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Galectin-3 Binding Protein in Cardiovascular Disease and Chronic Heart Failure

GALectin-3 Binding Protein for Risk Assessment in Coronary arTery dIsease and Chronic Heart Failure

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01210157
Acronym
GALACTIC
Enrollment
373
Registered
2010-09-28
Start date
2008-06-30
Completion date
2010-08-31
Last updated
2010-09-28

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

Conditions

Cardiomyopathies, Coronary Artery Disease, Heart Failure

Brief summary

The purpose of this study is to determine whether galectin-3 binding protein plasma levels can predict adverse cardiovascular events in patients with coronary artery disease and/or heart failure.

Detailed description

Chronic heart failure represents an important cause of disease burden in Western countries. Heart failure can be either caused by vascular disease (i.e. cardiomypathy (CMP) due to coronary artery disease (ischemic/ICMP)) or by myocardial conditions (i.e. dilated cardiomyopathies (DCMP) resulting from other causes like familial disposition, drug toxicity, etc.). Gold standard for the diagnosis of CMPs is the coronary angiography in conjunction with left ventricular angiography and myocardial biopsy, non-invasive markers include C-reactive protein (CRP) for ICMP and brain natriuretic protein (BNP) for DCMP. We have previously identified G3BP to be overexpressed in foam cells and plasma-derived microparticles, both potentially important in formation of atherosclerotic plaque. Galectin-3 binding protein (G3BP) is a secreted protein that is involved in cell adhesion and immune activation. The purpose of the current study is to test, whether G3BP plasma levels (a) are able to non-invasively differentiate causes of CMP and (b) are a suitable means for future risk assessment in CMP patients.

Interventions

None listed

Sponsors

Heidelberg University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* impaired ventricular function

Exclusion criteria

* neoplastic disease * infections with hepatitis C or HIV

Design outcomes

Primary

MeasureTime frame
Death from cardiac causesup to five years

Secondary

MeasureTime frame
diagnosis of cardiomypathy (CMP)up to five years
assessment of disease stage (CAD-1-3, NYHA I-IV)up to five years
non-fatal myocardial infarction or cerebrovascular accidentup to five years
revascularization (percutaneous coronary intervention (PCI) or coronary artery bypass graft (CABG))up to five years
rehospitalizationup to five years
implantation of ICD/biventricular pacemakerup to five years
heart transplantationup to five years
diagnosis of coronary artery disease (CAD)up to five years
correlation with physical examinationup to five years
correlation with routine lab valuesup to five years
correlation with ECGup to five years
correlation with echocardiographyup to five years
correlation with cardiac MRIup to five years
correlation with cardiac CTup to five years
correlation with chest X-rayup to five years
correlation with patient historyup to five years

Countries

Germany

Outcome results

None listed

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