Folic acid supplementation use and the MTHFR C677T polymorphism in orofacial clefts etiology: An individual participant data pooled-analysis
Birth Defects Research. Part A: Clinical and Molecular Teratology , Volume 97 - Issue 8 p. 509- 514
BACKGROUND: 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. METHODS: We used logistic regression to analyze the pooled sample of 1149 isolated cases and 1161 controls. Fetal and maternal MTHFR C677T genotypes, and maternal periconceptional exposure to smoking, alcohol, vitamin containing folic acid and folic acid supplements were contrasted between the cleft types [non-syndromic clefts lip or without cleft palate (CL(P)) and non-syndromic cleft palate (CP)] and control groups. RESULTS: There was a reduced risk of CL(P) with maternal folic acid use (p=0.008; OR=0.70, 95% CI: 0.65-0.94) and with supplements containing folic acid (p=0.028, OR=0.80, 95% CI: 0.65-0.94). Maternal smoking increased the risk of both CL(P) (p<10 e-3; OR=1.62, 95% CI: 1.35-1.95) and CP (p=0.028; OR=1.38, 95% CI: 1.04-1.83). No significant risk was observed with either maternal or fetal MTHFR C677T genotypes. CONCLUSION: This individual participant data (IPD) meta-analysis affords greater statistical power and can help alleviate the problems associated with aggregate-level data-sharing. The result of this IPD meta-analysis is consistent with previous reports suggesting that folic acid and smoking influence OFC outcomes. Birth Defects Research (Part A) 97:509-514, 2013.
|Cleft lip and palate, Folic acid, individual patient data, MTHFR, Pooled-analysis|
|Birth Defects Research. Part A: Clinical and Molecular Teratology|
|Organisation||Department of Gynaecology & Obstetrics|
Butali, A, Little, J, Chevrier, C, Cordier, S, Steegers-Theunissen, R.P.M, Juqessur, A, … Mossey, P.A. (2013). Folic acid supplementation use and the MTHFR C677T polymorphism in orofacial clefts etiology: An individual participant data pooled-analysis. Birth Defects Research. Part A: Clinical and Molecular Teratology, 97(8), 509–514. doi:10.1002/bdra.23133