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  • 1
    In: Caries Research, S. Karger AG, Vol. 51, No. 3 ( 2017), p. 209-215
    Abstract: The antimicrobial peptides human β-defensins (hBDs) are encoded by β-defensin genes (DEFBs) and are possibly involved in caries susceptibility. In this study we aimed (1) to investigate the relationship between salivary hBDs and caries and (2) to evaluate the association of genetic polymorphisms in DEFB1 and microRNA202 (miRNA202) with salivary levels of hBDs and caries experience. Two data sets were available for this study, totalizing 678 Brazilian children. Dental examination and saliva collection were performed in all included children. The salivary level for hDB1, hBD2, and hBD4 was assessed by ELISA sandwich technique in 168 children. The DNA was extracted from saliva, and polymorphisms in DEFB1 and miRNA202 were analyzed by real-time PCR. Statistical analysis was performed to investigate the associations between caries experience, hBD salivary level, genotype, and allele distribution, with an alpha of 0.05. The hBD1 level was significantly higher in caries-free children ( 〈 i 〉 p 〈 /i 〉 〈 0.0001). The miRNA202 was associated with a lower level of salivary hBD1 ( 〈 i 〉 p 〈 /i 〉 〈 0.05). Also, the polymorphic distribution of miRNA202 was associated with caries ( 〈 i 〉 p 〈 /i 〉 = 0.006). The polymorphisms in DEFB1 were not associated with hBD salivary level and caries experience ( 〈 i 〉 p 〈 /i 〉 〉 0.05). In conclusion, our results indicate that genetic polymorphism in miRNA202 is involved in hBD1 salivary level as well as caries experience in children.
    Type of Medium: Online Resource
    ISSN: 0008-6568 , 1421-976X
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2017
    detail.hit.zdb_id: 1482046-8
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  • 2
    In: Caries Research, S. Karger AG, Vol. 51, No. 3 ( 2017), p. 225-230
    Abstract: Saliva components play a crucial role in the integrity of the dental enamel and in caries susceptibility. The saliva characteristics are controlled by many factors, including genetic factors. Therefore, this study aimed to evaluate the association between the genetic variations in genes expressed in enamel development with calcium and phosphorus levels in saliva. We collected 276 unrelated 12-year-old children from private and public schools. Saliva was collected for DNA extraction from oral cells and for measurement of calcium and phosphorus. Inductively coupled plasma-mass spectrometry determined calcium and phosphorus levels in whole saliva. Fifteen genetic variations in 9 genes were analyzed. The genotype was determined by real-time polymerase chain reactions. Data were analyzed using Plink with an alpha of 5%. Genetic variations in 〈 i 〉 AMELX 〈 /i 〉 , 〈 i 〉 AMNB 〈 /i 〉 and 〈 i 〉 ESRRB 〈 /i 〉 were associated with the calcium level in saliva (p 〈 0.05). A borderline association was observed in 〈 i 〉 ENAM 〈 /i 〉 allele distribution shown with phosphate level in saliva (p = 0.049). In conclusion, our results are the first to report that genetic variations contribute to calcium and phosphorus levels in saliva.
    Type of Medium: Online Resource
    ISSN: 0008-6568 , 1421-976X
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2017
    detail.hit.zdb_id: 1482046-8
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  • 3
    In: Caries Research, S. Karger AG, Vol. 51, No. 2 ( 2017), p. 102-108
    Abstract: Polymorphisms in genes encoding the enzymes involved in the metabolism of homocysteine, such as methionine synthase ( 〈 i 〉 MTR 〈 /i 〉 ) and methionine synthase reductase ( 〈 i 〉 MTRR 〈 /i 〉 ), play an important function in the metabolism of folic acid and vitamin B 〈 sub 〉 12 〈 /sub 〉 . The present study aimed to evaluate the association of polymorphisms in genes 〈 i 〉 MTR 〈 /i 〉 (rs1805087) and 〈 i 〉 MTRR 〈 /i 〉 (rs1801394) with susceptibility of early childhood caries (ECC) and with body mass index alterations. A cross-sectional study was performed in 488 children aged from 2 to 6 years from 25 public day care centers in Rio de Janeiro, Brazil. Demographic data and oral health habits were obtained through a questionnaire. Anthropometric measurements and caries experience data were collected by 2 examiners ( & #x03BA; = 0.80). Genotyping of the selected polymorphisms was carried out by TaqMan real-time PCR using genomic DNA extracted from buccal cells. Allele and genotype frequencies were compared between groups with and without disease. The 〈 i 〉 t 〈 /i 〉 test, & #x03C7; 〈 sup 〉 2 〈 /sup 〉 test, odds ratio, Pearson correlation tests, and logistic regression analysis were used ( 〈 i 〉 p 〈 /i 〉 ≤ 0.05). The mean white spot lesion score was 1.18 (±2.57) in normal weight children and 2.50 (±3.87) in underweight children ( 〈 i 〉 p 〈 /i 〉 = 0.05). For 〈 i 〉 MTRR 〈 /i 〉 polymorphisms, significant differences were observed for allele and genotype frequency distributions between caries-free and caries-affected children ( 〈 i 〉 p 〈 /i 〉 = 0.03 and 0.04 for allele and genotype frequencies, respectively) and in the genotype frequencies between normal weight and underweight children ( 〈 i 〉 p 〈 /i 〉 = 0.04). Our results suggest an association between underweight and ECC; in addition it is suggested that 〈 i 〉 MTRR 〈 /i 〉 is a common genetic risk factor for ECC and underweight.
