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Epicardial Fat, Visceral Fat and Coronary Atherosclerosis

Conditions
Epicardial Fat
Visceral Fat
Atherosclerosis
Interventions
Other: patient with liver fat
Other: pts. with excess of visceral fat
Other: control
Registration Number
NCT01344694
Lead Sponsor
Ziv Hospital
Brief Summary

Background: Visceral fat is increasingly associated with metabolic syndrome and with fatty liver, a condition carrying a high risk of cardiovascular disease. The independent role of epicardial fat deposition in cardiovascular risk remains unclear.

Detailed Description

Background: Visceral fat is increasingly associated with metabolic syndrome and with fatty liver, a condition carrying a high risk of cardiovascular disease. The independent role of epicardial fat deposition in cardiovascular risk remains unclear. Aim: Evaluate the link between epicardial fat, visceral fat, liver fat accumulation and cardiovascular diseases and carotis atherosclerosis in patients with the major cardiovascular risk factors and with or without metabolic syndrome.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
110
Inclusion Criteria
  • Patients referred to cardiac CT will be the source of recruitment.
  • patients with excess of visceral fat,
  • 30 patients with liver fat accumulation
  • 30 sex-age-matched individual (controls) will be enrolled. All patients will undergo a complete family history, personal clinical history, physical examination and blood sampling for biochemical analysis.
  • Informed consent will be obtained from each individual.
Exclusion Criteria
  • subjects with severe morbid obesity (body mass index [BMI] > 40),
  • recent history of acute illness,
  • clinical history of ischemic heart disease and cerebrovascular disease,
  • typical chest pain,
  • previous coronary artery disease,
  • conventional coronary angiography, percutaneous interventions, coronary by pass grafting, renal failure, cancer patients,
  • subjects who take drugs that induces hepatic steatosis ( corticosteroids, estrogens, methotrexate, amiodarone and others)

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
patient with liver fatpatient with liver fat30 patients with liver fat
excess of visceral fatpts. with excess of visceral fat50 pts. with excess of visceral fat
controlcontrol30 control subjects
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Ziv MC

🇮🇱

Safed, Israel

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