Non Alcoholic Fatty Liver Disease Clinical Trial
Official title:
Prospective Clinical Study on the Role of the Immune Response, in Relation to Diet, in Patients With Either Chronic Hepatitis C Virus (HCV) Infection or Non Alcoholic Fatty Liver Disease (NAFLD). Director Prof. V. Barnaba, Head of Internal Medicine; Principal Investigator, Prof. C. Balsano
Chronic hepatitis C virus (HCV) infection and nonalcoholic fatty liver disease (NAFLD) are
characterized by a spectrum of pathological conditions ranging from an early stage of
inflammation and fibrosis up to more advanced disease conditions, such as hepatocellular
carcinoma. The prevalence of NAFLD is between 10 and 25% of the population, with large
differences in age and ethnic groups, while it is well known that HCV infection is a major
cause of chronic liver disease in Western countries.
For both diseases the progression of liver damage is in close correlation with the lifestyle
of patients (eg., nutrition, physical activity, ingestion of alcohol, etc.). In fact, it was
shown that feeding imbalances may have implications in altering the normal immune functions
of the subjects, suggesting that the metabolic and the immune systems are closely related to
each other. Although it is well known the negative role of obesity on the progression of
NAFLD and HCV liver diseases, the pathogenic mechanism underlying the alterations related to
the immune response is not yet fully understood. Insulin resistance, altered lipid
metabolism, lipid peroxidation, oxidative stress and mitochondrial alterations are
pathogenic mechanisms that induce liver damage and its progression, both in NAFLD and in HCV
infection.
Recent studies suggest that the evolution of viral infections and chronic inflammation in
NAFLD are deeply influenced by CD4+ T helper cells expressing IL-17 , defined as T helper 17
(Th17) cells. Broadening the knowledge on the role of diet in the course of NAFLD and HCV
infection in the activation of Th17 cells and in the alteration of some of their functions,
will allow to shed light on the pathogenic mechanisms underlying the progression of
immune-mediated diseases. Moreover, this investigation will allow to understand whether Th17
cells may have a role in the diminished response to therapy in patients who have high
cholesterol levels.
If the results will confirm our hypothesis, this study will provide useful informations for
the clinical management of patients with both steatosis and chronic HCV infection. The data
obtained can also be used for the development of new therapeutic strategies directed to
modulate the antiviral immune response.
All patients will undergo clinical and instrumental assessment depending on the type of
pathology. Patients will be required to follow a normocaloric low cholesterol diet for a
period of 30 days.
The prospective clinical study does not present any form of additional risk for the patients
and will be conducted in accordance with the principles established by the Declaration of
Helsinki and with the standards of Good Clinical Practice (GCP). The study does not require
any additional costs.
n/a
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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