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1.
Acta Stomatol Croat ; 51(4): 290-299, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29872234

RESUMEN

BACKGROUND: Congenitally missing permanent teeth (CMPT) was recognized as a clinical and public health problem in pediatric dentistry. AIM: To determine the prevalence of CMPT among orthodontic patients in Southern Croatia. MATERIALS AND METHODS: In a retrospective study, we analyzed CMPT in patients from three different regions in Southern Croatia (SC). Two orthodontic practices from each region were selected and a total of 4649 records of patients aged 6 - 15 years, who were clinically examined for orthodontic treatment between 2008 and 2015, were evaluated. We excluded 219 patients and 4430 patients remained for further analysis. RESULTS: There was no difference in prevalence of CMPT among regions in Southern Croatia, and the whole sample was evaluated. CMPT was found in 345(7.8%) patients. The highest proportion of CMPT was with one or two missing teeth 122 (81.9%) and 158 (80.6%), followed by those with three to five missing teeth or moderate hypodontia, 25(16.8%) and 35(17.9%), in males, and females respectively. Bilateral hypodontia of the lower second premolars and upper second incisors was more common than unilateral hypodontia. CONCLUSIONS: The obtained results of high prevalence of CMPT in Southern Croatia reinforce the need for a timely diagnostics and treatment of moderate and severe cases.

2.
Arch Oral Biol ; 66: 155-64, 2016 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-26954096

RESUMEN

AIMS: Pathogenic mechanisms involved in early submerged implant failure are poorly understood. In this study we immunohistochemically analyse differences in proliferation, apoptosis and inflammation in edentulous ridge oral mucosa (ERM) of successful and early failed submerged implants. MATERIALS AND METHODS: 30 samples of ERM covering successful and early failed submerged implants were obtained at the end of osseointegration period along with control samples of healthy ERM. Sections were stained with Ki-67 (proliferation), caspase-3 (apoptosis) and syndecan-1 (epithelial marker). Percentage of positive cells was analysed by Kruskal-Wallis test and Dunn's post hoc test. Co-localization of Ki-67 and caspase-3 with α-SMA, CD68 and TGF-ß was done by double immunofluorescence. RESULTS: There was no significant difference in number of Ki-67 positive cells within surface epithelium (SE) in all groups. Proliferation was significantly higher in underlying connective tissue (UCT) of ERM of early failed submerged implants (26%) compared to ERM of successful submerged implants (3%) and controls (4%). More apoptotic cells appeared in UCT of early failed submerged implants (8%) compared to UCT of successful submerged implants (4%) and UCT of control ERM (3%). Co-localization of Ki-67 and α-SMA in ERM of early failed submerged implants disclosed proliferating fibroblasts and pericytes of blood vessels. Macrophages and cells expressing TGF-ß appeared in UCT of failed implants. Expression of syndecan-1 was significantly weaker in SE of early failed submerged implants. CONCLUSIONS: Imbalance between proliferation and apoptosis, changes in syndecan-1 expression and inflammation are histopathological features of ERM of early failed submerged implants.


Asunto(s)
Actinas/biosíntesis , Implantes Dentales/efectos adversos , Fracaso de la Restauración Dental , Mucosa Bucal/metabolismo , Boca Edéntula/metabolismo , Sindecano-1/biosíntesis , Actinas/fisiología , Anciano , Antígenos CD/metabolismo , Antígenos de Diferenciación Mielomonocítica/metabolismo , Apoptosis/fisiología , Caspasa 3/metabolismo , Proliferación Celular/fisiología , Implantación Dental Endoósea , Femenino , Humanos , Macrófagos/metabolismo , Masculino , Persona de Mediana Edad , Mucosa Bucal/irrigación sanguínea , Mucosa Bucal/patología , Boca Edéntula/patología , Oseointegración , Sindecano-1/fisiología , Factor de Crecimiento Transformador beta/análisis , Factor de Crecimiento Transformador beta/biosíntesis , Factor de Crecimiento Transformador beta/fisiología
3.
Coll Antropol ; 38 Suppl 2: 173-80, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-25643546

