| Autor: |
Calvano Küchler E, Maschietto Pucinelli C, Carpio Horta K, Assed Bezerra da Silva R, de Castro Costa M, Rezende Vieira A, Nelson-Filho P, Assed Bezerra da Silva L, Santos Antunes L, Azeredo Antunes L |
| Jazyk: |
angličtina |
| Zdroj: |
The Journal of clinical pediatric dentistry [J Clin Pediatr Dent] 2020; Vol. 44 (1), pp. 35-40. |
| DOI: |
10.17796/1053-4625-44.1.6 |
| Abstrakt: |
Purpose : Recent studies have suggested that disruptions in the RANKL/RANK/OPG system might be involved in enamel conditions. The aim of this study was to test whether genetic polymorphisms in RANK, RANKL and OPG are associated with dental caries, developmental defects of enamel (DDE) and enamel microhardness. Study design : Saliva samples were collected from two subsets for the purpose of genomic DNA extraction. In the first subset, composed of 248 children, dental caries and DDE were evaluated during their clinical examination. In the second subset, composed of 72 children, enamel samples from the buccal surface of primary teeth were used for enamel microhardness analysis. Genetic polymorphisms in RANK, RANKL and OPG were genotyped by real-time polymerase chain reactions in all samples from both populations. The chi-square test was used for dental caries and DDE analysis while, one-way ANOVA with Tukey's post-test was used for microhardness analysis. Hardy-Weinberg equilibrium was also calculated. The established alpha was 5%. Results: Caries experience analysis demonstrated a statistically-significant difference for OPG allele distribution in primary dentition (p=0.033). The studied polymorphisms in RANK, RANKL and OPG were not associated with DDE or enamel microhardness (p>0.05). Conclusion: The genetic polymorphism rs2073618 in OPG is associated with dental caries experience in primary dentition. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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