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Cystathionine β-synthase genetic variant rs2124459 is associated with a reduced risk of cleft palate in French and Belgian populations.
- Source :
-
Journal of medical genetics [J Med Genet] 2016 Dec; Vol. 53 (12), pp. 828-834. Date of Electronic Publication: 2016 Aug 17. - Publication Year :
- 2016
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Abstract
- Background: Orofacial cleft (OFC) is the most prevalent craniofacial birth defect. Genes involved in one-carbon, folate and vitamin B <subscript>12</subscript> metabolisms have been associated with OFC but no study performed a concomitant assessment on genes involved in these three pathways.<br />Objective: We looked for potential genetic variants associated with OFC using an exhaustive gene panel of one-carbon metabolism.<br />Methods: We performed a case-control discovery study on children with OFC (236 cases, 145 controls) and their related mothers (186 cases, 127 controls). We performed a replication study on the top significant genetic variant in an independent group from Belgium (248 cases, 225 controls).<br />Results: In the discovery study on 'mothers', the CBS locus reached array-wide significance (p=9.13×10 <superscript>-6</superscript> ; Bonferroni p=4.77×10 <superscript>-3</superscript> ; OR 0.47 (0.33 to 0.66)) among the 519 haplotypes tested for their association with OFC risk. Within the CBS haplotype block (rs2124459, rs6586282, rs4920037, rs234705, rs234709), the rs2124459 was the most significantly associated with a reduced risk of OFC (p=1.77×10 <superscript>-4</superscript> ; Bonferroni p=2.00×10 <superscript>-2</superscript> ; OR 0.53 (0.38 to 0.74), minor allele). The rs2124459 was associated with a reduced risk of cleft palate (CP) (p=6.78×10 <superscript>-5</superscript> ; Bonferroni p=7.80×10 <superscript>-3</superscript> ; OR 0.40 (0.25 to 0.63)). In the 'children' group, the rs2124459 was associated with a reduced risk of CP (p=0.02; OR 0.61 (0.40 to 0.93), minor allele). The association between rs2124459 and reduced risk of CP was replicated in an independent children population from Belgium (p=0.02; OR 0.64 (0.44 to 0.93), minor allele).<br />Conclusions: The CBS rs2124459 was associated with a reduced risk of CP in both French and Belgian populations. These results highlight the prominent involvement of the vitamin B6-dependent transsulfuration pathway of homocysteine in OFC risk and the interest for evaluating vitamin B6 status in further population studies.<br /> (Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.)
- Subjects :
- Adult
Belgium
Case-Control Studies
Child
Child, Preschool
Cleft Lip complications
Cleft Lip metabolism
Cleft Palate complications
Cleft Palate metabolism
Female
France
Genetic Association Studies
Haplotypes
Humans
Infant
Male
Cleft Lip genetics
Cleft Palate genetics
Cystathionine beta-Synthase genetics
Genetic Predisposition to Disease
Polymorphism, Single Nucleotide
Subjects
Details
- Language :
- English
- ISSN :
- 1468-6244
- Volume :
- 53
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Journal of medical genetics
- Publication Type :
- Academic Journal
- Accession number :
- 27535090
- Full Text :
- https://doi.org/10.1136/jmedgenet-2016-104111