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1.
Br J Dermatol ; 171(6): 1386-90, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24807810

RESUMO

BACKGROUND: Foam sclerotherapy has been one of the most frequently applied therapeutic methods for the treatment of varicose veins and venous malformation. Few studies have investigated the sterile condition of the air used for foam creation. OBJECTIVES: To evaluate the bacterial conditions in foam created from the air in outpatient and operating rooms used for sclerotherapy treatment, in order to provide the basis for clinical applications in foam sclerotherapy. MATERIALS AND METHODS: In this study, we measured the amount of airborne microorganisms in the air in the operating room, and in the outpatient room, the polidocanol (POL) foam created using the air in the respective rooms, and the microorganisms present in the liquid POL. We used the settle plate method for air sampling. We used the Tessari method to generate foam. The experiment was repeated three times. RESULTS: Typical bacterial colonies were formed on nutrient agar plates in both the outpatient room and operating room air groups. No colonies were cultivated in the liquid POL. Although the use of sterile or nonsterile air in sclerotherapy produces significantly different results in the counts of colony-forming units, there was no difference in the foam created using sterile or nonsterile air (i.e. no colonies were cultivated on either foam). CONCLUSIONS: There is no increased risk of infection when using foam sclerotherapy in outpatient rooms compared with using foam created under sterile operating-room conditions.


Assuntos
Microbiologia do Ar , Contaminação de Medicamentos , Polietilenoglicóis/normas , Soluções Esclerosantes/normas , Escleroterapia/efeitos adversos , Escleroterapia/normas , Instituições de Assistência Ambulatorial/normas , Humanos , Salas Cirúrgicas/normas , Polidocanol
2.
Occup Med (Lond) ; 62(4): 295-7, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22232065

RESUMO

BACKGROUND: Return to work is an important outcome following traumatic work-related hand injuries. It is unclear how psychosocial factors affect the time to return to work following traumatic work-related hand injury. AIMS: To investigate the relationships between hand injury severity, self-perceived health, demographics and time off work (TOW) following traumatic work-related hand injuries and the influence of psychosocial factors on the readiness of return to work. METHODS: Data from 120 traumatic work-related hand injured patients were gathered. The Modified Hand Injury Severity Score (MHISS) and Short Form Health Survey (SF-36) were used to assess the severity of hand trauma and self-perceived health, respectively. The relationships between MHISS, SF-36, demographics and TOW were analysed by multiple regression analysis. RESULTS: Mean duration of TOW was 127 days for patients with a mild MHISS, 108 days for a moderate score, 160 days for a severe score and 236 days for those with a major score. A positive correlation between MHISS and duration of TOW was identified. Self-perceived physical functioning was found to have a negative correlation with TOW, whereas self-perceived mental health was positively correlated with TOW. CONCLUSIONS: This study highlights the importance of self-perceived health in considering return to work following traumatic work-related hand injury.


Assuntos
Absenteísmo , Acidentes de Trabalho , Autoavaliação Diagnóstica , Traumatismos da Mão/psicologia , Nível de Saúde , Adolescente , Adulto , Estudos Transversais , Feminino , Traumatismos da Mão/etiologia , Humanos , Escala de Gravidade do Ferimento , Masculino , Pessoa de Meia-Idade , Análise de Regressão , Taiwan , Adulto Jovem
3.
Clin Otolaryngol ; 36(2): 147-53, 2011 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21332670

RESUMO

OBJECTIVES: Previous studies have demonstrated a relationship between elevated serum C-reactive protein (CRP) levels and shorter survival in cancer patients. Few studies, however, have investigated the role of serum CRP levels in oral squamous cell carcinoma. The present study was conducted to analyze the relationship between preoperative CRP levels, clinicopathologic factors, and prognosis in oral squamous cell carcinoma patients. DESIGN: Retrospective clinical study. SETTING: University teaching hospital. PARTICIPANTS: Eighteen oral cavity leukoplakia and 59 oral squamous cell carcinoma patients between November 2006 and November 2009 from the Chang Gung Memorial Hospital. OUTCOME MEASURES: Clinicopathologic parameters, disease-free survival and overall survival were correlated with CRP levels. METHODS: Serum CRP levels were measured preoperatively, and all oral cavity cancer patients underwent curative intent radical surgery with or without postoperative adjuvant therapy. RESULTS: The CRP levels in leukoplakia patients were used to analyze if factors (including diabetes and liver cirrhosis, smoking, alcohol drinking and areca quid chewing) influence CRP levels, and the results demonstrated they were not associated with CRP elevation (> 5.0 mg/L) (P > 0.05). In oral cancer patients, elevated CRP levels were associated with tumor status (P = 0.005), tumor stage (P = 0.054), bone invasion (P = 0.033), lymph node metastasis (P = 0.004) and lymph node extra-capsular spread (P = 0.018). Patients with higher CRP levels showed poorer disease-free survival (log rank test, P < 0.001) and overall survival (log rank test, P = 0.013). CONCLUSIONS: Preoperative serum CRP levels are associated with advanced tumor stage, bone invasion, lymph node metastasis, lymph node extra-capsular spread and patients' survival. CRP is thus potentially a prognostic indicator, but studies with longer follow-up will be needed to confirm its reliability.


