Vitamin E and DHA-EE on NAFLD - Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Clinical Trial (PUVENAFLD)

Non-Alcoholic Fatty Liver Disease Clinical Trial

— PUVENAFLD  

Official title:

The Effect of Vitamin E and Docosahexaenoic Acid Ethyl Ester on Non-Alcoholic Fatty Liver Disease (NAFLD) - Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Clinical Trial (PUVENAFLD)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04198805
• Other study ID #: 2017-1088
• Status: Completed
• Phase: Phase 2
• Start date: January 3, 2020
• Est. completion date: September 1, 2022

Study information

• Verified date: April 2023
• Source: Indiana University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Multicenter, randomized, double-blinded, placebo-controlled clinical trial is focused on novel treatments for non-alcoholic fatty liver disease (NAFLD), the most common cause of chronic liver disease. The primary objective of the study is to determine the clinical efficacy and safety of Vitamin E [(all-rac)-α-tocopheryl acetate] and Omega-3 fatty acid (DHA EE) compared to placebo on reducing liver fat content in participants with NAFLD. There is currently no approved drug treatment for NAFLD or NASH. While several new targets are being evaluated, they are not sufficiently powered to provide definitive data. There is, therefore, a need for well-designed, appropriately powered efficacy (phase 2) trials to define the utility of newer therapies for NAFLD. The combination of Vitamin E and DHA may provide optimal benefit for patients with NAFLD due to their associated mechanisms of action, namely Vitamin E's antioxidant action, preventing lipid oxidation of long-chain fatty acids such as DHA and thus preventing the propagation of free radicals and ROS.

Description:

Background information

Non-alcoholic fatty liver disease (NAFLD) is characterized by excessive fat accumulation in the liver and is defined by evidence of hepatic steatosis (via imaging or histology) and is not due to secondary liver fat accumulation from excessive alcohol consumption or hereditary disorders (e.g., Wilson's disease). NAFLD is most commonly associated with metabolic syndrome, consisting of obesity, insulin resistance, elevated blood pressure, and dyslipidemia. NAFLD is one of the most common causes of chronic liver disease, globally with a prevalence as high as 30% in Western countries. It includes a spectrum of diseases from steatosis to non-alcoholic steatohepatitis (NASH), liver fibrosis, cirrhosis, and hepatocellular carcinoma. Non-alcoholic fatty liver does not involve hepatocellular injury in the form of ballooning hepatocytes, whereas NASH is defined by steatosis, inflammation, and hepatocyte injury (ballooning) with or without fibrosis. The causes of NAFLD are likely due to a combination of genetic and physiologic factors, namely those that promote oxidative stress and inflammation such as metabolic syndrome, visceral adiposity, and changes in intestinal microbiota. NAFLD is significantly associated with increased risk of Type II Diabetes and cardiovascular disease and increased overall mortality compared to age-matched controls. There is currently no approved drug treatment for NAFLD or NASH. Dietary restrictions for weight loss and increased physical activity are the recommended therapies, albeit with limited success.

Investigational products

Vitamin E [(all-rac)-α-tocopheryl acetate]

Vitamin E is a fat-soluble vitamin that is synthesized naturally in plants in four tocopheryl forms: α, β, γ, and δ. All-rac-α-tocopheryl acetate has the highest biological activity in animal models, and it is the α-tocopheryl form that is used to prevent and treat Vitamin E deficiency in humans. Functionally, Vitamin E is an anti-oxidant and peroxyl radical scavenger. It is an inhibitor of lipid peroxidation and can also inhibit and modulate intracellular signaling molecules, e.g., protein kinase C, and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase. α-tocopheryl regulates gene expression of several intracellular enzymes such as 5-lipoxygenase and cyclooxygenase and has anti-inflammatory activity (i.e., decreasing cytokine release and plasma C reactive protein). It is also known to inhibit platelet adhesion and aggregation. \

DHA Ethyl Ester

Long-chain polyunsaturated fatty acid (LC-PUFA), docosahexaenoic acid (DHA) is an essential omega-3 fatty acid for brain, eye and cardiovascular development and health. It significantly reduces triglycerides (TGs), lowers heart rate, lowers blood pressure, and reduces the risk of cardiac death by an overall 8%. Both DHA and eicosapentaenoic acid (EPA) have anti-thrombotic, anti-inflammatory, and anti-oxidative properties. As NAFLD patients are at significantly greater risk of cardiovascular disease and higher overall mortality, the cardioprotective effects of DHA are significant and may be beneficial in the NAFLD population.

