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1.
Rev. colomb. cardiol ; 28(6): 556-563, nov.-dic. 2021. tab, graf
Article in English | LILACS, COLNAL | ID: biblio-1357230

ABSTRACT

Abstract Introduction Until now, only few studies have reported the correlation between vesicle-associated membrane protein-8 (VAMP-8) A/G gene polymorphism and acute myocardial infarction. Whereas, theoretically, VAMP-8 plays a pivotal role in the pathogenesis of acute myocardial infarction through platelet activation, secretion, and aggregation. Objective To investigate the association between VAMP-8 A/G gene polymorphism and the risk of acute myocardial infarction. Methods A cross-sectional study was carried out at Saiful Anwar General Hospital during June 2013 - May 2014. A Mae II enzyme with restriction fragment length polymorphism method was used to genotype VAMP-8 A/G gene polymorphisms in acute myocardial infarction and control groups. A multiple logistic regression test was used to analyze the association between VAMP-8 A/G gene polymorphism and the risk of acute myocardial infarction. Results A total of 35 controls and 97 acute myocardial infarction patients from our Hospital during the period were enrolled for our study. Our results found that VAMP-8 A/G gene polymorphism was not associated with the risk of acute myocardial infarction. Moreover, we also failed to confer the association between VAMP-8 A/G gene polymorphism and both smoking and hypertension among patients with acute myocardial infarction. Furthermore, in the setting of premature acute myocardial infarction, the correlation also failed to confirm. Conclusion In our population, there is no association between VAMP-8 A/G gene polymorphism and the risk of acute myocardial infarction.


Resumen Introducción Hasta la fecha, solo unos pocos estudios han reportado la correlación entre el polimorfismo A/G del gen de la proteína de membrana asociada a vesículas-8 (VAMP-8, por sus siglas en inglés) y el infarto agudo de miocardio. Si bien, en teoría, VAMP-8 juega un papel fundamental en la patogénesis del infarto agudo de miocardio a través de la activación, secreción y agregación plaquetaria. Objetivo Investigar la relación entre el polimorfismo A/G del gen VAMP-8 y el riesgo de infarto agudo de miocardio. Métodos: Se llevó a cabo un estudio transversal en Siful Anwar General Hospital entre junio del 2013 y mayo del 2014. Se utilizó la técnica de polimorfismos de longitud de fragmentos de restricción con la enzima Mae II para genotipificar los polimorfismos A/G del gen VAMP-8 en grupos de infarto agudo de miocardio y de control. Se aplicó una prueba de regresión logística múltiple para analizar la relación entre el polimorfismo A/G del gen VAMP-8 y el riesgo de infarto agudo de miocardio. Resultados Se incluyeron un total de 35 controles y 97 pacientes con infarto agudo de miocardio de nuestro Hospital durante el periodo del estudio. Nuestros resultados encontraron que el polimorfismo A/G del gen VAMP-8 no estaba relacionado con el riesgo de infarto agudo de miocardio. Por otra parte, tampoco pudimos establecer una relación entre el polimorfismo A/G del gen VAMP-8 y tanto tabaquismo como hipertensión en pacientes con infarto agudo de miocardio. Asimismo, en el contexto de infarto agudo de miocardio prematuro, tampoco se confirmó la correlación. Conclusión: En nuestra población, no existe una relación entre el polimorfismo A/G del gen VAMP-8 y el riesgo de infarto agudo de miocardio.


Subject(s)
Humans , Myocardial Infarction , Polymorphism, Genetic , Membrane Proteins
2.
Biosci. j. (Online) ; 30(5 Supplement 2): 833-838, 2014. tab
Article in English | LILACS | ID: biblio-947982

