Determination of TNF-a Gene Polymorphisms on Skeletal Pattern in Class II Malocclusion.
Simone Carvalho LevyLivia Azeredo Alves AntunesJulia Guimaraes Barcellos de AbreuJullia Assis da Silva NascimentoAna Carolina KuntzWalter Luis Soares FialhoAmanda Silva RodriguesEllen Cardoso TeixeiraJosé de Albuquerque Calasans-MaiaMarcelo Calvo de AraújoErika C KüchlerLeonardo Dos Santos AntunesPublished in: Brazilian dental journal (2019)
Bone development and growth is a non-going, life-long process, varying greatly among individuals and much of this variation could be modulated by genetic factors. The purpose of this study was to evaluate the association between the polymorphisms in the TNF-a gene and skeletal class II malocclusion. Single nucleotide polymorphisms in TNF-a (rs1799724; rs1800629) gene were studied in 79 skeletal class II malocclusion and 102 skeletal class I malocclusion subjects from Straight Wire Group of Studies on Orthodontics and Functional Orthopedics for Maxillary from Rio de Janeiro, Brazil. The Genotyping of these selected polymorphisms was carried out by TaqMan real-time PCR using genomic DNA extracted from buccal cells. All allele and genotype frequencies were compared between the groups using the PLINK® software in a free, in a dominant and in a recessive model using a chi-square test (p≤0.05). There was no significant association of TNF-a (rs1799724; rs1800629) genotype and allele distribution with skeletal class II malocclusion. Regardless of the dominant or recessive genetic model, the preferential genotype associations for rs1799724 and rs1800629 was insignificant. In conclusion, no evidence of association is apparent between genetic polymorphisms involving TNF-a and skeletal class II malocclusion or the position of the maxilla and mandible in the postero-anterior direction.
Keyphrases
- rheumatoid arthritis
- genome wide
- copy number
- real time pcr
- intellectual disability
- dna methylation
- computed tomography
- bone mineral density
- gene expression
- circulating tumor
- cell death
- soft tissue
- genome wide identification
- single molecule
- transcription factor
- postmenopausal women
- magnetic resonance
- circulating tumor cells
- solid state