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1.
Aesthetic Plast Surg ; 43(4): 982-992, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-30963186

RESUMO

OBJECTIVE: The purpose of this study was to investigate the differences in facial profile development between unoperated adult cleft palate (UACP) patients and normal controls and to analyse the reasons for the differences. MATERIALS AND METHODS: A total of 50 individuals with a unilateral cleft palate and 20 normal controls were selected to undergo angular measurement of their facial profiles. Data with significant differences between the two groups were analysed. RESULTS: Seven angle measurements of the facial profile showed that the mid-facial protrusion of the UACP patients had no significant differences from the control group (p > 0.05). But their angle of the medium face (N'-Trg-Sn) was significantly lower than the non-cleft controls (p < 0.05), suggesting a worse vertical development of the middle face. A significantly larger nasal tip angle (Cm-Sn/N'-Prn) for UACP patients suggested they had a rounder and blunter nasal tip (p < 0.05). The soft tissue facial angle and chin-lip angle of UACP patients had significant differences from non-cleft controls (p < 0.05), but the head position angle (Sn-Sm-THP) had no significant difference between two groups (p > 0.05), which suggested a steep mandibular plane for UACP patients but without severe retraction of the chin. CONCLUSION: The development of facial protrusions in UACP patients is similar to that in normal adults, but the vertical development in the middle face is insufficient. Such hypoplasia may be related to the intrinsic deficiency of the maxilla. There is a tendency for flat nasal growth and insufficient development of the chin in UACP patients. LEVEL OF EVIDENCE IV: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors www.springer.com/00266 .


Assuntos
Cefalometria/métodos , Fissura Palatina/diagnóstico , Assimetria Facial/diagnóstico , Adulto , Estudos de Casos e Controles , China , Fissura Palatina/cirurgia , Face/anatomia & histologia , Assimetria Facial/etiologia , Músculos Faciais/anatomia & histologia , Feminino , Hospitais Universitários , Humanos , Masculino , Nariz/anatomia & histologia , Procedimentos Cirúrgicos Ortognáticos/efeitos adversos , Procedimentos Cirúrgicos Ortognáticos/métodos , Seleção de Pacientes , Procedimentos de Cirurgia Plástica/métodos , Valores de Referência
2.
Cranio ; 41(5): 416-422, 2023 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-33355036

RESUMO

OBJECTIVE: To investigate the relationship between upper airway morphology and the severity of obstructive sleep apnea (OSA) in patients with anatomically small retruded mandibles. METHODS: Fifty-two patients with small retruded mandibles underwent polysomnography and airway computed tomography. The airway morphology parameters and sleep assessment were compared between the patients with or without OSA. RESULTS: Twenty-eight patients diagnosed with OSA, according to polysomnography, had a higher distance between the hyoid bone and mandibular plane (HMP), lateral dimension (LAT)/anteroposterior dimension (AP), but lower minimum cross-sectional area (mCSA), AP, surface area, volume, avgCSA, and airway uniformity (U). The apnea-hypopnea index had negative correlations with mCSA, AP, surface area, volume, avgCSA, and U, and had a positive correlation with HMP and LAT/AP. CONCLUSION: OSA is common among patients with small retruded mandibles and is associated with a more compressed upper airway shape and longer HMP.


Assuntos
Apneia Obstrutiva do Sono , Humanos , Apneia Obstrutiva do Sono/diagnóstico por imagem , Sistema Respiratório , Sono , Tomografia Computadorizada por Raios X/métodos , Mandíbula/diagnóstico por imagem
3.
Anim Biotechnol ; 20(3): 124-32, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19544208