ABSTRACT

The objective of this research was to compare the results obtained by the Microscopic Agglutination Test (MAT) and indirect ELISA using outer membrane proteins (OMP) of the serovar Hardjo as antigen (ELISA/OMP-Hardjo). Ninety-three samples of blood serum from 3 to 6-year-old cattle of both sexes with no history of vaccination for leptospirosis were used. To perform the MAT, live cultures of 14 Leptospira serovars representing 11 serogroups of L. interrogans were used as antigen. Outer membrane proteins (OMP) of the serovar Hardjo (ELISAOMP/ Hardjo) were used as the ELISA antigen. Of the 93 samples tested by MAT, 37 (40%) were positive. None of the samples testing positive in the MAT were negative in the ELISA. Sensitivity was 100% and specificity 64%. A comparison of the MAT and ELISA-OMP/Hardjo tests showed 78% agreement and the Kappa index was 0.58 (p<0.0001). The ELISA-OMP/Hardjo proved to be a sensitive test for the diagnosis of bovine leptospirosis, indicating its potential use as a screening test and for epidemiological studies. The titration results obtained by MAT and by optical density (OD) in the ELISA-OMP/Hardjo test showed a positive correlation, and as the antibody titers in the MAT increased, so did the OD in ELISA, demonstrating the correspondence between the tests evaluated here.


O objetivo desta pesquisa foi comparar os resultados obtidos pela Soroaglutinação Microscópica (SAM) e pelo ELISA indireto empregando proteínas de membrana externa (PME) do sorovar Hardjo como antígeno (ELISA/PME-Hardjo). Utilizou-se 93 amostras de soro sanguíneo de bovinos de ambos os sexos com idade entre três a seis anos e sem histórico de vacinação para leptospirose. Para a realização da SAM utilizou-se como antígeno culturas vivas de 14 sorovares de Leptospira, representando 11 sorogrupos de L. interrogans. Empregou-se como antígeno do ELISA, proteínas de membrana externa (PME) do sorovar Hardjo (ELISA-PME/Hardjo). Das 93 amostras testadas na SAM, 37 (40%) foram positivas. Já o ELISA-PME/Hardjo identificou 57 (62%) positivas e 36 (38%) negativas. Nenhuma amostra positiva na SAM foi negativa no ELISA. A sensibilidade foi de 100% e especificidade 64%. A comparação dos testes de SAM e ELISA-PME/Hardjo demonstrou concordância de 78% e índice Kappa de 0,58 (p<0,0001). O ELISAPME/ Hardjo revelou-se como um teste sensível para o diagnóstico da leptospirose bovina, indicando seu uso potencial como exame de triagem e para estudos epidemiológicos. A correlação dos resultados obtidos pela titulação na SAM e DO no ELISA-PME/Hardjo foi positiva, sendo que a medida que os títulos de anticorpos na SAM aumentaram, a DO no ELISA também aumentou, demonstrando haver correspondência entre os exames avaliados.


Subject(s)
Immunologic Tests , Cattle , Enzyme-Linked Immunosorbent Assay , Leptospira
3.
Ciênc. rural ; 39(9): 2539-2543, dez. 2009. ilus
Article in English | LILACS | ID: lil-534740

ABSTRACT

The protein profile of the outer membrane of Leptospira interrogans serovar Hardjo subtype hardjoprajitno associated with the bovine natural immune response was investigated. The outer membrane proteins were extracted utilizing Triton X114 and precipitated with acetone. The protein sample was then resolved by SDS-PAGE and reacted in western blot against sera from a hyperimmune rabbit and from naturally infected bovines. In silver stained gels, 14 protein bands were observed, among which four proteins, with 22, 29, 47 and 63kDa, appeared as major constituents. Western blot tests with hyperimmune rabbit antiserum detected bands corresponding to proteins with 35; 27; 24; 21; 17 and 14kDa, while 32kDa and 45kDa proteins were the most immunoreactive with sera from naturally infected bovines.


Estudou-se o perfil proteico da membrana externa da Leptospira interrogans sorovariedade Hardjo, amostra hardjoprajitno, associado à resposta imune natural de bovinos infectados. Foram utilizados Triton X114 para a extração das proteínas de membrana externa e acetona para precipitá-las. As proteínas extraídas foram analisadas por SDS-PAGE e western blot contra soro de coelhos hiperimunes e de bovinos naturalmente infectados. Em géis corados com nitrato de prata, 14 bandas proteicas foram identificadas, e quatro dessas bandas, com 22, 29, 47 e 63kDa, foram as mais proeminentes. Os western blots com soro hiperimune de coelho detectaram bandas correspondentes a proteínas com pesos moleculares de 35, 27, 24, 21, 17 e 14kDa, e bandas de 32 e 45kDa destacaram-se nos testes com soros de bovinos naturalmente infectados.

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