Assuntos
Biomarcadores Tumorais/análise , Proteína C-Reativa/análise , Carcinoma de Células Escamosas/patologia , Leucoplasia Oral/patologia , Neoplasias Bucais/patologia , Lesões Pré-Cancerosas/patologia , Adulto , Idoso , Areca/efeitos adversos , Carcinoma de Células Escamosas/mortalidade , Carcinoma de Células Escamosas/cirurgia , Feminino , Humanos , Leucoplasia Oral/mortalidade , Leucoplasia Oral/cirurgia , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Neoplasias Bucais/mortalidade , Neoplasias Bucais/cirurgia , Esvaziamento Cervical , Estadiamento de Neoplasias , Lesões Pré-Cancerosas/mortalidade , Lesões Pré-Cancerosas/cirurgia , Prognóstico , Estudos Retrospectivos , Estatística como Assunto , Análise de Sobrevida , Taiwan , Tomografia Computadorizada por Raios X
4.
J Int Med Res ; 37(2): 479-90, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19383243

RESUMO

Herpes simplex virus thymidine kinase (HSV-TK) and Escherichia coli cytosine deaminase (CD) can convert innocuous prodrugs into cytotoxic metabolites and are being investigated for use in gene therapy for cancer. Human adenoid cystic carcinoma (ACC-2) cells transduced with a CD/HSV-TK fusion gene (ACC-2/CD-TK cells) were found to be more sensitive to radiation than ACC-2 cells when exposed to 5-fluorocytosine (5-FC; 40 microg/ml) plus ganciclovir (0.1 microg/ml) for 48 h before irradiation. Analysis of radiation survival curves for cells exposed to 5-FC plus ganciclovir before irradiation showed that ACC-2 cells had a higher capacity for sublethal damage repair (D(q) value) and greater cellular radiosensitivity (D(0) value) than ACC-2/CD-TK cells. Colony formation rate after 2 Gy of irradiation was significantly greater for ACC-2 than for ACC-2/CD-TK cells when cells were treated with 5-FC plus ganciclovir before irradiation. This study, therefore, indicates that addition of radiation might substantially improve the therapeutic potential of CD-TK fusion gene therapy of human adenoid cystic carcinomas.


Assuntos
Fusão Gênica Artificial , Carcinoma Adenoide Cístico/patologia , Citosina Desaminase/metabolismo , Genes Transgênicos Suicidas , Tolerância a Radiação , Timidina Quinase/metabolismo , Western Blotting , Carcinoma Adenoide Cístico/genética , Morte Celular/efeitos dos fármacos , Morte Celular/efeitos da radiação , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Sobrevivência Celular/efeitos da radiação , Ensaios de Seleção de Medicamentos Antitumorais , Flucitosina/farmacologia , Ganciclovir/farmacologia , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Regulação Neoplásica da Expressão Gênica/efeitos da radiação , Genes Transgênicos Suicidas/efeitos dos fármacos , Genes Transgênicos Suicidas/efeitos da radiação , Humanos , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Tolerância a Radiação/efeitos dos fármacos , Tolerância a Radiação/efeitos da radiação , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Raios X
5.
Eur Rev Med Pharmacol Sci ; 23(16): 7016-7023, 2019 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-31486502

