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1.
Caries Res ; 52(4): 263-271, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29393149

RESUMO

Dental caries is a multifactorial infectious disease and a major public health problem estimated to affect 60-90% of school children as well as a vast number of adults. The aim of this work was to define patterns of progression of the disease based on longitudinal data in contrast to using a cross-sectional assessment. dmft/DMFT scores were collected at ages 5, 12, 14, 16, 17, and 18 from 876 individuals. We tested our newly defined phenotypes for association with genetic variants in genes shown to be associated with caries. We generated genotyping data using Taqman chemistry in markers of genes involved in processes such as enamel formation and salivary contributions. Kallikrein 4 (KLK4) was found to show a significant association with the created phenotypes (p = 0.0008 in a recessive model for low caries experience in the primary dentition vs. high caries experience in the primary dentition, and p = 0.0004 in a recessive model for caries free primary dentition vs. high caries experience in the primary dentition).


Assuntos
Cárie Dentária/genética , Fenótipo , Polimorfismo de Nucleotídeo Único , Adolescente , Criança , Pré-Escolar , Índice CPO , Cárie Dentária/prevenção & controle , Progressão da Doença , Feminino , Genótipo , Humanos , Calicreínas/genética , Estudos Longitudinais , Masculino , Fatores de Risco
2.
BMC Med Genet ; 15: 81, 2014 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-25023176

RESUMO

BACKGROUND: Congenital forms of hearing impairment can be caused by mutations in the estrogen related receptor beta (ESRRB) gene. Our initial linkage studies suggested the ESRRB locus is linked to high caries experience in humans. METHODS: We tested for association between the ESRRB locus and dental caries in 1,731 subjects, if ESRRB was expressed in whole saliva, if ESRRB was associated with the microhardness of the dental enamel, and if ESRRB was expressed during enamel development of mice. RESULTS: Two families with recessive ESRRB mutations and DFNB35 hearing impairment showed more extensive dental destruction by caries. Expression levels of ESRRB in whole saliva samples showed differences depending on sex and dental caries experience. CONCLUSIONS: The common etiology of dental caries and hearing impairment provides a venue to assist in the identification of individuals at risk to either condition and provides options for the development of new caries prevention strategies, if the associated ESRRB genetic variants are correlated with efficacy.


Assuntos
Cárie Dentária/genética , Perda Auditiva Neurossensorial/patologia , Receptores de Estrogênio/genética , Desmineralização do Dente/genética , Adolescente , Adulto , Animais , Linhagem Celular Tumoral , Criança , Pré-Escolar , Cromossomos Humanos Par 14 , Esmalte Dentário/crescimento & desenvolvimento , Feminino , Estudos de Associação Genética , Perda Auditiva Neurossensorial/genética , Humanos , Desequilíbrio de Ligação , Masculino , Camundongos , Linhagem , Polimorfismo de Nucleotídeo Único , Receptores de Estrogênio/fisiologia , Adulto Jovem
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