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Introducción: el desarrollo esquelético y dental es una condición determinante como factor principal de mala oclusión e influye en la evaluación, diagnóstico y planificación de los tratamientos de ortodoncia. Objetivo: estimar la correlación entre la edad cronológica y dental con los estadios de maduración vertebral. Material y métodos: la edad cronológica y dental se estimó por los métodos de Baccetti y el de Demirjian, con la lectura de 400 radiografías panorámicas y laterales de cráneo de 205 mujeres y 195 varones, con edades entre 4 y 17 años. La significancia estadística se estableció con el valor p < 0.05 del coeficiente de correlación de Pearson utilizando el programa SPSS v.24. Resultados: se observó un mayor porcentaje entre el estadio D de Demirjian con el estadio I de madurez de las vértebras cervicales (CVM) de Baccetti, seguido del estadio de calcificación dentaria E con el estadio CVM II. Además, existió una correlación moderada entre el método de Baccetti y el método de Demirjian en la pieza 37 (R2 = 0.3741) para la apreciación de la edad cronológica de un individuo. Conclusión: existe una buena correlación entre la edad cronológica y dental con los estadios de la maduración vertebral cervical, sin existir diferencias significativas por el sexo del individuo (AU)

Introduction: skeletal and dental development is a determining condition as the main factor of malocclusion and influences the evaluation, diagnosis, and planning of orthodontic treatments. Objective: to estimate the correlation between chronological and dental age with vertebral maturation stages. Material and methods: chronological and dental age was estimated by the Baccetti and Demirjian methods, with the reading of 400 panoramic and lateral skull radiographs of 205 women, and 195 men, aged between 4 and 17 years. Statistical significance was established with the value p < 0.05 of the Pearson correlation coefficient using the SPSS v.24 program. Results: a higher percentage was observed between Demirjian stage D with Baccetti cervical vertebral maturation (MVC) stage I, followed by dental calcification stage E with MVC stage II. In addition, there was a moderate correlation between the Baccetti method and the Demirjian method in piece 37 (R2 = 0.3741) for the assessment of the CD of an individual. Conclusion: there is a good correlation between chronological and dental age with the stages of cervical vertebral maturation, without significant differences due to the sex of the individual (AU)

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BACKGROUND: Changes in bone age and tooth development are late side effects of cancer therapy and can be identified by imaging examination. AIM: To evaluate the late effects of antineoplastic treatment on bone age and dental development in childhood cancer survivors. DESIGN: This is a retrospective case-control study on paediatric cancer survivors of both sexes who underwent antineoplastic treatment with 5-15 years of survival. Carpal radiographs were assessed for bone age and growth curve, and panoramic radiographs were used to evaluate dental development and alterations. Carpal radiographs were analyzed using the Greulich and Pyle inspection method, and the Martins and Sakima method was used to analyze the growth curve. All tests were applied with a confidence level of 95%. RESULTS: The study and control groups comprised 28 and 56 patients, respectively. There was no significant difference in bone age and growth curve between the study and control groups. Nonetheless, when sex was compared to chronological and bone ages, there was a significant difference in bone age (p = 0.019) and an underestimation in both groups and sexes in the Greulich and Pyle method. As to late dental effects, dental agenesia, microdontia, gyroversion, and unerupted teeth were found. Dental shape alterations mainly involve the root region. CONCLUSION: Close multidisciplinary collaboration is necessary during the follow-up period of young patients who have survived cancer.

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Marine teleost species of commercial interest are often reported with hyperostosis, an osteological condition that results in bone thickening. Various specimens of Atlantic Spadefish Chaetodipterus faber (n = 86) obtained from artisanal fishermen in Rio de Janeiro, Brazil, were radiographed and assessed to detect the occurrence of hyperostosis across four different size classes. Of the examined individuals, 58.62% displayed signs of hyperostosis, which manifested in eight skeletal regions, notably in the supraoccipital crest, cleithrum and supraneural areas. In the vertebral column, hyperostosis was more frequently observed in haemal spines than in neural spines, predominantly between the sixth and eighth caudal vertebrae. The smallest size class (<200 mm total length) showed a low frequency of hyperostosis at 7.89%. This frequency escalated for larger classes, reaching 94.12% in individuals measuring 200-300 mm in total length and was observed in all individuals exceeding 300 mm. Hyperostosis exhibited an ontogenetic development pattern, where both the occurrence frequencies and the sizes of the affected bones expanded in proportion to the fish size. This is the first description of the hyperostosis pattern of development for the species, an important commercial resource.

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Purpose: To evaluate the inductive capacity of F18 bioglass putty on the induced membrane technique in a segmental bone defect of the rabbit's radius. Methods: Ten female Norfolk at 24 months of age were used. The animals were randomly separated based on postoperative time points: five rabbits at 21 and four at 42 days. A 1-cm segmental bone defect was created in both radii. The bone defects were filled with an F18 bioglass putty. Results: Immediate postoperative radiographic examination revealed the biomaterial occupying the segmental bone defect as a well-defined radiopaque structure with a density close to bone tissue. At 21 and 42 days after surgery, a reduction in radiopacity and volume of the biomaterial was observed, with particle dispersion in the bone defect region. Histologically, the induced membrane was verified in all animals, predominantly composed of fibrocollagenous tissue. In addition, chondroid and osteoid matrices undergoing regeneration, a densely vascularized tissue, and a foreign body type reaction composed of macrophages and multinucleated giant cells were seen. Conclusions: the F18 bioglass putty caused a foreign body-type inflammatory response with the development of an induced membrane without expansion capacity to perform the second stage of the Masquelet technique.