RESUMO

OBJECTIVE: Kinesin superfamily member 4 (Kif4), a conventional kinesin, is a microtubule-dependent molecular motor. The active movement of Kif4 participates in several cellular functions, including DNA repair, mitosis, the transport of macromolecules, survival of neurons and even tumorigenesis and progression. However, the role of Kif4 in monocyte/macrophage cells has not been reported. Our work aimed to increase understanding and further investigations of Kif4 in monocyte/macrophage cells. MATERIALS AND METHODS: RAW264.7 cells were transfected with Kif4 small interfering RNA (siRNA), and whole genome expression microarray analysis was employed to analyze gene expression after cells treatment with or without Kif4 siRNA. RESULTS: Our data found multiple differentially expressed genes which were enriched in the top 5 biological processes about innate immune response, immune response, response to interferon-beta, immune system process and cellular response to interferon-beta. 23 most significant pathways had been identified and enriched pathways indicated enrichment in peroxisome, lysosome, fatty acid metabolism, cell adhesion molecules and so on. CONCLUSIONS: Our work may help understand the roles of Kif4 in monocyte/macrophage cells and would give useful information on basic research and the function of monocyte/macrophage cells.


Assuntos
Cinesinas/genética , Macrófagos/metabolismo , Monócitos/metabolismo , Análise de Sequência com Séries de Oligonucleotídeos , Animais , Células Cultivadas , Cinesinas/metabolismo , Camundongos , Células RAW 264.7
6.
Eur Rev Med Pharmacol Sci ; 22(14): 4542-4550, 2018 07.
Artigo em Inglês | MEDLINE | ID: mdl-30058692

RESUMO

OBJECTIVE: Kinesin family member 5b (Kif5b), a conventional kinesin, mainly participates in lysosome and mitochondria transportation. Some studies have indicated that Kif5b may be associated with the development of a variety of tumors. However, the role Kif5b plays in oral squamous cell carcinoma (OSCC) has yet to be determined. Our study aimed at investigating the expression level of Kif5b in primary OSCC and discussing its clinical significance in patients' outcomes. PATIENTS AND METHODS: We measured Kif5b expression in 82 OSCC tissue samples with immunohistochemistry. The associations between the expression level of Kif5b and clinicopathological characteristics as well as patients' survival were statistically assessed. RESULTS: Kif5b level was significantly associated with tumor size (p=0.034), histological differentiation (p=0.028), disease recurrence (p=0.018), surrounding tissue invasion (p=0.045), recurrence time (p=0.036) and survival status (p=0.030). Kaplan-Meier cumulative survival analyses indicated that high expression of Kif5b was linked to worse overall survival (p=0.0112) and disease-free survival (p=0.0085). The univariate and multivariate Cox proportional hazard analysis further identified the expression status of Kif5b as an independent variable that correlated with patients' survival and recurrence. Furthermore, in 54 early-stage, clinically node negative OSCC patients, Kif5b expression were correlated with histological differentiation (p=0.034), disease recurrence (p=0.038) and surrounding tissue invasion (p=0.029). Univariate and multivariable logistic regression results showed that only Kif5b expression level could influence the probability of recurrence. CONCLUSIONS: Our results reveal that Kif5b expression is associated with poor clinical outcome in OSCC and even in early-stage, clinically node negative OSCC and may be a potential target for OSCC treatment.


Assuntos
Cinesinas/metabolismo , Neoplasias Bucais/patologia , Recidiva Local de Neoplasia/diagnóstico , Carcinoma de Células Escamosas de Cabeça e Pescoço/patologia , Progressão da Doença , Intervalo Livre de Doença , Feminino , Seguimentos , Humanos , Estimativa de Kaplan-Meier , Masculino , Pessoa de Meia-Idade , Mucosa Bucal/patologia , Mucosa Bucal/cirurgia , Neoplasias Bucais/mortalidade , Neoplasias Bucais/cirurgia , Recidiva Local de Neoplasia/patologia , Prognóstico , Carcinoma de Células Escamosas de Cabeça e Pescoço/mortalidade , Carcinoma de Células Escamosas de Cabeça e Pescoço/cirurgia , Taxa de Sobrevida
7.
Transplant Proc ; 39(10): 3030-1, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18089315

