Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/107560
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dc.contributorDepartment of Health Technology and Informatics-
dc.creatorChiyanika, C-
dc.creatorChan, DFY-
dc.creatorHui, SCN-
dc.creatorSo, HK-
dc.creatorDeng, M-
dc.creatorYeung, DKW-
dc.creatorNelson, EAS-
dc.creatorChu, WCW-
dc.date.accessioned2024-07-04T01:54:45Z-
dc.date.available2024-07-04T01:54:45Z-
dc.identifier.issn2047-6302-
dc.identifier.urihttp://hdl.handle.net/10397/107560-
dc.language.isoenen_US
dc.publisherWiley-Blackwell Publishing Ltd.en_US
dc.rights© 2020 The Authors. Pediatric Obesity published by John Wiley & Sons Ltd on behalf of World Obesity Federationen_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following publication Chiyanika C, Chan DFY, Hui SCN, et al. The relationship between pancreas steatosis and the risk of metabolic syndrome and insulin resistance in Chinese adolescents with concurrent obesity and non-alcoholic fatty liver disease. Pediatric Obesity. 2020; 15:e12653 is available at https://doi.org/10.1111/ijpo.12653.en_US
dc.subjectFatty liveren_US
dc.subjectInsulin resistanceen_US
dc.subjectMagnetic resonance imagingen_US
dc.subjectMetabolic syndromeen_US
dc.subjectPancreasen_US
dc.titleThe relationship between pancreas steatosis and the risk of metabolic syndrome and insulin resistance in Chinese adolescents with concurrent obesity and non-alcoholic fatty liver diseaseen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume15-
dc.identifier.issue9-
dc.identifier.doi10.1111/ijpo.12653-
dcterms.abstractBackground: The incidence of childhood obesity and associated comorbidities are on an increasing trend worldwide. More than 340 million children and adolescents aged between 5 and 19 years old were overweight or had obesity in 2016, from which over 124 million children and adolescents (6% of girls and 8% of boys) had obesity.-
dcterms.abstractObjective: To describe the relationship between pancreas steatosis, body fat and the risk of metabolic syndrome, insulin resistance in Hong Kong Chinese adolescents with both obesity and non-alcoholic fatty liver disease (NAFLD).-
dcterms.abstractMethods: Fifty two adolescents with obesity and NAFLD were analysed (14-18 years), stratified into fatty and non-fatty pancreas groups using chemical shift encoded MRI-pancreas proton density fat fraction ≥5%. Pancreatic, abdominal subcutaneous adipose tissue (SAT)/visceral adipose tissue (VAT) volumes, biochemical and anthropometric parameters were measured. Mann-Whitney U test, multiple linear/binary logistic regression analyses and odds ratios were used.-
dcterms.abstractResults: Fifty percent had fatty pancreas, 38% had metabolic syndrome and 81% had insulin resistance. Liver proton density fat fraction (PDFF) and VAT were independent predictors of insulin resistance (P =.006,.016). Pancreas and liver PDFF were both independent predictors of beta cells dysfunction (P =.015,.050) and metabolic syndrome (P =.021,.041). Presence of fatty pancreas in obesity was associated with insulin resistance (OR = 1.58, 95% CI = 0.39-6.4) and metabolic syndrome (OR = 1.70, 95% CI = 0.53-5.5).-
dcterms.abstractConclusion: A significant causal relationship exists between fatty pancreas, fatty liver, body fat and the risk of developing metabolic syndrome and insulin resistance.-
dcterms.abstractKey Points: Fatty pancreas is a common finding in adolescents with obesity, with a prevalence rate of 50% in this study cohort.-
dcterms.abstractLiver PDFF and VAT are independent predictors of insulin resistance while pancreas PDFF and liver PDFF are independent predictors of both beta cells dysfunction and metabolic syndrome.-
dcterms.abstractPresence of fatty pancreas at imaging should not be considered as a benign finding but rather as an imaging biomarker of emerging pancreatic metabolic and endocrine dysfunction.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationPediatric obesity, Sept. 2020, v. 15, no. 9, e12653-
dcterms.isPartOfPediatric obesity-
dcterms.issued2020-09-
dc.identifier.scopus2-s2.0-85083966268-
dc.identifier.pmid32351030-
dc.identifier.eissn2047-6310-
dc.identifier.artne12653-
dc.description.validate202407_ada-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera2932 [non PolyU]en_US
dc.identifier.SubFormID48819en_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextDirect Grant for Research, Grant/Award Number: 2014.1.065; Health and Medical Research Fund, Food and Health Bureau, Grant/Award Number: 11122981en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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