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Abstract Objective: To validate a deep learning (DL) model for bone age estimation in individuals in the city of São Paulo, comparing it with the Greulich and Pyle method. Materials and Methods: This was a cross-sectional study of hand and wrist radiographs obtained for the determination of bone age. The manual analysis was performed by an experienced radiologist. The model used was based on a convolutional neural network that placed third in the 2017 Radiological Society of North America challenge. The mean absolute error (MAE) and the root-mean-square error (RMSE) were calculated for the model versus the radiologist, with comparisons by sex, race, and age. Results: The sample comprised 714 examinations. There was a correlation between the two methods, with a coefficient of determination of 0.94. The MAE of the predictions was 7.68 months, and the RMSE was 10.27 months. There were no statistically significant differences between sexes or among races (p > 0.05). The algorithm overestimated bone age in younger individuals (p = 0.001). Conclusion: Our DL algorithm demonstrated potential for estimating bone age in individuals in the city of São Paulo, regardless of sex and race. However, improvements are needed, particularly in relation to its use in younger patients.

Resumo Objetivo: Validar em indivíduos paulistas um modelo de aprendizado profundo (deep learning - DL) para estimativa da idade óssea, comparando-o com o método de Greulich e Pyle. Materiais e Métodos: Estudo transversal com radiografias de mão e punho para idade óssea. A análise manual foi feita por um radiologista experiente. Foi usado um modelo baseado em uma rede neural convolucional que ficou em terceiro lugar no desafio de 2017 da Radiological Society of North America. Calcularam-se o erro médio absoluto (mean absolute error - MAE) e a raiz do erro médio quadrado (root mean-square error - RMSE) do modelo contra o radiologista, com comparações entre sexo, etnia e idade. Resultados: A amostra compreendia 714 exames. Houve correlação entre ambos os métodos com coeficiente de determinação de 0,94. O MAE das predições foi 7,68 meses e a RMSE foi 10,27 meses. Não houve diferenças estatisticamente significantes entre sexos ou raças (p > 0,05). O algoritmo superestimou a idade óssea nos mais jovens (p = 0,001). Conclusão: O nosso algoritmo de DL demonstrou potencial para estimar a idade óssea em indivíduos paulistas, independentemente do sexo e da raça. Entretanto, há necessidade de aprimoramentos, particularmente em pacientes mais jovens.

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Alendronate, a nitrogen-containing bisphosphonate, has reported long-term clinical success in the management of distinct bone-related conditions, particularly in the modulation of post-menopausal osteoporosis. Nonetheless, whether the inhibitory activity over osteoclastic cells' functionality is widely acknowledged, contradictory evidence arises from the assessment of alendronate activity over osteoblastic populations. This may be of particular relevance in situations in which bone formation exceeds bone resorption, with further emphasis on embryonic development, since alendronate can cross the placental barrier and alendronate-based therapies are being extended into women of reproductive age. Accordingly, the present study aims to assess the effects of alendronate, at distinct concentrations (1.5E-10M to 1.5E-7M) on bone tissue development, within a translational animal model - the embryonic chicken development model. Embryos, at the beginning of osteogenesis (day 7) were exposed to different alendronate concentrations for 4 days. Embryos were following characterized for skeletal development by histomorphometric analysis upon histochemical staining, microtomographic analysis, and gene expression assessment of genes related to osteoclastogenic/osteoclastic and osteoblastogenic/osteogenic differentiation, as well as to the immuno-inflammatory activation. The findings revealed that exposure to alendronate had a dose-dependent impact on skeletal growth and mineralization. This effect was evidenced by diminished bone volume and reduced bone surface parameters, with the 1.5E-7M concentration leading to a remarkable reduction of over 50%. Additionally, a decreased osteoclastogenic/osteoclastic gene expression was verified, associated with a diminished osteoblastogenic/osteogenic program - within the 30-50% range for 1.5E-7 M, supporting the diminished bone formation process. An increased inflammatory activation may contribute, at least in part, to the attained outcomes. Overall present findings suggest a negative influence of alendronate on the embryonic bone development process in a dose-dependent manner, highlighting the potential risk of alendronate use during embryonic development.

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Objective: To validate a deep learning (DL) model for bone age estimation in individuals in the city of São Paulo, comparing it with the Greulich and Pyle method. Materials and Methods: This was a cross-sectional study of hand and wrist radiographs obtained for the determination of bone age. The manual analysis was performed by an experienced radiologist. The model used was based on a convolutional neural network that placed third in the 2017 Radiological Society of North America challenge. The mean absolute error (MAE) and the root-mean-square error (RMSE) were calculated for the model versus the radiologist, with comparisons by sex, race, and age. Results: The sample comprised 714 examinations. There was a correlation between the two methods, with a coefficient of determination of 0.94. The MAE of the predictions was 7.68 months, and the RMSE was 10.27 months. There were no statistically significant differences between sexes or among races (p > 0.05). The algorithm overestimated bone age in younger individuals (p = 0.001). Conclusion: Our DL algorithm demonstrated potential for estimating bone age in individuals in the city of São Paulo, regardless of sex and race. However, improvements are needed, particularly in relation to its use in younger patients.

