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Effect of Spironolactone and Vitamin E in Patients With Nonalcoholic Fatty Liver Disease (NAFLD)

Primary Purpose

Fatty Liver, Steatohepatitis

Status
Completed
Phase
Phase 2
Locations
Greece
Study Type
Interventional
Intervention
Spironolactone/Vitamin E
Sponsored by
Aristotle University Of Thessaloniki
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fatty Liver focused on measuring nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, adipokines, spironolactone, vitamin E, adiponectin, visfatin, leptin, resistin, TNF-alpha, IL-6, IL-1

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Bright liver on ultrasound imaging and increased liver function tests for at least 6 months before liver biopsy
  • Biopsy-proven NAFLD (either NAFL or NASH) according to NAFLD Activity Score (NAS)

Exclusion Criteria:

  • Ethanol consumption more than 20 g/day
  • Known intolerance to spironolactone or vitamin E
  • History of liver disease (chronic viral hepatitis, autoimmune hepatitis, drug-induced liver disease, primary biliary cirrhosis, hemochromatosis, Wilson's disease and α1-antitrypsin deficiency)
  • Previous exposure to hepatotoxic drugs
  • Spironolactone or vitamin E administration within one year before screening
  • Type I Diabetes Mellitus
  • Pancreatitis
  • Uncontrolled hypothyroidism or hyperthyroidism
  • Adrenal Insufficiency
  • Renal Failure
  • Cancer
  • Pregnancy

Exclusion criteria were generally the same as those proposed for PIVENS trial design with two modifications: a) known intolerance to spironolactone as an exclusion criterion and b) the inclusion of patients with T2DM not receiving thiazolidinediones or insulin.

Sites / Locations

  • Second Medical Clinic, Medical School, Aristotle University of Thessaloniki, Ippokration Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Vitamin E

Arm Description

Vitamin E, capsules 400 mg daily, for 52 weeks

Outcomes

Primary Outcome Measures

Serum adipocytokines levels
Adiponectin; visfatin; leptin; resistin; omentin; vaspin; RBP4; TNF-alpha, IL-6; IL-1

Secondary Outcome Measures

Serum homocysteine levels
Homocysteine; vitamin B12; folate
Liver histology
Repeat biopsy, if patients provide their consent
Insulin resistance
Serum insulin; serum glucose; HOMA and QUICKI indexes
Hormonal profile
DHEAS; testosterone; estradiol; TSH; free T4; cortisol (serum levels)
Serum biochemistry
ALT; AST; ggt; Potassium; Sodium; urea; creatinin; cholesterol; triglycerides; HDL; LDL
Reactive Oxygen Metabolites (ROMs)
Serum dROMs leves

Full Information

First Posted
June 17, 2010
Last Updated
January 19, 2012
Sponsor
Aristotle University Of Thessaloniki
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1. Study Identification

Unique Protocol Identification Number
NCT01147523
Brief Title
Effect of Spironolactone and Vitamin E in Patients With Nonalcoholic Fatty Liver Disease
Acronym
NAFLD
Official Title
The Effect of Spironolactone and Vitamin E Versus Vitamin E on Serum Adipocytokines Levels in Patients With Biopsy-proven Nonalcoholic Fatty Liver Disease-A Phase II Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2012
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
November 2010 (Actual)
Study Completion Date
December 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aristotle University Of Thessaloniki

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary aim of the study is the effect of spironolactone and vitamin E versus vitamin E on serum levels of adipokines 52 weeks post-treatment.
Detailed Description
Unlike other chronic liver diseases (e.g., hepatitis C), there are no effective treatment strategy for NAFLD. Currently, the management of NAFLD includes modification of underlying risk factors, detection of patients that have progressed to cirrhosis, management of cirrhosis-related morbidity and transplantation in patients with end-stage liver disease. Diet, exercise, bariatric surgery and pharmacologic treatment, including weight loss agents, insulin sensitizers, lipid-lowering agents, ursodeoxycholic acid and vitamin E have been investigated with some promising results. The renin-angiotensin-aldosterone system (RAAS) has been implicated in the pathogenesis of insulin resistance (IR) and nonalcoholic fatty liver disease (NAFLD). Recently, low-dose (25-50 mg/day) aldosterone antagonists in patients with heart failure diminish mortality, possibly by reducing cardiac and vascular fibrosis. Moreover, the beneficial effect of spironolactone in a mouse model with diet-induced diabetes and NAFLD has been reported. However, to our knowledge, the role of spironolactone in NAFLD patients has not been investigated yet. The primary aim of the study is the effect of spironolactone and vitamin E versus vitamin E on serum levels of adipokines 52 weeks post-treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fatty Liver, Steatohepatitis
Keywords
nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, adipokines, spironolactone, vitamin E, adiponectin, visfatin, leptin, resistin, TNF-alpha, IL-6, IL-1