Potential mechanisms for DHA's effects in NAFLD include the reduction of TG synthesis via activation of peroxisome proliferator-activated receptors (PPAR-α and γ), which accelerates fatty acid oxidation in liver mitochondria. DHA is also known to have an integral role in maintaining and improving cell membrane fluidity, as a fatty acid that is incorporated into the phospholipids of the membrane, thereby optimizing surface receptors and signal transduction pathways in liver cells. The anti-inflammatory role of DHA in NAFLD may be mediated through activation of adiponectin secretion through adults with NAFLD. MRI-PDFF is also an appropriate technique to diagnose and stage disease in those with metabolic syndrome and NAFLD. The clinical trial is designed to test the combination of Vitamin E and DHA against placebo, to demonstrate efficacy and safety.

Rationale for conducting the clinical study

The combination of Vitamin E and DHA has not been tested in previous clinical trials of adults with NAFLD. This combination may provide optimal benefit for patients with NAFLD due to their associated mechanisms of action, namely Vitamin E's antioxidant action, preventing lipid oxidation of long-chain fatty acids such as DHA and thus preventing the propagation of free radicals and ROS. Vitamin E's protection of LC-PUFA DHA, therefore, assists it in maintaining cell membrane stability and optimal signaling. Their combined anti-inflammatory effects (e.g., inhibiting pro-inflammatory cytokines, increasing adiponectin, and producing docosanoids to resolve inflammation) may also be efficacious for those with metabolic syndrome and NAFLD. The combination of Vitamin E and DHA will correctly be used in this study to determine if a reduction in liver fat occurs after six months of co-administration, using a magnetic resonance imaging (MRI) technique, proton density fat fraction (PDFF). PDFF imaging is non-invasive and highly sensitive to detect liver steatosis in patients with NAFLD.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 205
• Est. completion date: September 1, 2022
• Est. primary completion date: September 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female gender

• =18 years of age

• A new diagnosis or reconfirmation of previously known fatty liver by imaging (ultrasound or CT or MRI), or by liver biopsy within = 4 years

• Fibroscan CAP score >300db

• Hepatic fat fraction =12% by MRI PDFF

• ALT= 40 U/L

• eGFR/Creatinine Clearance = 60ml/min

• Participants with previously diagnosed Type 2 diabetes (up to 50% of sample): they must either be taking anti-diabetic medications, or their fasting (>10 hours) glucose must be = 100 mg/dL at the time of screening

• Stable weight (±5%) for at least 3 months

• Subjects willing and able to give written informed consent and to understand, to participant and to comply with the clinical study requirements.

Exclusion Criteria:

• Evidence of alternative causes of hepatic steatosis or other forms of chronic liver disease, e.g. Hep.B, Hep.C

• Evidence of acute Hepatitis A

• Serum ALT or AST = 250 U/L

• Serum Alkaline Phosphatase > 2 ULN

• Total bilirubin > 2 ULN in the absence of Gilbert's Syndrome [In patients with Gilbert's Syndrome, direct bilirubin must not exceed 2 ULN]

• HbA1c=9.5%

• Decompensated acute or chronic liver disease

• Clinical, imaging or histological evidence of cirrhosis

• Use of anti-NASH drugs (e.g. thiazolidinediones) in the 3 months prior to randomization

• Use of a non-stable dose of statins or fibrates in the 3 months prior to randomization

• Use of fish oil, algal oil or Krill oil supplements, drugs or foods fortified with omega-3s in the 2 months prior to randomization (>200mg DHA/d and/or >60mg EPA/d by FFQ)

• Known intolerance to vitamin E or DHA

• Malabsorption of Vit E (e.g. due to steatorrhea, chronic pancreatitis, severe cholestasis)

• Vitamin E supplementation of greater than 100 IU/day in the 3 months prior to randomization

• History of bariatric surgery (jejunoileal bypass or gastric weight loss surgery) or currently undergoing evaluation for bariatric surgery

• History of biliary diversion

• Known positivity for antibody to Human Immunodeficiency Virus (HIV)

• Patients with coagulopathy (PT =3 sec.from ULN), thrombocytopenia (<70K)

• Contraindication to MRI (implants, metal…)

• Active, serious medical disease or disease diagnosis of a life-expectancy less than 5 years

• Ongoing or recent alcohol consumption > 21 drinks (1 drink= 12 oz regular beer, or 5 oz wine, or 1.5 oz distilled spirits) per week in men and > 14 drinks per week in women as per subject self-report as part of medical history.

