Paula Cristina Trevilatto

Dr. Paula Cristina Trevilatto


Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 September 2010 in Oral Diseases
Verified
Journal Article
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RWRi Werneck
Ri Werneck
MMMt Mira
Mt Mira
PTPaula Cristina Trevilatto
Paula Cristina Trevilatto

15 April 2004 in Journal of Clinical Periodontology
Verified
Journal Article
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RCRaquel M. Scarel Caminaga
Raquel M. Scarel Caminaga
PTPaula Cristina Trevilatto
Paula Cristina Trevilatto
ASAna P Souza
Ana P Souza
RBRui B Brito
Rui B Brito
LCLuis Eduardo Camargo
Luis Eduardo Camargo
SLSergio Roberto Peres Line
Sergio Roberto Peres Line

24 September 2012 in PLOS ONE
Verified
Journal Article
Open access
PDF file
TSTakehiko Shimizu
Takehiko Shimizu
BHBao Ho
Bao Ho
KDKathleen Deeley
Kathleen Deeley
JBJessica Briseño-Ruiz
Jessica Briseño-Ruiz
IFItalo M. Faraco
Italo M. Faraco
AVAlexandre Vieira
Alexandre Vieira
There is evidence for a genetic component in caries susceptibility, and studies in humans have suggested that variation in enamel formation genes may contribute to caries. For the present study, we used DNA samples collected from 1,831 individuals from various population data sets. Single nucleotide polymorphism markers were genotyped in selected genes (ameloblastin, amelogenin, enamelin, tuftelin, and tuftelin interacting protein 11) that influence enamel formation. Allele and genotype frequencies were compared between groups with distinct caries experience. Associations with caries experience can be detected but they are not necessarily replicated in all population groups and the most expressive results was for a marker in AMELX (p = 0.0007). To help interpret these results, we evaluated if enamel microhardness changes under simulated cariogenic challenges are associated with genetic variations in these same genes. After creating an artificial caries lesion, associations could be seen between genetic variation in TUFT1 (p = 0.006) and TUIP11 (p = 0.0006) with enamel microhardness. Our results suggest that the influence of genetic variation of enamel formation genes may influence the dynamic interactions between the enamel surface and the oral cavity.

1 August 2004 in Journal of Periodontology
Verified
Journal Article
Closed access
RJRui Barbosa de Brito Junior
Rui Barbosa de Brito Junior
RCRaquel M. Scarel Caminaga
Raquel M. Scarel Caminaga
PTPaula Cristina Trevilatto
Paula Cristina Trevilatto
ASAna Paula Souza
Ana Paula Souza
SBSilvana Pereira Barros
Silvana Pereira Barros
Background: Genetic polymorphisms in the vitamin D receptor (VDR) gene are associated with bone homeostasis and diseases in which bone loss is a cardinal sign. The aim of this study was to determine whether chronic periodontal disease in a Brazilian population is associated with polymorphisms in the VDR gene.Methods: Clinical examination and recordings of probing depth and clinical attachment level were performed in 113 unrelated adults who were divided into two groups: 44 healthy individuals (control group) and 69 subjects with chronic periodontitis (CP). DNA was obtained from the subjects' epithelial cells by scraping the buccal mucosa. Two polymorphisms in the VDR gene were analyzed by polymerase chain reaction, followed by TaqI and BsmI restriction endonuclease digestion.Results: Frequencies of VDR/TaqI and VDR/BsmI showed significant differences between the control group and the CP group (P <0.05). The “Tb” haplotype was prevalent in the control group (43.2%), and the “TB” haplotype in the CP group (36.6%). The “TB” haplotype seemed to increase susceptibility to periodontal disease (odds ratio [OR] = 2.19). The heterozygous haplotype “TB/tb” was predominant in the CP group (OR = 4.32; P = 0.005).Conclusions:TaqI and BsmI polymorphisms of the VDR gene are associated with clinical attachment loss due to periodontal disease in a Brazilian population. These findings suggest that VDR genotype might be a risk indicator for susceptibility to chronic periodontitis. J Periodontol 2004;75:1090‐1095.

1 December 2007 in Implant Dentistry
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Journal Article
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CMClaudia Cristina Montes
Claudia Cristina Montes
FPFabiano Alvim Dds Pereira
Fabiano Alvim Dds Pereira
GTGeninho Dds Thomé
Geninho Dds Thomé
EAEdson Durval Menezes Dds Alves
Edson Durval Menezes Dds Alves
RARogéria Vieira Dds Acedo
Rogéria Vieira Dds Acedo
PTPaula Cristina Trevilatto
Paula Cristina Trevilatto
Purpose: Dental implants are currently the aesthetic and functional alternative for tooth replacement. Despite the high success rate shown by longitudinal studies, failures do occur, even in patients who present appropriate clinical conditions. The aim of the present study was to identify factors related to, or determinant of, dental implant loss in patients of the Latin-American Dental Research Institute, Curitiba, PR, Brazil. Materials and Methods: Retrospective analysis of 3578 records of patients who had implants placed in this institute during the period of 1996 to 2006 was performed. Beyond records, panoramic and periapical radiographs were analyzed. Results: Of the 3578 individuals implant treated, failures occurred in 126 (3.5%) patients (mean age 52.2 ± 10.6 years). Men lost more implants (4.5%) than did women (3.1%) (P = 0.05). Most failure occurred before loading (88.2%). Failure was more frequent when the implant was installed in the posterior jaw (58.5%). The main detectable causes of implant loss were evaluated. Most implant losses (75%) did not have an apparent clinical cause. Identified causes were 17.5% iatrogenic conditions (surgical technique, contamination, and/or occlusal trauma), poor bone quality and quantity (3%), peri-implantitis (1%), and 3.5% missing data. Conclusions: The results obtained in this study suggest that host factors can be contributing to the failure of implants.

1 February 2003 in Journal of Clinical Periodontology
Verified
Journal Article
Closed access
ASA. P. De Souza
A. P. De Souza
PTPaula Cristina Trevilatto
Paula Cristina Trevilatto
RCRaquel M. Scarel Caminaga
Raquel M. Scarel Caminaga
RBR. B. Brito
R. B. Brito
SLSergio Roberto Peres Line
Sergio Roberto Peres Line