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Correlation of Clinical Types and Complexity of Coronary Artery Disease With Patients' Metabolic Profile

Correlation of Clinical Types and Complexity of Coronary Artery Disease With Patients' Metabolic Profile

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04580173
Acronym
CorLipid
Enrollment
1050
Registered
2020-10-08
Start date
2019-07-12
Completion date
2021-08-31
Last updated
2020-10-12

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

Conditions

Coronary Artery Disease

Keywords

coronary artery disease, metabolomics

Brief summary

The purpose of the research project is to investigate the potential association of the complexity and the severity of coronary artery disease (as assessed via SYNTAX score) with patients' metabolic profile. The aim of the study is to combine biochemical, clinical and laboratory data in order to create an algorithm that will enable an individualized therapeutic patient approach.

Detailed description

The objective of this observational study is to expand our knowledge on the biochemical process and pathogenesis of atherogenesis and to recognize clinically important metabolic biomarkers correlated with the severity and clinical presentation of Coronary Artery Disease (CAD). 1050 patients who will undergo coronary angiography will be enrolled in the study. SYNTAX score will be calculated for all participants and their blood samples will be collected before coronary angiography. Metabolomics-based analysis will be performed in order to confirm CAD prognostic biomarkers previously reported in the literature and to investigate their correlations with CAD clinical data. The ultimate aim of this study is to predict the risk of cardiovascular events by incorporating metabolomic information into the SYNTAX score and provide personalized therapeutic guidance to patients.

Interventions

DIAGNOSTIC_TESTmetabolomics analysis

Targeted and untargeted metabolomics-based analysis will be performed using Gas Chromatography tandem Mass Spectometry and Liquid Chromatography tandem Mass Spectrometry, in order to quantify serum biomarkers.

Sponsors

ANALYSIS MEDICAL SA
CollaboratorUNKNOWN
Aristotle University Of Thessaloniki
CollaboratorOTHER
AHEPA University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients giving voluntary written consent to participate in the study 2. Adults 3. Patients without previous history of coronary artery disease 4. Patients who are admitted in the Department of Cardiology in the AHEPA University General Hospital of Thessaloniki and undergo coronary angiography for clinical purposes

Exclusion criteria

1. Cardiac Arrest at admission 2. Patients with serious concurrent disease and life expectancy of \< 1 year

Design outcomes

Primary

MeasureTime frameDescription
Relationship between metabolic profile and the SYNTAX score12 monthsSerum metabolomic biomarkers (ceramides, acyl-carnitines, total fatty acids and protein markers: Galectin-3, Neutrophil Gelatinase-Associated Lipocalin, Adiponectin, ApolipoproteinB/ ApolipoproteinΑ-Ι) will be quantified using metabolomics-based methods and enzyme-linked immunosorbent assay. The SYNTAX score will be calculated for all patients. Correlation between patients' metabolic profile and the SYNTAX score will be performed.

Secondary

MeasureTime frameDescription
Concentration of serum ceramide species12 monthsQuantification of serum ceramide species (C18:0/16:0, C18:0/18:0, C18:0/24:0 and C18:0/24:1) using a developed Ultra-high performance liquid chromatography tandem mass spectrometry method.
Concentration of serum acyl-carnitines12 monthsQuantification of serum acyl-carnitines (C2, C3, C4, isoC4, C5, isoC5, C6, C8, C10, C12, C14, C16, C18, C18:1 C18:2) using a developed hydrophilic interaction chromatography tandem mass spectrometry method.
Concentration of serum total fatty acids12 monthsQuantification of total fatty acids (C10:0, C12:0, C14:0, C15:0, C16:0, C16:1, C17:0, C18:0, C18:1 cis, C18:2 cis, C20:0, C18:3 n6, C18:3 n3, C20:1, C20:2, C22:0, C20:3 n6, C22:1 & C20:4, C23:0, C20:5, C24:0, C24:1, C22:6) using a developed gas chromatography with flame-ionization method.
Concentration of serum selective protein markers12 monthsQuantification of selective protein markers (Galectictin-3, NGAL, Adiponectin, ApoB/ ApoΑ-Ι)
Major Adverse Cardiovascular and Cerebrovascular Events12 monthsCardiovascular death, myocardial infarction, stent thrombosis, revascularization and stroke

Countries

Greece

Contacts

Primary ContactGeorgios Sianos, PhD
gsianos@auth.gr2310994837

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026