NASH and Coronary Disease
- Conditions
- Non-Alcoholic Fatty Liver Disease
- Interventions
- Diagnostic Test: Hepatic evaluation
- Registration Number
- NCT03819283
- Lead Sponsor
- Assistance Publique - Hôpitaux de Paris
- 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.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 260
- 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.
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Hepatic evaluation Hepatic evaluation -
- Primary Outcome Measures
Name Time Method NAFLD and significant fibrosis (≥ F2) 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 Outcome Measures
Name Time Method Correlation between the histological severity of NAFLD and the severity of coronary lesions 51 months after the start of the study The severity of the coronary lesions will be defined as follows : absent, stable coronary lesions (significant \>=50% or non significant coronary atheroma), acute coronary syndrome
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 The severity of the coronary lesions will be defined as follows : absent, stable coronary lesions (significant \>= 50% or non significant coronary atheroma), acute coronary syndrome
Severity of the coronary lesions Visit 1 Based on the results of the coronary angiography, patients will be classified according to the severity of CAD as follows: no CAD, stable CAD (less than 50% stenosis, 1 vessel CAD with \> 50% stenosis, 2 vessels CAD with \> 50% stenosis, 3 vessels CAD with \> 50% stenosis), and acute coronary syndrome.
Analyse of the metabolomic signature associated with the severity of coronary lesions according to the presence and severity of NAFLD Visit 1 and 2 The severity of the coronary lesions will be defined as follows : absent, stable coronary lesions (significant \>=50%or non significant coronary atheroma), acute coronary syndrome
Trial Locations
- Locations (1)
Pitié Salpêtrière Hospital
🇫🇷Paris, France