Nonalcoholic Fatty Liver Disease (NAFLD) Clinical Trial
Official title:
Predictors of Improvement of Nonalcoholic Fatty Liver Disease in Morbidly Obese Patients Undergoing Bariatric Surgery
Nonalcoholic fatty liver disease (NAFLD) is the most common cause of abnormal liver biochemistry tests in the world. The prevalence rate of NAFLD has been reported to be 30-40% in men and 15-20% in women, up to 70% of people with type 2 diabetes mellitus (Type 2 DM) and even surpassing 74% to 90% of morbidly obese patients with body mass index (BMI) higher than 35 kg/m^2. The primary aims of this prospective cohort study would evaluate the predictive factors of successful weight reduction, NAFLD and nonalcoholic steatohepatitis (NASH) improvement in a large cohort of morbidly obese patients undergoing bariatric surgery. Secondarily, the diagnostic accuracy of noninvasive serum markers, doppler ultrasonography and transient elastography would be validated. Thirdly, we would conduct gene expression analyses to elucidate biological pathways underlying NAFLD phenotypes in this unique cohort.
This prospective study have been approved by Taipei Medical University-Joint Institutional
Review Board. The starting point for each patient is the day of surgery and the end-point is
1 year after the operation. During bariatric surgery, all patients would undergo a liver
biopsy under laparoscopic guidance. The diagnosis of NASH and liver fibrosis would be made
histologically. For histological examinations, liver tissue specimens would be fixed in 10 %
formalin, embedded in paraffin, and then stained with hematoxylin and eosin. A detailed
history wound be obtained including history of alcohol use, type 2 DM, hypertension, or
hyperlipidemia. Written informed consents would be obtained from all patients who would agree
to undergo surgery. A histologic assessment would be planned approximately 1 year after
bariatric surgery, if patient would agree.
In this study, excess weight loss (EWL) is defined as the excess weight over the ideal body
weight calculated according to the Metropolitan Life Weight Tables. The weight reduction
success would be defined as the percentage of excess weight loss (%EWL) >50% at the point of
1 year after operation. Diagnosis and classification of type 2 DM is based on criteria
established by the American Diabetes Association. The individual components of glycemic
control (levels of serum glucose, HbA1c levels) body weight, waist circumference, and blood
pressure would be examined. Additionally, the levels of total cholesterol, LDL-C,
triglyceride, uric acid, aspartate aminotransferase (AST),alanine aminotransferase (ALT),
albumin, insulin, C-peptide, iron, calcium, complete blood cell counts would be assessed 1
day before surgery and 12 months post-operatively. All patients would receive abdominal
ultrasonography, duplex doppler ultrasonography, transient elastography (FibroScan®) before
and 12 months after bariatric surgery. The diagnosis accuracy of transient elastography
(FibroScan®) would be validated. Transient elastography (FibroScan®) appears to be a
non-invasive, reproducible, and reliable method for predicting liver fibrosis, in patients
with hepatitis B virus, hepatitis C virus, NAFLD and alcoholic liver disease.
Patients body weight would be measured in light clothing without shoes to the nearest 0.1 kg,
and body height would be measured to the nearest 0.1 cm. BMI is calculated as weight in
kilograms divided by height in meters squared. Waist circumference would be measured midway
between the lateral lower rib margin and the superior anterior iliac crest.
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