Intra-abdominal fat is related to metabolic syndrome and non-alcoholic fat liver disease in obese youth
Previous studies have shown an association between adiposity, especially intra-abdominal adipose tissue, and hemodynamic/metabolic comorbidities in adults, however it is not clear in pediatric population. The aim of the study was to analyze the relationship between non-alcoholic fatty liver disease...
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creator | Silveira, Loreana Sanches Monteiro, Paula Alves Antunes, Bárbara de Moura Mello Seraphim, Patrícia Monteiro Fernandes, Rômulo Araújo Christofaro, Diego G Destro Freitas Júnior, Ismael F |
description | Previous studies have shown an association between adiposity, especially intra-abdominal adipose tissue, and hemodynamic/metabolic comorbidities in adults, however it is not clear in pediatric population. The aim of the study was to analyze the relationship between non-alcoholic fatty liver disease (NAFLD) and components of metabolic syndrome (MS) with values of intra-abdominal (IAAT) and subcutaneous (SCAT) adipose tissue in obese children and adolescents.
Cross-sectional study.
182 obese sedentary children and adolescents (aged 6 to 16 y), identified by the body mass index (BMI).
Body composition and trunk fat by dual-energy X-ray absorptiometry- DXA; lipid profile, blood pressure and pubertal stage were also assessed. NAFLD was classified as absent (0), mild (1), moderate (2) and severe (3), and intra-abdominal and subcutaneous abdominal fat thickness were identified by ultrasound. The MS was identified according to the cut offs proposed by World Health Organization adapted for children and adolescents. The chi-square test was used to compare categorical variables, and the binary logistic regression indicated the magnitude of the associations adjusted by potential cofounders (sex, age, maturation, NAFLD and HOMA-IR).
Higher quartile of SCAT was associated with elevated blood pressure (p = 0.015), but not associated with NAFLD (p = 0.665). Higher IAAT was positively associated with increased dyslipidemia (p = 0.001), MS (p = 0.013) and NAFLD (p = 0.005). Intermediate (p = 0.007) and highest (p = 0.001) quartile of IAAT were also associated with dyslipidemia, independently of age, sex, maturation, NAFLD and HOMA-IR (homeostatic model assessment-insulin resistance).
Obese children and adolescents, with higher IAAT are more prone to develop MS and NAFLD than those with higher values of SCAT, independent of possible confounding variables. |
doi_str_mv | 10.1186/1471-2431-13-115 |
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Cross-sectional study.
182 obese sedentary children and adolescents (aged 6 to 16 y), identified by the body mass index (BMI).
Body composition and trunk fat by dual-energy X-ray absorptiometry- DXA; lipid profile, blood pressure and pubertal stage were also assessed. NAFLD was classified as absent (0), mild (1), moderate (2) and severe (3), and intra-abdominal and subcutaneous abdominal fat thickness were identified by ultrasound. The MS was identified according to the cut offs proposed by World Health Organization adapted for children and adolescents. The chi-square test was used to compare categorical variables, and the binary logistic regression indicated the magnitude of the associations adjusted by potential cofounders (sex, age, maturation, NAFLD and HOMA-IR).
Higher quartile of SCAT was associated with elevated blood pressure (p = 0.015), but not associated with NAFLD (p = 0.665). Higher IAAT was positively associated with increased dyslipidemia (p = 0.001), MS (p = 0.013) and NAFLD (p = 0.005). Intermediate (p = 0.007) and highest (p = 0.001) quartile of IAAT were also associated with dyslipidemia, independently of age, sex, maturation, NAFLD and HOMA-IR (homeostatic model assessment-insulin resistance).
