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Assessment of Endothelial Function in Patients With Non Alcoholic Fatty Liver Disease and the Impact of Statin Treatment

Assessment of Endothelial Function in Patients With Non Alcoholic Fatty Liver Disease and the Impact of Statin Treatment

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01987310
Enrollment
0
Registered
2013-11-19
Start date
2015-12-31
Completion date
2015-12-31
Last updated
2017-04-27

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

Conditions

Non Alcoholic Fatty Liver Disease

Keywords

non alcoholic fatty liver disease, endothelial function, liver steatosis, liver fibrosis, statin treatment

Brief summary

The aim of the current study is to evaluate the association of fatty liver severity and endothelial function in Non-Alcoholic Fatty Liver Disease (NAFLD) patients and to find the impact of statin treatment compared to usual care or life style modification on endothelial function, liver steatosis and fibrosis.

Detailed description

The study cohort will include 150 patients with fatty liver per ultrasound or histology. The patients will be divided randomly to one of three arms: follow up group, lifestyle modification group, and statins therapy (Atorvastatin 20mg/d for 6 months). at screening, after 6 months (end of treatment), and 12 months the patients will undergo: 1. complete physical examination 2. blood pressure measurement 3. assessment of height and weight, body mass index and waist circumference 4. blood samples for complete blood count, fasting plasma glucose, fasting plasma insulin, lipid profile, liver enzymes, albumin, bilirubin, Prothrombin time (PT INR), Hemoglobin A1c, ferritin, adiponectin, C-reactive protein, Tumor necrosis factor alpha, Lipoprotein-phospholipase A2, Apolipoproteins B100, A1, C3, C4, ceruloplasmin 5. Liver elastography and sonographic liver fat quantification 6. Brachial artery flow-mediated dilatation (FMD) measurement

Interventions

DRUGatorvastatin

atorvastatin 20 mg per day for 6 months

BEHAVIORALlifestyle counseling

lifestyle modification by dietician counseling and follow up

Sponsors

Sheba Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* subjects willing to comply with study requirements and have signed an informed consent form * fatty liver per abdominal ultrasound or liver biopsy

Exclusion criteria

* alcohol drinking \>140g/week * presence of hepatitis B or C or HIV * known liver disease other than fatty liver * usage of drugs known to cause liver steatosis * subjects with known allergies or hypersensitivity to statins * subjects with known cardiovascular/cerebrovascular disease * subjects with known dyslipidemia requiring drug treatment * subjects with diabetes mellitus * history of drug or alcohol abuse * refusal to sig the informed consent form

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in liver steatosis at 6 monthsbaseline, 6 months and 12 monthsImpact of statin treatment(which will be given for 6 months) compared to no intervention or lifestyle modification on liver steatosis and fibrosis. Liver steatosis will be assessed by sonographic liver fat quantification (hepatorenal sonographic index.
change from baseline in liver fibrosis at 6 monthsbaseline, 6 months and 12 monthsImpact of statin treatment(which will be given for 6 months) compared to no intervention or lifestyle modification on liver fibrosis. Liver fibrosis will be assessed by Real-Time shear wave elastography.

Secondary

MeasureTime frameDescription
endothelial function in Non-Alcoholic Fatty Liver Disease (NAFLD) patients12 monthsmeasurement of endothelial function in NAFLD patients and finding the correlation between the degree of endothelial dysfunction and the severity of fatty liver disease. Endothelial function will be assessed by brachial artery flow-mediated (FMD) measurement at diagnosis and after 6 and 12 months. The severity of fatty liver disease will be assessed by liver elastography and sonographic liver fat quantification
relationship between blood parameters and liver steatosis and fibrosis12 monthslevels of liver enzymes, liver synthetic function, blood lipids, insulin resistance, ferritin, adiponectin, C reactive protein, Tumor necrosis factor alpha and ceruloplasmin and their correlation with liver steatosis and fibrosis
relationship between blood parameters and endothelial functionat diagnosis and after 6 months and 12 monthslevels of liver enzymes, liver synthetic function, blood lipids, insulin resistance, ferritin, adiponectin, C reactive protein, tumor necrosis factor alpha and ceruloplasmin and their correlation with endothelial function
change from baseline in endothelial function at 6 monthsat diagnosis 6 months and 12 monthsImpact of statin treatment(which will be given for 6 months) compared to no intervention or lifestyle modification on endothelial function. Endothelial function will be assessed by flow mediated dilatation (FMD) of brachial artery.

Countries

Israel

Outcome results

None listed

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