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1.
Community Dent Health ; 37(2): 110-114, 2020 May 29.
Artigo em Inglês | MEDLINE | ID: mdl-32212438

RESUMO

OBJECTIVE: To assess associations between caregiver oral health literacy (OHL) and socioeconomic factors, child and caregiver's oral health behaviors and perceptions of oral health status. BASIC RESEARCH DESIGN: Cross-sectional study. CLINICAL SETTING: University pediatric dentistry clinic. PARTICIPANTS: 205 pairs of caregivers and children aged 6 to 12-years undergoing dental treatment. METHOD: A questionnaire was sent to caregivers enquiring about socioeconomic factors, oral health behaviors, perceptions of own and child oral health. The clinical dental status of the children was recorded with the DMFT/dmft index. MAIN OUTCOME MEASURE: OHL was measured by the Brazilian version of the Rapid Estimate of Adult Literacy in Dentistry (BREALD-30). Descriptive analysis, unadjusted and adjusted logistic regression, odds ratio and confidence interval were calculated considering a significance level of 5%. RESULTS: The frequency of poor OHL was 21%. In adjusted analysis caregivers with 8 years or less of schooling had a 3.72 (95% CI 1.74-7.95) times greater chance of have poor OHL. Caregivers who perceived their child to have poor oral health were 2.70 (95% CI 1.10-6.63) times more likely to have poor OHL. CONCLUSIONS: Poor oral health literacy was more common among caregivers with less schooling and a poor perception of their child's oral health. OHL was unrelated to monthly family income, child dental health status, perception of own oral health or child or caregiver oral health behaviors.


Assuntos
Letramento em Saúde , Saúde Bucal , Adulto , Brasil , Cuidadores , Criança , Estudos Transversais , Comportamentos Relacionados com a Saúde , Humanos , Fatores Socioeconômicos
2.
Med Oral Patol Oral Cir Bucal ; 23(6): e639-e645, 2018 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-30341262

RESUMO

BACKGROUND: The objective of this study was to evaluate the dental and oral manifestations in patients with celiac disease. MATERIAL AND METHODS: The sample consisted of 40 patients with the disease and 40 without the disease matched by age in southern Brazil. The CD group included patients previously diagnosed by positive anti-endomysial (IgA) examination and confirmed by small intestine biopsy. The presence of dental enamel defects and dental caries was evaluated by a calibrated researcher according to AINE's and WHO's criteria, respectively. The history of recurrent aphthous ulcers and dry mouth was obtained through reporting. For the evaluation of the salivary flow, the saliva samples were obtained through the non-stimulated and stimulated saliva collection method. RESULTS: There was a significant association between CD and dental enamel defects (OR=2.38, P=0.045) and dry mouth (OR=9.15, P=0.002). No difference was found for the report of recurrent aphthous ulcers and caries experience between the two groups. Patients with CD had normal pattern of unstimulated and stimulated saliva flow rates (0.67 ± 0.38 ml / min and 1.14 ± 0.47 ml / min, respectively). A higher occurrence of dental enamel defects was observed in patients with classic CD (P=0.054). Of the 1,962 permanent teeth, 59 presented dental enamel defects, 71.8% of which were in patients with CD (P=0.001), predominantly in molars (P=0.009). CONCLUSIONS: CD increased the likelihood of dental enamel defects and dry mouth sensation. The oral examination can be an important auxiliary tool for the identification of cases of the disease.


Assuntos
Doença Celíaca/complicações , Doenças da Boca/etiologia , Doenças Dentárias/etiologia , Adolescente , Criança , Feminino , Humanos , Masculino , Doenças da Boca/epidemiologia , Prevalência , Doenças Dentárias/epidemiologia
3.
Pesqui Odontol Bras ; 15(3): 201-7, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11705267

RESUMO

The present study investigated the factors associated with the development of dental caries in preschool children who receive regular dental care and follow-up. The research was carried out at the Baby Clinic, Londrina State University, and comprised two hundred preschool children, whose ages ranged from 24 to 48 months, as well as their mothers, who had already taken part in a dental program at the Baby Clinic during, at least, the previous twelve months. Regarding oral hygiene habits, there was no significant difference between the preschool children who presented with caries and those who did not present with caries. However, the presence of visible bacterial plaque on the upper incisors was strongly associated with the presence of dental caries. Other factors associated with the presence of caries were: period of formal education of the father or of both parents equal or inferior to 8 years, high sugar consumption and bottle-feeding during sleep. In the studied population, the dietary pattern is still the main cause of carious lesions. In addition, the presence of visible bacterial plaque on the labial surface of the upper incisors must be considered as an important clinical sign, often associated with inadequate patterns of diet and oral hygiene.