Objetivo: Validar em indivíduos paulistas um modelo de aprendizado profundo (deep learning - DL) para estimativa da idade óssea, comparando-o com o método de Greulich e Pyle. Materiais e Métodos: Estudo transversal com radiografias de mão e punho para idade óssea. A análise manual foi feita por um radiologista experiente. Foi usado um modelo baseado em uma rede neural convolucional que ficou em terceiro lugar no desafio de 2017 da Radiological Society of North America. Calcularam-se o erro médio absoluto (mean absolute error - MAE) e a raiz do erro médio quadrado (root mean-square error - RMSE) do modelo contra o radiologista, com comparações entre sexo, etnia e idade. Resultados: A amostra compreendia 714 exames. Houve correlação entre ambos os métodos com coeficiente de determinação de 0,94. O MAE das predições foi 7,68 meses e a RMSE foi 10,27 meses. Não houve diferenças estatisticamente significantes entre sexos ou raças (p > 0,05). O algoritmo superestimou a idade óssea nos mais jovens (p = 0,001). Conclusão: O nosso algoritmo de DL demonstrou potencial para estimar a idade óssea em indivíduos paulistas, independentemente do sexo e da raça. Entretanto, há necessidade de aprimoramentos, particularmente em pacientes mais jovens.

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ABSTRACT Introduction Incomplete skeletal development in adolescents and children depends on several factors such as genetic load, diet, and environment. Appropriate physical exercise can improve youth's physical fitness, but its effect on bone density is still questioned. Objective Verify the influence of appropriate physical activity on adolescents' bone development. Methods Among 3240 students aged 12 to 16 years from 4 schools, 96 students (52 males) were selected for observation. They were divided into a control and an experimental group, with a sports activity protocol inserted into the latter. Family and student questionnaires, physical examinations, and X-rays were used for data collection. Statistical analysis of factors including sports and development of adolescents' height quality was extensively documented. Results The skeletal development in adolescents on regular participation in sports is better than that in adolescents not involved in sports. Conclusion Physical exercise can promote skeletal development in adolescents. Evidence Level II; Therapeutic Studies - Investigating the result.

RESUMO Introdução O desenvolvimento incompleto do esqueleto de adolescentes e crianças depende de vários fatores como carga genética, alimentação e ambiente. O exercício físico apropriado pode melhorar a aptidão física do jovem, porém ainda há interrogações de seu efeito sobre a densidade óssea. Objetivo Verificar a influência da atividade física apropriada sobre o desenvolvimento ósseo em adolescentes. Métodos Entre 3240 estudantes com 12 a 16 anos de 4 escolas, selecionou-se 96 estudantes (52 homens) para observação. Divididos entre grupo controle e experimental, com protocolo de atividades esportivas inseridos nesse último. Para a coleta de dados foram utilizados questionários familiares e estudantis, exames físicos e radiografia. A análise estatística de fatores como esportes e desenvolvimento da qualidade da altura dos adolescentes foi amplamente documentada. Resultados O desenvolvimento esquelético de adolescentes que participam regularmente de esportes é melhor do que o de adolescentes que não participam de esportes. Conclusão O exercício físico pode promover o desenvolvimento ósseo nos adolescentes. Nível de evidência II; Estudos Terapêuticos - Investigação de Resultados.

RESUMEN Introducción El desarrollo incompleto del esqueleto de los adolescentes y los niños depende de varios factores como la carga genética, la nutrición y el entorno. Un ejercicio físico adecuado puede mejorar la forma física de los jóvenes, pero su efecto sobre la densidad ósea sigue siendo cuestionado. Objetivo Comprobar la influencia de una actividad física adecuada en el desarrollo óseo de los adolescentes. Métodos Entre 3240 estudiantes de 12 a 16 años de 4 escuelas, se seleccionaron 96 estudiantes (52 varones) para observación. Se dividieron entre los grupos de control y los experimentales, insertando el protocolo de actividad deportiva en estos últimos. Para la recogida de datos se utilizaron cuestionarios de la familia y de los alumnos, exámenes físicos y radiografías. El análisis estadístico de factores como el deporte y el desarrollo de la calidad de la estatura de los adolescentes se documentó ampliamente. Resultados El desarrollo del esqueleto de los adolescentes que practican regularmente un deporte es mejor que el de los adolescentes que no lo practican. Conclusión El ejercicio físico puede promover el desarrollo óseo en los adolescentes. Nivel de evidencia II; Estudios terapéuticos - Investigación de resultados.

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La hipocondroplasia es una displasia esquelética caracterizada por baja estatura, constitución robusta, brazos y piernas desproporcionadamente cortos, manos y pies anchos y cortos, leve laxitud articular y macrocefalia. Los niños generalmente se presentan como pequeños, con velocidad de crecimiento disminuida, que conduce a una baja estatura y desproporción de las extremidades. La hipocondroplasia en la mayoría de los casos se hereda con carácter autosómico dominante, aunque se detectan numerosos casos esporádicos. El diagnóstico requiere una exhaustiva anamnesis y adecuada exploración física. Es importante valorar algunos indicadores de crecimiento como: peso para la edad, longitud/talla para la edad, relación entre peso y longitud/talla, velocidad de crecimiento, talla diana genética, medidas de segmentos corporales, entre otros. Las radiografías esqueléticas permiten diagnosticar la mayoría de las displasias óseas. Los estudios moleculares suelen ser la prueba de confirmación y se solicitan ante una sospecha diagnóstica. Es importante incluir las displasias óseas en el diagnóstico diferencial de la talla baja y tenerlas en cuenta ante cualquier caso de talla baja disarmónica con alteraciones fenotípicas. La hipocondroplasia en la actualidad, no es una indicación aprobada para tratamiento con hormona del crecimiento. Se presenta un caso clínico de una niña de 14 meses, con talla baja severa, desproporcionada, que presentó dificultades para llegar al diagnóstico definitivo de hipocondroplasia.

