Effect of High-protein High-fiber Diet in Patients With Autoimmune Hepatitis

Sponsor
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran (Other)
Overall Status
Completed
CT.gov ID
NCT01655121
Collaborator
(none)
40
1
2
30
1.3

Study Details

Study Description

Brief Summary

Autoimmune hepatitis is a chronic disease of the liver caused by an alteration of the immune response that attacks the body's own hepatocytes, progressively, leading to cirrhosis and liver failure.

There are few studies on dietary management in hepatitis and most of theme have focused on micronutrients specifically vitamin D to prevent osteoporosis, and decreased symptoms of other diseases associated, but few recommendations have been made regarding a complete dietary approach. Fiber has been proven to increase the excretion of nitrogen products and consequently reduce its blood levels and an adequate protein intake (1.2g/kg) has shown to decrease endogenous catabolism in cirrhotics patients.

The implementation of a high protein high fiber nutrition plan and improves nutritional status of patients with autoimmune cirrhosis.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: High protein high fiber diet
N/A

Detailed Description

Each participant will receive a high protein (1.2g/kg/day) and high fiber (30g/day) dietary plan. The monitoring of adherence to the diet will be once a month for the duration of the study period.

There will be an nutritional assessment by anthropometric techniques: arm circumference, triceps skinfold, weight, height and body mass index as parameters of malnutrition by taking the standard for cirrhotic patients. Body composition was measured by bioelectric impedance to obtain fat mass, lean and total fluid content.

The presence of minimal hepatic encephalopathy will be assessed by PHES and CFF and applied three times during the study and the quality of life questionnaire SF-36 CLDQ and will be held in direct interview at the first visit and at study end.

Were also measured serum concentrations of ammonium, TNF-alpha, IL-1, IL-6, IL-10, renin, angiotensin and aldosterone.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Effect of a High-protein High-fiber Diet and Nutritional Status, Serum Ammonia Concentration and Plasma Cytokines in Patients With Autoimmune Hepatitis
Study Start Date :
Jan 1, 2012
Actual Primary Completion Date :
Jul 1, 2014
Actual Study Completion Date :
Jul 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Autoimmune hepatitis (Non-cirrhotic)

A personalized high protein high fiber dietary plan will be provided to each participant from both groups. Each participant will receive nutritional counseling once a month during six months.

Dietary Supplement: High protein high fiber diet
A personalized high protein high fiber dietary plan will be provided to each participant from both groups. Each participant will receive nutritional counseling once a month during six months. Each participant will receive nutritional counseling once month during six months.

Experimental: Autoimmune hepatitis (Cirrhotic)

A personalized high protein high fiber dietary plan will be provided to each participant from both groups. Each participant will receive nutritional counseling once a month during six months.

Dietary Supplement: High protein high fiber diet
A personalized high protein high fiber dietary plan will be provided to each participant from both groups. Each participant will receive nutritional counseling once a month during six months. Each participant will receive nutritional counseling once month during six months.

Outcome Measures

Primary Outcome Measures

  1. Nutritional Status [Participants will be assessed for six months]

    Measured with the following parameters:body weight and height (to calculate BMI), triceps skinfold and mid-arm circumference (to calculated mid-arm muscle circumference, fat mass, fat free mass total, intracellular and extracellular body water obtained by bioelectrical impedance analysis and individual vectors obtained by bioelectrical impedance vector analysis.

Secondary Outcome Measures

  1. Minimal hepatic encephalopathy [Participants will be assessed for six months]

    Assessed by psychometric Hepatic Encephalopathy (PHES) and Critical Flicker Frequency (CFF), at visit 0 months and 6 months visit.

  2. Quality of life [Participants will be assessed for six months]

    Assessed by CLDQ and SF-36 questionnaires, at visit 0 months and 6 months visit.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Autoimmune hepatitis (Non cirrhotic)

  • Diagnose of Autoimmune hepatitis

  • Presence of antinuclear antibody (ANA, SMA)

  • Biochemical evidence, based on elevation of transaminases

  • Biopsy compatible with Autoimmune hepatitis

  • Ambulatory patients

Autoimmune hepatitis (Cirrhotic)

  • Presence of antinuclear antibody (ANA, SMA)

  • Biochemical evidence, based on elevation of transaminases

  • Biopsy compatible with autoimmune cirrhosis

  • Hepatic cirrhosis by USD

  • Ambulatory patients

  • Diagnose of Autoimmune cirrhosis by two or more of the following criteria:

  • Albumin <3.4g/dl

  • INR>1.2

  • Total bilirubin >2mg/dl

  • Presence of esophageal varices by endoscopy

Exclusion Criteria:
  • Hospitalized patients

  • Overlapping syndrome with predominant primary biliary cirrhosis

  • Chronic renal failure

  • Hepatocellular carcinoma

  • Neuropsychiatric disorders

Contacts and Locations

Locations

Site City State Country Postal Code
1 Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán Mexico City D.f. Mexico 14000

Sponsors and Collaborators

  • Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Investigators

  • Principal Investigator: Aldo Torre Delgadillo, M.D. M.Sc, INCMNSZ

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
ALDO TORRE DELGADILLO, Principal Investigator, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
ClinicalTrials.gov Identifier:
NCT01655121
Other Study ID Numbers:
  • GAS-501-11/12-1
First Posted:
Aug 1, 2012
Last Update Posted:
Aug 20, 2014
Last Verified:
Aug 1, 2014
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 20, 2014