| Literature DB >> 30149392 |
Senda Charone1, Erika Calvano Küchler2, Aline de Lima Leite1, Mileni Silva Fernandes1, Vinicius Taioqui Pelá1, Tatiana Martini1, Bárbara Margarido Brondino3, Ana Carolina Magalhães1, Thiago J Dionisio1, Carlos F Santos1, Marília Afonso Rabelo Buzalaf4.
Abstract
Genes expressed during amelogenesis are candidates to increase the risk of dental fluorosis (DF). Thus, this study aimed to evaluate the association between polymorphisms in enamel development genes and susceptibility to DF in mice. Mice of both sexes, representing strains 129P3/J (n = 20; resistant to DF) and A/J (n = 20; susceptible to DF), were divided into 2 groups. Each strain received a diet with a low concentration of fluoride (F) and drinking water containing 0 or 50 mg/L of F for 6 weeks. Clinical evaluation and analysis of Vickers enamel microhardness of the incisors were performed. Livers were collected for genomic DNA extraction. Seventeen genetic polymorphisms in Amelx, Ambn, Ambn, Col14a1, Col1a1, Col5a2, Enam, Fam20a, Fam83h, Foxo1, Klk4, Mmp20, Serpinf1, Serpinh1, Smad3, Tuft1, and Wdr72 were genotyped by real-time PCR using Taqman chemistry. Overrepresentation of alleles and genotypes in DF was evaluated using the χ2 test with an alpha of 5%. The clinical aspects of the enamel and the surface enamel microhardness confirmed the DF condition. In the polymorphisms rs29569969, rs13482592, and rs13480057 in Ambn, Col14a1, and Mmp20, respectively, genotype and allele distributions were statistically significantly different between A/J and 129P3/J strains (p < 0.05). In conclusion, polymorphisms in Ambn, Col14a1, and Mmp20 are associated with the susceptibility to DF.Entities:
Keywords: Dental fluorosis; Gene; Polymorphisms
Year: 2018 PMID: 30149392 DOI: 10.1159/000491554
Source DB: PubMed Journal: Caries Res ISSN: 0008-6568 Impact factor: 4.056