RESUMO

BACKGROUND: Tissue-engineered bone is the most perspective and ideal prosthesis for bone defects. But the immunological reaction in allograft is unavoidable. To date there has not been an analysis of the effect of cryopreservation on osteoblast immunogenicity. In this study, we investigated the effects of fluid nitrogen cryopreservation on immunogenicity of osteoblasts. MATERIALS AND METHODS: The osteoblasts were harvested and cultured from the tibial periosteum of New Zealand rabbits, examined by alkaline phosphatase (ALP) and alizarin red S stains, and then cryopreserved for 90 days. Cryopreserved (group C) and fresh (group F) osteoblasts were labeled by the immunofluorescene technique, and the MHC class I antigen was examined by flow cytometric (FC) assay. At the same time, by establishing an osteoblast and lymphocyte mixed culture model (OLMC), the immunogenicity of osteoblasts was examined. RESULTS: The positive rate of MHC class I antigen in group F was 46.36%+/-3.15%, while in group C it was 26.43%+/-2.57%. The MHC I antigen expression was significantly stronger in fresh cells than that in cryopreserved ones (P<.01). In the OLMC assay, the stimulation index (SI) of group F was 3.55+/-0.78, which was significantly higher than that of group C (1.83+/-0.41; P<.01). CONCLUSIONS: The FC assay and OLMC experiments showed that osteoblasts surface antigen expression and allostimulatory function were greatly reduced by cryopreservation. Fluid nitrogen cryopreservation is an ideal method to reduce the immunogenicity in allograft.


Assuntos
Criopreservação/métodos , Osteoblastos/citologia , Osteoblastos/imunologia , Animais , Citometria de Fluxo , Teste de Cultura Mista de Linfócitos , Modelos Animais , Coelhos
8.
Int J Oral Maxillofac Surg ; 36(8): 756-8, 2007 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-17369025

RESUMO

The case is presented of 16 supernumerary teeth in an 11-year-old Chinese female patient with congenital cardiopathy. It was found that the patient's mother had the same clinical manifestation. A detailed investigation into the family history was carried out. Though the etiology of this dental anomaly remains unclear, genetics as a key factor in the development of supernumerary teeth is highlighted.


Assuntos
Transtornos Cromossômicos/genética , Dente Supranumerário/genética , Adulto , Criança , Feminino , Genes Dominantes/genética , Humanos , Prolapso da Valva Mitral/complicações , Linhagem , Radiografia , Dente Supranumerário/complicações , Dente Supranumerário/diagnóstico por imagem
9.
Int J Oral Maxillofac Surg ; 36(4): 350-3, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17223311

RESUMO

Mucoepidermoid carcinoma (MEC) is common in the salivary glands, but alterations of the p16(INK4a) tumour suppressor gene are largely unknown. The aim of this study was to analyse p16(INK4a) gene alterations in MEC, and evaluate their significance for carcinogenesis. Thirty-eight salivary glands with MEC and six normal salivary glands were studied for p16(INK4a) alterations. In the MEC-affected group, there were 23.7% (9/38) and 13.2% (5/38) cases of homozygous deletion, and 5.3% (2/38) and 2.6% (1/38) cases of point mutation in p16(INK4a) exon 1 and exon 2, respectively. Hypermethylation of the p16(INK4a) gene promoter was found in 13 cases (13/38, 34.2%). Alterations of the p16(INK4a) gene were not found in the normal salivary glands. These findings suggest that the main mechanisms of inactivation of the p16(INK4a) gene in MEC of the salivary glands are promoter hypermethylation and homozygous deletion.


Assuntos
Carcinoma Mucoepidermoide/genética , Genes p16/fisiologia , Mutação/genética , Neoplasias das Glândulas Salivares/genética , Adolescente , Adulto , Idoso , Criança , Éxons/genética , Feminino , Deleção de Genes , Regulação Neoplásica da Expressão Gênica/genética , Homozigoto , Humanos , Masculino , Metilação , Pessoa de Meia-Idade , Mutação Puntual/genética , Reação em Cadeia da Polimerase , Polimorfismo Conformacional de Fita Simples , Regiões Promotoras Genéticas/genética , Glândulas Salivares/patologia
10.
Int J Oral Maxillofac Surg ; 36(7): 615-9, 2007 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-17499479

RESUMO

Oral submucous fibrosis can result in progressive closure of the mouth. A total of 10 patients with advanced oral submucous fibrosis were surgically treated. The procedure consisted of (1) release of all the intraoral fibrotic tissue, (2) masticatory muscle myotomy and coronoidotomy, and (3) reconstruction with a bipaddled radial forearm flap. Preoperative mouth opening was 0-5mm (mean 2.3mm). The intraoperative mouth opening was 12-20mm (mean 16 mm) after submucous release, and 32-42 mm (mean 35.5mm) after further release via myotomy and coronoidotomy. The proximal flap included one perforator in four patients and two perforators in the remaining six patients. The flaps were 8-9 cm in length and 2-2.5 cm in width. Nine flaps survived uneventfully. Arterial thrombosis was noted in one flap, which was successfully salvaged. Temporomandibular joint subluxation developed in one patient. Two patients needed flap revision due to bulkiness. The postoperative mouth opening was 18-38 mm (mean 28.2mm) after a mean of 21 months' follow-up, and the mean increase was 25.9 mm. A bipaddled radial forearm flap, using a single donor site, can cover two separate buccal defects after release of oral submucosal fibrosis and obviate the need for a second free flap.