Hypochondroplasia is a skeletal dysplasia characterized by short height, robust build, disproportionately short arms and legs, short and broad hands and feet, mild joint laxity, and macrocephaly. Children generally show slow growth rate, which leads to short stature and limb disproportion. Hypochondroplasia is mostly inherited with an autosomal dominant character, although many sporadic cases have been detected. Diagnosis requires a thorough history and adequate physical examination. It is important to assess some growth indicators such as: weight for age, length/height for age, relationship between weight and length/height, growth speed, genetic target height, measurements of body segments, among others. Skeletal XRs can diagnose most bone dysplasias. Molecular studies are usually the confirmatory test and are requested when a diagnosis is suspected. It is important to include bone dysplasias in the differential diagnosis of short stature and to take them into account for any disharmonious short stature with phenotypic alterations. Hypochondroplasia is currently not an approved indication for growth hormone therapy. We present a clinical case of a 14-month-old girl, with a severe, disproportionate short stature, who presented difficulties in her definitive hypochondroplasia diagnosis.

A hipocondroplasia é uma displasia esquelética caracterizada por baixa estatura, constituição robusta, braços e pernas desproporcionalmente curtos, mãos e pés largos e curtos, frouxidão articular leve e macrocefalia. As crianças geralmente são pequenas, com diminuição da velocidade de crescimento, o que leva à baixa estatura e desproporção dos membros. A hipocondroplasia na maioria dos casos é herdada com caráter autossômico dominante, embora sejam detectados numerosos casos esporádicos. O diagnóstico requer uma história completa e um exame físico adequado. É importante avaliar alguns indicadores de crescimento como: peso para idade, comprimento/altura para idade, relação entre peso e comprimento/altura, taxa de crescimento, estatura alvo genético, medidas de segmentos corporais, entre outros. As radiografias esqueléticas permitem o diagnóstico da maioria das displasias ósseas. Os estudos moleculares são geralmente o teste de confirmação e são solicitados quando há suspeita de diagnóstico. É importante incluir as displasias ósseas no diagnóstico diferencial da baixa estatura e considerá-las em qualquer caso de baixa estatura desarmônica com alterações fenotípicas. A hipocondroplasia não é atualmente uma indicação aprovada para o tratamento com hormônio de crescimento. Apresenta-se o caso clínico de uma menina de 14 meses, com baixa estatura grave e desproporcional, que apresentou dificuldades em chegar ao diagnóstico definitivo de hipocondroplasia.

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Aim: Facial orthopaedic treatments based on the stimulation or restrictions of craniofacial bone growth are more effective when carried out during the pubertal growth spurt. The aim of this cross-sectional study was to evaluate the reproducibility of two cervical vertebrae methods (CVM) with manual tracing and direct visual inspection. Methods: A sample of 60 lateral cephalometric radiographs (10 of each of the 6 CVM stages) was randomly selected from 171 records. 5 orthodontists classified these radiographs according to the skeletal maturation stage in 2002 and 2005, and the application of both methods was conducted by direct visual inspection and evaluation through manual tracing. Results: The average reliability of the two methods determination and the two forms of evaluation was substantial. The direct visual inspection evaluation showed the highest reliability and agreement interexaminer values for both methods, as well as the intraexaminers evaluation. Conclusion: The reproducibility of CVM method was substantial, indicating its clinical use to determine the skeletal maturity and the ideal moment for treatment execution

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Objetivo: A proposta deste estudo foi investigar a composição óssea em ratos tratados com dieta suplementada com farinha de taro (Colocasia esculenta) até eles completarem 90 dias de idade. Métodos: No momento do desmame, os ratos foram divididos em grupo controle (C, n = 11) e experimental (T, n = 12) ­ composto por animais tratados com farinha de taro até os 90 dias de idade. Ingestão alimentar, massa e comprimento corporal foram avaliados semanalmente ao longo de todo o período experimental. Dimensões ósseas, bem como a densidade mineral óssea (DMO), conteúdo mineral ósseo (CMO), área óssea total e propriedades biomecânicas foram determinadas no final de 90 dias. Resultados: Grupo T apresentou elevados valores (P<0.05) para massa e comprimento corporal; DMO, CMO e área óssea da coluna vertebral; DMO na quarta vértebra lombar; massa femoral, distância entre as epífises, largura do ponto médio da diáfise, DMO, força máxima e concentrações séricas de osteocalcina, quando comparado ao grupo controle. Conclusões: A ingestão da farinha de taro apresentou efeito positivo na saúde óssea. (AU)

Objective: This study aimed to investigate bone composition in male rats treated with diet supplemented with taro (Colocasia esculenta) flour until their 90 days. Methods: Weanling male rats were divided into control (C, n=11) and experimental group (T, n=12); the latter comprised animals treated with taro flour until their 90 days. Food intake, body mass and length were evaluated on a weekly basis throughout the experimental period. Spine bone dimension, as well as bone mineral density (BMD), mineral content (BMC), total area and biomechanical properties were determined after 90 days. Results: T group recorded higher values for (P<0.05) body mass and length; BMD, BMC and total spinal area; BMD of the fourth lumbar vertebra; femoral mass, distance between epiphysis, medial point of diaphysis width, BMD, maximum strength and osteocalcin concentrations than the control. Conclusion: Taro flour intake had positive effect on bone health. (AU)