RESUMEN

The purpose of this study was to estimate unmet orthodontic treatment needs of adolescents in Zagreb, Croatia, compare normative and self-perceived need and investigate factors influencing the reason why untreated subjects with severe malocclusions have not been treated before. One thousand and forty-two non-orthodontically treated subjects in age groups of 12 and 18 years, from sixteen randomly selected public schools in Zagreb, Croatia were examined. The Dental Aesthetic Index, Aesthetic Component of Index of Orthodontic Treatment Need and a questionnaire concerning self-perceived orthodontic treatment need, perception of aesthetics, function, behaviors and socioeconomic status were used. Around one third of untreated adolescent population had an objective need, less than 20 percent had aesthetic need, and self-perceived need was reported in one third of population. Associations and agreements between objective, aesthetic and self-perceived need were weak (r = 0.27-0.48; p < 0.001 and κ in range from 0.05 (p > 0.05) to 0.32 (p < 0.05), respectively). Satisfaction with personal dental appearance and awareness of malocclusion were better related in persons with no treatment need or minor need (r = 0.53-0.59) than in those with major need (r = 0.31-0.40). Multiple logistic regression analyses confirmed that objective, aesthetic and self-perceived needs were better related between themselves than to socio-economic status of subjects, function, activities of daily living and oral health-related behaviors. It appears that self-perceived treatment need has low role in predicting objective need, but relation between satisfaction and awareness of malocclusion could be one of basic factors in process of making decision to go for treatment and maybe could serve in predicting patient's compliance.


Asunto(s)
Atención Odontológica/estadística & datos numéricos , Maloclusión/epidemiología , Maloclusión/terapia , Evaluación de Necesidades/estadística & datos numéricos , Ortodoncia/estadística & datos numéricos , Aceptación de la Atención de Salud/estadística & datos numéricos , Adolescente , Niño , Croacia/epidemiología , Femenino , Humanos , Masculino , Prevalencia
4.
Acta Histochem ; 115(2): 144-50, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-22748563

RESUMEN

Chronic renal failure is often associated with skin itching (pruritus) in dialysis patients. In order to investigate the possible causes of pruritus, the epidermis of the thigh of 12 dialysis patients and 4 controls from patients without renal disease were examined. The sections of the epidermis were measured and immunohistochemically analyzed using antibodies to Bcl-2, Bax, caspase-3 proteins and TUNEL method. While the mean thickness of normal epidermis was 53 µm, in dialysis patients it ranged between 23 and 34 µm during the 3-5 year period on dialysis. Compared to normal skin, the fine balance between the Bcl-2 and Bax proteins did not greatly change in the epidermis of dialysis patients during the three years of dialysis. Following five-year dialysis, the epidermis displayed increased Bax and decreased Bcl-2 expression in the basal and intermediate epidermal layers, as well as the presence of apoptotic cells (TUNEL and caspase-3 positive) both in the superficial and intermediate epidermal layers. Our study demonstrated the predominant expression of cell death Bax proteins over cell survival Bcl-2 proteins, and apoptotic cells in the deeper layers of the epidermis in patients on long-term dialysis. We speculate that the thinning of the epidermis might be associated with the appearance of dead cells in the deeper epidermal layers, while the changed internal milieu of epidermal cells could possibly affect the intra-epidermal nerve endings thus leading to the sensation of pruritus.


Asunto(s)
Apoptosis , Epidermis/patología , Fallo Renal Crónico/metabolismo , Proteínas Proto-Oncogénicas c-bcl-2/metabolismo , Prurito/metabolismo , Piel/patología , Proteína X Asociada a bcl-2/metabolismo , Anciano , Biopsia , Caspasa 3/metabolismo , Muerte Celular , Supervivencia Celular , Epidermis/metabolismo , Células Epiteliales/citología , Humanos , Inmunohistoquímica/métodos , Etiquetado Corte-Fin in Situ , Microscopía Fluorescente , Persona de Mediana Edad , Diálisis Renal
5.
Acta Histochem ; 114(5): 469-79, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-22113177