Assuntos
Mucosa Bucal/cirurgia , Fibrose Oral Submucosa/cirurgia , Procedimentos de Cirurgia Plástica/métodos , Retalhos Cirúrgicos , Adulto , Idoso , Bochecha/cirurgia , Feminino , Fibrose , Seguimentos , Antebraço/cirurgia , Sobrevivência de Enxerto , Humanos , Masculino , Mandíbula/cirurgia , Músculo Masseter/cirurgia , Pessoa de Meia-Idade , Complicações Pós-Operatórias , Reoperação , Retalhos Cirúrgicos/irrigação sanguínea , Retalhos Cirúrgicos/patologia , Músculo Temporal/cirurgia , Trombose/etiologia
11.
AJNR Am J Neuroradiol ; 27(8): 1617-21, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16971598

RESUMO

BACKGROUND: A model of toe-to-finger transplantation has been used in studying peripheral nerve regeneration and central reorganization. It was found that recovery of sensory perception depends not only on peripheral reinnervation but also on central integrative mechanisms. OBJECTIVE: Our aim was to investigate functional changes of the brain and somatotopic representation of the transplanted toes after toe-to-finger transplantation. MATERIALS AND METHODS: Six patients who had toe-to-finger transplantation from 3 to 8 years earlier underwent motor and sensory functional MR imaging studies of transplanted toes and opposite corresponding normal fingers. The motor task was performed by repetitively tapping of the transplanted toe or finger against the thumb, whereas the sensory task was applied by tactilely stimulating the pulp of the transplanted toe or finger. RESULTS: The main activation areas from both types of stimulations were located in the expected location of the finger homunculus of the primary sensorimotor cortex. In addition, activated volumes from the transplanted toes were significantly greater than those from the opposite fingers (P = .017 for motor task and P = .005 for tactile sensory task, paired samples Student t test). CONCLUSIONS: Functional recruitment in the primary sensorimotor cortex seemed to have occurred following toe-to-finger transplantation. The transplanted toe was somatotopically represented in the hand area.


Assuntos
Amputação Traumática/cirurgia , Dominância Cerebral/fisiologia , Traumatismos dos Dedos/cirurgia , Dedos/inervação , Imageamento por Ressonância Magnética , Córtex Motor/fisiopatologia , Regeneração Nervosa/fisiologia , Plasticidade Neuronal/fisiologia , Nervos Periféricos/fisiopatologia , Complicações Pós-Operatórias/fisiopatologia , Córtex Somatossensorial/fisiopatologia , Dedos do Pé/transplante , Adolescente , Adulto , Amputação Traumática/fisiopatologia , Mapeamento Encefálico , Criança , Potencial Evocado Motor/fisiologia , Potenciais Somatossensoriais Evocados/fisiologia , Feminino , Traumatismos dos Dedos/fisiopatologia , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Atividade Motora/fisiologia , Exame Neurológico , Dedos do Pé/inervação
12.
Breast ; 15(2): 158-66, 2006 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-16061383

RESUMO

From March 2000 to June 2002, 74 deep inferior epigastric perforator (DIEP) flaps were performed in 73 female patients for oncological post-mastectomy breast reconstruction in Chang Gung Memorial Hospital. The mean age was 44.2 years and mean body weight was 56.6 kg. Twenty-five breast reconstructions were immediate and 49 were delayed. The average size of the flap was 30.1x12.0 cm and the mean number of perforators was 2.2. The average weight of the harvested flap was 595 g and 85.6% (mean: 509 g) of the flap was used for shaping the new breast mound. Zone IV was not discarded, except in one case. Total flap failure and donor site morbidity was not encountered. Only one flap was revised due to venous congestion (1.4%) and successfully salvaged. Partial flap loss occurred in two patients (2.7%). Fat necrosis was detected in 10 cases (13.5%) and sizes ranged from 2x2 to 4x5 cm. The numbers of perforators and the percentage of the used flap weight/total flap weight were not related to the complications. The free DIEP flap and inclusion of zone IV is a reliable and valuable method of breast reconstruction and provides superior aesthetic outcomes.