    Type of Medium: Online Resource
    ISSN: 0008-6568 , 1421-976X
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2017
    detail.hit.zdb_id: 1482046-8
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  • 4
    In: Caries Research, S. Karger AG, Vol. 53, No. 4 ( 2019), p. 441-446
    Abstract: The aim of this study was to investigate the association between genetic polymorphisms in 〈 i 〉 MMP8 〈 /i 〉 , 〈 i 〉 MMP13 〈 /i 〉 , and 〈 i 〉 MMP20 〈 /i 〉 with caries experience and developmental defects of enamel (DDE) in children from the Amazon region of Brazil. Den tal caries and DDE data were collected through clinical examination from 216 children. Genomic DNA was extracted from saliva, and genotyping of selected polymorphisms in 〈 i 〉 MMP8 〈 /i 〉 (rs17099443 and rs3765620), 〈 i 〉 MMP13 〈 /i 〉 (rs478927 and rs2252070), and 〈 i 〉 MMP20 〈 /i 〉 (rs1784418) was performed using TaqMan chemistry and endpoint analysis. χ 〈 sup 〉 2 〈 /sup 〉 or Fisher’s exact tests were used to compare allele and genotype distributions between children with caries experience and caries-free children and between DDE-affected and -unaffected children with an established alpha of 5%. The polymorphism rs478927 in 〈 i 〉 MMP13 〈 /i 〉 was associated with caries experience and DDE ( 〈 i 〉 p 〈 /i 〉 & #x3c; 0.05). The analysis performed comparing children with both conditions (caries experience plus DDE) and children with neither of the conditions (caries-free chil dren without DDE) demonstrated that children carrying the 〈 i 〉 MMP13 〈 /i 〉 rs478927 TT genotype were more likely to have concomitant occurrence of these two conditions (OR = 5.8, 95% CI 2.1–15.8; 〈 i 〉 p 〈 /i 〉 = 0.0003). In conclusion, the genetic polymorphism rs478927 in 〈 i 〉 MMP13 〈 /i 〉 was associated with caries experience and DDE.
    Type of Medium: Online Resource
    ISSN: 0008-6568 , 1421-976X
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2019
    detail.hit.zdb_id: 1482046-8
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  • 5
    In: Caries Research, S. Karger AG, Vol. 52, No. 1-2 ( 2018), p. 1-6
    Abstract: The aim of this study was to evaluate whether genetic polymorphisms in 〈 i 〉 AMELX 〈 /i 〉 , 〈 i 〉 AMBN 〈 /i 〉 , 〈 i 〉 ENAM 〈 /i 〉 , 〈 i 〉 TFIP11 〈 /i 〉 , and 〈 i 〉 TUFT1 〈 /i 〉 genes are associated with dental fluorosis (DF). A total of 1,017 children from 2 Brazilian cohorts were evaluated. These populations lived in cities with fluoridation of public water supplies. DF was assessed in erupted permanent teeth using the modified Dean index. The polymorphisms rs946252, rs12640848, rs4694075, rs5997096, and rs4970957 were analyzed by real-time PCR from genomic DNA. Associations between DF, genotype, and allele distribution were evaluated using the & #x03C7; 〈 sup 〉 2 〈 /sup 〉 test, with an alpha of 5%. The polymorphisms rs4694075, rs5997096, and rs4970957 in 〈 i 〉 AMBN 〈 /i 〉 , 〈 i 〉 TFIP11 〈 /i 〉 , and 〈 i 〉 TUFT1 〈 /i 〉 were associated with DF ( 〈 i 〉 p 〈 /i 〉 〈 0.05). In conclusion, enamel matrix genes are associated with DF.
