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1.
Sci Rep ; 14(1): 4116, 2024 02 19.
Artículo en Inglés | MEDLINE | ID: mdl-38374382

RESUMEN

Air pollution has become a significant concern for human health, and its impact on influenza, has been increasingly recognized. This study aims to explore the spatiotemporal heterogeneity of the impacts of air pollution on influenza and to confirm a better method for infectious disease surveillance. Spearman correlation coefficient was used to evaluate the correlation between air pollution and the influenza case counts. VIF was used to test for collinearity among selected air pollutants. OLS regression, GWR, and STWR models were fitted to explore the potential spatiotemporal relationship between air pollution and influenza. The R2, the RSS and the AICc were used to evaluate and compare the models. In addition, the DTW and K-medoids algorithms were applied to cluster the county-level time-series coefficients. Compared with the OLS regression and GWR models, STWR model exhibits superior fit especially when the influenza outbreak changes rapidly and is able to more accurately capture the changes in different regions and time periods. We discovered that identical air pollutant factors may yield contrasting impacts on influenza within the same period in different areas of Fuzhou. NO2 and PM10 showed opposite impacts on influenza in the eastern and western areas of Fuzhou during all periods. Additionally, our investigation revealed that the relationship between air pollutant factors and influenza may exhibit temporal variations in certain regions. From 2013 to 2019, the influence coefficient of O3 on influenza epidemic intensity changed from negative to positive in the western region and from positive to negative in the eastern region. STWR model could be a useful method to explore the spatiotemporal heterogeneity of the impacts of air pollution on influenza in geospatial processes. The research findings emphasize the importance of considering spatiotemporal heterogeneity when studying the relationship between air pollution and influenza.


Asunto(s)
Contaminantes Atmosféricos , Contaminación del Aire , Gripe Humana , Humanos , Gripe Humana/epidemiología , Contaminación del Aire/efectos adversos , Contaminación del Aire/análisis , Contaminantes Atmosféricos/efectos adversos , Contaminantes Atmosféricos/análisis , Material Particulado/efectos adversos , Material Particulado/análisis , Monitoreo del Ambiente , China/epidemiología
2.
Zhongguo Yi Liao Qi Xie Za Zhi ; 29(1): 19-22, 2005 Jan.
Artículo en Zh | MEDLINE | ID: mdl-15875687

RESUMEN

A new computer-assisted vector-cardiogram analyzing system Model TJ-IV developed based on Model TJ-III, has been using in the routine clinical work in order to evaluate its features and performances. The system employs a 586 computer with a CPU of 120 MHz, a special low-noise amplifier, a 12 bit A/D tranducer and the C language for programming. The examinations of 206 cases were performed and all the vector-cardiograms were analyzed by the computer system and by manipulative methods respectively. In comparison with the manipulative methods the system has a very high accuracy of picture-recognition. The accuracy for distinguishing the onsets and terminals of orthogonal ECG waves is 98% while that for distinguishing the peaks and troughs of the waves is 100%. These waves include P, Q, R, S, R' and S' waves. The new system is capable to provide the parameters of more than 591 items, including 46 newly-developed diagnostic parameters. The testing and analyzing of 12 parameters of orthogonal ECG and plane VCG have proved that the results of the aboved two methods have no difference. The new system has a very high accuracy of picture-recognition and index calculation with many technical problems existing in the old versions, solved--a great improvement of safety and anti-interference and an increase of the detecting & diagnostic speed.


Asunto(s)
Diagnóstico por Computador/instrumentación , Infarto del Miocardio/diagnóstico , Procesamiento de Señales Asistido por Computador , Vectorcardiografía/instrumentación , Adolescente , Adulto , Anciano , Sistemas de Computación , Procesamiento Automatizado de Datos , Femenino , Humanos , Masculino , Persona de Mediana Edad , Valores de Referencia , Reproducibilidad de los Resultados , Programas Informáticos
3.
Mol Med Rep ; 7(2): 466-70, 2013 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-23229085

RESUMEN

The present study aimed to determine the effect of small interfering RNA (siRNA)­induced inhibition of cyclin­dependent kinase 2 (Cdc2) expression on osteosarcoma MG63 cell proliferation and apoptosis. An siRNA expression plasmid, psilencer 2.1­U6/Cdc2, targeting the Cdc2 gene, and a control psilencer 2.1­U6/Scramble plasmid were constructed and transfected into MG63 cells using liposomes. Cdc2 expression in the MG63 cells was investigated by western blot analysis and real­time polymerase chain reaction. Cell morphology was also examined. The effects of psilencer 2.1­U6/Cdc2 on MG63 cell proliferation and the cell cycle were detected via MTT and flow cytometry, respectively. Expression levels of apoptosis­related molecules, B­cell lymphoma 2 (Bcl­2) and Bcl­2­associated X (Bax) were determined by western blot analysis. MG63 cells stably transfected with the psilencer 2.1­U6/Cdc2 plasmid (MG63­siRNA/Cdc2) and negative control cells, MG63­siRNA/Scramble, were successfully obtained. The silencing efficiencies of the Cdc2­expressing mRNA and protein in MG63­siRNA/Cdc2 were 86 and 89% of that of the control MG63­siRNA/Scramble cells, respectively. Interference of Cdc2 expression inhibited MG63 cell proliferation and was demonstrated to significantly increase and decrease cells in the G2/M and S phases, respectively. Cdc2 expression silencing had negligible effects on Bcl­2 and Bax expression in MG63 cells. In conclusion, silencing of Cdc2 expression suppresses proliferation of osteosarcoma MG63 cells but has negligible effects on apoptosis.


Asunto(s)
Apoptosis , Quinasa 2 Dependiente de la Ciclina/genética , ARN Interferente Pequeño/metabolismo , Línea Celular Tumoral , Proliferación Celular , Quinasa 2 Dependiente de la Ciclina/antagonistas & inhibidores , Quinasa 2 Dependiente de la Ciclina/metabolismo , Humanos , Proteínas Proto-Oncogénicas c-bcl-2/metabolismo , Interferencia de ARN , Proteína X Asociada a bcl-2/metabolismo
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