2020
Matrix metalloproteinases gene variants and dental caries in Czech children
BOŘILOVÁ LINHARTOVÁ, Petra, Tereza DEISSOVÁ, Martina KUKLETOVÁ a Lydie IZAKOVIČOVÁ HOLLÁZákladní údaje
Originální název
Matrix metalloproteinases gene variants and dental caries in Czech children
Autoři
BOŘILOVÁ LINHARTOVÁ, Petra (203 Česká republika, domácí), Tereza DEISSOVÁ (203 Česká republika, domácí), Martina KUKLETOVÁ (203 Česká republika, domácí) a Lydie IZAKOVIČOVÁ HOLLÁ (203 Česká republika, garant, domácí)
Vydání
BMC Oral Health, LONDON, BMC, 2020, 1472-6831
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30208 Dentistry, oral surgery and medicine
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.757
Kód RIV
RIV/00216224:14110/20:00116012
Organizační jednotka
Lékařská fakulta
UT WoS
000535616700001
Klíčová slova anglicky
Polymorphism; Association study; Caries; Oral disease; Genetic predisposition; ELSPAC
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 23. 1. 2021 18:09, doc. RNDr. Petra Bořilová Linhartová, Ph.D., MBA
Anotace
V originále
Background Matrix metalloproteinases (MMPs) play an important role in tooth formation and the mineralization of dental tissue. The aim of the study was to analyse Czech children with primary/permanent dentition polymorphisms in those genes encoding MMP2, MMP3, MMP9, MMP13, MMP16, and MMP20, which had been previously associated with dental caries in other populations. Methods In total, 782 Czech children were included in this case-control study. DNA samples were taken from 474 subjects with dental caries (with decayed/missing/filled teeth, DMFT >= 1) and 155 caries free children (DMFT = 0) aged 13-15 years, as well as 101 preschool children with early childhood caries (ECC, dmft >= 1) and 52 caries free children (dmft = 0), were analyzed for nine MMPs single nucleotide polymorphisms (SNPs) using real time polymerase chain reaction TaqMan assays. Results There were no significant differences in the allele and/or genotype frequencies of all the studied MMPs SNPs among children with dental caries in primary/permanent dentition and the healthy controls (P > 0.05). In addition, similar allele or genotype frequencies of the studied MMPs SNPs were found in children with severe dental caries in their permanent teeth (children with DMFT >= 6) and the healthy controls (DMFT = 0, P > 0.05). Conclusions This study demonstrated the lack of association between the selected SNPs in candidate genes of MMPs and the susceptibility to or severity of dental caries in both primary and permanent dentitions in Czech children.
Návaznosti
EF16_013/0001761, projekt VaV |
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MUNI/A/1428/2019, interní kód MU |
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NV17-30439A, projekt VaV |
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ROZV/23/LF1/2019, interní kód MU |
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