Journal
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY MEDICINE AND PATHOLOGY
Volume 27, Issue 6, Pages 782-785Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajoms.2015.04.008
Keywords
Homocysteine; Folate; Methylation; Orofacial cleft; SNP; Genetics
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Objective: Non-syndromic cleft lip with or without cleft palate (NSCL/P) is a common complex birth defect with complex etiology. Elevated levels of plasma homocysteine have been found to be associated with intrauterine growth retardation, preterm birth, intrauterine fetal death, neural tube defects and NSCL/P. The aim of the present study was to evaluate the role of A2756G SNP and MTRR A66G polymorphisms in the pathogenesis of NSCL/P in South Indian subjects. Methods: In the present study we genotyped MTR A2756G SNP and MTRR A66G polymorphisms in 142 patients with NSCL/P and 141 healthy controls using PCR-RFLP assay. Results: The genotype frequencies of the control group were in agreement with the Hardy-Weinberg equilibrium for the MTR A2756G (p = 0.096), but not for MTRR A66G (p < 0.001). The MTRR A66G is polymorphic, but the homozygous GG genotype was not observed in both control and NSCL/P groups. MTRR A66G heterozygous genotype significantly increased the risk of CL/P (OR = 1.65, 95% CI = 1.00-2.72) and CPO (OR = 3.21, 95% CI = 1.01-10.15) in codominant model suggesting a possible link with NSCL/P predisposition; however, the more stringent Yates' test suggests no significance. There are no clear differences in risk for CL/P or CPO was observed for different MTR-MTRR genotype combinations. Conclusions: The present study failed to show an association between the MTR A2756G gene and NSCL/P and provides possible evidence regarding MTRR A66G risk for non-syndromic cleft lip and palate possibly due to abnormal folate and homocysteine status in Indian population. (C) 2015 Asian AOMS, ASOMP, JSOP, JSOMS, JSOM, and JAMI. Published by Elsevier Ltd. All rights reserved.
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