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Safety and Efficacy of Long-Term Treatment With Atorvastatin in Patients With Primary Biliary Cirrhosis

Primary Purpose

Primary Biliary Cirrhosis, Hypercholesterolemia

Status
Completed
Phase
Phase 3
Locations
Austria
Study Type
Interventional
Intervention
Atorvastatin
Sponsored by
Medical University of Graz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Primary Biliary Cirrhosis focused on measuring Cholestasis, Atherosclerosis, Statins, Vascular function

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • LDL-cholesterol > 130 mg/dl
  • Primary biliary cirrhosis (AMA positive or biopsy proven)
  • Male or female gender
  • Age 18-70 years
  • Normal kidney function

Exclusion Criteria:

  • Primary biliary cirrhosis Stage III-IV (Ludwig Score)
  • Liver cirrhosis
  • Decompensated liver disease ( > Child-Pugh class B, ascites, esophageal varices)
  • ALT or AST > 2x ULN
  • Pregnancy or breastfeeding
  • Premenopausal women without certain contraception
  • Known hypersensitivity to HMG-CoA reductase inhibitors
  • Current treatment with lipid-lowering agents other than atorvastatin; immunosuppressants, macrolides

Sites / Locations

  • Department of Internal Medicine, Medical University of Graz

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Atorvastatin

Arm Description

Atorvastatin 10 mg per day for 48 weeks

Outcomes

Primary Outcome Measures

Low-density lipoprotein cholesterol (LDL-C)

Secondary Outcome Measures

Intima-media thickness of the common carotid artery (IMT), vascular wall stiffness (stiffness index SI), flow-mediated dilation of the brachial artery (FMD)
Total cholesterol, triglycerides, VLDL-C, HDL-C, lipid profile, hs-CRP, AP, GGT, bilirubin, bile acids, immunoglobins
AST, ALT, CK, PZ, AT, albumin, creatinine, blood cell count

Full Information

First Posted
February 13, 2009
Last Updated
February 13, 2009
Sponsor
Medical University of Graz
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1. Study Identification

Unique Protocol Identification Number
NCT00844402
Brief Title
Safety and Efficacy of Long-Term Treatment With Atorvastatin in Patients With Primary Biliary Cirrhosis
Official Title
Safety and Efficacy of Long-Term Treatment With Atorvastatin in Patients With Primary Biliary Cirrhosis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
November 2007 (Actual)
Study Completion Date
November 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Medical University of Graz

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Primary biliary cirrhosis (PBC) is frequently associated with hypercholesterolemia and possibly with an increased cardiovascular morbidity and mortality. Statins lower serum cholesterol levels and may thus improve the cardiovascular risk in PBC patients. The aim of our study therefore was to prospectively examine the efficacy of low-dose atorvastatin on indicators of cardiovascular risk such as dyslipidemia and vascular function as well as safety in patients with PBC.
Detailed Description
Primary biliary cirrhosis (PBC) is often associated with abnormalities in serum lipids. Hypercholesterolemia is an established risk factor for cardiovascular morbidity and mortality. Since many PBC patients have a very slow progression of their underlying liver disease cardiovascular risk factors may become more relevant as prognostic facors. Whether statins lower serum cholesterol levels and reduce the cardiovascular risk in PBC patients remains to be determined. Statins are generally well tolerated and are not associated with an increased risk of hepatotoxicity in patients with nonalcoholic fatty liver disease (NAFLD). However only limited data on safety on statins in chronic cholestatic liver diseases are available. In a recent pilot study at the Medical University of Graz atorvastatin did not statistically increase liver enzymes in PBC patients. However, data on long-term treatment with atorvastatin in these patients are not yet available. Moreover, long-term treatment with statins may have potential beneficial immunomodulatory effects on the disease course of PBC in analogy to other immune-mediated disorders such as rheumatoid arthritis and multiple sclerosis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Primary Biliary Cirrhosis, Hypercholesterolemia
Keywords
Cholestasis, Atherosclerosis, Statins, Vascular function

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Atorvastatin
Arm Type
Experimental
Arm Description
Atorvastatin 10 mg per day for 48 weeks
Intervention Type
Drug
Intervention Name(s)
Atorvastatin
Other Intervention Name(s)
Sortis10 mg, 1-21927, C10AA05
Intervention Description
oral, 10 mg, daily, 48 weeks
Primary Outcome Measure Information:
Title
Low-density lipoprotein cholesterol (LDL-C)
Time Frame
week 0, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 60
Secondary Outcome Measure Information:
Title
Intima-media thickness of the common carotid artery (IMT), vascular wall stiffness (stiffness index SI), flow-mediated dilation of the brachial artery (FMD)
Time Frame
week 0, 48
Title
Total cholesterol, triglycerides, VLDL-C, HDL-C, lipid profile, hs-CRP, AP, GGT, bilirubin, bile acids, immunoglobins
Time Frame
week 0, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 60
Title
AST, ALT, CK, PZ, AT, albumin, creatinine, blood cell count
Time Frame
week 0, 4, 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 60

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: LDL-cholesterol > 130 mg/dl Primary biliary cirrhosis (AMA positive or biopsy proven) Male or female gender Age 18-70 years Normal kidney function Exclusion Criteria: Primary biliary cirrhosis Stage III-IV (Ludwig Score) Liver cirrhosis Decompensated liver disease ( > Child-Pugh class B, ascites, esophageal varices) ALT or AST > 2x ULN Pregnancy or breastfeeding Premenopausal women without certain contraception Known hypersensitivity to HMG-CoA reductase inhibitors Current treatment with lipid-lowering agents other than atorvastatin; immunosuppressants, macrolides
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Trauner, M.D.
Organizational Affiliation
Medical University of Graz, Department of Internal Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Internal Medicine, Medical University of Graz
City
Graz
ZIP/Postal Code
8036
Country
Austria

12. IPD Sharing Statement

Citations:
PubMed Identifier
19782361
Citation
Stojakovic T, Claudel T, Putz-Bankuti C, Fauler G, Scharnagl H, Wagner M, Sourij H, Stauber RE, Winkler K, Marz W, Wascher TC, Trauner M. Low-dose atorvastatin improves dyslipidemia and vascular function in patients with primary biliary cirrhosis after one year of treatment. Atherosclerosis. 2010 Mar;209(1):178-83. doi: 10.1016/j.atherosclerosis.2009.08.052. Epub 2009 Sep 6.
Results Reference
derived

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Safety and Efficacy of Long-Term Treatment With Atorvastatin in Patients With Primary Biliary Cirrhosis

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