2016
Polymorphisms in genes encoding purinoreceptor and osteoprotegerin and external apical root resorption in children after orthodontic treatment
VRANKOVÁ, Zuzana, Martina SIROTKOVÁ, Petra BOŘILOVÁ LINHARTOVÁ, Pavlína ČERNOCHOVÁ, Jakub KAŠTOVSKÝ et. al.Základní údaje
Originální název
Polymorphisms in genes encoding purinoreceptor and osteoprotegerin and external apical root resorption in children after orthodontic treatment
Autoři
VRANKOVÁ, Zuzana (703 Slovensko, domácí), Martina SIROTKOVÁ (703 Slovensko, domácí), Petra BOŘILOVÁ LINHARTOVÁ (203 Česká republika, garant, domácí), Pavlína ČERNOCHOVÁ (203 Česká republika, domácí), Jakub KAŠTOVSKÝ (203 Česká republika, domácí) a Lydie IZAKOVIČOVÁ HOLLÁ (203 Česká republika, domácí)
Vydání
15th Euro Congress on Dental & Oral Health, Rome, 2016
Další údaje
Jazyk
angličtina
Typ výsledku
Prezentace na konferencích
Obor
Genetika a molekulární biologie
Stát vydavatele
Itálie
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14110/16:00088272
Organizační jednotka
Lékařská fakulta
Klíčová slova anglicky
polymorphism; purinoreceptor; osteoprotegerin; external apical root resorption; orthodontic treatment
Štítky
Změněno: 20. 12. 2016 13:28, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Orthodontically induced external apical root resoption (EARR) is a multifactorial inflammatory disease. Genes encoding proteins, which are involved in the modulation of inflammatory response and bone remodeling, are considered as the “candidate” for EARR. The aim of this study was to analyze possible associations of single nucleotide polymorphisms (SNPs) in the P2RX7 (encoding purinoreceptor) and TNFRSF11B (encoding osteoprotegerin) genes with EARR in Czech children after orthodontic treatment. A total, 99 orthodontically treated patients (69 healthy and 30 with EARR) were enrolled in this case-control study. Genotype determination of P2RX7 +489C/T (rs208294, Tyr155His) and +1068C/T (rs1718119, Thr348Ala), TNFRSF11B -163C/T (rs3102735) and TNFRSF11B +1181C/G (rs2073618, Lys3Asn) was based on polymerase chain reaction using 5 nuclease TaqMan® assays. While no significant differences were observed in allele or genotype frequencies of all four studied SNPs, specific combinations of variants in P2RX7 may be associated with lower/higher risk of EARR development (P<0.05). In addition, the length of treatment by orthodontic appliances positively correlated with the presence of EARR (P<0.05). Although the effect of P2RX7 SNPs themselves to the development EARR was not confirmed in the Czech population, haplotype analysis suggests, that variability in the P2RX7 gene, as well as the length of treatment, may be important factors contributing to the etiopathogenesis of post-orthodontic EARR.
Návaznosti
GB14-37368G, projekt VaV |
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MUNI/A/1258/2015, interní kód MU |
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ROZV/24/LF/2016, interní kód MU |
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