- Measured H-ficolin levels using immunoassay at rest, peak stress, and 2 hours post-stress.
- Assessed cardiovascular death and non-fatal myocardial infarction over a 5-year follow-up period.
Main Results:
- H-ficolin levels did not differ significantly between patients with and without fCAD (AUC 0.53).
- H-ficolin was not a predictor of cardiovascular events in the overall cohort.
- A potential association was observed between H-ficolin and non-fatal myocardial infarction in patients without fCAD.
Conclusions:
- H-ficolin concentration lacks diagnostic and prognostic value for patients undergoing evaluation for fCAD.
- No significant correlation was found between H-ficolin and the presence of fCAD.
- Further research may be needed to clarify the specific role of H-ficolin in certain subgroups, such as patients without fCAD.
Background:
We aimed to test the diagnostic and prognostic ability of H-ficolin, an initiator of the lectin pathway of the complement system, for functionally relevant coronary artery disease (fCAD), and explore its determinants.
Methods:
The presence of fCAD was adjudicated using myocardial perfusion imaging single-photon emission tomography and coronary angiography. H-ficolin levels were measured by a sandwich-type immunoassay at rest, peak stress-test, and 2 h after stress-test. Cardiovascular death and non-fatal myocardial infarction were assessed during 5-year follow-up.
Results:
Among 1,571 patients (32.3 % women), fCAD was detected in 462 patients (29.4 %). H-ficolin concentration at rest was 18.6 (15.3-21.8) µg/ml in patients with fCAD versus 17.8 (15.4-21.5) µg/ml, p = 0.33, in patients without fCAD, resulting in an AUC of 0.53 (95 %CI 0.48-0.56). During follow-up, 107 patients (6.8 %) had non-fatal myocardial infarction and 99 patients (6.3 %) experienced cardiovascular death. In Cox regression analysis, H-ficolin was not a predictor of events in the overall cohort. Subgroup analysis suggested a potential link between H-ficolin and non-fatal myocardial infarction in patients without fCAD (adjusted HR 1.03, 95 % CI 1.02-1.15, p = 0.005). H-ficolin concentration showed a weak positive correlation with systolic (r = 0.069, p < 0.001) and diastolic blood pressure (r = 0.111, p < 0.001).
Conclusion:
H-ficolin concentration did not have diagnostic and/or prognostic value in patients referred for fCAD work-up.
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