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1.
Caries Res ; 51(1): 79-84, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28088794

RESUMO

The aim of this study was to examine the association of single-nucleotide polymorphisms (SNPs) in the gene encoding ficolin-2 protein (FCN2 gene) at positions -986 (rs17514136), -602 (rs3124953), and -4 (rs3124952) with dental caries in Polish children. Two hundred and sixty Polish Caucasian children aged 15 years were enrolled in this study: 82 with "higher" caries experience (DMFT >5) and 178 with "lower" caries experience (DMFT ≤5). In addition, subjects with caries experience (DMFT ≥1) and caries-free subjects (DMFT = 0) were compared. FCN2 SNPs were genotyped with PCR-RFLP methods. There were no significant differences in the genotype, allele, or haplotype distributions in 3 analyzed SNPs of the FCN2 gene between children with "higher" and those with "lower" caries experience as well as between children with caries experience and caries-free children. In conclusion, we did not find any association of FCN2 promoter polymorphisms at positions -986, -602, and -4 with dental caries in Polish children.


Assuntos
Cárie Dentária/etnologia , Cárie Dentária/epidemiologia , Predisposição Genética para Doença/etnologia , Lectinas/genética , Polimorfismo de Nucleotídeo Único , Regiões Promotoras Genéticas/genética , Adolescente , Alelos , Índice CPO , Cárie Dentária/genética , Feminino , Frequência do Gene , Técnicas de Genotipagem , Haplótipos , Humanos , Masculino , Polônia/epidemiologia , Ficolinas
2.
Oral Dis ; 18(4): 389-95, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22221294

RESUMO

OBJECTIVE: The aim of the study was to examine whether the MBL2 C(-290)G and G161A, MASP2 A359G, AMELX C287T and C522T, and ENAM C2452T polymorphisms are associated with dental caries. SUBJECTS AND METHODS: Genomic DNA of 95 Polish children with 'higher caries experience' (HC) and 84 subjects with 'lower caries experience' (LC) belonging to two age-groups (5 and 13 years old) was extracted from the buccal mucosa. SNPs were genotyped with PCR-RFLP methods. RESULTS: Among 5-year-old children, we found significantly higher percentage of subjects carrying MBL2 (-290)G allele in HC group compared with LC group (43.2%vs 17.6%, P = 0.023). MBL2 C(-290)G-G161A C-G haplotype was overrepresented in LC group in 5-year-olds (P = 0.01), while the opposite association was observed in 13-year-olds, where C-G was overrepresented in HC group (P = 0.028). In 5-year-old children, the frequency of MBL2 G-G haplotype was higher in HC group compared with LC subjects (P = 0.045), while the opposite association (with borderline significance) was observed in 13-year-old children (P = 0.057). SNPs in MASP2, AMELX, and ENAM were not associated with dental caries. CONCLUSION: MBL2 gene polymorphism is associated with caries experience in Polish children, but the direction of this association seems to be opposite in primary and permanent dentition.


Assuntos
Amelogenina/genética , Cárie Dentária/genética , Lectina de Ligação a Manose/genética , Serina Proteases Associadas a Proteína de Ligação a Manose/genética , Polimorfismo de Nucleotídeo Único/genética , Proteínas/genética , Adenina , Adolescente , Alelos , Estudos de Casos e Controles , Pré-Escolar , Citosina , Índice CPO , Proteínas da Matriz Extracelular , Feminino , Frequência do Gene/genética , Genoma Humano/genética , Guanina , Haplótipos/genética , Heterozigoto , Humanos , Masculino , Mutação/genética , Polônia , Timina
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