Assuntos
Neoplasias da Mama/cirurgia , Mamoplastia/métodos , Retalhos Cirúrgicos/estatística & dados numéricos , Abdome/cirurgia , Adulto , Idoso , Neoplasias da Mama/epidemiologia , Feminino , Humanos , Mamoplastia/estatística & dados numéricos , Mastectomia/métodos , Mastectomia/estatística & dados numéricos , Prontuários Médicos , Pessoa de Meia-Idade , Estudos Retrospectivos , Taiwan/epidemiologia , Resultado do Tratamento
13.
Br J Oral Maxillofac Surg ; 54(10): 1090-1094, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27516164

RESUMO

We have evaluated the survival of dental implants placed in vascularised fibular flap onlay grafts placed over marginal mandibulectomies and the effects on marginal bone loss of different types of soft tissue around implants under functional loading. From 2001-2009 we studied a total of 11 patients (1 woman and10 men), three of whom had had ameloblastoma and eight who had had squamous cell carcinomas resected. A total of 38 dental implants were placed either at the time of transfer of the vascularised fibular ostoseptocutaneous flaps (nine patients with 30 implants) or secondarily (two patients with eight implants). Four patients were given palatal mucosal grafts to replace intraoral skin flaps around the dental implants (n=13), and the other seven had the skin flaps around the dental implants thinned (n=25) at the second stage of implantation of the osteointegrated teeth. All vascularised fibular osteoseptocutaneous flaps were successfully transferred, and all implants survived a mean (range) of 73 (33-113) months after occlusal functional loading. The mean (SD) marginal bone loss was 0.5 (0.3) mm on both mesial and distal sides in patients who had palatal mucosal grafts, but 1.8 (1.6) mm, and 1.7 (1.5) mm, respectively, on the mesial and distal sides in the patients who had had thinning of their skin flaps. This difference is significant (p=0.008) with less resorption of bone in the group who had palatal mucosal grafts. Palatal mucosa around the implants helps to reduce resorption of bone after functional loading of implants.


Assuntos
Implantação Dentária Endóssea , Implantes Dentários , Osteotomia Mandibular , Perda do Osso Alveolar , Prótese Dentária Fixada por Implante , Feminino , Humanos , Restaurações Intracoronárias , Masculino , Retalhos Cirúrgicos
14.
Am J Psychiatry ; 156(8): 1273-5, 1999 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10450274

RESUMO

OBJECTIVE: Catechol O-methyltransferase (COMT) is involved in the degradation of catecholamine neurotransmitters. Recent linkage studies of schizophrenia and molecular studies of velocardiofacial syndrome suggest that the COMT gene might be a candidate gene for schizophrenia. METHOD: The authors systematically searched for mutations and microdeletion of the COMT gene in 177 Chinese schizophrenic patients from Taiwan; 99 comparison subjects were also studied. RESULTS: Five molecular variants were identified: c.186C > T at exon 3, c.408C > G at exon 4, c.472G > A at exon 4, c.597G > A at exon 5, and c.821-827insC at the 3' untranslated region. However, no differences in the genotype and haplotype frequencies of these molecular variants between the schizophrenic and comparison subjects were detected. Furthermore, no microdeletion was identified among the patients. CONCLUSIONS: These data suggest that the COMT gene does not play a major role in the pathogenesis of schizophrenia, and the genotypic overlap between schizophrenia and velocardiofacial syndrome was rare in this cohort.


Assuntos
Catecol O-Metiltransferase/genética , Cromossomos Humanos Par 22/genética , Esquizofrenia/genética , Aberrações Cromossômicas/genética , Estudos de Coortes , Análise Mutacional de DNA , Éxons/genética , Feminino , Deleção de Genes , Marcadores Genéticos , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Polimorfismo Genético/genética , Taiwan
15.
Mech Ageing Dev ; 54(2): 103-20, 1990 May 30.
Artigo em Inglês | MEDLINE | ID: mdl-2362469

RESUMO

The selenium level and activity of glutathione peroxidase in blood of children living in Kaschin-Beck disease (KBD) endemic areas were lower than that in nonendemic areas. KBD children were deficient in selenium, their lipid components, structure and function of the red cell membrane and cartilage tissue were abnormal. That is, the phospholipid (PL) content in the tissues of the patient was less than that of the controls in endemic and non-endemic areas. Especially as the phosphatidylcholine (PC) content decreased significantly, but sphingomyelin (SM) increased, the molar ratio of SM/PC and cholesterol (Ch)/PL increased. Increase of acanthocyte content was seen under the electron microscope and the fragility of erythrocytes was also increased. It indicated that there were membrane defects and membrane damage in KBD. At the same time, the sulfation extent of mucopolysaccharides in cartilage of patients was lower, and the collagen content was higher than that of controls. The presenile changes in lipid composition, structure and function of biomembranes and cartilage metabolism of KBD are very significant in studies on the aetiological pathogenesis of KBD and other ageing diseases.