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin E
Arm Type
Experimental
Arm Description
Vitamin E, capsules 400 mg daily, for 52 weeks
Intervention Type
Drug
Intervention Name(s)
Spironolactone/Vitamin E
Other Intervention Name(s)
Aldactone tab 25, Eviol caps 100
Intervention Description
Spironolactone, tablets, 25 mg daily plus Vitamin E, capsules, 400 mg daily, for 52 weeks
Primary Outcome Measure Information:
Title
Serum adipocytokines levels
Description
Adiponectin; visfatin; leptin; resistin; omentin; vaspin; RBP4; TNF-alpha, IL-6; IL-1
Time Frame
52 weeks
Secondary Outcome Measure Information:
Title
Serum homocysteine levels
Description
Homocysteine; vitamin B12; folate
Time Frame
52 weeks
Title
Liver histology
Description
Repeat biopsy, if patients provide their consent
Time Frame
52 weeks
Title
Insulin resistance
Description
Serum insulin; serum glucose; HOMA and QUICKI indexes
Time Frame
52 weeks
Title
Hormonal profile
Description
DHEAS; testosterone; estradiol; TSH; free T4; cortisol (serum levels)
Time Frame
52 weeks
Title
Serum biochemistry
Description
ALT; AST; ggt; Potassium; Sodium; urea; creatinin; cholesterol; triglycerides; HDL; LDL
Time Frame
52 weeks
Title
Reactive Oxygen Metabolites (ROMs)
Description
Serum dROMs leves
Time Frame
52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Bright liver on ultrasound imaging and increased liver function tests for at least 6 months before liver biopsy Biopsy-proven NAFLD (either NAFL or NASH) according to NAFLD Activity Score (NAS) Exclusion Criteria: Ethanol consumption more than 20 g/day Known intolerance to spironolactone or vitamin E History of liver disease (chronic viral hepatitis, autoimmune hepatitis, drug-induced liver disease, primary biliary cirrhosis, hemochromatosis, Wilson's disease and α1-antitrypsin deficiency) Previous exposure to hepatotoxic drugs Spironolactone or vitamin E administration within one year before screening Type I Diabetes Mellitus Pancreatitis Uncontrolled hypothyroidism or hyperthyroidism Adrenal Insufficiency Renal Failure Cancer Pregnancy Exclusion criteria were generally the same as those proposed for PIVENS trial design with two modifications: a) known intolerance to spironolactone as an exclusion criterion and b) the inclusion of patients with T2DM not receiving thiazolidinediones or insulin.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stergios A Polyzos, MD, MSc
Organizational Affiliation
Second Medical Clinic, Medical School, Aristotle University of Thessaloniki, Ippokration Hospital, Thessaloniki, Greece
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jannis Kountouras, MD, Prof
Organizational Affiliation
Second Medical Clinic, Medical School, Aristotle University of Thessaloniki, Ippokration Hospital, Thessaloniki, Greece
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Efthimia Zafeiriadou, MD, PhD
Organizational Affiliation
Department of Radiology, Ippokration Hospital, Thessaloniki, Greece
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Kalliopi Patsiaoura, MD, PhD
Organizational Affiliation
Department of Pathology, Ippokration Hospital, Thessaloniki, Greece
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Evangelia Katsiki, MD
Organizational Affiliation
Department of Pathology, Ippokration Hospital, Thessaloniki, Greece
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Aristidis Slavakis, MD, MSc
Organizational Affiliation
Department of Biochemistry, Ippokration Hospital, Thessaloniki, Greece
Official's Role
Study Director
Facility Information:
Facility Name
Second Medical Clinic, Medical School, Aristotle University of Thessaloniki, Ippokration Hospital
City
Thessaloniki
ZIP/Postal Code
54642
Country
Greece