• Active substance abuse, such as oral, inhaled or injected illicit drugs (except marijuana), in the year prior to screening

• Women of childbearing potential: positive pregnancy test during screening or at randomization or unwillingness to use an effective form of birth control during the trial

• Women who are breastfeeding

• Any other condition which, in the opinion of the investigator would impede compliance or hinder completion of the study

• Subjects who are enrolled in an interventional clinical study or have received an investigational new drug or product within the last 30 days prior to screening

• Participants diagnosed with type 1 diabetes

Related Conditions & MeSH terms

• Fatty Liver
• Liver Diseases
• Non-Alcoholic Fatty Liver
• Non-Alcoholic Fatty Liver Disease
• Non-Alcoholic Steatohepatitis

Intervention

Dietary Supplement:
• Vitamin E [(all-rac)-a-tocopheryl acetate]
Vitamin E (1000 mg) once daily for 6 months (1 capsule) and matching placebos (2 matched capsules) for 6 months
• Omega-3 fatty acid (DHA EE)
DHA EE (1.89 g) once daily for 6 months (2 capsules) and matching placebo for DHA EE (1 matched capsule for 6 months)

Combination Product:
• Omega-3 fatty acid (DHA EE) & Vitamin E [(all-rac)-a-tocopheryl acetate]
DHA EE (1.89 g) once daily for 6 months and Vitamin E (1000 mg) once daily for 6 months

Other:
• Placebo
Matching soybean placebo (3 capsules) of all arms daily for 6 months.

Locations

Country	Name	City	State
United States	Summit Clinical Research LLC	Athens	Georgia
United States	Arizona Liver Health	Chandler	Arizona
United States	Integrity Clinical Research LLC	Doral	Florida
United States	Indago Research and Health Center, Inc.	Hialeah	Florida
United States	Centex Studies, Inc.	Houston	Texas
United States	Liver Specialists of Texas/Mt. Olympus Medical Research	Houston	Texas
United States	Indiana University School of Medicine	Indianapolis	Indiana
United States	Florida Research Institute	Lakewood Ranch	Florida
United States	Advanced Pharma CR LLC	Miami	Florida
United States	Med-Care Research	Miami	Florida
United States	Arkansas Gastroenterology	North Little Rock	Arkansas
United States	M3 Wake Research Associates	Raleigh	North Carolina
United States	Inland Empire Clinical Trials, LLC	Rialto	California
United States	American Research Corporation at the Texas Liver Institute	San Antonio	Texas
United States	Arizona Liver Health	Tucson	Arizona

Sponsors (2)

