Nonalcoholic Fatty Liver Disease in Morbidly Obese Patients
Mo kle
Abstrè
Deskripsyon
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.
Dat
Dènye verifye: | 08/31/2016 |
Premye Soumèt: | 12/21/2016 |
Enskripsyon Estimasyon Soumèt: | 08/14/2019 |
Premye afiche: | 08/15/2019 |
Dènye Mizajou Soumèt: | 08/14/2019 |
Dènye Mizajou afiche: | 08/15/2019 |
Dat aktyèl kòmanse etid la: | 09/30/2016 |
Dat Estimasyon Prensipal Estimasyon an: | 06/30/2020 |
Dat estime fini etid la: | 06/30/2021 |
Kondisyon oswa maladi
Entèvansyon / tretman
Procedure: Morbidly obese patients with NAFLD
Faz
Gwoup bra
Bra | Entèvansyon / tretman |
---|---|
Morbidly obese patients with NAFLD Morbidly obese patient with Nonalcoholic fatty liver disease. 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 wedge liver biopsy under laparoscopic guidance. The diagnosis of NASH would be made histologically. | Procedure: Morbidly obese patients with NAFLD During bariatric surgery, all patients would undergo a wedge liver biopsy under laparoscopic guidance. |
Kritè kalifikasyon yo
Laj ki kalifye pou etid | 20 Years Pou 20 Years |
Sèks ki kalifye pou etid | All |
Metòd echantiyonaj | Probability Sample |
Aksepte Volontè Healthy | Wi |
Kritè | Inclusion Criteria: - Adult male and female Morbidly obese patients age 20-65 years with BMI over 37.5 kg/m^2, or BMI over 32.5 kg/m^2 with comorbidity other than diabetes (hypertension, NASH, dyslipidemia, obstructive sleep apnea, osteoarthritis joint…etc.) or BMI over 27.5 kg/m^2 with poor control diabetes undergoing bariatric surgery Exclusion Criteria: - The presence of end organ damage - Previous bariatric surgery - Women who are pregnant or nursing - Prolonged exposure to known hepatotoxins such as alcohol or drugs - Concurrent hepatitis B virus, hepatitis C virus, hepatitis D virus, or human immunodeficiency virus infection - Concurrent autoimmune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis - Wilson disease or hemochromatosis |
Rezilta
Mezi Rezilta Prensipal yo
1. Change from body mass index (BMI) at 12 months after surgery [pre-surgery and 12 months after surgery]
Mezi Rezilta Segondè
1. Change from alanine aminotransferase at 12 months after surgery [pre-surgery and 12 months after surgery]
2. Change from aspartate aminotransferase at 12 months after surgery [pre-surgery and 12 months after surgery]
3. Nonalcoholic steatohepatitis [1 day of surgery]