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Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/70835

Type: Journal article
Title: Fetal and maternal candidate single nucleotide polymorphism associations with Cerebral Palsy: a case-control study
Author: O'Callaghan, M.
MacLennan, A.
Gibson, C.
McMichael, G.
Haan, E.
Broadbent, J.
Goldwater, P.
Painter, J.
Montgomery, G.
Dekker, G.
Citation: Pediatrics, 2012; 129(2):E414-E423
Publisher: Amer Acad Pediatrics
Issue Date: 2012
ISSN: 0031-4005
1098-4275
Organisation: Australian Collaborative Cerebral Palsy Research Group
Statement of
Responsibility: 
Michael E. O’Callaghan, Alastair H. MacLennan, Catherine S. Gibson, Gai L. McMichael, Eric A. Haan, Jessica L. Broadbent, Paul N. Goldwater, Jodie N. Painter, Grant W. Montgomery and Gus A. Dekker for the Australian Collaborative Cerebral Palsy Research Group
Abstract: OBJECTIVE: Previous studies have suggested associations between certain genetic variants and susceptibility to cerebral palsy (CP). This study was designed to assess established and novel maternal and child genetic and epidemiologic risk factors for CP along with their interactions. METHODS: DNA from 587 case and 1154 control mother-child pairs was analyzed. A panel of 35 candidate single nucleotide polymorphisms (SNPs) were examined and included SNPs in genes associated with (1) thrombophilia, (2) inflammation, and (3) risk factors for CP (eg, preterm birth). Comparisons were specified a priori and made by using a χ(2) test. RESULTS: There were 40 fetal and 28 maternal associations with CP when analyzed by CP subtype, gestational age, genotypes of apolipoprotein E, and haplotypes of mannose-binding-lectin. After Bonferroni correction for multiple testing, no fetal or maternal candidate SNP was associated with CP or its subtypes. Only fetal carriage of prothrombin gene mutation remained marginally associated with hemiplegia in term infants born to mothers with a reported infection during pregnancy. Odds ratio directions of fetal SNP associations were compared with previously reported studies and confirmed no trend toward association. CONCLUSIONS: Except for the prothrombin gene mutation, individual maternal and fetal SNPs in our candidate panel were not found to be associated with CP outcome. Past reported SNP associations with CP were not confirmed, possibly reflecting type I error from small numbers and multiple testing in the original reports.
Keywords: Cerebral palsy; candidate gene; SNP association; case-control
Rights: Copyright © 2012 by the American Academy of Pediatrics
RMID: 0020116737
DOI: 10.1542/peds.2011-0739
Appears in Collections:Cerebral Palsy Research Group publications
Obstetrics and Gynaecology publications
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