RESUMEN

The spatial and temporal distribution of epithelial membrane antigen (EMA), mesothelin and nestin was immunohistochemically analyzed in developing and adult human serous membranes and mesotheliomas in order to detect possible differences in the course of mesenchymal to epithelial transformation, which is associated with differentiation of mesothelial cells during normal development and tumorigenesis. Pleura and pericardium developing from the visceral mesoderm gradually transform into mesothelial cells and connective tissue. EMA appeared in mesothelium of both serous membranes during the early fetal period, whereas during further development, EMA expression was retained only in the pericardial mesothelium. It increased in both pleural mesothelium and connective tissue. Mesothelin appeared first in pericardial submesothelial cells and later in surface mesothelium, while in pleura it was immediately localized in mesothelium. In adult serous membranes, EMA and mesothelin were predominantly expressed in mesothelium. Nestin never appeared in mesothelium, but in connective tissues and myocardial cells and subsequently decreased during development, apart from in the walls of blood vessels. Mesothelial cells in the two serous membranes developed in two separate developmental pathways. We speculate that submesothelial pericardial and mesothelial pleural cells might belong to a population of stem cells. In epithelioid mesotheliomas, 13% of cells expressed nestin, 39% EMA and 7% mesothelin.


Asunto(s)
Proteínas Ligadas a GPI/análisis , Proteínas de Filamentos Intermediarios/análisis , Mesotelioma/metabolismo , Mucina-1/análisis , Proteínas del Tejido Nervioso/análisis , Membrana Serosa/embriología , Membrana Serosa/metabolismo , Anciano , Femenino , Humanos , Inmunohistoquímica , Masculino , Mesotelina , Mesotelioma/patología , Persona de Mediana Edad , Nestina
6.
Eur J Oral Sci ; 118(6): 537-46, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21083614

RESUMEN

The regulators of apoptosis Bcl-2, Bax, caspase-3, p53, and Hsp70 were analyzed immunohistochemically in the developing human mandible of eight human conceptuses from weeks 5 to 10 of gestation. During this period, all proteins displayed an increased pattern of expression in the mandible ectomesenchyme and in newly formed bone, except for caspase-3, which showed decreased expression in the ectomesenchyme, but appeared first in the ossification zone at the 7th wk of development. Simultaneously, the oral epithelium showed weak (p53) to strong (hsp70) expression of all proteins investigated, while in Meckel's cartilage cells, bcl-2 was expressed weakly and hsp70 was expressed moderately. Cells on the surface of the forming bone were predominantly bax positive, and only occasionally bcl-2 positive. Only a few cells on the surface and inside the bony spicules co-expressed bax and bcl-2. Terminal deoxynucleotidyl transferase (TdT)-mediated biotin-dUTP nick-end labelling (TUNEL)-positive cells were found to be apoptotic osteoblasts. The expression of all proteins investigated changed dynamically during early mandible development and the subsequent differentiation of Meckel's cartilage and bone. While interactions between those factors might be associated with the survival of Meckel's cartilage, in the ossification zone they might participate in the control of cell numbers, mineralization, and bone remodelling. Among many other factors, precise orchestration of pro- and anti-apoptotic factors contributes to normal mandible development.


Asunto(s)
Factor Inductor de la Apoptosis/análisis , Proteínas Inhibidoras de la Apoptosis/análisis , Mandíbula/embriología , Matriz Ósea/embriología , Remodelación Ósea/fisiología , Calcificación Fisiológica/fisiología , Cartílago/embriología , Caspasa 3/análisis , Recuento de Células , Ectodermo/embriología , Epitelio/embriología , Técnica del Anticuerpo Fluorescente , Edad Gestacional , Proteínas HSP70 de Choque Térmico/análisis , Humanos , Etiquetado Corte-Fin in Situ , Mesodermo/embriología , Mucosa Bucal/embriología , Osteoblastos/citología , Osteocitos/citología , Osteogénesis/fisiología , Proteínas Proto-Oncogénicas c-bcl-2/análisis , Proteína p53 Supresora de Tumor/análisis , Proteína X Asociada a bcl-2/análisis
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