0 419

Cited 32 times in

Apolipoprotein B/A1 ratio is associated with free androgen index and visceral adiposity and may be an indicator of metabolic syndrome in male children and adolescents

DC Field Value Language
dc.contributor.author이용호-
dc.date.accessioned2018-05-10T06:33:27Z-
dc.date.available2018-05-10T06:33:27Z-
dc.date.issued2011-
dc.identifier.issn0300-0664-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/158191-
dc.description.abstractOBJECTIVE : A high apolipoprotein B/apolipoprotein A1 (apoB/A1) ratio is strongly associated with cardiometabolic diseases. However, few studies have examined this ratio in children and adolescents. The aim of our study was to determine significant factors related to the apoB/A1 ratio and examine its association with paediatric metabolic syndrome. PATIENTS AND METHODS : Sixty-seven male children and adolescents were recruited. We measured anthropometric parameters, fat areas by abdominal computed tomography, fasting glucose, insulin, lipid profiles, apoB, apoA1, adiponectin, free androgen index (FAI) and oestradiol. RESULTS : Thirty per cent of participants (n = 20) were identified as having paediatric metabolic syndrome. The apoB/A1 ratio was significantly correlated with BMI z-score, waist circumference, waist-to-hip ratio (WHR), waist-to-height ratio, abdominal fat areas, total cholesterol, triglycerides, LDL-cholesterol, HDL-cholesterol, adiponectin and leptin. In addition to lipid profiles, WHR was identified as a significant independent variable correlated with the apoB/A1 ratio. Obese boys with a high FAI (>75th percentile) had significantly lower adiponectin and higher apoB/A1 ratios than those with a low FAI. The apoB/A1 ratio was higher in subjects with high visceral fat (>50th percentile) and a high FAI when compared with subjects with low visceral fat and a low FAI. The prevalence of paediatric metabolic syndrome was significantly associated with increasing tertiles of the apoB/A1 ratio (highest tertile; odds ratio = 18·8 [95% confidence interval = 1·8-198·8], P < 0·05). CONCLUSION : ApoB/A1 ratio was significantly higher in viscerally obese male children and adolescents with high levels of FAI and was associated with increased frequency of paediatric metabolic syndrome.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherBlackwell Publishing-
dc.relation.isPartOfCLINICAL ENDOCRINOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdolescent-
dc.subject.MESHAndrogens/blood*-
dc.subject.MESHAnthropometry-
dc.subject.MESHApolipoprotein A-I/blood*-
dc.subject.MESHApolipoproteins B/blood*-
dc.subject.MESHBiomarkers-
dc.subject.MESHBody Composition-
dc.subject.MESHChild-
dc.subject.MESHHumans-
dc.subject.MESHIntra-Abdominal Fat-
dc.subject.MESHMale-
dc.subject.MESHMetabolic Syndrome/blood-
dc.subject.MESHMetabolic Syndrome/diagnosis*-
dc.titleApolipoprotein B/A1 ratio is associated with free androgen index and visceral adiposity and may be an indicator of metabolic syndrome in male children and adolescents-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Internal Medicine-
dc.contributor.googleauthorYong-ho Lee-
dc.contributor.googleauthorSung Hee Choi-
dc.contributor.googleauthorKwan Woo Lee-
dc.contributor.googleauthorDae Jung Kim-
dc.identifier.doi10.1111/j.1365-2265.2010.03953.x-
dc.contributor.localIdA02989-
dc.relation.journalcodeJ00571-
dc.identifier.eissn1365-2265-
dc.identifier.pmid21138461-
dc.identifier.urlhttp://onlinelibrary.wiley.com/doi/10.1111/j.1365-2265.2010.03953.x/abstract-
dc.contributor.alternativeNameLee, Yong Ho-
dc.contributor.affiliatedAuthorLee, Yong Ho-
dc.citation.volume74-
dc.citation.number5-
dc.citation.startPage579-
dc.citation.endPage586-
dc.identifier.bibliographicCitationCLINICAL ENDOCRINOLOGY, Vol.74(5) : 579-586, 2011-
dc.identifier.rimsid48945-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.