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This study investigated the impact and non-impact sports on bone mineral density accrual in adolescents over 18 months. The impact sports were beneficial for bone health (accrual of bone density). In contrast, swimmers had similar or lower bone mineral density compared with the control group depending on the skeletal site. PURPOSE: To investigate the impact and non-impact sports on bone mineral density (BMD) accrual in adolescents over a period of 18 months METHODS: The sample was composed of 71 adolescents, avarage age of 12.7 (± 1.7) years old at baseline. Bone outcomes were compared according to the loading of the sports practiced (impact sports, n = 33 [basketball, karate, and judo], non-impact sport, n = 18 [swimming], and control group, n = 20). Areal bone mineral density (aBMD) was measured by dual-energy X-ray absorptiometry (DXA) and bone mineral apparent density (BMAD) estimated through equation. The results were compared between the groups using analysis of variance and analysis of covariance. RESULTS: Adjusted aBMD at lower limbs, whole body less head (WBLH), and adjusted WBLH BMAD were significantly greater in the impact sport group than the non-impact sport group at all time points. Adjusted upper limbs aBMD was significantly higher at the impact sports group compared to the non-impact sport group at 9 months and 18 months, besides compared to the control group at baseline and 18 months. Non-impact sport group presented a significant lower adjusted aBMD compared with control group at lower limbs and WBLH at 9 months, and at 9 months and 18 months in WBLH BMAD. There was a significant interaction (time × sport group) at upper limbs (p = 0.042) and WBLH aBMD (p = 0.006), and WBLH BMAD (p < 0.001). CONCLUSION: Impact sports were more beneficial on accumulating aBMD and BMAD over a period of 18 months, while non-impact group (swimmers) had similar and lower aBMD and BMAD compared with the control group.

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BACKGROUND: The epiphyseal growth plate is an important anatomical segment localized on the ends of a long bone. Despite the abovementioned atractive reasons for alendronate's use, few data on the effect of alendronate during epiphyseal growth exist. AIM: Verify the effect of alendronate on the growth epiphyseal plate, and compare its effect with the size of the femur during the double-staining of the immunolocalization of transforming growth factor-ß1 (TGF-ß1) and bone morphogenetic protein-2 (BMP2) in endochondral ossifing in specimens that have received alendronate. METHODS: Forty newborn rats were randomly divided into two groups: a control group (were given applications of 1 mg/kg physiologic saline) and a group that received Alendronate (a dose of 2.5 mg/kg). These groups were then divided into two subgroups for euthanasia in two and 12 d of life. After euthanasia, the femurs were removed, and the femoral bones were measured linearly between the apex of the greater trochanter until the lower intercondylar midlle face to verify the probable bone growth between 3 and 12 d in control and alednroanto treated rats. Posteriorly, the surgical pieces were also sent to the histopathology laboratory to produce histological slides. The obtained slides were stained with hematoxylin and eosin to measure each of the cartilage zones in endochondral development. and other slides were immunohistochemically tested for anti- TGF-ß1 and BMP-2 antibodies to investigate the immunolocalization of these proteins in the epiphyseal plaque area. RESULTS: On the third day, some diferences between the control group and specimens treated with alendronate were verified. Macroscopiccaly, we found similarities in size between the femoral bones when we compared the control group with the specimens that received alendronate. On the 12th day, the bone size of the mice receiving the drug was significantly smaller than those of the control group. These results coincide with changes in the TGF-ß1 and BMP-2 expression. In the specimens that received alendronate, the TGF-ß1 was expressed in some sites of trabecular bone that was neoformed, peripherally to the bone marrow area. The BMP-2 was also positive in proliferative chondrocytes and hypertrofic chondrocytes. On the 12th day, all layers of chondrocytes exhibited positivity for BMP-2 in the specimens that received alendronate. In the interface between the trabecular bone and cartilage, an area of disorganized bone deposition was evident. Neoformed bone also appeared to be different at 12 d. In the control group, BMP-2 was positive in an intense area of bone trabeculae, whereas the alendronate-treated group showed TGF-ß1 positive trabeculae and a greater bone area. CONCLUSION: Alendronate alters the immunolocalization of TGF-ß1 and BMP-2 simultaneously, a condition that changes the usual histological aspects of the cartilage zone and impairs epiphysis growth and femur growth.

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Ao tratar pacientes em crescimento, especialmente os portadores de más-oclusões esqueléticas de classes II e III, onde espera-se redirecioná-lo, é fundamental a determinação do estágio de crescimento do indivíduo. Para tal, existem diversas técnicas, como as radiográficas e as enzimáticas. O objetivo deste estudo determinar a fase de crescimento através dos níveis e da correlação dos valores de um biomarcador ósseo (fosfatase alcalina óssea) e duas técnicas radiográfica. Foram selecionados 65 pacientes de ambos os sexos, com idade média de 12,7 anos, em busca de tratamento ortodôntico nos setores de Ortodontia e Odontopediatria da Universidade do Estado do Rio de Janeiro e que se enquadraram nos critérios de inclusão/exclusão. Os indicadores de crescimento ósseo radiográficos escolhidos foram os estágios de maturação das vértebras cervicais, avaliados através da radiografia cefalométrica lateral, e os da maturação da falange média do terceiro dedo, obtida em exame da área de interesse, na mão direita. Após a obtenção e o devido processamento das radiografias, estas foram avaliadas por dois avaliadores previamente calibrados, utilizando os métodos de Bacetti e Perinetti para as radiografias cefalométrica e do terceiro dedo, respectivamente. O índice de concordância kappa demonstrou boa reprodutibilidade intra e inter-examinadores. Na avaliação intra-examinador, o resultado de kappa foi de 0,711 para a maturação vertebral e 0,893 para a maturação da falange. Quanto a correlação inter-examinador, a avaliação da maturação da falange média, o valor de kappa ponderado foi de 0,923 enquanto para o da maturação das vértebras cervicais foi de 0,864. O terceiro indicador de crescimento avaliado neste trabalho foi a quantificação da fosfatase alcalina óssea na saliva. A coleta da saliva foi realizada entre 9 e 11 horas da manhã, sem estímulo químico ou mecânico. O processamento da saliva foi feito através de um ensaio de imunoabsorção enzimática, com posterior determinação da densidade óptica através de um espectrofotômetro. Os valores obtidos neste ensaio foram então correlacionados aos estágios de crescimento pré-pico, pico e pós-pico de crescimento puberal, determinados por ambas as radiografias. Após a aplicação do teste ANOVA, não foi encontrada diferença estatisticamente significativa entre os estágios de crescimento puberal. Como não houve variação dos níveis da fosfatase alcalina entre os diferentes estágios maturacionais, pode-se inferir que a avaliação desta enzima na saliva pode não ser um indicador confiável do crescimento ósseo. A quantificação desta enzima pode ser avaliada em outros fluidos corpóreos, como sangue ou fluido gengival(AU)