12. IPD Sharing Statement

Citations:
PubMed Identifier
19355912
Citation
Polyzos SA, Kountouras J, Zavos C. Nonalcoholic fatty liver disease: the pathogenetic roles of insulin resistance and adipocytokines. Curr Mol Med. 2009 Apr;9(3):299-314. doi: 10.2174/156652409787847191.
Results Reference
background
PubMed Identifier
19162411
Citation
Polyzos SA, Kountouras J, Zavos C. Insulin resistance and therapy: cross-talk between phosphatidylinositol-3 kinase and mitogen-activated protein kinase pathways. Med Hypotheses. 2009 May;72(5):610. doi: 10.1016/j.mehy.2008.12.019. Epub 2009 Jan 21. No abstract available.
Results Reference
background
PubMed Identifier
19561788
Citation
Polyzos SA, Kountouras J, Zavos Ch. The multi-hit process and the antagonistic roles of tumor necrosis factor-alpha and adiponectin in non alcoholic fatty liver disease. Hippokratia. 2009 Apr;13(2):127; author reply 128. No abstract available.
Results Reference
background
PubMed Identifier
19770674
Citation
Polyzos SA, Kountouras J, Zavos C. Nonlinear distribution of adiponectin in patients with nonalcoholic fatty liver disease limits its use in linear regression analysis. J Clin Gastroenterol. 2010 Mar;44(3):229-30; author reply 230-1. doi: 10.1097/MCG.0b013e3181b5ce68. No abstract available.
Results Reference
background
PubMed Identifier
20080361
Citation
Polyzos SA, Kountouras J, Zavos C, Stergiopoulos C. Adipocytokines in insulin resistance and non-alcoholic fatty liver disease: the two sides of the same coin. Med Hypotheses. 2010 Jun;74(6):1089-90. doi: 10.1016/j.mehy.2009.12.028. Epub 2010 Jan 18. No abstract available.
Results Reference
background
PubMed Identifier
20394676
Citation
Polyzos SA, Kountouras J, Zavos C. Adiponectin as a potential therapeutic agent for nonalcoholic steatohepatitis. Hepatol Res. 2010 Apr;40(4):446-7. doi: 10.1111/j.1872-034X.2010.00632.x. No abstract available.
Results Reference
background
PubMed Identifier
20415685
Citation
Polyzos SA, Kountouras J, Zavos C, Tsiaousi E. The role of adiponectin in the pathogenesis and treatment of non-alcoholic fatty liver disease. Diabetes Obes Metab. 2010 May;12(5):365-83. doi: 10.1111/j.1463-1326.2009.01176.x.
Results Reference
background
PubMed Identifier
20717042
Citation
Polyzos SA, Kountouras J, Zavos C, Deretzi G. The potential adverse role of leptin resistance in nonalcoholic fatty liver disease: a hypothesis based on critical review of the literature. J Clin Gastroenterol. 2011 Jan;45(1):50-4. doi: 10.1097/MCG.0b013e3181ec5c66.
Results Reference
background
PubMed Identifier
21040935
Citation
Polyzos SA, Toulis KA, Goulis DG, Zavos C, Kountouras J. Serum total adiponectin in nonalcoholic fatty liver disease: a systematic review and meta-analysis. Metabolism. 2011 Mar;60(3):313-26. doi: 10.1016/j.metabol.2010.09.003. Epub 2010 Oct 30.
Results Reference
background
PubMed Identifier
21314876
Citation
Polyzos SA, Kountouras J, Zavos C. Adiponectin in non-alcoholic fatty liver disease treatment: therapeutic perspectives and unresolved dilemmas. Int J Clin Pract. 2011 Mar;65(3):373-4. doi: 10.1111/j.1742-1241.2010.02594.x. No abstract available.
Results Reference
background
PubMed Identifier
21435084
Citation
Polyzos SA, Kountouras J, Zavos C, Deretzi G. The association between Helicobacter pylori infection and insulin resistance: a systematic review. Helicobacter. 2011 Apr;16(2):79-88. doi: 10.1111/j.1523-5378.2011.00822.x.
