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1.
Clin Oral Investig ; 21(5): 1457-1464, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-27401181

RESUMEN

OBJECTIVE: The objective of this study was to develop a simple tool for the assessment of possible dental treatment needs (DTN) for non-dental professionals (Mini Dental Assessment, MDA). To keep the assessment universal, we aimed to base it on the patient's history and a simple chewing efficiency test (CET) as the dental status is a known determinant for chewing efficiency. MATERIALS & METHODS: The assessment was developed using data from 169 patients from two sites (University Hospital Giessen, St. Bonifatius Hospital Lingen, both Germany). In all patients, a dental examination was performed, the denture status was evaluated (based on the California Dental Association criteria; CDA criteria), and the DTN was determined. In addition, the time since the patient's last visit to a dentist (TLVD) and denture age (DA) were assessed. Furthermore, a CET was carried out and the comminution score was determined (CETS). RESULTS: In total, 108 patients required dental treatment. The mean value (±SD) was 2.9 ± 0.9 score points for the DTN, 2.5 ± 3.8 years for the TLVD, and 10.8 ± 8.9 years for the DA. There was a significant correlation (Spearman, P < .05) between the DTN and degree of comminution (3.4 ± 1.8). Based on the results of the statistical analysis, the intended assessment tool was developed using the variables CETS, TLVD, and DA weighed by their respective regression coefficients (10:3:1). Subsequently, the resulting MDA score (51.32 ± 28.14) was calculated. A sensitivity/specificity analysis was conducted and a receiver operating characteristic curve was calculated (SPSS 17.0, area under curve 0.805; 95 % CI 0.738-0.873). CONCLUSION: It can be concluded that the dental status of elderly patients is reflected in the outcome of the MDA. However, ongoing validation is needed. TRIAL REGISTRATION: DRKS00003219.


Asunto(s)
Atención Odontológica , Evaluación Geriátrica , Necesidades y Demandas de Servicios de Salud , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Alemania , Humanos , Masculino , Masticación/fisiología , Persona de Mediana Edad , Sensibilidad y Especificidad
2.
Digestion ; 63(4): 214-9, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11435720

RESUMEN

BACKGROUND/AIMS: Early weaning has been shown to induce intestinal ornithine decarboxylase (ODC) activities and cell proliferation in rats. No information is available about the effect of early weaning on ODC activity in the stomach. METHODS: Suckling rats were prematurely weaned on postnatal day 15 and followed through day 21. Oxyntic gland mucosa of stomach was obtained on postnatal days 15, 16, 18 and 21 (days 0, 1, 3 and 6 after early weaning) and assayed for ODC activity, DNA, protein and pepsinogen activity. alpha-Difluoromethyl ornithine (DFMO), a specific ODC inhibitor, was given orally to early-weaned pups and its resultant effects were assessed on days 1 and 6 after early weaning. RESULTS: Stomach mucosal wet weight, DNA, protein and pepsinogen activities significantly increased on day 6 after early weaning. ODC activity increased on days 1, 3, and 6 after early weaning, with the highest increase (3-fold) on day 1 when compared to controls. The increases of ODC activity, DNA and protein contents as induced by early weaning were significantly suppressed when pups were exposed to DFMO. However, no suppression of pepsinogen activity was observed. CONCLUSIONS: Our study shows that early weaning induces ODC activity and functional growth in the stomach. Gastric ODC activity is essential in gastric mucosal growth processes but not in differentiation. The induction of stomach ODC may act as an early marker in the growth of stomach mucosa induced by early weaning in rats.


Asunto(s)
Inducción Enzimática/efectos de los fármacos , Inducción Enzimática/fisiología , Mucosa Gástrica/metabolismo , Ornitina Descarboxilasa/biosíntesis , Ornitina Descarboxilasa/efectos de los fármacos , Ratas Sprague-Dawley/fisiología , Destete , Animales , Peso Corporal/efectos de los fármacos , Peso Corporal/fisiología , Eflornitina/antagonistas & inhibidores , Inhibidores Enzimáticos/farmacología , Femenino , Mucosa Gástrica/efectos de los fármacos , Mucosa Gástrica/enzimología , Modelos Animales , Pepsinógenos/biosíntesis , Pepsinógenos/efectos de los fármacos , Embarazo , Ratas , Estómago/efectos de los fármacos , Estómago/crecimiento & desarrollo , Factores de Tiempo
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