When treating growing patients, especially those who have a skeletal class II or III condition, where the willing is to redirect growth, it is indispensable to determine the individual's growing stage. For this determination, there are different methods, radiographic or enzymatic. The aim of this study was to assess the levels of a bone biomarker (bone-alkaline phosphatase) and its correlation to two different radiographic techniques. Sixty-five patients of both sex and mean age of 12.7 years old looking for treatment at Orthodontics and Pediatric Dentistry sectors in the State University of Rio de Janeiro were selected for filling the inclusion/exclusion criteria. The radiographic growing indicators chosen for this study were the maturational stages of cervical vertebrae (CVM), assessed in lateral cephalometric radiograph, and maturational stages of the middle phalanx of the third finger (MP3), acquired in a radiograph taken from the interested area on the right hand. After obtaining and processing the X-rays, those were assessed by two calibrated examiners. They have used the methods proposed by Baccetti and Perinetti to assess lateral and third finger X-rays, respectively. The Cohen's kappa index of agreement showed a good reproducibility intra and inter-examiner. The intra-observer rater, the result was a kappa of 0,711 to cervical vertebrae maturation and 0,893 to third finger middle phalanx maturation. Inter-observer weighted and unweighted kappa values were 0.864 and 0.693 for and 0.923 and 0.868, respectively, for MP3 method. The third maturational growth indicator analyzed in this study was the quantification of salivary bone-alkaline phosphatase, a biomarker of bone metabolism. The patients were asked to expel unstimulated whole saliva between nine and eleven in the morning. Those samples were collected and stored according to the orientations of the analysis kit. Saliva were processed through an immunosorbent assay, with posterior determination of optical density by spectrophotometry. The resulting values of this assay were then correlated to the three stages of pubertal growth: pre-, pubertal and post-pubertal. An ANOVA test was used to correlate that information and as a result, it was not found a statistically significant correlation between bone alkaline phosphatase levels and maturational stages. As no difference was found, quantification of this enzyme in saliva may not be a reliable maturational growth indicator. The assessment of bone alkaline phosphatase should be done in other body fluids, as blood serum or gingival fluid(AU)

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SUMMARY BACKGROUND Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disease characterized by multisystem involvement including low bone mineral density (BMD). OBJECTIVE To assess the bone phenotype of individuals with NF1 and verify its association with nutrient intake. METHODS Twenty-six adults with NF1 underwent bone phenotype assessments using dual-energy X-ray absorptiometry (DXA) and food intake evaluations. They were compared to 26 unaffected matched control patients. Weight, height, and waist circumference (WC) were measured. DXA provided total body, spine, and hip BMDs and bone mineral content (BMC) for all patients. Food intake was evaluated for energy, macro- and micro-nutrients. RESULTS Height (1.68 ± 0.1; 1.61 ± 0.1 cm; P = 0.003) and BMC (2.3 ± 0.4; 2.0 ± 0.5 kg; P = 0.046) were lower in the NF1 group. Individuals with NF1 also presented lower total body and spine BMDs (g/cm2) (1.1 ± 0.1, 1.0 ± 0.1, P = 0.036; 1.0 ± 0.1, 0.9 ± 0.1; P = 0.015, respectively). The frequency of total body bone mass below the expected level for patients' ages was higher in the NF1 group (7.7%; 34.6%, P = 0.016). There were no differences in energy consumption. No correlations between BMC and BMD with nutrient intake were observed in the NF1 group. CONCLUSIONS The NF1 group presented lower BMCs and BMDs. Although a lower consumption of calcium, iron, and vitamin A, and a higher intake of sodium and omega-6 were observed, there was no relationship between bone phenotype and nutrient intake.