    Type of Medium: Online Resource
    ISSN: 0008-6568 , 1421-976X
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2018
    detail.hit.zdb_id: 1482046-8
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  • 6
    In: Caries Research, S. Karger AG, Vol. 53, No. 2 ( 2019), p. 228-233
    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 ( 〈 i 〉 n 〈 /i 〉 = 20; resistant to DF) and A/J ( 〈 i 〉 n 〈 /i 〉 = 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 〈 i 〉 Amelx 〈 /i 〉 , 〈 i 〉 Ambn 〈 /i 〉 , 〈 i 〉 Ambn 〈 /i 〉 , 〈 i 〉 Col14a1 〈 /i 〉 , 〈 i 〉 Col1a1 〈 /i 〉 , 〈 i 〉 Col5a2 〈 /i 〉 , 〈 i 〉 Enam 〈 /i 〉 , 〈 i 〉 Fam20a 〈 /i 〉 , 〈 i 〉 Fam83h 〈 /i 〉 , 〈 i 〉 Foxo1 〈 /i 〉 , 〈 i 〉 Klk4 〈 /i 〉 , 〈 i 〉 Mmp20 〈 /i 〉 , 〈 i 〉 Serpinf1 〈 /i 〉 , 〈 i 〉 Serpinh1 〈 /i 〉 , 〈 i 〉 Smad3 〈 /i 〉 , 〈 i 〉 Tuft1 〈 /i 〉 , 〈 i 〉 〈 /i 〉 and 〈 i 〉 Wdr72 〈 /i 〉 were genotyped by real-time PCR using Taqman chemistry. Overrepresentation of alleles and genotypes in DF was evaluated using the χ 〈 sup 〉 2 〈 /sup 〉 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 〈 i 〉 Ambn 〈 /i 〉 , 〈 i 〉 Col14a1 〈 /i 〉 , and 〈 i 〉 Mmp20 〈 /i 〉 , respectively, genotype and allele distributions were statistically significantly different between A/J and 129P3/J strains ( 〈 i 〉 p 〈 /i 〉 & #x3c; 0.05). In conclusion, polymorphisms in 〈 i 〉 Ambn, Col14a1 〈 /i 〉 , and 〈 i 〉 Mmp20 〈 /i 〉 are associated with the susceptibility to DF.
    Type of Medium: Online Resource
    ISSN: 0008-6568 , 1421-976X
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2019
    detail.hit.zdb_id: 1482046-8
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  • 7
    In: Caries Research, S. Karger AG, Vol. 49, No. 1 ( 2015), p. 70-77
    Abstract: Early childhood caries (ECC) is a chronic, infectious disease that affects the primary dentition of young children. It is the result of an imbalance of risk factors and protective factors that influence the disease. The aim of this study was to assess genetic and environmental factors that may contribute to ECC. Two hundred and fifty-nine unrelated children were evaluated using a cross-sectional design. Data on oral habits were obtained through a questionnaire, and caries experience data were collected by clinical examination. Twenty-three markers in 10 genes were studied. Genotyping of the selected polymorphisms was carried out by real-time PCR. Regression analyses were performed comparing individuals with and without caries experience. Of 259 subjects, 123 were caries free. The genotype TT in 〈 i 〉 ALOX15 〈 /i 〉 (rs7217186) was a risk factor for ECC, whereas the genotypes GG in 〈 i 〉 ENAM 〈 /i 〉 (rs1264848), AG and GG in 〈 i 〉 KLK4 〈 /i 〉 (rs198968), CT in 〈 i 〉 LTF 〈 /i 〉 (rs4547741), and GG in 〈 i 〉 TUFT1 〈 /i 〉 (rs3790506) were protective for EEC. 〈 b 〉 〈 /b 〉 In conclusion, environmental factors and gene interactions can act as protective or risk factors for ECC. These factors together contribute to the presence and severity of the disease.
    Type of Medium: Online Resource
    ISSN: 0008-6568 , 1421-976X
    RVK:
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2015
    detail.hit.zdb_id: 1482046-8
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