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dc.contributor.authorPangilinan, Faith
dc.contributor.authorMolloy, Anne M
dc.contributor.authorMills, James L
dc.contributor.authorTroendle, James F
dc.contributor.authorParle-McDermott, Anne
dc.contributor.authorKay, Denise M
dc.contributor.authorBrowne, Marilyn L
dc.contributor.authorMcGrath, Emily C
dc.contributor.authorAbaan, Hatice O
dc.contributor.authorSutton, Marie
dc.contributor.authorKirke, Peadar N
dc.contributor.authorCaggana, Michele
dc.contributor.authorShane, Barry
dc.contributor.authorScott, John M
dc.contributor.authorBrody, Lawrence C
dc.date.accessioned2014-11-20T10:11:57Z
dc.date.available2014-11-20T10:11:57Z
dc.date.issued2014-10-08
dc.identifier.citationPangilinan, F. et al., 2014. Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects. BMC Medical Genetics, 15 (1) p 102en_GB
dc.identifier.urihttp://dx.doi.org/10.1186/s12881-014-0102-9
dc.identifier.urihttp://hdl.handle.net/10147/335868
dc.description.abstractAbstract Background Neural tube defects (NTDs), which are among the most common congenital malformations, are influenced by environmental and genetic factors. Low maternal folate is the strongest known contributing factor, making variants in genes in the folate metabolic pathway attractive candidates for NTD risk. Multiple studies have identified nominally significant allelic associations with NTDs. We tested whether associations detected in a large Irish cohort could be replicated in an independent population. Methods Replication tests of 24 nominally significant NTD associations were performed in racially/ethnically matched populations. Family-based tests of fifteen nominally significant single nucleotide polymorphisms (SNPs) were repeated in a cohort of NTD trios (530 cases and their parents) from the United Kingdom, and case–control tests of nine nominally significant SNPs were repeated in a cohort (190 cases, 941 controls) from New York State (NYS). Secondary hypotheses involved evaluating the latter set of nine SNPs for NTD association using alternate case–control models and NTD groupings in white, African American and Hispanic cohorts from NYS. Results Of the 24 SNPs tested for replication, ADA rs452159 and MTR rs10925260 were significantly associated with isolated NTDs. Of the secondary tests performed, ARID1A rs11247593 was associated with NTDs in whites, and ALDH1A2 rs7169289 was associated with isolated NTDs in African Americans. Conclusions We report a number of associations between SNP genotypes and neural tube defects. These associations were nominally significant before correction for multiple hypothesis testing. These corrections are highly conservative for association studies of untested hypotheses, and may be too conservative for replication studies. We therefore believe the true effect of these four nominally significant SNPs on NTD risk will be more definitively determined by further study in other populations, and eventual meta-analysis.
dc.language.isoenen
dc.subjectGENETICSen_GB
dc.subjectNEONATEen_GB
dc.subject.otherBIRTH DEFECTSen_GB
dc.titleReplication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defectsen_GB
dc.language.rfc3066en
dc.rights.holderFaith Pangilinan et al.; licensee BioMed Central Ltd.
dc.description.statusPeer Reviewed
dc.date.updated2014-10-14T11:12:52Z
refterms.dateFOA2018-08-08T14:11:00Z
html.description.abstractAbstract Background Neural tube defects (NTDs), which are among the most common congenital malformations, are influenced by environmental and genetic factors. Low maternal folate is the strongest known contributing factor, making variants in genes in the folate metabolic pathway attractive candidates for NTD risk. Multiple studies have identified nominally significant allelic associations with NTDs. We tested whether associations detected in a large Irish cohort could be replicated in an independent population. Methods Replication tests of 24 nominally significant NTD associations were performed in racially/ethnically matched populations. Family-based tests of fifteen nominally significant single nucleotide polymorphisms (SNPs) were repeated in a cohort of NTD trios (530 cases and their parents) from the United Kingdom, and case–control tests of nine nominally significant SNPs were repeated in a cohort (190 cases, 941 controls) from New York State (NYS). Secondary hypotheses involved evaluating the latter set of nine SNPs for NTD association using alternate case–control models and NTD groupings in white, African American and Hispanic cohorts from NYS. Results Of the 24 SNPs tested for replication, ADA rs452159 and MTR rs10925260 were significantly associated with isolated NTDs. Of the secondary tests performed, ARID1A rs11247593 was associated with NTDs in whites, and ALDH1A2 rs7169289 was associated with isolated NTDs in African Americans. Conclusions We report a number of associations between SNP genotypes and neural tube defects. These associations were nominally significant before correction for multiple hypothesis testing. These corrections are highly conservative for association studies of untested hypotheses, and may be too conservative for replication studies. We therefore believe the true effect of these four nominally significant SNPs on NTD risk will be more definitively determined by further study in other populations, and eventual meta-analysis.


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