PEMT variants are associated with nonsyndromic cleft lip with or without cleft palate in Chile

Author:

Suazo José1ORCID,Salamanca Carlos123,González-Hormazábal Patricio4,Cáceres-Rojas Gabriela1,Pantoja Roberto56,Leiva Noemi7,Pardo Rosa89

Affiliation:

1. Institute for Research in Dental Sciences, School of Dentistry, Universidad de Chile, Santiago, Chile

2. Research Center in Dental Sciences (CICO), Dental School, Universidad de La Frontera, Temuco, Chile

3. Universidad Adventista de Chile, Chillán, Chile

4. Human Genetics Program, Institute of Biomedical Sciences, School of Medicine, Universidad de Chile, Santiago, Chile

5. Unit of Oral & Maxillofacial Surgery, Hospital Clínico San Borja-Arriaran, Santiago, Chile

6. Department of Oral & Maxillofacial Surgery, School of Dentistry, Universidad de Chile, Santiago, Chile

7. Unit of Maxillofacial Malformations, School of Dentistry, Universidad de Chile, Santiago, Chile

8. Section of Genetics, Hospital Clínico Universidad de Chile, Santiago, Chile

9. Unit of Neonatology, Hospital Clínico Universidad de Chile, Santiago, Chile

Abstract

Aim: To assess the association between PEMT variants and nonsyndromic cleft lip with or without cleft palate in Chile and the effects of these variants on global DNA methylation. Subjects & methods: The authors obtained genotypes for nine variants from 247 cases and 453 controls for genotype–phenotype associations. The effect of significant polymorphisms on global DNA methylation (percentage of long interspersed element-1 methylation) was evaluated in a subsample of 95 controls. Results: After multiple comparison corrections, variants rs7649 and rs4646409 were associated with nonsyndromic cleft lip with or without cleft palate. Carriers of risk alleles presented lower DNA methylation levels than noncarriers. Conclusion: According to functional analysis for risk variants from previous reports, the authors infer that a decrease of methyl group availability is occurring in affected subjects.

Funder

Fondo Nacional de Desarrollo Científico y Tecnológico

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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