Obese children and adolescents, with higher IAAT are more prone to develop MS and NAFLD than those with higher values of SCAT, independent of possible confounding variables.</description><identifier>ISSN: 1471-2431</identifier><identifier>EISSN: 1471-2431</identifier><identifier>DOI: 10.1186/1471-2431-13-115</identifier><identifier>PMID: 23919592</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Absorptiometry, Photon ; Adipose tissues ; Adiposity ; Adolescent ; Analysis ; Body mass index ; Child ; Cholesterol ; Comorbidity ; Complications and side effects ; Cross-Sectional Studies ; Development and progression ; Fatty liver ; Fatty Liver - diagnosis ; Fatty Liver - etiology ; Fatty Liver - pathology ; Female ; Humans ; Insulin resistance ; Intra-Abdominal Fat - pathology ; Logistic Models ; Male ; Metabolic syndrome ; Metabolic Syndrome - diagnosis ; Metabolic Syndrome - etiology ; Metabolic Syndrome - pathology ; Metabolic syndrome X ; Multivariate Analysis ; Non-alcoholic Fatty Liver Disease ; Obesity ; Obesity in adolescence ; Pediatric Obesity - complications ; Pediatric Obesity - pathology ; Physiological aspects ; Risk Factors ; Studies ; Subcutaneous Fat - pathology</subject><ispartof>BMC pediatrics, 2013-08, Vol.13 (1), p.115-115, Article 115</ispartof><rights>COPYRIGHT 2013 BioMed Central Ltd.</rights><rights>2013 Silveira et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2013 Silveira et al.; licensee BioMed Central Ltd. 2013 Silveira et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b615t-e15ac30ccb33b1ebf853ce67ffa480093c28f92709d4c9963836059581e8004f3</citedby><cites>FETCH-LOGICAL-b615t-e15ac30ccb33b1ebf853ce67ffa480093c28f92709d4c9963836059581e8004f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751250/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751250/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23919592$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Silveira, Loreana Sanches</creatorcontrib><creatorcontrib>Monteiro, Paula Alves</creatorcontrib><creatorcontrib>Antunes, Bárbara de Moura Mello</creatorcontrib><creatorcontrib>Seraphim, Patrícia Monteiro</creatorcontrib><creatorcontrib>Fernandes, Rômulo Araújo</creatorcontrib><creatorcontrib>Christofaro, Diego G Destro</creatorcontrib><creatorcontrib>Freitas Júnior, Ismael F</creatorcontrib><title>Intra-abdominal fat is related to metabolic syndrome and non-alcoholic fat liver disease in obese youth</title><title>BMC pediatrics</title><addtitle>BMC Pediatr</addtitle><description>Previous studies have shown an association between adiposity, especially intra-abdominal adipose tissue, and hemodynamic/metabolic comorbidities in adults, however it is not clear in pediatric population. The aim of the study was to analyze the relationship between non-alcoholic fatty liver disease (NAFLD) and components of metabolic syndrome (MS) with values of intra-abdominal (IAAT) and subcutaneous (SCAT) adipose tissue in obese children and adolescents.
Cross-sectional study.
182 obese sedentary children and adolescents (aged 6 to 16 y), identified by the body mass index (BMI).
Body composition and trunk fat by dual-energy X-ray absorptiometry- DXA; lipid profile, blood pressure and pubertal stage were also assessed. NAFLD was classified as absent (0), mild (1), moderate (2) and severe (3), and intra-abdominal and subcutaneous abdominal fat thickness were identified by ultrasound. The MS was identified according to the cut offs proposed by World Health Organization adapted for children and adolescents. The chi-square test was used to compare categorical variables, and the binary logistic regression indicated the magnitude of the associations adjusted by potential cofounders (sex, age, maturation, NAFLD and HOMA-IR).
Higher quartile of SCAT was associated with elevated blood pressure (p = 0.015), but not associated with NAFLD (p = 0.665). Higher IAAT was positively associated with increased dyslipidemia (p = 0.001), MS (p = 0.013) and NAFLD (p = 0.005). Intermediate (p = 0.007) and highest (p = 0.001) quartile of IAAT were also associated with dyslipidemia, independently of age, sex, maturation, NAFLD and HOMA-IR (homeostatic model assessment-insulin resistance).
