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      Is Open Access
      BMC Gastroenterology
      BioMed Central
      fatty liver disease, risk factors, metabolic syndrome, obesity

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          Abstract

          Background

          Nonalcoholic fatty liver disease (NAFLD) is a common problem across the world. We aimed to determine the prevalence of NAFLD and its associations in Sri Lankan adolescents living in an urban Sri Lankan community .

          Method

          The study population consisted of the birth cohort of the year 2000, residing in the Ragama Medical Officer of Health area. Socio-demographic and anthropometric data [anthropometric measurements, blood pressure and total body fat distribution] of these adolescents were collected by trained data collectors. Fasting blood sugar, serum insulin, fasting serum lipids and serum alanine aminotransferase (ALT) levels were measured and an abdominal ultrasound was performed. NAFLD was diagnosed on established ultrasound criteria for fatty liver and absent alcohol consumption.

          Results

          The study sample consisted of 499 adolescents [263 (51.8%) girls]. Forty two (8.4%) had NAFLD. NAFLD was significantly associated with being breast fed for less than 4 months (33.3% vs. 17.1 in controls, p = 0.02), higher waist circumference (prevalence risk ratio 83.3/20.3, 4.1, p < 0.0001), higher body mass index (prevalence risk ratio 40.5/4.8, 8.4, p < 0/0001),higher HOMA-IR (3.7 vs. 1.9, p < 0.0001) and high triglycerides (prevalence risk ratio 14.3/5.8, 2.5, p = 0.033). Adolescents with NAFLD also had a higher amount of total body fat ( p < 0.001) and subcutaneous fat ( p < 0.001) than those without NAFLD. The number of children with metabolic derangements was higher among adolescents with NAFLD than those without (85.8 vs 26.3 in controls, p < 0.0001), but a family history of hypertension, diabetes, myocardial infarction or dyslipidaemia were not.

          Conclusion

          Prevalence of NAFLD was high in Sri Lankan adolescents, and was associated with metabolic derangements, especially obesity, insulin resistance and early cessation of breast feeding.

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          Most cited references20

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          The metabolic syndrome in children and adolescents.

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            Cardiovascular risk factors and the metabolic syndrome in pediatric nonalcoholic fatty liver disease.

            Nonalcoholic fatty liver disease (NAFLD), the most common cause of liver disease in children, is associated with obesity and insulin resistance. However, the relationship between NAFLD and cardiovascular risk factors in children is not fully understood. The objective of this study was to determine the association between NAFLD and the presence of metabolic syndrome in overweight and obese children. This case-control study of 150 overweight children with biopsy-proven NAFLD and 150 overweight children without NAFLD compared rates of metabolic syndrome using Adult Treatment Panel III criteria. Cases and controls were well matched in age, sex, and severity of obesity. Children with NAFLD had significantly higher fasting glucose, insulin, total cholesterol, low-density lipoprotein cholesterol, triglycerides, systolic blood pressure, and diastolic blood pressure than overweight and obese children without NAFLD. Subjects with NAFLD also had significantly lower high-density lipoprotein cholesterol than controls. After adjustment for age, sex, race, ethnicity, body mass index, and hyperinsulinemia, children with metabolic syndrome had 5.0 (95% confidence interval, 2.6 to 9.7) times the odds of having NAFLD as overweight and obese children without metabolic syndrome. NAFLD in overweight and obese children is strongly associated with multiple cardiovascular risk factors. The identification of NAFLD in a child should prompt global counseling to address nutrition, physical activity, and avoidance of smoking to prevent the development of cardiovascular disease and type 2 diabetes.
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              Gender-specific differences in adipose distribution and adipocytokines influence adolescent nonalcoholic fatty liver disease.

              Nonalcoholic fatty liver disease (NAFLD) is a predominantly adult-diagnosed disorder. Knowledge regarding the epidemiology, phenotype, and metabolic risk factors, during adolescence is limited. We sought to determine the prevalence, phenotype, and predictors of NAFLD in 1170 community-based adolescents in the Western Australian Pregnancy Cohort (Raine) Study (the Raine Cohort) who underwent a cross-sectional assessment that included questionnaires, anthropometry, cardiovascular examinations, blood tests, and abdominal ultrasound examinations. Among the 1170 adolescents assessed, the prevalence of NAFLD was 12.8%. Females compared with males had a significantly higher prevalence of NAFLD (16.3% versus 10.1%, P = 0.004) and central obesity (33.2% versus 9.9%, P 0.05); however, in comparison with females with NAFLD, males with NAFLD had greater VAT, a more severe metabolic phenotype with higher glucose levels and systolic blood pressure and lower adiponectin and high-density lipoprotein cholesterol levels (P < 0.001 for all), and greater measures of liver injury (alanine aminotransferase and aspartate aminotransferase, P < 0.001 for all). Similarly, metabolic syndrome was more common in males than females with NAFLD (24% versus 8%, P = 0.01). Suprailiac skinfold thickness predicted NAFLD independently of the body mass index, insulin resistance, and VAT. Gender differences in adolescent NAFLD are related to differences in adipose distribution and adipocytokines. The male phenotype of NAFLD is associated with more adverse metabolic features and greater visceral adiposity than the female phenotype despite the lower prevalence of NAFLD. Copyright © 2010 American Association for the Study of Liver Diseases.
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                Author and article information

                Contributors
                +94-112-958039 , shamanr0@lycos.com
                pathmes@gmail.com
                chamilkajayasinghe@yahoo.com
                dulanik@kln.ac.lk
                akasturiratne@gmail.com
                shamiladp@hotmail.com
                maduniln@yahoo.co.uk
                anuradhadassa@gmail.com
                apdsilva@yahoo.com
                hjanakadesilva@gmail.com
                Journal
                BMC Gastroenterol
                BMC Gastroenterol
                BMC Gastroenterology
                BioMed Central (London )
                1471-230X
                29 November 2017
                29 November 2017
                2017
                : 17
                : 135
                Affiliations
                [1 ]ISNI 0000 0000 8631 5388, GRID grid.45202.31, Department of Paediatrics, Faculty of Medicine, , University of Kelaniya, ; Ragama, 11010 Sri Lanka
                [2 ]ISNI 0000 0000 8631 5388, GRID grid.45202.31, Department of Public Health, Faculty of Medicine, , University of Kelaniya, ; Ragama, 11010 Sri Lanka
                [3 ]ISNI 0000 0000 8631 5388, GRID grid.45202.31, Department of Physiology, Faculty of Medicine, , University of Kelaniya, ; Ragama, 11010 Sri Lanka
                [4 ]ISNI 0000 0000 8631 5388, GRID grid.45202.31, Department of Medicine, Faculty of Medicine, , University of Kelaniya, ; Ragama, 11010 Sri Lanka
                [5 ]ISNI 0000 0000 8631 5388, GRID grid.45202.31, Department of Pharmacology, Faculty of Medicine, , University of Kelaniya, ; Ragama, 11010 Sri Lanka
                Article
                677
                10.1186/s12876-017-0677-7
                5708084
                29187144
                8e31f363-3601-49c9-b694-714fe42b7f7f
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 1 June 2017
                : 15 November 2017
                Funding
                Funded by: Ministry of Higher Education of Sri Lanka
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2017

                Gastroenterology & Hepatology
                fatty liver disease,risk factors,metabolic syndrome,obesity
                Gastroenterology & Hepatology
                fatty liver disease, risk factors, metabolic syndrome, obesity

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