Lead Sponsor	Collaborator
Naga P. Chalasani	DSM Nutritional Products, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Hepatic Fat Fraction [%] Between of Vitamin E and DHA EE vs Placebo	A change in liver fat content relative to baseline between Vitamin E and DHA EE vs placebo. This will be measured by MRI-PDFF at baseline and after 6 months of intervention (value at 6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Hepatic Fat Fraction [%] Between Vitamin E vs Placebo Arm	Change in liver fat content relative to baseline between Vitamin E vs placebo arm. This will be measured by MRI-PDFF at baseline and after 6 months of intervention (value at 6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Hepatic Fat Fraction [%] Between DHA EE vs Placebo Arm	Change in liver fat content relative to baseline between DHA EE vs placebo arm. This will be measured by MRI-PDFF at baseline and after 6 months of intervention (value at 6 months minus value at baseline).	Baseline to 6 months
Secondary	Change After 6 Months of DHA EE and/ or Vitamin E Intervention in the Anthropometric Measure, Waist Circumference.	Evaluation of baseline and 6 month measurements of waist circumference in the DHA EE and /or Vitamin E intervention over a 6 month period.	Baseline to 6 months
Secondary	Change After 6 Months of DHA EE and /or Vitamin E Intervention in the Anthropometric Measure, Bodyweight.	Evaluation of baseline and 6-month measurements of body weight in the DHA EE and /or Vitamin E intervention over a 6 month period.	Baseline to 6 months
Secondary	Change After 6 Months of DHA EE and/ or Vitamin E Intervention in the Anthropometric Measure, Waist-to-hip Ratio .	Evaluation of baseline and 6-month measurements of waist-to-hip ratio (the circumference of the waist divided by the circumference of the hips) in the DHA EE and /or Vitamin E intervention over a 6 month period.	Baseline to 6 months
Secondary	Change After 6 Months of DHA EE and/ or Vitamin E Intervention in the Anthropometric Measure, Body Mass Index (BMI)	Evaluation of baseline and 6-month measurements of body mass index (BMI) in the DHA EE and /or Vitamin E intervention over a 6 month period.	Baseline to 6 months
Secondary	Change in Insulin Levels to Determine Insulin Resistance		Baseline to 6 months
Secondary	Change in Liver Enzymes (ALT) in the DHA EE and /or Vitamin E Intervention Over a 6 Month Period.	Evaluation of baseline and 6-month liver enzymes: alanine transaminase (ALT) in the DHA EE and /or Vitamin E intervention over a 6 month period value at (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Liver Enzymes (AST) in the DHA EE and /or Vitamin E Intervention Over a 6 Month Period.	Evaluation of baseline and 6-month liver enzymes: aspartate aminotransferase (AST) in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Liver Enzymes Bilirubin in the DHA EE and /or Vitamin E Intervention Over a 6 Month Period.	Evaluation of baseline and 6-month liver enzymes: Bilirubin in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Liver Enzymes Alkaline Phosphatase in the DHA EE and /or Vitamin E Intervention Over a 6 Month Period.	Evaluation of baseline and 6-month liver enzymes: Alkaline Phosphatase in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Fibrosis-4 (FIB-4) Score	The formula for FIB-4 is: Age ([yr] x AST [U/L]) / ((PLT [10(9)/L]) x (ALT [U/L])(1/2)). A value of FIB-4 below 1.30 is considered as low risk for advanced fibrosis; a value of FIB-4 over 2.67 is considered as high risk for advanced fibrosis	Baseline to 6 months
Secondary	Change in Plasma Vitamin E Concentration	Evaluation of baseline and 6-month plasma Vitamin E concentration in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Plasma DHA EE Concentration	Evaluation of baseline and 6-month plasma DHA EE concentration in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Lipid Profile (HDL-C)	Evaluation of baseline and 6-month lipid profile (HDL-C) in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Lipid Profile (Low Density Lipoprotein (LDL-C))	Evaluation of baseline and 6-month lipid profile (low density lipoprotein (LDL-C))in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Lipid Profile (Triglycerides)	Evaluation of baseline and 6-month lipid profile (TGs)in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Lipid Profile (Oxidized LDL)	Evaluation of baseline and 6-month lipid profile (oxidized LDL) in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Health Related Quality of Life Score (Short Form (SF-36))	Evaluation of baseline and 6-month quality of life score (SF-36) in the DHA EE and /or Vitamin E intervention over a 6 month period (value at 6 months minus value at baseline). The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability	Baseline to 6 months
Secondary	Change in Dietary Intake Levels of Long-chain Polyunsaturated Fatty Acids (LC-PUFA ) (i.e. DHA and EPA) as Measured by the Food Frequency Questionnaire (FFQ)	Evaluation of baseline and 6-month dietary intake levels of LC-PUFA (i.e. DHA and EPA) as measured by the Food Frequency Questionnaire (FFQ)in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Inflammatory Markers (Cytokeratin 18 (CK-18))	Evaluation of baseline and 6-month inflammatory markers (cytokeratin 18) in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Inflammatory Markers (IL-1ß)	Evaluation of baseline and 6-month inflammatory markers (IL-1ß) in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months
Secondary	Change in Inflammatory Markers (TNFa)	Evaluation of baseline and 6-month inflammatory markers (TNFa) in the DHA EE and /or Vitamin E intervention over a 6 month period (6 months minus value at baseline).	Baseline to 6 months