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1.
Int J Oral Maxillofac Implants ; 0(0): 1-27, 2024 May 24.
Artigo em Inglês | MEDLINE | ID: mdl-38788135

RESUMO

PURPOSE: The study aimed to evaluate the clinical and radiographic results of simultaneous implant placements using transcrestal sinus floor elevation (TSFE) with and without enamel matrix derivative (EMD) application. MATERIAL AND METHODS: Twenty-four patients were randomly assigned into two groups: EMD+TSFE Group was defined as (n=13 patients, 20 implants) TSFE with EMD application, and TSFE Group was defined as (n=11 patients, 20 implants) TSFE without EMD application. The patients recalled at 3- (T3) and 12- (T12) months after surgery. The residual bone height (RBH), implant protrusion length (IPL), peri-implant sinus bone level (SBL), endo-sinus bone gain (ESBG), and implant stability (ISQ) were measured. Multivariable regressions were performed for the groups. RESULTS: The ESBG was 3.72±0.85 mm in the EMD+TSFE group and, was 3.10±0.05 mm in the TSFE group at T3 and there were statistically significant differences. (p<0.05). However, there were no statistically significant differences in ESBG at T12 between the groups. (p>0.05) ISQ values did not show a statistical difference between the groups at T1 and T3, but in the TSFE+EMD group, it showed a statistical increase at T3 in the intra-group evaluation compared to the TSFE group. CONCLUSION: In this study, it can be mentioned that the use of EMD in TSFE operations is effective in new bone formation in the apical part of the implant during the early healing period, but in the long term, no significant difference was shown between cases in which EMD was used or not in terms of new bone formation and primary and secondary stabilization. The study was submitted at ClinicalTrials.com; the clinical trial number is ###.

2.
J Periodontal Res ; 58(2): 456-464, 2023 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-36755315

RESUMO

BACKGROUND AND OBJECTIVES: Recently, the terms autophagy and apoptosis have been studied on implants, especially in cell culture and in vitro studies, but in vivo evaluations are limited. The aim of this study was to compare the differences in apoptosis and autophagy intensity at the molecular and cellular level in periodontal and peri-implant diseases. METHODS: Sixty-four biopsy samples were obtained from 52 patients, 36 female and 16 male, whose mean age was between 18 and 75, and were included in the study. The periodontitis group was defined as PG (n:30 sample) and the peri-implantitis group as IG (n:34 samples). Granulation tissues as biopsy materials were collected, and immunohistochemical analysis was performed with hematoxylin-eosin, Masson's trichrome, anti-MAP1LC3A, anti-beclin, and anti-active caspase-3 antibodies and terminal TdT-mediated dUTP-biotin nick end labeling (TUNEL) methods. The histological slide images were evaluated with the ImageJ software program. Inflammatory cell density in epithelial tissue, inflammatory cell density in connective tissue, the density of necrotic tissue debris, and collagen density in connective tissue were scored between 0 and 3 (0: none, 1: minimal, 2: moderate, 3: severe by hematoxylin-eosin and Masson's trichrome). The antibody binding reaction areas were evaluated per unit area (mm2 ) in connective tissue by immunohistochemical examination. RESULTS: As histochemical evaluations, there was no statistically significant differences the mean inflammatory cell density value in the epithelial tissue, inflammatory cell density value in the connective tissue, density value of necrotic tissue debris, collagen density value in the connective tissue between the groups. There was no statistically significant difference on immunohistochemical staining with LC3, caspase-3, Beclin-1 and TUNEL between the two groups (p > .05). CONCLUSIONS: A higher rate of inflammatory accumulation was shown on peri-implantitis, but no difference was found between periodontitis and peri-implantitis according to autophagy and apoptosis markers. Studies with high sample sizes with different markers are needed.


Assuntos
Implantes Dentários , Peri-Implantite , Periodontite , Humanos , Masculino , Feminino , Peri-Implantite/metabolismo , Caspase 3 , Amarelo de Eosina-(YS) , Hematoxilina , Periodontite/metabolismo , Colágeno , Apoptose , Autofagia
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