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1.
Dementia and Neurocognitive Disorders ; : 129-138, 2014.
Artigo em Inglês | WPRIM | ID: wpr-204661

RESUMO

BACKGROUND: The purpose of this study was to evaluate the value of phosphorylated tau with epitopes threonine 181(p-tau181) in cerebrospinal fluid (CSF) for the differential diagnosis of Alzheimer's disease typed dementia from other type of dementia. METHODS: A systematic literature search was performed to identify studies on p-tau181. Two evaluators independently evaluated the quality of the ten studies using the Scottish Intercollegiate Guidelines Network (SIGN) tool. The literature review covered from October 27, 1946 to October 22, 2013, and eight domestic databases including KoreaMed and international databases including Ovid-MEDLINE, EMBASE, and Cochrane Library were used. Tau concentrations were compared to healthy controls and to subjects with Alzheimer's disease (AD) using random effect meta-analysis. Outcome measures were Cohen's delta, sensitivity and specificity. RESULTS: Finally, 8 studies (8 diagnostic evaluation studies) were identified to evaluate CSF p-tau181. The effectiveness of this test was evaluated based on diagnostic accuracy. The diagnostic accuracy for identifying AD by ELISA was high which revealed pooled sensitivity as 0.843 (95% CI 0.818-0.867), pooled specificity as 0.799(95% CI 0.768-0.828) and summary receiver operating characteristic area under the curve 0.9082+/-0.0236. CONCLUSIONS: CSF p-tau181 concentrations in other type of dementia are intermediate between controls and AD patients. Overlap between both controls and AD patients results in insufficient diagnostic accuracy, and the development of more specific biomarkers for these disorders is needed.


Assuntos
Humanos , Doença de Alzheimer , Biomarcadores , Líquido Cefalorraquidiano , Demência , Diagnóstico Diferencial , Ensaio de Imunoadsorção Enzimática , Epitopos , Avaliação de Resultados em Cuidados de Saúde , Curva ROC , Sensibilidade e Especificidade , Proteínas tau , Treonina
2.
Journal of the Korean Medical Association ; : 704-709, 2014.
Artigo em Coreano | WPRIM | ID: wpr-210259

RESUMO

The evaluation of fibrosis is crucial in the assessment of chronic liver disease. Liver biopsy has been a reference standard for assessing liver fibrosis. However, it has some drawbacks - invasiveness, risk of complications, and intra-observer/inter-observer variability. One of the promising tools for evaluating liver fibrosis is the Multivariate Index Assay, which combines the values of three biomarkers (hyaluronic acid, amino-terminal propeptide of type III procollagen, and tissue inhibitor of matrix metalloproteinase-1) from serum samples. A systematic review was conducted to determine whether the test would be a safe and effective method for assessing liver fibrosis. A total of 16 diagnostic studies on the serum liver fibrosis test have been reported. Based on the literature published until January 2013, this test is safe and can be used as an adjunct tool for detecting liver fibrosis in a wide range of chronic liver diseases.


Assuntos
Biomarcadores , Biópsia , Colágeno Tipo III , Fibrose , Ácido Hialurônico , Fígado , Cirrose Hepática , Hepatopatias , Inibidor Tecidual de Metaloproteinase-1
3.
Yonsei Medical Journal ; : 852-861, 2006.
Artigo em Inglês | WPRIM | ID: wpr-141741

RESUMO

This study investigated that whether a 2 mT, 60 Hz, sinusoidal electromagnetic field (EMF) alters the structure and function of cells. This research compared the effects of EMF on four kinds of cell lines: hFOB 1.19 (fetal osteoblast), T/G HA-VSMC (aortic vascular smooth muscle cell), RPMI 7666 (B lymphoblast), and HCN-2 (cortical neuronal cell). Over 14 days, cells were exposed to EMF for 1, 3, or 6 hours per day (hrs/d). The results pointed to a cell type-specific reaction to EMF exposure. In addition, the cellular responses were dependent on duration of EMF exposure. In the present study, cell proliferation was the trait most sensitive to EMF. EMF treatment promoted growth of hFOB 1.19 and HCN-2 compared with control cells at 7 and 14 days of incubation. When the exposure time was 3 hrs/d, EMF enhanced the proliferation of RPMI 7666 but inhibited that of T/G HA- VSMC. On the other hand, the effects of EMF on cell cycle distribution, cell differentiation, and actin distribution were unclear. Furthermore, we hardly found any correlation between EMF exposure and gap junctional intercellular communication in hFOB 1.19. This study revealed that EMF might serve as a potential tool for manipulating cell proliferation.


Assuntos
Humanos , Transdução de Sinais , Citoesqueleto de Actina/efeitos da radiação , Junções Comunicantes/metabolismo , Campos Eletromagnéticos , Proliferação de Células/efeitos da radiação , Fenômenos Fisiológicos Celulares/efeitos da radiação , Linhagem Celular , Diferenciação Celular/efeitos da radiação , Ciclo Celular/efeitos da radiação
4.
Yonsei Medical Journal ; : 852-861, 2006.
Artigo em Inglês | WPRIM | ID: wpr-141740

RESUMO

This study investigated that whether a 2 mT, 60 Hz, sinusoidal electromagnetic field (EMF) alters the structure and function of cells. This research compared the effects of EMF on four kinds of cell lines: hFOB 1.19 (fetal osteoblast), T/G HA-VSMC (aortic vascular smooth muscle cell), RPMI 7666 (B lymphoblast), and HCN-2 (cortical neuronal cell). Over 14 days, cells were exposed to EMF for 1, 3, or 6 hours per day (hrs/d). The results pointed to a cell type-specific reaction to EMF exposure. In addition, the cellular responses were dependent on duration of EMF exposure. In the present study, cell proliferation was the trait most sensitive to EMF. EMF treatment promoted growth of hFOB 1.19 and HCN-2 compared with control cells at 7 and 14 days of incubation. When the exposure time was 3 hrs/d, EMF enhanced the proliferation of RPMI 7666 but inhibited that of T/G HA- VSMC. On the other hand, the effects of EMF on cell cycle distribution, cell differentiation, and actin distribution were unclear. Furthermore, we hardly found any correlation between EMF exposure and gap junctional intercellular communication in hFOB 1.19. This study revealed that EMF might serve as a potential tool for manipulating cell proliferation.


Assuntos
Humanos , Transdução de Sinais , Citoesqueleto de Actina/efeitos da radiação , Junções Comunicantes/metabolismo , Campos Eletromagnéticos , Proliferação de Células/efeitos da radiação , Fenômenos Fisiológicos Celulares/efeitos da radiação , Linhagem Celular , Diferenciação Celular/efeitos da radiação , Ciclo Celular/efeitos da radiação
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