Results Reference
background
PubMed Identifier
21789399
Citation
Polyzos SA, Kountouras J, Zavos C, Deretzi G. The potentially dual-faceted nature of fetuin-A in Helicobacter pylori infection and insulin resistance. Clinics (Sao Paulo). 2011;66(5):911-2. doi: 10.1590/s1807-59322011000500031. No abstract available.
Results Reference
background
PubMed Identifier
22064347
Citation
Polyzos SA, Kountouras J, Zavos C, Deretzi G. Helicobacter pylori and insulin resistance association: not just a myth, not yet a fact. Saudi J Gastroenterol. 2011 Nov-Dec;17(6):425-6. doi: 10.4103/1319-3767.87190. No abstract available.
Results Reference
background
PubMed Identifier
22082482
Citation
Polyzos SA, Kountouras J, Deretzi G, Zavos C, Mantzoros CS. The emerging role of endocrine disruptors in pathogenesis of insulin resistance: a concept implicating nonalcoholic fatty liver disease. Curr Mol Med. 2012 Jan;12(1):68-82. doi: 10.2174/156652412798376161.
Results Reference
background
PubMed Identifier
22166563
Citation
Polyzos SA, Kountouras J, Patsiaoura K, Katsiki E, Zafeiriadou E, Deretzi G, Zavos C, Gavalas E, Katsinelos P, Mane V, Slavakis A. Serum homocysteine levels in patients with nonalcoholic fatty liver disease. Ann Hepatol. 2012 Jan-Feb;11(1):68-76.
Results Reference
background
PubMed Identifier
22229957
Citation
Polyzos SA, Kountouras J, Patsiaoura K, Katsiki E, Zafeiriadou E, Zavos C, Deretzi G, Tsiaousi E, Slavakis A. Serum vitamin B12 and folate levels in patients with non-alcoholic fatty liver disease. Int J Food Sci Nutr. 2012 Sep;63(6):659-66. doi: 10.3109/09637486.2011.649249. Epub 2012 Jan 9.
Results Reference
background
PubMed Identifier
21436212
Citation
Polyzos SA, Kountouras J, Zafeiriadou E, Patsiaoura K, Katsiki E, Deretzi G, Zavos C, Tsarouchas G, Rakitzi P, Slavakis A. Effect of spironolactone and vitamin E on serum metabolic parameters and insulin resistance in patients with nonalcoholic fatty liver disease. J Renin Angiotensin Aldosterone Syst. 2011 Dec;12(4):498-503. doi: 10.1177/1470320311402110. Epub 2011 Mar 24.
Results Reference
result
PubMed Identifier
21974769
Citation
Polyzos SA, Kountouras J, Zavos C, Deretzi G. Spironolactone revisited. J Clin Hypertens (Greenwich). 2011 Oct;13(10):783-4. doi: 10.1111/j.1751-7176.2011.00484.x. Epub 2011 Jul 18. No abstract available.
Results Reference
result
PubMed Identifier
30467685
Citation
Polyzos SA, Kountouras J, Anastasilakis AD, Makras P, Hawa G, Sonnleitner L, Missbichler A, Doulberis M, Katsinelos P, Terpos E. Noggin levels in nonalcoholic fatty liver disease: the effect of vitamin E treatment. Hormones (Athens). 2018 Dec;17(4):573-579. doi: 10.1007/s42000-018-0083-8. Epub 2018 Nov 22.
Results Reference
derived
PubMed Identifier
28452101
Citation
Polyzos SA, Kountouras J, Mantzoros CS, Polymerou V, Katsinelos P. Effects of combined low-dose spironolactone plus vitamin E vs vitamin E monotherapy on insulin resistance, non-invasive indices of steatosis and fibrosis, and adipokine levels in non-alcoholic fatty liver disease: a randomized controlled trial. Diabetes Obes Metab. 2017 Dec;19(12):1805-1809. doi: 10.1111/dom.12989. Epub 2017 Jul 10.
Results Reference
derived

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Effect of Spironolactone and Vitamin E in Patients With Nonalcoholic Fatty Liver Disease

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