Genetic determinants and postorthodontic external apical root resorption in Czech children
Language English Country Denmark Media print-electronic
Document type Journal Article
PubMed
27493142
DOI
10.1111/odi.12564
Knihovny.cz E-resources
- Keywords
- gene polymorphism, orthodontic treatment, root resorption,
- MeSH
- Gene Frequency genetics MeSH
- Genetic Predisposition to Disease genetics MeSH
- Interleukin-17 genetics physiology MeSH
- Polymorphism, Single Nucleotide genetics MeSH
- Humans MeSH
- Adolescent MeSH
- Orthodontics, Corrective adverse effects MeSH
- Osteopontin genetics physiology MeSH
- Osteoprotegerin genetics physiology MeSH
- Receptors, Purinergic P2X7 genetics physiology MeSH
- Root Resorption etiology genetics MeSH
- Case-Control Studies MeSH
- Check Tag
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- Interleukin-17 MeSH
- Osteopontin MeSH
- Osteoprotegerin MeSH
- P2RX7 protein, human MeSH Browser
- Receptors, Purinergic P2X7 MeSH
- SPP1 protein, human MeSH Browser
- TNFRSF11B protein, human MeSH Browser
OBJECTIVE: Genes, involved in the modulation of inflammatory response and bone remodeling, play a role in the development of postorthodontic external apical root resorption (EARR). The aim of our study was to analyze possible associations between seven single nucleotide polymorphisms (SNPs) in interleukin-17A (IL-17), osteopontin (SPP1), purinoreceptor P2X7 (P2RX7), and tumor necrosis factor receptor superfamily member 11B (TNFRSF11B) genes and EARR in children after orthodontic treatment. SUBJECTS AND METHODS: This case-control study comprised 99 orthodontically treated patients (69 controls and 30 subjects with EARR). Genotype determinations of rs2275913, rs11730582, rs9138, rs208294, rs1718119, rs3102735, and rs2073618 were based on polymerase chain reaction using 5' nuclease TaqMan® assays. RESULTS: While no significant differences were observed in allele or genotype frequencies of all seven studied SNPs, specific haplotype of P2RX7 (rs208294 and rs1718119) modified the risk of EARR development (P < 0.05). In addition, the length of treatment with a fixed orthodontic appliance positively correlated with the presence of EARR (P < 0.05). CONCLUSIONS: Although the effect of individual SNPs studied on the EARR development was not confirmed in the Czech population, complex analysis suggested that variability in the P2RX7 gene and the length of orthodontic treatment may be important factors contributing to the etiopathogenesis of postorthodontic EARR.
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