Examination of OPG, RANK, RANKL and HIF1A polymorphisms in temporomandibular joint ankylosis patients

被引:10
作者
Cotait de Lucas Corso, Paola Fernanda [1 ]
Meger, Michelle Nascimento [1 ]
Ferreira Petean, Igor Bassi [2 ]
de Souza, Juliana Feltrin [3 ]
Brancher, Joao Armando [1 ]
Bezerra da Silva, Lea Assed [4 ]
Barbosa Rebelatto, Nelson Luis [3 ]
Kluppel, Leandro Eduardo [3 ]
Sousa-Neto, Manoel Damiao [2 ]
Kuchler, Erika Calvano [1 ,4 ]
Scariot, Rafaela [1 ,3 ]
机构
[1] Positivo Univ, Sch Hlth Sci, 5300 Prof Pedro Viriato Parigot de Souza St, BR-81280330 Curitiba, Parana, Brazil
[2] Univ Sao Paulo, Sch Dent, Dept Restorat Dent, Ave Cafe,Campus USP, BR-14040904 Ribeirao Preto, SP, Brazil
[3] Univ Fed Parana, Sch Dent, Dept Stomatol, 632 Prefeito Lothario Meissner Ave, BR-80210170 Curitiba, PR, Brazil
[4] Univ Sao Paulo, Sch Dent, Dept Pediat Dent, Ave Cafe,Campus USP, BR-14040904 Ribeirao Preto, SP, Brazil
关键词
Genetics; Temporomandibular joint; Ankylosis; HYPOXIA-INDUCIBLE FACTOR; BONE-MINERAL DENSITY; SKELETAL MORPHOGENESIS; OSTEOPROTEGERIN GENE; SURGICAL-MANAGEMENT; OSTEOGENESIS; HIF-1-ALPHA; TNFRSF11B; MUTATIONS; PATHWAY;
D O I
10.1016/j.jcms.2019.01.024
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: To evaluate the association between polymorphisms in genes that regulate bone metabolism, such as OPG, RANK, RANKL, and HIFIA, in patients with temporomandibular joint (TMJ) ankylosis. Methods: The sample consisted of 181 individuals, the study included 17 individuals with TMJ ankylosis and 164 controls. DNA was extracted from buccal epithelial cells. The genotyping of genetic poly-morphisms in OPG (rs2073618), RANK (rs3826620), RANKL (rs9594738), and HIFIA (rs2301113 and rs2057482) was performed by real-time PCR using TaqMan (TM) technology (Applied Biosystems). The data were subjected to statistical analysis with a level of significance of 0.05. Results: The OPG (rs2073618) polymorphism was associated with TMJ ankylosis, both in the additive model and in the dominant model (p < 0.05). In the additive model, when the individuals carried the CC genotype, they presented as 10.80 times more likely to develop the condition (p = 0.03). In the dominant model, individuals that carried at least one C allele were 5.76 times more likely to have TMJ ankylosis, than those with the G allele (p = 0.01). Conclusion: The polymorphism rs2073618 of OPG is a possible marker that is associated with the risk of manifestation of TMJ ankylosis. (C) 2019 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:766 / 770
页数:5
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