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

Primary Purpose

Non Alcoholic Fatty Liver Disease

Status
Withdrawn
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
atorvastatin
lifestyle counseling
Sponsored by
Sheba Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non Alcoholic Fatty Liver Disease focused on measuring non alcoholic fatty liver disease, endothelial function, liver steatosis, liver fibrosis, statin treatment

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Sheba Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

No Intervention

Active Comparator

Arm Label

Statin

usual care

lifestyle counseling

Arm Description

statin therapy (atorvastatin 20 mg/d) for 6 months

follow up group with no intervention

lifestyle modification by dietician counseling and follow-up

Outcomes

Primary Outcome Measures

Change from baseline in liver steatosis at 6 months
Impact 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 months
Impact 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 Outcome Measures

endothelial function in Non-Alcoholic Fatty Liver Disease (NAFLD) patients
measurement 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 fibrosis
levels 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 function
levels 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 months
Impact 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.

Full Information

First Posted
October 27, 2013
Last Updated
April 25, 2017
Sponsor
Sheba Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01987310
Brief Title
Assessment of Endothelial Function in Patients With Non Alcoholic Fatty Liver Disease and the Impact of Statin Treatment
Official Title
Assessment of Endothelial Function in Patients With Non Alcoholic Fatty Liver Disease and the Impact of Statin Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Withdrawn
Why Stopped
the study was stopped because of lack of interest
Study Start Date
December 2015 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sheba Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

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: complete physical examination blood pressure measurement assessment of height and weight, body mass index and waist circumference 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 Liver elastography and sonographic liver fat quantification Brachial artery flow-mediated dilatation (FMD) measurement

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non Alcoholic Fatty Liver Disease
Keywords
non alcoholic fatty liver disease, endothelial function, liver steatosis, liver fibrosis, statin treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Statin
Arm Type
Active Comparator
Arm Description
statin therapy (atorvastatin 20 mg/d) for 6 months
Arm Title
usual care
Arm Type
No Intervention
Arm Description
follow up group with no intervention
Arm Title
lifestyle counseling
Arm Type
Active Comparator
Arm Description
lifestyle modification by dietician counseling and follow-up
Intervention Type
Drug
Intervention Name(s)
atorvastatin
Other Intervention Name(s)
Atorvastatin Teva, Lipitor, Litorva
Intervention Description
atorvastatin 20 mg per day for 6 months
Intervention Type
Behavioral
Intervention Name(s)
lifestyle counseling
Intervention Description
lifestyle modification by dietician counseling and follow up
Primary Outcome Measure Information:
Title
Change from baseline in liver steatosis at 6 months
Description
Impact 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.
Time Frame
baseline, 6 months and 12 months
Title
change from baseline in liver fibrosis at 6 months
Description
Impact 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.
Time Frame
baseline, 6 months and 12 months
Secondary Outcome Measure Information:
Title
endothelial function in Non-Alcoholic Fatty Liver Disease (NAFLD) patients
Description
measurement 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
Time Frame
12 months
Title
relationship between blood parameters and liver steatosis and fibrosis
Description
levels 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
Time Frame
12 months
Title
relationship between blood parameters and endothelial function
Description
levels 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
Time Frame
at diagnosis and after 6 months and 12 months
Title
change from baseline in endothelial function at 6 months
Description
Impact 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.
Time Frame
at diagnosis 6 months and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ziv Ben-Ari, MD
Organizational Affiliation
Sheba Medical Center, Ramat Gan, Israel
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sheba Medical Center
City
Ramat Gan
ZIP/Postal Code
5265601
Country
Israel

12. IPD Sharing Statement

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

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