Assuntos
Envelhecimento/metabolismo , Osteoartrite/metabolismo , Cartilagem/metabolismo , Criança , Pré-Escolar , DNA/metabolismo , Eritrócitos/metabolismo , Eritrócitos/ultraestrutura , Feminino , Glutationa Peroxidase/sangue , Humanos , Lactente , Metabolismo dos Lipídeos , Masculino , Lipídeos de Membrana/sangue , Microscopia Eletrônica de Varredura , Osteoartrite/etiologia , Selênio/metabolismo
16.
Am J Med Genet ; 74(1): 40-3, 1997 Feb 21.
Artigo em Inglês | MEDLINE | ID: mdl-9034004

RESUMO

Dopamine D3 receptor (DRD3) was demonstrated to have important implications in schizophrenia, because it binds antipsychotic drugs and is abundant in the limbic system of the brain. Several groups attempted to find an association between a serine-to-glycine polymorphism at codon 9 of the DRD3 gene (Ser9Gly) and schizophrenia; however, the results were inconsistent. We conducted a case-control association study in Han Chinese schizophrenic patients from Taiwan, to examine the relationship of this serine-to-glycine polymorphism and schizophrenia. We noted no significant differences of genotype distribution, allele frequencies, or homozygosity proportion of this polymorphism between schizophrenic patients (N = 178) and controls (N = 100). When patients were divided according to sex, or presence or absence of family history, the differences were still not significant. Our study does not support the contention that the Ser9Gly polymorphism of the DRD3 gene plays a major role in schizophrenia.


Assuntos
Polimorfismo Genético , Receptores de Dopamina D2/genética , Esquizofrenia/genética , Alelos , Povo Asiático , Estudos de Casos e Controles , Feminino , Genótipo , Glicina , Humanos , Masculino , Pessoa de Meia-Idade , Receptores de Dopamina D3 , Serina , Taiwan
17.
Am J Med Genet ; 67(6): 556-9, 1996 Nov 22.
Artigo em Inglês | MEDLINE | ID: mdl-8950414

RESUMO

Several linkage studies suggested chromosome 22q11-13 may harbor susceptible genes for schizophrenia. Catechol-O-methyl-transferase (COMT), which is involved in the metabolism of catecholamines, was mapped to 22q11 and is considered a possible candidate gene for schizophrenia. Recently, we identified a polymorphic marker, a single nucleotide C insertion at the 3' untranslated region of the COMT gene, which obliterates a BglI site. Using this BglI polymorphism, we conducted a case-control association study in Chinese patients with schizophrenia. No significant differences of allele and genotype frequencies were noted between patients (N = 177) and controls (N = 99). When patients were subgrouped according to sex, no significant differences of genotype and allele frequencies were noted in either male or female patients compared to normal controls. Our results do not support an association between the BglI polymorphism of COMT gene and schizophrenia.


Assuntos
Catecol O-Metiltransferase/genética , Desoxirribonucleases de Sítio Específico do Tipo II/metabolismo , Polimorfismo Genético , Esquizofrenia/genética , Feminino , Genótipo , Humanos , Masculino , Reação em Cadeia da Polimerase
18.
J Clin Psychiatry ; 57(7): 298-302, 1996 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-8666571

