Evaluation of The Effectiveness of Ellagic Acid on Liver Steatosis in Overweight/Obese Non-Alcoholic Fatty Liver Disease Patients: Study Protocol for A Randomized Controlled Trial | ||
| Journal of Nutrition,Fasting and Health | ||
| مقالات آماده انتشار، پذیرفته شده، انتشار آنلاین از تاریخ 13 دی 1402 | ||
| نوع مقاله: Protocol Study | ||
| شناسه دیجیتال (DOI): 10.22038/jnfh.2024.77183.1492 | ||
| نویسندگان | ||
| Mohammad Mahmoudi Azar1؛ Motahare Bateni1؛ Fateme Tafaghodi Piadeh Gheibi2؛ farnood rajabzadeh3؛ Ali Jafarzadeh Esfahani4؛ Ladan Goshayeshi5، 6؛ Vahidreza Askari* 7، 8؛ Mohsen Nematy1، 4 | ||
| 1Department of Nutrition, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. | ||
| 2Department of Nutrition, Varastegan Institute for Medical Sciences, Mashhad, Iran. | ||
| 3Department of Radiology, Mashhad Medical Sciences Branch, Islamic Azad University, Mashhad, Iran. | ||
| 4Metabolic Syndrome Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. | ||
| 5Department of Gastroenterology and Hepatology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. | ||
| 6Gastroenterology and Hepatology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. | ||
| 7Pharmacological Research Center of Medicinal Plants, Mashhad University of Medical Sciences, Mashhad, Iran. | ||
| 8Neurogenic Inflammation Research Centre, Mashhad University of Medical Sciences, Mashhad, Iran. | ||
| چکیده | ||
| Introduction: Non-alcoholic fatty liver (NAFLD) is a condition that can lead to liver fibrosis, cirrhosis, and hepatocellular carcinoma. There is no definite treatment for NAFLD. Ellagic acid (EA) is natural polyphenol with proven pharmacological properties, but its effectiveness on NAFLD in patients is not clear. The aim of this study is to evaluate the effect of ellagic acid on liver fibrosis in NAFLD patients. Method: This randomized, double-blind, controlled, and parallel clinical trial will be conducted on 60 patients with NAFLD (grade 2 or above) who will be allocated in intervention or placebo groups with 1:1 ratio. The intervention group will receive capsules containing 200 mg EA while the placebo group will receive avicel as placebo for 8 weeks. Body composition and anthropometric indices will be measured at baseline, end of 4th and 8th week. Transient elastography, 3-day food record, International Physical Activity Questionnaire (IPAQ), and laboratory tests (CBC/diff, uric acid, creatinine, lipid profile (total cholesterol, triglyceride [TG], low-density lipoprotein cholesterol [LDL-c], and high-density lipoprotein cholesterol [HDL-c]), aspartate aminotransferase [AST], alanine aminotransferase [ALT], alkaline phosphatase [ALP], and gamma-glutamyl transpeptidase [GGT], albumin, high sensitive C-reactive protein [hs-CRP] and insulin) will be performed for both groups at baseline and end of the study. Conclusion: We expect that 200 mg EA ellagic acid administration for 8 weeks will improve liver steatosis, clinical and paraclinical outcomes in NAFLD patients. | ||
| کلیدواژهها | ||
| Non-alcoholic fatty liver؛ Ellagic acid؛ Transient elastography؛ Anthropometric insides؛ Liver enzymes | ||
| مراجع | ||
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