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1.
Forensic Sci Int ; 301: e8-e13, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31196583

RESUMEN

An evaluation of the development of a child's skeleton and estimation of bone age provides an insight into a child's overall maturation. This study aimed to introduce a contemporary method for assessing bone age of Australian children using formulae incorporating carpal areal measurements. The standards introduced in this study can be used to assess the developmental status of Australian children who may be affected by growth-related illnesses. Additionally, in situations where the living age of a subadult is unknown, methodologies to accurately estimate age are required, particularly in the Western world where knowledge of the age of an individual is necessary for legal reasons. The sample consisted of retrospective hand and wrist radiographs acquired from 541 children (females: 246, males: 295) aged from birth to 20 years. Using the DICOM viewer Weasis, the carpal area ratio (B.Ar/T.Ar) was calculated for each individual radiograph by measuring the carpal bone area (B.Ar) and total tissue area of the carpus (T.Ar). A changepoint regression model demonstrated that the model constructed in this study was the most accurate in the younger age groups and was able to accurately determine whether a child was under 12 years if female and 13 years if male. A rapid acceleration of growth was observed at approximately 12-13 years in our sample, which may represent the onset of the pubertal growth spurt; this resulted in a high data variance and low model prediction accuracy in female and male children older than 12 and 13 years, respectively.


Asunto(s)
Determinación de la Edad por el Esqueleto/métodos , Huesos de la Mano/diagnóstico por imagen , Huesos de la Mano/crecimiento & desarrollo , Osteogénesis , Adolescente , Australia , Niño , Preescolar , Femenino , Antropología Forense , Humanos , Lactante , Recién Nacido , Masculino , Radiografía , Radio (Anatomía)/diagnóstico por imagen , Radio (Anatomía)/crecimiento & desarrollo , Análisis de Regresión , Reproducibilidad de los Resultados , Estudios Retrospectivos , Cúbito/diagnóstico por imagen , Cúbito/crecimiento & desarrollo , Adulto Joven
2.
Calcif Tissue Int ; 80(3): 176-83, 2007 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-17334881

RESUMEN

Fracture healing is retarded in the presence of cyclooxygenase-2 (COX-2) inhibitors, demonstrating an important role of COX-2 in trauma-induced woven bone adaptation. The aim of this experiment was to determine the influence of COX-2 inhibition on the remodeling and consolidation of nontraumatic woven bone produced by mechanical loading. A periosteal woven bone callus was initiated in the right tibia of female Wistar rats following a single bout of four-point bending, applied as a haversine wave for 300 cycles at a frequency of 2 Hz and a magnitude of 65 N. Daily injections of vehicle (VEH, polyethylene glycol) or the COX-2 inhibitor 5,5-dimethyl-3-3(3 fluorophenyl)-4-(4-methylsulfonal)phenyl-2(5H)-furanone (DFU, 2.0 mg . kg(-1) and 0.02 mg . kg(-1) i.p.), commenced 7 days postloading, and tibiae were examined 2, 3, 4, and 5 weeks postloading. Tibiae were dissected, embedded in polymethylmethacrylate, and sectioned for histomorphometric analysis of periosteal woven bone. No significant difference in peak woven bone area was observed between DFU-treated and VEH rats. However, treatment with DFU resulted in a temporal defect in woven bone formation, where the achievement of peak woven bone area was delayed by 1 week. Woven bone remodeling was observed in DFU-treated rats at 21 days postloading, demonstrating that remodeling of the periosteal callus is not prevented in the presence of a COX-2 inhibitor in the rat. We conclude that COX-2 inhibition does not significantly disrupt the mechanism of woven bone remodeling but alters its timing.


Asunto(s)
Huesos/patología , Inhibidores de la Ciclooxigenasa 2/farmacología , Ciclooxigenasa 2/metabolismo , Animales , Desarrollo Óseo/efectos de los fármacos , Huesos/metabolismo , Femenino , Curación de Fractura , Masculino , Osteogénesis , Periostio/patología , Isoformas de Proteínas , Ratas , Ratas Wistar , Tibia/patología , Factores de Tiempo
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