Effects of Alanine in Patients With Nonalcoholic Steatohepatitis

Not Applicable

Completed

• Conditions: Nonalcoholic Steatohepatitis
• Interventions: Drug: L-alanine

• Registration Number: NCT00586885
• Lead Sponsor: Keith D Lindor, M.D.

Brief Summary

Purpose of this study is to assess the therapeutic efficacy of L-alanine in improving biological and histological findings by administrating 6-18g/day L-alanine for one year. We will also assess the safety and toxicity profile of long-term administration of L-alanine.

Detailed Description

Not available

Study Timeline

• Study Start: 2004-02
• Primary Completion: 2006-06
• Study Completion: 2006-06
• Study First Submitted: 2007-12-21
• Study First Submitted QC: 2007-12-21
• Study First Posted: 2008-01-07
• Status Verified: 2012-10
• Last Update Submitted: 2012-10-09
• Last Update Posted: 2012-10-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 9

Inclusion Criteria

• Males and females, age between 18 and 75
• Histological diagnosis of steatohepatitis with or without fibrosis made within one year of entry
• Transaminase levels (ALT or AST) more than 1.5 times the upper normal limit on at least two occasions with one assessment in three months or more prior to treatment of this study
• Previous and current alcohol consumption less than 20g per day by patient-provided information.
• Written informed consent specific for this protocol available prior to entry.
• Patients with diabetes and on stable medical management for six months prior to entry and an anticipated stable program throughout the study will be eligible. Medications that may be used include insulin, biguanides and sulfonylureas.
• Patients with congestive heart failure, hypertension and arrhythmia controlled by medications and without cardiac episodes during the past 6 months will be eligible.

Exclusion Criteria

• Any causes for liver disease other than nonalcoholic steatohepatitis that are confirmed by patient history, laboratory data, or histological data

• Decompensated liver disease based on laboratory data, or clinical manifestations

  1. Hemoglobin <11.0g/dl for male, <10.0 g/dl for female
  2. White blood cells <2000 /mm3
  3. Platelet count <50,000/mm3
  4. Prothrombin time >INR 1.5
  5. Total Bilirubin >2.0 g/dl
  6. Albumin <3.0/dl
  7. The presence of ascites
  8. The presence of bleeding varices
  9. The presence of spontaneous encephalopathy

• Any previous experimental treatment of NASH within the past 3 months such as betaine, thiazolidinediones, α-tocopherol, or UDCA

• Pre-existing diseases/situations that could interfere with the results or the completion of this trial.

• Uncontrolled diabetes mellitus meeting following criteria in previous 3 months

  1. Fasting blood sugar >200 mg/dl
  2. Hemoglobin A1c >12%

• Renal or liver transplant patients

• Renal dysfunction in previous 3 months

  a) CCr <50ml/min

• Severe cardiovascular dysfunction in previous 6 months

• Congestive heart failure

• Uncontrolled hypertension

• Uncontrolled arrhythmia

• Patients with hyperlipidemia on a medical program for control of lipids which has had a change in drug treatment in the proceeding six months or with anticipated changes in the year of the study.

• Chronic pulmonary disease such as COPD requiring corticosteroid therapy in previous 3 months

• Active autoimmune or immunologically mediated diseases including systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel diseases in previous 12 months

• Previous (in three years) or present malignant disease except for non-melanoma skin cancer

• Untreated hyperthyroidism and hypothyroidism

• Substance abuse of oral, I.V., or inhaled drugs.

• If patients with history of substance abuse are considered as participants in this trial, patients must have abstained from using the abused substance for at least one year.

• Patients receiving methadone within the past 6 months are also excluded.

• Any other conditions that would make the patients unsuitable for enrollment in the opinion of the investigator in terms of interference in completing the trial and/or results of trial.

• Pregnant women

• Unwillingness of patients and /or partner to use contraceptive during treatment and for 3 months after discontinuation of treatment.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
1	L-alanine	Single arm, active treatment

Primary Outcome Measures

Name	Time	Method
To assess the safety and tolerability of long-term L-alanine supplementation and the therapeutic efficacy of long-term L-alanine supplementation by evaluating liver biochemistry and histological findings.	1 year

Secondary Outcome Measures

Name	Time	Method
Determine the effect of L-alanine on gene profiles, anti-oxidant response and inflammatory response in hepatocytes. Evaluate possible correlation between therapeutic efficacy and gene profiles altered by L-alanine supplementation	1 year

Trial Locations

Locations (1)

Mayo Clinic; 🇺🇸 Rochester, Minnesota, United States