Skip to main content
Clinical Trials/NCT03819283
NCT03819283
Unknown
Not Applicable

Prevalence and Impact of NAFLD in Patients With Symptomatic Coronary Artery Disease

Assistance Publique - Hôpitaux de Paris1 site in 1 country260 target enrollmentApril 19, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non-Alcoholic Fatty Liver Disease
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
260
Locations
1
Primary Endpoint
NAFLD and significant fibrosis (≥ F2)
Last Updated
3 years ago

Overview

Brief Summary

Although the clinical relationship between NAFLD/NASH and cardiovascular (CV) risk is now well established, there is very little awareness of the hepatic disease and the way it may contribute to increased CV risk in patients seen in cardiology clinics for complications of coronary artery disease. Our clinical hypothesis is that NAFLD, possibly at a stage of advanced fibrosis, is common in patients with symptomatic coronary artery disease (CAD) and increases the risk of severe atherosclerotic lesions. The primary aim of this study is to determine (a) the prevalence and (b) the severity spectrum of NAFLD among patients with symptomatic coronary artery disease. The secondary aims are: to analyze the impact of the presence and the severity spectrum of NAFLD (steatosis, steatohepatitis and fibrosis) on the severity of CAD ; To determine the profile of NAFLD patients at risk to develop coronary lesions; To explore the mechanistic link between NAFLD and CAD beyond common metabolic risk factors.

Detailed Description

Because of shared metabolic risk factors and pathogenic pathways (insulin resistance, chronic low grade inflammation, atherogenic dyslipidemia) non-alcoholic fatty liver disease is frequently associated with cardiovascular (CV) disease. Despite a lot of transversal studies showing a frequent association between NAFLD and CV disease, it is difficult to determine if NAFLD plays an active role in atherogenesis or is just a marker of common risk factors. Some longitudinal studies, although retrospectives, showed that NAFLD favors the progression of early atherosclerosis, suggesting that NAFLD is an independent CV risk factor beyond the association driven by metabolic syndrome. Although the clinical relationship between NAFLD/NASH and CV risk is now well established, there is very little awareness of the hepatic disease and the way it may contribute to increased CV risk in patients seen in cardiology clinics for complications of coronary artery disease (CAD). Our clinical hypothesis is that NAFLD, possibly at a stage of advanced fibrosis, is common in patients with symptomatic CAD and increases the risk of severe atherosclerotic lesions. The primary aim of this study is to determine (a) the prevalence of NAFLD among patients with symptomatic CAD. The secondary aims are: * To determine the severity spectrum of NAFLD among patients with coronary artery disease. * To analyze the impact of the presence and the severity spectrum of NAFLD (steatosis, steatohepatitis and fibrosis) on the severity of CAD and long term clinical outcomes (ancillary studies) * To determine the clinical profile of NAFLD patients at risk to develop coronary lesions * To explore the mechanistic link between NAFLD and CAD beyond common metabolic risk factors. * Establish a cohort of patients with NAFLD and coronary disease allowing future subsequent ancillary studies.

Registry
clinicaltrials.gov
Start Date
April 19, 2019
End Date
July 19, 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult patients (\>18 years old) that undergo coronary angiography for suspected CAD for: acute coronary syndrome (ACS) with ST-elevation ACS (STE-ACS) or non-ST elevation (NSTE-ACS) with or without troponin elevation OR suspicion of stable coronary artery disease after stress imaging techniques and/or symptoms of angina.
  • Patients with one or more of traditional cardiovascular risk factors.

Exclusion Criteria

  • Patients unable to sign the informed consent
  • Morbidly obese patients (BMI \> 40kg/m2)
  • Excessive alcohol consumption of more than 50 g/day
  • Patients with known other causes of chronic liver disease (viral hepatitis, autoimmune, hemochromatosis...)
  • Active neoplastic pathology
  • Pregnant or breastfeeding women
  • Protected adults

Outcomes

Primary Outcomes

NAFLD and significant fibrosis (≥ F2)

Time Frame: Visit 2

NAFLD will be defined by the presence of steatosis at ultrasound concomitant with at least one metabolic risk factor among overweight/obesity, type 2 diabetes, dyslipidemia. The severity of NAFLD will be determined by the presence of significant fibrosis (≥F2) by noninvasive measures (either serum markers or transient elastography).

Secondary Outcomes

  • Correlation between the histological severity of NAFLD and the severity of coronary lesions(51 months after the start of the study)
  • Analyse of clinical factors associated with the severity of coronary lesions according to the presence or absence of NAFLD(51 months after the start of the study)
  • Severity of the coronary lesions(Visit 1)
  • Analyse of the metabolomic signature associated with the severity of coronary lesions according to the presence and severity of NAFLD(Visit 1 and 2)

Study Sites (1)

Loading locations...

Similar Trials