Nonalcoholic fatty liver disease (NAFLD) is the most common and harmful chronic liver disease. NAFLD accounts for 49.3% of the total number of chronic liver disease patients in China. It is important to effectively prevent and control NAFLD and its related diseases. Previous studies show the level of serum uric acid is significantly elevated in patients with NAFLD. Xanthine oxidase is a key enzyme in uric acid metabolism. It is a new therapeutic target for NAFLD. This study is aimed to further confirm that hyperuricemia is a new risk factor for NAFLD through a large sample prospective study. Furthermore, this study explore whether Xanthine oxidase (XO), a key enzyme in uric acid metabolism, plays an important role in regulating NAFLD.
Nonalcoholic fatty liver disease (NAFLD) is the most common and harmful chronic liver disease. NAFLD accounts for 49.3% of the total number of chronic liver disease patients in China. It is important to effectively prevent and control NAFLD and its related diseases. Previous studies show the level of serum uric acid is significantly elevated in patients with NAFLD. In a large cross-sectional study, the researcher were the first to confirm that serum uric acid level was significantly increased in patients with NAFLD. The results were published in J Hepatol. Xanthine oxidase is a key enzyme in uric acid metabolism. It is a new therapeutic target for NAFLD. This study is aimed to further confirm that hyperuricemia is a new risk factor for NAFLD through a large sample prospective study. Furthermore, this study explore whether Xanthine oxidase (XO), a key enzyme in uric acid metabolism, plays an important role in regulating NAFLD.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
200
According to NAFLD guidelines, participants accept febuxostat treatment (40mg, once a day, orally)
According to NAFLD guidelines, participants receive lifestyle intervention (diet and exercise).
Ningbo first hospital
Ningbo, Zhejiang, China
Liver fat content of subjects in different groups
Liver fat was assessed based on Magnetic Resonance Imaging (MRI).
Time frame: at the first week.
Liver fat content of subjects in different groups
Liver fat was assessed based on Magnetic Resonance Imaging (MRI).
Time frame: at the 24th week .
Liver fat content of subjects in different groups
Liver fat was assessed based on Magnetic Resonance Imaging (MRI).
Time frame: at the 48th week.
Serum uric acid levels of subjects in different groups
blood samples was assessed after 12 hours overnight fasting for the determination of hematological and biochemical variables, which were measured using an automated hematology analyzer by standard methods.
Time frame: at the first week
Serum uric acid levels of subjects in different groups
blood samples was assessed after 12 hours overnight fasting for the determination of hematological and biochemical variables, which were measured using an automated hematology analyzer by standard methods.
Time frame: at the forth week.
Serum uric acid levels of subjects in different groups
blood samples was assessed after 12 hours overnight fasting for the determination of hematological and biochemical variables, which were measured using an automated hematology analyzer by standard methods.
Time frame: at the twelfth week.
Serum uric acid levels of subjects in different groups
blood samples was assessed after 12 hours overnight fasting for the determination of hematological and biochemical variables, which were measured using an automated hematology analyzer by standard methods.
Time frame: at the 24th week.
Serum uric acid levels of subjects in different groups
blood samples was assessed after 12 hours overnight fasting for the determination of hematological and biochemical variables, which were measured using an automated hematology analyzer by standard methods.
Time frame: at the 36th week.
Serum uric acid levels of subjects in different groups
blood samples was assessed after 12 hours overnight fasting for the determination of hematological and biochemical variables, which were measured using an automated hematology analyzer by standard methods.
Time frame: at the 48th week.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.