RESUMO

To improve animal growth, growth hormone-releasing hormone (GHRH) expression vectors that maintain constant GHRH expression can be directly injected into muscles. To deliver the GHRH expression vectors, biodegradable microspheres have been used as a sustained release system. Although administering GHRH through microspheres is a common practice, the intergenerational effects of this delivery system are unknown. To investigate the intergenerational effects of polylactic-co-glycolic acid (PLGA) encapsulated plasmid-mediated GHRH supplements, pCMV-Rep-GHRH microspheres were injected into pregnant mice. Growth and expression of GHRH were measured in the offspring. RT-PCR and immunohistochemistry reveal GHRH expression 3-21 days post-injection. The proportion of GH-positive cells in the GHRH treated offspring was 48.2% higher than in the control group (P < 0.01). The GHRH treated offspring were 6.15% (P < 0.05) larger than the control offspring. At day 49 post-injection, IGF-I serum levels were significantly higher in the treatment group than in the control group. This study confirms that intramuscular expression of GHRH mediated by PLGA microspheres significantly enhances intergenerational growth.


Assuntos
Hormônio Liberador de Hormônio do Crescimento/biossíntese , Hormônio Liberador de Hormônio do Crescimento/genética , Plasmídeos/administração & dosagem , Plasmídeos/genética , Animais , Sequência de Bases , Primers do DNA/genética , Preparações de Ação Retardada , Sistemas de Liberação de Medicamentos , Feminino , Expressão Gênica , Hormônio Liberador de Hormônio do Crescimento/metabolismo , Imuno-Histoquímica , Fator de Crescimento Insulin-Like I/metabolismo , Ácido Láctico , Camundongos , Microesferas , Músculo Esquelético/efeitos dos fármacos , Músculo Esquelético/metabolismo , Adeno-Hipófise/crescimento & desenvolvimento , Adeno-Hipófise/metabolismo , Ácido Poliglicólico , Copolímero de Ácido Poliláctico e Ácido Poliglicólico , Gravidez , Efeitos Tardios da Exposição Pré-Natal , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Aumento de Peso/genética
4.
Talanta ; 84(1): 71-7, 2011 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-21315900

RESUMO

A novel matrix, gold nanoparticles-bacterial cellulose nanofibers (Au-BC) nanocomposite was developed for enzyme immobilization and biosensor fabrication due to its unique properties such as satisfying biocompatibility, good conductivity and extensive surface area, which were inherited from both gold nanoparticles (AuNPs) and bacterial cellulose nanofibers (BC). Heme proteins such as horseradish peroxidase (HRP), hemoglobin (Hb) and myoglobin (Mb) were successfully immobilized on the surface of Au-BC nanocomposite modified glassy carbon electrode (GCE). The immobilized heme proteins showed electrocatalytic activities to the reduction of H(2)O(2) in the presence of the mediator hydroquinone (HQ), which might be due to the fact that heme proteins retained the near-native secondary structures in the Au-BC nanocomposite which was proved by UV-vis and IR spectra. The response of the developed biosensor to H(2)O(2) was related to the amount of AuNPs in Au-BC nanocomposite, indicating that the AuNPs in BC network played an important role in the biosensor performance. Under the optimum conditions, the biosensor based on HRP exhibited a fast amperometric response (within 1s) to H(2)O(2), a good linear response over a wide range of concentration from 0.3 µM to 1.00 mM, and a low detection limit of 0.1 µM based on S/N=3. The high performance of the biosensor made Au-BC nanocomposite superior to other materials as immobilization matrix.


Assuntos
Técnicas Biossensoriais/métodos , Celulose/química , Ouro/química , Hemeproteínas/química , Peróxido de Hidrogênio/análise , Nanopartículas Metálicas/química , Nanocompostos/química , Animais , Calibragem , Catálise , Bovinos , Eletroquímica , Gluconacetobacter xylinus/química , Hemeproteínas/metabolismo , Hemoglobinas/química , Hemoglobinas/metabolismo , Peróxido de Hidrogênio/química , Proteínas Imobilizadas/química , Proteínas Imobilizadas/metabolismo , Mioglobina/química , Mioglobina/metabolismo , Nanofibras/química , Análise Espectral
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