Obese children and adolescents, with higher IAAT are more prone to develop MS and NAFLD than those with higher values of SCAT, independent of possible confounding variables.</description><subject>Absorptiometry, Photon</subject><subject>Adipose tissues</subject><subject>Adiposity</subject><subject>Adolescent</subject><subject>Analysis</subject><subject>Body mass index</subject><subject>Child</subject><subject>Cholesterol</subject><subject>Comorbidity</subject><subject>Complications and side effects</subject><subject>Cross-Sectional Studies</subject><subject>Development and progression</subject><subject>Fatty liver</subject><subject>Fatty Liver - diagnosis</subject><subject>Fatty Liver - etiology</subject><subject>Fatty Liver - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Insulin resistance</subject><subject>Intra-Abdominal Fat - pathology</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Metabolic syndrome</subject><subject>Metabolic Syndrome - diagnosis</subject><subject>Metabolic Syndrome - etiology</subject><subject>Metabolic Syndrome - pathology</subject><subject>Metabolic syndrome X</subject><subject>Multivariate Analysis</subject><subject>Non-alcoholic Fatty Liver Disease</subject><subject>Obesity</subject><subject>Obesity in adolescence</subject><subject>Pediatric Obesity - complications</subject><subject>Pediatric Obesity - pathology</subject><subject>Physiological aspects</subject><subject>Risk Factors</subject><subject>Studies</subject><subject>Subcutaneous Fat - pathology</subject><issn>1471-2431</issn><issn>1471-2431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFklFrFDEQxxdRbK2--yQBQXzZmtlks5sXoRytFgq-6HPIZmfvUrJJ3WQL9-2b9ep5JxXJQ4aZ3_wzmZmieAv0HKAVn4A3UFacQQmsBKifFad71_MD-6R4FeMtpdC0XLwsTiomQdayOi3W1z5NutRdH0brtSODTsRGMqHTCXuSAhkx6S44a0jc-n4KIxLte-KDL7UzYfMrtKQ5e48T6W1EHZFYT0KH2diGOW1eFy8G7SK-ebzPih9Xl99XX8ubb1-uVxc3ZSegTiVCrQ2jxnSMdYDd0NbMoGiGQfOWUslM1Q6yaqjsuZFSsJYJWsu6BcxhPrCz4vNO927uRuwNLt9z6m6yo562KmirjiPebtQ63CvW1FDVNAusdgKdDf8QOI6YMKql0WpptAKm8hyyysfHMqbwc8aY1GijQee0xzBHBa1s8ouyFf9HeSUoVEAho-__Qm_DPOWp7SjBG8bbP9RaO1TWDyHXaRZRdVEzLkBIxjN1_gSVT4-jNcHjYLP_KOHDQcIGtUubGNycbPDxGKQ70EwhxgmHffOAqmVtn2rXu8Op7RN-7yl7AKK_5bY</recordid><startdate>20130807</startdate><enddate>20130807</enddate><creator>Silveira, Loreana Sanches</creator><creator>Monteiro, Paula Alves</creator><creator>Antunes, Bárbara de Moura Mello</creator><creator>Seraphim, Patrícia Monteiro</creator><creator>Fernandes, Rômulo Araújo</creator><creator>Christofaro, Diego G Destro</creator><creator>Freitas Júnior, Ismael F</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7TS</scope><scope>5PM</scope></search><sort><creationdate>20130807</creationdate><title>Intra-abdominal fat is related to metabolic syndrome and non-alcoholic fat liver disease in obese youth</title><author>Silveira, Loreana Sanches ; Monteiro, Paula Alves ; Antunes, Bárbara de Moura Mello ; Seraphim, Patrícia Monteiro ; Fernandes, Rômulo Araújo ; Christofaro, Diego G Destro ; Freitas Júnior, Ismael F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b615t-e15ac30ccb33b1ebf853ce67ffa480093c28f92709d4c9963836059581e8004f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Absorptiometry, Photon</topic><topic>Adipose tissues</topic><topic>Adiposity</topic><topic>Adolescent</topic><topic>Analysis</topic><topic>Body mass index</topic><topic>Child</topic><topic>Cholesterol</topic><topic>Comorbidity</topic><topic>Complications and side effects</topic><topic>Cross-Sectional Studies</topic><topic>Development and progression</topic><topic>Fatty liver</topic><topic>Fatty Liver - diagnosis</topic><topic>Fatty Liver - etiology</topic><topic>Fatty Liver - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Insulin resistance</topic><topic>Intra-Abdominal Fat - pathology</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Metabolic syndrome</topic><topic>Metabolic Syndrome - diagnosis</topic><topic>Metabolic Syndrome - etiology</topic><topic>Metabolic Syndrome - pathology</topic><topic>Metabolic syndrome X</topic><topic>Multivariate Analysis</topic><topic>Non-alcoholic Fatty Liver Disease</topic><topic>Obesity</topic><topic>Obesity in adolescence</topic><topic>Pediatric Obesity - complications</topic><topic>Pediatric Obesity - pathology</topic><topic>Physiological aspects</topic><topic>Risk Factors</topic><topic>Studies</topic><topic>Subcutaneous Fat - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silveira, Loreana Sanches</creatorcontrib><creatorcontrib>Monteiro, Paula Alves</creatorcontrib><creatorcontrib>Antunes, Bárbara de Moura Mello</creatorcontrib><creatorcontrib>Seraphim, Patrícia Monteiro</creatorcontrib><creatorcontrib>Fernandes, Rômulo Araújo</creatorcontrib><creatorcontrib>Christofaro, Diego G Destro</creatorcontrib><creatorcontrib>Freitas Júnior, Ismael F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Physical Education Index</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silveira, Loreana Sanches</au><au>Monteiro, Paula Alves</au><au>Antunes, Bárbara de Moura Mello</au><au>Seraphim, Patrícia Monteiro</au><au>Fernandes, Rômulo Araújo</au><au>Christofaro, Diego G Destro</au><au>Freitas Júnior, Ismael F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intra-abdominal fat is related to metabolic syndrome and non-alcoholic fat liver disease in obese youth</atitle><jtitle>BMC pediatrics</jtitle><addtitle>BMC Pediatr</addtitle><date>2013-08-07</date><risdate>2013</risdate><volume>13</volume><issue>1</issue><spage>115</spage><epage>115</epage><pages>115-115</pages><artnum>115</artnum><issn>1471-2431</issn><eissn>1471-2431</eissn><abstract>Previous studies have shown an association between adiposity, especially intra-abdominal adipose tissue, and hemodynamic/metabolic comorbidities in adults, however it is not clear in pediatric population. The aim of the study was to analyze the relationship between non-alcoholic fatty liver disease (NAFLD) and components of metabolic syndrome (MS) with values of intra-abdominal (IAAT) and subcutaneous (SCAT) adipose tissue in obese children and adolescents.
Cross-sectional study.
182 obese sedentary children and adolescents (aged 6 to 16 y), identified by the body mass index (BMI).
Body composition and trunk fat by dual-energy X-ray absorptiometry- DXA; lipid profile, blood pressure and pubertal stage were also assessed. NAFLD was classified as absent (0), mild (1), moderate (2) and severe (3), and intra-abdominal and subcutaneous abdominal fat thickness were identified by ultrasound. The MS was identified according to the cut offs proposed by World Health Organization adapted for children and adolescents. The chi-square test was used to compare categorical variables, and the binary logistic regression indicated the magnitude of the associations adjusted by potential cofounders (sex, age, maturation, NAFLD and HOMA-IR).
Higher quartile of SCAT was associated with elevated blood pressure (p = 0.015), but not associated with NAFLD (p = 0.665). Higher IAAT was positively associated with increased dyslipidemia (p = 0.001), MS (p = 0.013) and NAFLD (p = 0.005). Intermediate (p = 0.007) and highest (p = 0.001) quartile of IAAT were also associated with dyslipidemia, independently of age, sex, maturation, NAFLD and HOMA-IR (homeostatic model assessment-insulin resistance).
Obese children and adolescents, with higher IAAT are more prone to develop MS and NAFLD than those with higher values of SCAT, independent of possible confounding variables.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>23919592</pmid><doi>10.1186/1471-2431-13-115</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Absorptiometry, Photon Adipose tissues Adiposity Adolescent Analysis Body mass index Child Cholesterol Comorbidity Complications and side effects Cross-Sectional Studies Development and progression Fatty liver Fatty Liver - diagnosis Fatty Liver - etiology Fatty Liver - pathology Female Humans Insulin resistance Intra-Abdominal Fat - pathology Logistic Models Male Metabolic syndrome Metabolic Syndrome - diagnosis Metabolic Syndrome - etiology Metabolic Syndrome - pathology Metabolic syndrome X Multivariate Analysis Non-alcoholic Fatty Liver Disease Obesity Obesity in adolescence Pediatric Obesity - complications Pediatric Obesity - pathology Physiological aspects Risk Factors Studies Subcutaneous Fat - pathology |
title | Intra-abdominal fat is related to metabolic syndrome and non-alcoholic fat liver disease in obese youth |
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