RESUMO INTRODUÇÃO A Neurofibromatose tipo 1 (NF1) é uma doença genética autossômica dominante caracterizada por envolvimento neurocutâneo e multissistêmico, incluindo baixa densidade mineral óssea (DMO). OBJETIVOS Avaliar características ósseas em indivíduos com NF1 e verificar associação com a ingestão de nutrientes. METODOLOGIA 26 adultos com NF1 submeteram-se a avaliação dos parâmetros ósseos usando absorciometria com raios-X de dupla energia (DXA), além da avaliação da ingestão alimentar. O grupo NF1 foi comparado e pareado com 26 indivíduos sem a doença. Peso, estatura e circunferência da cintura foram avaliados. DXA forneceu o conteúdo mineral ósseo (CMO) e a DMO do corpo total, coluna e fêmur. A ingestão de calorias, macronutrientes e micronutrientes foi avaliada. RESULTADOS O grupo NF1 apresentou redução da estatura (1,68 ± 0,1; 1,61 ± 0,1 cm; P=0,003) e do CMO (2,3 ± 0,4; 2,0 ± 0,5 kg; P=0,046). Indivíduos com NF1 também apresentaram redução da DMO de corpo total e coluna (g/cm2) (1,1 ± 0,1, 1,0 ± 0,1, P=0,036; 1,0 ± 0,1, 0,9 ± 0,1; P=0,015, respectivamente). A frequência de indivíduos com massa óssea abaixo do esperado para a idade foi maior no grupo NF1 (7,7%; 34,6%, P=0,016). Não houve diferenças no consumo energético. Não houve correlação entre CMO e DMO com a ingestão de nutrientes no grupo NF1. CONCLUSÕES O grupo NF1 apresentou redução do CMO e da DMO. Apesar de menor consumo de cálcio, ferro e vitamina A, e maior consumo de sódio e ômega-6, não foi observada relação entre o fenótipo ósseo e a ingestão de nutrientes.

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OBJECTIVE: To assess the effect of chronic alcohol consumption on the longitudinal growth of the tibia and bone quality parameters in young rats under an experimental setup. METHODS: The control (n=10) rats received only water. The ethanol (n=10) rats received ethyl alcohol at concentrations established in the protocol for the induction of chronic alcohol consumption. The blood samples were immediately collected via cardiac puncture and processed to evaluate the levels of alkaline phosphatase by automated spectrophotometry. Following blood sample collection, both tibias were dissected, and weighed; the tibial length was measured., and the samples were stored in a freezer for future analysis of the bone mineral content and mechanical resistance, known as maximal load and stiffness. RESULTS: Compromised bone health, with a 35.3% decrease in the serum alkaline phosphatase levels (p < 0.01), a 10% decrease in the tibial mass (p < 0.05), and a 5.3% decrease in the tibial length (p < 0.0001) were noted. Furthermore, a 10% decrease in the bone mineral density was observed (p < 0.01), which led to a 17.2% decrease in the maximum strength (p < 0.01) and 22.6% decrease in stiffness (p < 0.001). CONCLUSION: Chronic consumption of alcohol affected the bones of young rats, making them weaker and osteopenic. In addition, the long bones were shorter, suggesting interference with growth. Level of Evidence III, Case Control Study.

OBJETIVO: Verificar a influência do consumo experimental crônico de álcool no crescimento longitudinal da tíbia e em parâmetros de qualidade óssea de ratos jovens. MÉTODOS: Dez ratos controle receberam água, outros dez receberam álcool etílico nas concentrações estabelecidas no protocolo para indução. Após eutanásia, as amostras de sangue foram coletadas por punção cardíaca e processadas para avaliar os níveis de fosfatase alcalina por espectrofotometria automatizada. Após a coleta de sangue, ambas as tíbias foram dissecadas, pesadas e medidas em comprimento. Foram realizadas análises do conteúdo mineral ósseo e resistência mecânica, por meio da análise da força máxima e rigidez. RESULTADOS: Houve comprometimento da saúde óssea, com redução de 35,3% no nível de fosfatase alcalina no plasma (p<0,01), redução de 10% na massa da tíbia (p<0,05) e queda de 5,3% no comprimento das tíbias (p<0,0001). Também foi observada redução de 10% na densidade mineral óssea (p<0,01), que levou à redução de 17,2% na força máxima (p<0,01) e 22,6% na rigidez (p<0,001). CONCLUSÃO: O consumo crônico de álcool afetou os ossos de ratos jovens, tornando-os mais fracos e osteopênicos. Ainda, os ossos longos eram mais curtos, sugerindo interferência no crescimento. Nível de evidência III, Estudo caso-controle.

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The formation of the vertebrate skeleton is orchestrated in time and space by a number of gene regulatory networks that specify and position all skeletal tissues. During embryonic development, bones have two distinct origins: bone tissue differentiates directly from mesenchymal progenitors, whereas most long bones arise from cartilaginous templates through a process known as endochondral ossification. Before endochondral bone development takes place, chondrocytes form a cartilage analgen that will be sequentially segmented to form joints; thus, in the cartilage template, either the cartilage maturation programme or the joint formation programme is activated. Once the cartilage differentiation programme starts, the growth plate begins to form. In contrast, when the joint formation programme is activated, a capsule begins to form that contains special articular cartilage and synovium to generate a functional joint. In this review, we will discuss the mechanisms controlling the earliest molecular events that regulate cell fate during skeletogenesis in long bones. We will explore the initial processes that lead to the recruitment of mesenchymal stem/progenitor cells, the commitment of chondrocyte lineages, and the formation of skeletal elements during morphogenesis. Thereafter, we will review the process of joint specification and joint morphogenesis. We will discuss the links between transcription factor activity, cell-cell interactions, cell-extracellular matrix interactions, growth factor signalling, and other molecular interactions that control mesenchymal stem/progenitor cell fate during embryonic skeletogenesis.