Assuntos
Cárie Dentária/epidemiologia , Adulto , Fatores Etários , Alimentação com Mamadeira , Pré-Escolar , Cárie Dentária/microbiologia , Sacarose Alimentar , Feminino , Humanos , Masculino , Pais
4.
Biochem J ; 330 ( Pt 2): 881-8, 1998 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-9480905

RESUMO

An enzyme activity splitting FAD to AMP and riboflavin 4',5'-cyclic phosphate (4',5'-cFMN), with a Km of 6-8 microM, was partially purified from the cytosolic fraction of rat liver homogenates. 4', 5'-cFMN was characterized by enzyme, HPLC, UV-visible and NMR spectroscopic analyses. The data suggest that a novel enzyme, tentatively named FAD-AMP lyase (cyclizing) or FMN cyclase, is involved. Also, 4',5'-cFMN was hydrolysed to 5'-FMN by a rat liver cyclic phosphodiesterase. The results indicate a novel enzymic pathway for flavins in mammals, and support the biological relevance of 4',5'-cFMN, perhaps as a flavocoenzyme or a regulatory signal.


Assuntos
Mononucleotídeo de Flavina/análogos & derivados , Flavina-Adenina Dinucleotídeo/metabolismo , Fígado/enzimologia , Pirofosfatases/metabolismo , Monofosfato de Adenosina/metabolismo , Animais , Cromatografia Líquida de Alta Pressão , Citosol/enzimologia , Feminino , Mononucleotídeo de Flavina/metabolismo , Cinética , Manganês/metabolismo , Modelos Químicos , Fósforo-Oxigênio Liases , Ratos , Ratos Wistar
5.
Biochemistry ; 40(45): 13710-22, 2001 Nov 13.
Artigo em Inglês | MEDLINE | ID: mdl-11695920

RESUMO

An enzyme with FAD-AMP lyase (cyclizing) activity, splitting FAD to AMP and riboflavin 4',5'-phosphate (cFMN), was recently identified [Fraiz, F., et al. (1998) Biochem. J. 330, 881-888]. Now, it has been purified to apparent homogeneity from a rat liver supernatant, by a procedure that includes affinity for ADP-agarose (adsorption required the activating cation Mn2+ and desorption required its removal), to a final activity of 2.2 units/mg after a 240-fold purification with a 15% yield. By SDS-PAGE, only one protein band was observed (Mr = 59 000). The correspondence between protein and enzyme activity was demonstrated by renaturation after SDS-PAGE, by gradient ultracentrifugation followed by analytical SDS-PAGE, and by native PAGE with visualization of enzyme activity by fluorescence. A native Mr of 100 000 (ultracentrifugation) or 140 000 (gel filtration) indicated that FAD-AMP lyase could be a dimer. The enzyme required millimolar concentrations of Mn2+ or Co2+, exhibited different optimum pH values with these cations (pH 8.5 or 7.3, respectively), and was strongly inhibited by ADP or ATP, but not by dADP, dATP, or the reaction products AMP and cFMN. A specificity study was conducted with 35 compounds related to FAD, mostly nucleoside diphosphate-X (NDP-X) derivatives. Besides FAD, the enzyme split 11 of these compounds with the pattern NDP-X --> NMP + P=X. Structure-activity correlations of substrates, nonsubstrates, and inhibitors, and the comparison of the enzymic reactivities of NDP-X compounds with their susceptibilities to metal-dependent chemical degradation, pinpointed the following specificity pattern. FAD-AMP lyase splits ribonucleoside diphosphate-X compounds in which X is an acyclic or cyclic monosaccharide or derivative bearing an X-OH group that is able to attack internally the proximal phosphorus with the geometry necessary to form a P=X product, either a five-atom monocyclic phosphodiester or a cis-bicyclic phosphodiester-pyranose fusion. For instance, NDP-glucose and GDP-alpha-L-fucose were substrates, but dTDP-glucose, NDP-mannose, and GDP-beta-L-fucose were not. Judging from kcat/Km ratios, we found the best substrate to be FAD, followed closely by ADP-glucose (kcat/Km only 2-fold lower, but not a physiological compound in mammals), whereas other substrates exhibited 50-500-fold lower kcat/Km values. However, there was no evidence for specific flavin recognition. Instead, what seems to be recognized is the NDP moiety of NDP-X, with a strong preference for ADP-X. Splitting would then depend on the presence of an adequate X-OH group. The possibility that, besides FAD, there could be in mammals other ADP-X substrates of FAD-AMP lyase is discussed, with emphasis placed on some ADP-ribose derivatives.


Assuntos
Flavina-Adenina Dinucleotídeo/metabolismo , Fígado/enzimologia , Pirofosfatases/isolamento & purificação , Difosfato de Adenosina/química , Difosfato de Adenosina/farmacologia , Trifosfato de Adenosina/química , Trifosfato de Adenosina/farmacologia , Animais , Cátions/metabolismo , Eletroforese em Gel de Poliacrilamida , Inibidores Enzimáticos/química , Inibidores Enzimáticos/farmacologia , Feminino , Flavina-Adenina Dinucleotídeo/química , Galactose/química , Galactose/metabolismo , Glucose/química , Glucose/metabolismo , Concentração de Íons de Hidrogênio , Cinética , Peso Molecular , Fósforo-Oxigênio Liases , Renaturação Proteica , Pirofosfatases/antagonistas & inibidores , Pirofosfatases/metabolismo , Ratos , Ratos Wistar , Relação Estrutura-Atividade , Especificidade por Substrato , Difosfato de Uridina/química , Difosfato de Uridina/farmacologia , Xilose/química , Xilose/metabolismo
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