Analysis of association of gene variants with obesity traits in New Zealand European children at 6 years of age

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dc.contributor.author Krishnan, Mohanraj en
dc.contributor.author Thompson, John en
dc.contributor.author Mitchell, Edwin en
dc.contributor.author Murphy, Rinki en
dc.contributor.author McCowan, Lesley en
dc.contributor.author Shelling, Andrew en
dc.contributor.author On Behalf Of The Children Of Scope Study Group, G en
dc.date.accessioned 2017-09-12T03:30:57Z en
dc.date.issued 2017-08 en
dc.identifier.citation Molecular BioSystems 13(8):1524-1533 Aug 2017 en
dc.identifier.issn 1742-206X en
dc.identifier.uri http://hdl.handle.net/2292/35620 en
dc.description.abstract Childhood obesity is a public health problem, which is associated with a long-term increased risk of cardiovascular disease and premature mortality. Several gene variants have previously been identified that have provided novel insights into biological factors that contribute to the development of obesity. As obesity tracks through childhood into adulthood, identification of the genetic factors for obesity in early life is important. The objective of this study was to identify putative associations between genetic variants and obesity traits in children at 6 years of age. We recruited 1208 children of mothers from the New Zealand centre of the international Screening for Pregnancy Endpoints (SCOPE) study. Eighty common genetic variants associated with obesity traits were evaluated by the Sequenom assay. Body mass index standardised scores (BMI z-scores) and percentage body fat (PBF; measured by bio-impedance assay (BIA)) were used as anthropometric measures of obesity. A positive correlation was found between BMI z-scores and PBF (p < 0.001, r = 0.756). Two subsets of gene variants were associated with BMI z-scores (HOXB5-rs9299, SH2B1-rs7498665, NPC1-rs1805081 and MSRA-rs545854) and PBF (TMEM18-rs6548238, NPY-rs17149106, ETV-rs7647305, NPY-rs16139, TIMELESS-rs4630333, FTO-rs9939609, UCP2-rs659366, MAP2K5-rs2241423 and FAIM2-rs7138803) in the genotype models. However, there was an absence of overlapping association between any of the gene variants with BMI z-scores and PBF. A further five variants were associated with BMI z-scores (TMEM18-rs6548238, FTO-rs9939609 and MC4R-rs17782313) and PBF (SH2B1-rs7498665 and FTO-rs1421085) once separated by genetic models (additive, recessive and dominant) of inheritance. This study has identified significant associations between numerous gene variants selected on the basis of prior association with obesity and obesity traits in New Zealand European children. en
dc.format.medium Print en
dc.language eng en
dc.publisher RSC en
dc.relation.ispartofseries Molecular BioSystems en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.title Analysis of association of gene variants with obesity traits in New Zealand European children at 6 years of age en
dc.type Journal Article en
dc.identifier.doi 10.1039/c7mb00104e en
pubs.issue 8 en
pubs.begin-page 1524 en
pubs.volume 13 en
dc.rights.holder Copyright: RSC en
dc.identifier.pmid 28636007 en
pubs.end-page 1533 en
pubs.publication-status Published en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 632403 en
pubs.org-id Medical and Health Sciences en
pubs.org-id School of Medicine en
pubs.org-id Medicine Department en
pubs.org-id Obstetrics and Gynaecology en
pubs.org-id Paediatrics Child & Youth Hlth en
pubs.org-id Science en
pubs.org-id Science Research en
pubs.org-id Maurice Wilkins Centre (2010-2014) en
dc.identifier.eissn 1742-2051 en
pubs.record-created-at-source-date 2017-09-12 en
pubs.dimensions-id 28636007 en


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