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1.
West China Journal of Stomatology ; (6): 566-569, 2021.
Article in English | WPRIM | ID: wpr-921375

ABSTRACT

OBJECTIVES@#This study aims to investigate the incidence and severity of obstructive sleep apnea (OSA) in cleft patients with velopharyngeal insufficiency (VPI) after pharyngeal flap surgery (PFS) and explore the influence of operation age.@*METHODS@#A retrospective study was conducted in 82 cleft patients after PFS. The patients were divided into two groups according to their age at the time of surgery. The incidence and severity of OSA were assessed at least 1.2 years (mean 6.0 years) postoperatively by polysomnography (PSG).@*RESULTS@#The incidence rates of OSA were 20% in the adult group and 31% in the child group. No significant difference was found between the two groups (@*CONCLUSIONS@#Some patients still have OSA average of 6.0 years after PFS, and operation ageis unrelated to the incidence and severity of OSA.


Subject(s)
Adult , Child , Humans , Pharynx , Polysomnography , Retrospective Studies , Sleep Apnea, Obstructive/epidemiology , Velopharyngeal Insufficiency/etiology
2.
Chinese Journal of Stomatology ; (12): 615-620, 2013.
Article in Chinese | WPRIM | ID: wpr-274190

ABSTRACT

<p><b>OBJECTIVE</b>To explore the signal transduction mechanism of p38 mitogen activated protein kinase (p38MAPK) in human facial hypertrophic scar fibroblast (FB) differentiation into myofibroblasts (MFB).</p><p><b>METHODS</b>Fibroblasts of primary culture were simple randomly assigned into two groups: cyclic stretch (control group) and cyclic stretch pre-treated with SB203580(experimental group). Expression of P-p38MAPK and α-smooth muscle actin (α-SMA) protein were examined using Western blotting and expression of transforming growth factor β1 (TGF-β1) mRNA and α-SMA mRNA were examined using reverse transcription PCR (RT-PCR).</p><p><b>RESULTS</b>In control group, the expressions of α-SMA, p38MAPK, TGF-β1 mRNA and α-SMA mRNA (0 h: 0.134 ± 0.011, 0.239 ± 0.015, 0.214 ± 0.018, 0.252 ± 0.010; 6 h: 0.152 ± 0.014, 0.287 ± 0.016, 0.288 ± 0.011, 0.277 ± 0.013; 12 h: 0.172 ± 0.017, 0.320 ± 0.017, 0.335 ± 0.013, 0.297 ± 0.006) , were significantly increased with loading time (6 h>0 h; 12 h>0 and 6 h). In experimental group (pre-treated with SB203580), the expressions of α-SMA, p38MAPK, TGF-β1 mRNA,α-SMA mRNA (6 h: 0.116 ± 0.017,0.128 ± 0.016,0.134 ± 0.014,0.163 ± 0.009; 12 h: 0.149 ± 0.013,0.136 ± 0.018,0.144 ± 0.013,0.187 ± 0.010) on corresponding time decreased sharply compared with those in control groups (6, 12 h).</p><p><b>CONCLUSIONS</b>The human facial hypertrophic scar fibroblasts differentiation in response to cyclic stretch was mediated by p38MAPK phosporylation.</p>


Subject(s)
Adolescent , Adult , Child , Female , Humans , Male , Young Adult , Actins , Genetics , Metabolism , Cell Transdifferentiation , Cells, Cultured , Cicatrix, Hypertrophic , Metabolism , Pathology , Enzyme Inhibitors , Pharmacology , Fibroblasts , Metabolism , Pathology , Imidazoles , Pharmacology , Myofibroblasts , Pathology , Phosphorylation , Pyridines , Pharmacology , RNA, Messenger , Metabolism , Random Allocation , Signal Transduction , Stress, Mechanical , Transforming Growth Factor beta1 , Genetics , Metabolism , p38 Mitogen-Activated Protein Kinases , Metabolism
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