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Cystathionine β-synthase genetic variant rs2124459 is associated with a reduced risk of cleft palate in French and Belgian populations.

Authors :
Goffinet L
Oussalah A
Guéant-Rodriguez RM
Chery C
Basha M
Avogbe PH
Josse T
Jeannesson E
Rouyer P
Flayac J
Gerard P
Le Touze A
Bonin-Goga B
Goga D
Simon E
Feillet F
Vikkula M
Guéant JL
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

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/.)

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