Long-Term Treatment with n-3 Polyunsaturated Fatty Acids as a Monotherapy in Children with Nonalcoholic Fatty Liver Disease
Autor: | Mehmet Boyraz, Bumin Dündar, Ferhat Cekmez, Ozgur Pirgon, Nihal Hatipoglu |
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Rok vydání: | 2015 |
Předmět: |
Male
obesity Pediatric Obesity medicine.medical_specialty Long term treatment Adolescent Endocrinology Diabetes and Metabolism medicine.medical_treatment Aspartate Aminotransferases digestive system Body Mass Index Endocrinology Insulin resistance Non-alcoholic Fatty Liver Disease Internal medicine Fatty Acids Omega-3 Nonalcoholic fatty liver disease medicine insulin sensitivity Humans Insulin Child Life Style Ultrasonography chemistry.chemical_classification biology business.industry Alanine Transaminase medicine.disease Long-Term Care digestive system diseases n-3 polyunsaturated fatty acids Diet Treatment Outcome chemistry Alanine transaminase Pediatrics Perinatology and Child Health Fatty Acids Unsaturated biology.protein Original Article Female Insulin Resistance business Body mass index Polyunsaturated fatty acid |
Zdroj: | Journal of Clinical Research in Pediatric Endocrinology |
ISSN: | 1308-5727 |
Popis: | Objective: To investigate the efficacy and safety of n-3 polyunsaturated fatty acids (PUFA) treatment in obese children with nonalcoholic fatty liver disease (NAFLD). Methods: One hundred and eight obese (body mass index (BMI) >95th percentile for age and sex) adolescents with NAFLD were included in the study. Mean age of the subjects was 13.8±3.9 years (9-17 yrs). The diagnosis of NAFLD was based on the presence of liver steatosis with high transaminases. The subjects were randomly divided into two groups. Group 1 (PUFA group, n=52) received a 1000 mg dose of PUFA once daily for 12 months and lifestyle intervention. Group 2 (placebo group, n=56) received a recommended diet plus placebo and lifestyle intervention for 12 months. Insulin resistance was evaluated by homeostasis model assessment of insulin resistance (HOMA-IR) from fasting samples. Results: BMI, fasting insulin levels and HOMA-IR values in both groups decreased significantly at the end of the study. In group 1, 67.8% of the patients had a decrease from baseline in the prevalence of steatosis (p0.05). Conclusion: Our results indicated that n-3 PUFA treatment is safe and efficacious in obese children with NAFLD and can improve ultrasonographic findings and the elevated transaminase levels. |
Databáze: | OpenAIRE |
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