Folic acid supplementation use and the MTHFR C677T polymorphism in orofacial clefts etiology: An individual participant data pooled‐analysis
Identifieur interne : 004A59 ( Main/Exploration ); précédent : 004A58; suivant : 004A60Folic acid supplementation use and the MTHFR C677T polymorphism in orofacial clefts etiology: An individual participant data pooled‐analysis
Auteurs : Azeez Butali [États-Unis] ; Julian Little [Canada] ; Cécile Chevrier [France] ; Sylvian Cordier [France] ; Regine Steegers-Theunissen [Pays-Bas] ; Astanand Jugessur [Norvège, Australie] ; Bola Oladugba [Nigeria] ; Peter A. Mossey [Royaume-Uni]Source :
- Birth Defects Research Part A: Clinical and Molecular Teratology [ 1542-0752 ] ; 2013-08.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Birth defects, Birth defects research, Cleft, Cleft lip, Cleft palate, Congenital cleft, Data analysis, Defect, Dietary folate, Environmental factors, Epidemiol, Etiology, Folate, Folic, Folic acid, Folic acid supplements, Genet, Genetic variability, Genotype, Human, Jugessur, Logistic regression, Maternal, Maternal folic acid, Maternal mthfr, Maternal smoking, Methylenetetrahydrofolate reductase (NADPH), Mthfr, Neural tube defects, Orofacial, Orofacial clefts, Palate, Parent triads, Polymorphism, Several studies, Similar methods, Supplementation, Triad.
- Teeft :
- Birth defects, Birth defects research, Cleft, Cleft palate, Defect, Dietary folate, Environmental factors, Epidemiol, Etiology, Folate, Folic, Folic acid, Folic acid supplements, Genet, Genotype, Jugessur, Logistic regression, Maternal, Maternal folic acid, Maternal mthfr, Maternal smoking, Mthfr, Neural tube defects, Orofacial, Orofacial clefts, Palate, Parent triads, Polymorphism, Several studies, Similar methods, Supplementation, Triad.
Abstract
This study examines gene–environment interaction between the MTHFR C667T polymorphism and folic acid in the etiology of orofacial clefts (OFC). We used a pooled‐analytical approach on four studies that used similar methods.
Url:
- https://api.istex.fr/document/1E9E11668A3D3D7D29FB2B340495AA6E7061CDC1/fulltext/pdf
- http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745533
DOI: 10.1002/bdra.23133
Affiliations:
- Australie, Canada, France, Nigeria, Norvège, Pays-Bas, Royaume-Uni, États-Unis
- Gueldre, Hollande-Méridionale, Iowa, Région Bretagne, Østlandet
- Nimègue, Oslo, Rennes, Rotterdam
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Le document en format XML
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<term>Cleft lip</term>
<term>Cleft palate</term>
<term>Congenital cleft</term>
<term>Data analysis</term>
<term>Defect</term>
<term>Dietary folate</term>
<term>Environmental factors</term>
<term>Epidemiol</term>
<term>Etiology</term>
<term>Folate</term>
<term>Folic</term>
<term>Folic acid</term>
<term>Folic acid supplements</term>
<term>Genet</term>
<term>Genetic variability</term>
<term>Genotype</term>
<term>Human</term>
<term>Jugessur</term>
<term>Logistic regression</term>
<term>Maternal</term>
<term>Maternal folic acid</term>
<term>Maternal mthfr</term>
<term>Maternal smoking</term>
<term>Methylenetetrahydrofolate reductase (NADPH)</term>
<term>Mthfr</term>
<term>Neural tube defects</term>
<term>Orofacial</term>
<term>Orofacial clefts</term>
<term>Palate</term>
<term>Parent triads</term>
<term>Polymorphism</term>
<term>Several studies</term>
<term>Similar methods</term>
<term>Supplementation</term>
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<term>Fissure congénitale</term>
<term>Génotype</term>
<term>Homme</term>
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<term>Mutation C677T</term>
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<term>Supplémentation</term>
<term>Variabilité génétique</term>
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<front><div type="abstract">This study examines gene–environment interaction between the MTHFR C667T polymorphism and folic acid in the etiology of orofacial clefts (OFC). We used a pooled‐analytical approach on four studies that used similar methods.</div>
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