RESUMO

BACKGROUND: Haloperidol decanoate is a long-acting depot antipsychotic agent used for the treatment of schizophrenic patients. The decanoate formulation was developed to treat schizophrenics who have a history of noncompliance with oral medication. Studies of techniques to convert from oral to depot therapy have not utilized the pharmacokinetics of the decanoate formulation. This study is a prospective evaluation for converting patients from oral to depot treatment. METHOD: Twenty-one patients meeting DSM-III-R criteria for schizophrenia participated in the study. Patients were treated with oral haloperidol for 6 weeks and then were switched to decanoate. Haloperidol decanoate 100 mg was administered on a weekly basis for the first 4 weeks. Afterward, injection intervals were increased to every 2 weeks and then to every 4 weeks. Plasma haloperidol concentrations were obtained prior to the next injection and assayed by HPLC with electrochemical detection. Patients were monitored by the psychiatrists and nursing staff for symptoms of clinical deterioration. RESULTS: All patients completed the conversion trial during the first 4 weeks without any problems or adverse side effects. By the third week, mean plasma haloperidol concentrations from the decanoate injections were comparable with those of the 10-mg oral haloperidol treatment (7.95 +/- 4.94 ng/mL vs. 7.79 +/- 4.79 ng/mL). Steady-state conditions for the decanoate therapy were achieved by the fourth week. CONCLUSION: These findings suggest that schizophrenic patients can be easily converted from oral to depot therapy without problems. Further studies with haloperidol decanoate and its conversion from oral treatment utilizing plasma concentrations are needed.


Assuntos
Antipsicóticos/administração & dosagem , Haloperidol/análogos & derivados , Haloperidol/administração & dosagem , Esquizofrenia/tratamento farmacológico , Administração Oral , Adulto , Antipsicóticos/sangue , Antipsicóticos/farmacocinética , Doença Crônica , Esquema de Medicação , Feminino , Haloperidol/sangue , Haloperidol/farmacocinética , Humanos , Injeções Intramusculares , Masculino , Cooperação do Paciente , Estudos Prospectivos , Recidiva , Esquizofrenia/sangue , Resultado do Tratamento
19.
Psychiatr Genet ; 11(3): 153-5, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11702057

RESUMO

Debrisoquine 4-hydroxylase (CYP2D6) is one of the cytochrome P450 enzyme families that metabolize many compounds. Polymorphic activities of debrisoquine 4-hydroxylase were suggested to be associated with some complex diseases, such as cancer and Parkinson's disease. Schizophrenia is also a complex disorder, and hence we are interested in understanding if the CYP2D6 gene is a susceptibility gene for schizophrenia in Chinese. We determined the genotype and allele frequencies of four molecular variants of CYP2D6 gene (i.e. 188C/T, 1934G/A, 2938C/T and 4268C/G) in 162 Chinese schizophrenic patients and 94 non-psychotic control subjects from Taiwan. No significant differences of allele or genotype frequencies of three polymorphisms (i.e. 188T/C, 2938C/T and 4268C/G) were detected between patients and control subjects. The 1934A allele, which accounts for the majority of poor metabolizers in Caucasians, was not detected in either patients or control subjects, indicating that the 1934A allele is very rare in Chinese. Our data suggest that the CYP2D6 gene may not be a susceptibility gene for schizophrenia in Chinese schizophrenic patients.


Assuntos
Povo Asiático/genética , Citocromo P-450 CYP2D6/genética , Polimorfismo Genético , Esquizofrenia/genética , Alelos , Feminino , Frequência do Gene , Predisposição Genética para Doença , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Polimorfismo de Nucleotídeo Único , Valores de Referência , Esquizofrenia/enzimologia , Taiwan , População Branca/genética
20.
Psychiatr Genet ; 7(1): 35-8, 1997.
Artigo em Inglês | MEDLINE | ID: mdl-9264136

RESUMO

Recent studies have reported an association between a 102T/C polymorphism of serotonin receptor type 2A gene (5-HT2A) and schizophrenia. In addition, an association was detected between a 102T/C polymorphism of the 5-HT2A receptor gene and drug response to clozapine in the treatment of schizophrenic patients. These studies suggest an important role of the 5-HT2A gene in schizophrenia. To study the possible involvement of the 5-HT2A gene in the pathogenesis of schizophrenia, a case-control association study was carried out in a Chinese population from Taiwan. No significant differences of genotype distributions, allele frequencies and homozygosity were detected between schizophrenic patients (n = 177) and nonpsychiatric controls (n = 98). When subjects were divided into subgroups according to sex, still no differences of allele frequencies or genotype distributions were noted between patients and controls. Our data do not support an allelic association between the 102T/C polymorphism of the 5-HT2A receptor gene and schizophrenia in Chinese population.


Assuntos
Povo Asiático/genética , Etnicidade/genética , Receptores de Serotonina/genética , Esquizofrenia/genética , Alelos , China/etnologia , Suscetibilidade a Doenças , Feminino , Frequência do Gene , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Receptor 5-HT2A de Serotonina , Receptores de Serotonina/fisiologia , Taiwan/epidemiologia
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