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ABSTRACT Objective: To assess the effect of chronic alcohol consumption on the longitudinal growth of the tibia and bone quality parameters in young rats under an experimental setup. METHODS: The control (n=10) rats received only water. The ethanol (n=10) rats received ethyl alcohol at concentrations established in the protocol for the induction of chronic alcohol consumption. The blood samples were immediately collected via cardiac puncture and processed to evaluate the levels of alkaline phosphatase by automated spectrophotometry. Following blood sample collection, both tibias were dissected, and weighed; the tibial length was measured., and the samples were stored in a freezer for future analysis of the bone mineral content and mechanical resistance, known as maximal load and stiffness. RESULTS: Compromised bone health, with a 35.3% decrease in the serum alkaline phosphatase levels (p < 0.01), a 10% decrease in the tibial mass (p < 0.05), and a 5.3% decrease in the tibial length (p < 0.0001) were noted. Furthermore, a 10% decrease in the bone mineral density was observed (p < 0.01), which led to a 17.2% decrease in the maximum strength (p < 0.01) and 22.6% decrease in stiffness (p < 0.001). CONCLUSION: Chronic consumption of alcohol affected the bones of young rats, making them weaker and osteopenic. In addition, the long bones were shorter, suggesting interference with growth. Level of Evidence III, Case Control Study.

RESUMO Objetivo: Verificar a influência do consumo experimental crônico de álcool no crescimento longitudinal da tíbia e em parâmetros de qualidade óssea de ratos jovens. Métodos: Dez ratos controle receberam água, outros dez receberam álcool etílico nas concentrações estabelecidas no protocolo para indução. Após eutanásia, as amostras de sangue foram coletadas por punção cardíaca e processadas para avaliar os níveis de fosfatase alcalina por espectrofotometria automatizada. Após a coleta de sangue, ambas as tíbias foram dissecadas, pesadas e medidas em comprimento. Foram realizadas análises do conteúdo mineral ósseo e resistência mecânica, por meio da análise da força máxima e rigidez. Resultados: Houve comprometimento da saúde óssea, com redução de 35,3% no nível de fosfatase alcalina no plasma (p<0,01), redução de 10% na massa da tíbia (p<0,05) e queda de 5,3% no comprimento das tíbias (p<0,0001). Também foi observada redução de 10% na densidade mineral óssea (p<0,01), que levou à redução de 17,2% na força máxima (p<0,01) e 22,6% na rigidez (p<0,001). Conclusão: O consumo crônico de álcool afetou os ossos de ratos jovens, tornando-os mais fracos e osteopênicos. Ainda, os ossos longos eram mais curtos, sugerindo interferência no crescimento. Nível de evidência III, Estudo caso-controle.

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Este trabalho teve como objetivo realizar uma avaliação fisioterapêutica em um voluntário com malformação congênita do membro inferior direito, a fim de conhecer seus aspectos motores e funcionais, devido ao fato de ser um caso peculiar com incidência de 1 a cada 100.000 nascidos vivos. Tratou-se de um relato de caso, realizado na clínica escola de fisioterapia de uma universidade do interior do Estado de São Paulo. Os procedimentos consistiram em: anamnese, exame físico, escalas e instrumentos de avaliação do controle, índice de Barthel modificado, plataforma de força e avaliação postural. Pode-se observar através da avaliação fisioterapêutica alterações posturais relevantes com assimetrias entre os hemicorpos, déficit de equilíbrio e diminuição de força muscular no membro inferior direito, o que acarreta uma alteração biomecânica importante no participante avaliado. Essas informações coletadas durante as avaliações são essenciais para conhecer as alterações físicas decorrentes da malformação congênita para promover um melhor direcionamento em seu tratamento.

A physiotherapy evaluation has been undertaken with a voluntary subject with congenital malformation of the right lower limber to understand motor and functional aspects of the issue. The fact has an occurrence of 1/100000 live births. The case study has been undertaken in a physiotherapy school at a university clinical in the interior of the state of São Paulo, Brazil. Procedures included anamnesis, physical examination, scales and instruments for control assessment, modified Barthel Index, force platform and posture evaluation. Physiotherapeutic evaluation revealed significant posture changes with asymmetry between the hemibodies, deficit in equilibrium and lessening of muscular force in the right lower member, with subsequent important biomechanical changes in the patient. Information collected during evaluations is essential to understand the physical alternations due to congenital malformation for better results through treatment.

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Growth is one of the most important traits from both a physiological and economic perspective in aquaculture species. Thus, identifying the genomic regions and genes underpinning genetic variation for this trait is of particular interest in several fish species, including rainbow trout. In this work, we perform a genome-wide association study (GWAS) to identify the genomic regions associated with body weight at tagging (BWT) and at 18 months (BW18M) using a dense SNP panel (57 k) and 4596 genotyped rainbow trout from 105 full-sib families belonging to a Chilean breeding population. Analysis was performed by means of single-step GBLUP approach. Genetic variance explained by 20 adjacent SNP windows across the whole genome is reported. To further explore candidate genes, we focused on windows that explained the highest proportion of genetic variance in the top 10 chromosomes for each trait. The main window from the top 10 chromosomes was explored by BLAST using the first and last SNP position of each window to determine the target nucleotide sequence. As expected, the percentage of genetic variance explained by windows was relatively low, due to the polygenic nature of body weight. The most important genomic region for BWT and BW18M were located on chromosomes 15 and 24 and they explained 2.14% and 3.02% of the genetic variance for each trait, respectively. Candidate genes including several growth factors, genes involved in development of skeletal muscle and bone tissue and nutrient metabolism were identified within the associated regions for both traits BWT and BW18M. These results indicate that body weight is polygenic in nature in rainbow trout, with the most important loci explaining as much as 3% of the genetic variance for the trait. The genes identified here represent good candidates for further functional validation to uncover biological mechanisms underlying variation for growth in rainbow trout.

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