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1.
J Int Med Res ; 48(7): 300060520943428, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-32721184

RESUMO

OBJECTIVE: With the development of human genomics, the genetic factors associated with dental caries have receiving increasing attention. This study was performed to evaluate the relationship between lactoferrin (LTF) and mannose-binding lectin 2 (MBL2) gene single nucleotide polymorphisms (SNPs) and dental caries susceptibility in Chinese children. METHODS: This prospective case-control study included 360 unrelated children (aged 12-15 years) who received oral health examinations and questionnaire surveys. The children were divided into two groups by counting the numbers of decayed, missing, and filled teeth (DMFT/dmft): case group (n = 162, DMFT/dmft ≥ 1) and control group (n = 198, DMFT/dmft = 0); non-invasive saliva samples were collected to extract genomic DNA. Six SNPs (rs2073495C/G, rs1042073C/T, rs10865941C/T, and rs1126477A/G in LTF; rs7096206C/G and rs7095891G/A in MBL2) were tested by mass spectrometry. RESULTS: The study included 360 individuals with (85 boys and 77 girls) and without a history of caries (96 boys and 102 girls). There were no statistically significant differences in alleles and genotypes among the six SNPs between the two groups. CONCLUSION: There is no evidence that polymorphisms of LTF and MBL2 genes are associated with dental caries susceptibility in populations from northwest China; further confirmation is needed with larger sample sizes.


Assuntos
Cárie Dentária , Lectina de Ligação a Manose , Adolescente , Estudos de Casos e Controles , Criança , China , Índice CPO , Cárie Dentária/genética , Suscetibilidade à Cárie Dentária , Feminino , Humanos , Lactoferrina/genética , Masculino , Lectina de Ligação a Manose/genética , Lectinas de Ligação a Manose , Polimorfismo de Nucleotídeo Único , Estudos Prospectivos
2.
J Int Med Res ; 47(4): 1696-1704, 2019 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-30803280

RESUMO

OBJECTIVE: To investigate the association between single nucleotide polymorphisms (SNPs) in six candidate genes (enamelin [ ENAM]; tuftelin 1 [ TUFT1]; matrix metallopeptidase 13 [ MMP13]; interleukin 1 beta [ IL1B]; interleukin 10 [ IL10]; interleukin 1 receptor antagonist [ IL1RN]) and dental caries in children from northwest China. METHODS: This case-control study enrolled children (12-15 years) who underwent routine dental examinations. The children were divided into two groups based on the presence of dental caries. A saliva sample was collected and seven SNPs (rs3806804A/G in ENAM, rs3811411T/G in TUFT1, rs2252070A/G and rs597315A/T in MMP13, rs1143627C/T in IL1B, rs1800872A/C in IL10 and rs956730G/A in IL1RN) were genotyped. RESULTS: A total of 357 children were enrolled in the study: 161 with dental caries and 196 without dental caries. No significant difference was found in the alleles and genotypes of five genes ( ENAM, TUFT1, MMP13, IL10 and IL1RN) between those with and without dental caries. A significant relationship was found between the IL1B rs1143627C/T polymorphism and dental caries susceptibility with those carrying the rs1143627CT genotype having a lower risk of dental caries compared with those carrying the CC genotype (odds ratio 0.557; 95% confidence interval 0.326, 0.952). CONCLUSION: The IL1B rs1143627C/T polymorphism may be associated with dental caries susceptibility in children from northwest China.


Assuntos
Cárie Dentária/genética , Proteínas do Esmalte Dentário/genética , Proteínas da Matriz Extracelular/genética , Proteína Antagonista do Receptor de Interleucina 1/genética , Interleucina-10/genética , Interleucina-1beta/genética , Metaloproteinase 13 da Matriz/genética , Polimorfismo de Nucleotídeo Único , Adolescente , Povo Asiático/genética , Estudos de Casos e Controles , Criança , Cárie Dentária/patologia , Feminino , Seguimentos , Predisposição Genética para Doença , Genótipo , Humanos , Masculino , Prognóstico
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