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1.
Can Vet J ; 52(4): 394-7, 2011 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-21731092

RESUMEN

Porcine circovirus type 2 systemic infection was diagnosed in 2 slaughter-weight pigs based on postmortem examination. The infection was associated with unusual central nervous system lesions characterized by a multifocal lymphohistiocytic to granulomatous meningoencephalomyelitis with giant cell formation. The role of these nervous system lesions in the development of the clinical signs in these pigs remains uncertain.


Asunto(s)
Sistema Nervioso Central/patología , Infecciones por Circoviridae/veterinaria , Circovirus/aislamiento & purificación , Enfermedades de los Porcinos/patología , Animales , Infecciones por Circoviridae/diagnóstico , Infecciones por Circoviridae/patología , Resultado Fatal , Inmunohistoquímica/veterinaria , Reacción en Cadena de la Polimerasa/veterinaria , Porcinos , Enfermedades de los Porcinos/diagnóstico
2.
Atherosclerosis ; 240(2): 351-4, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-25875387

RESUMEN

OBJECTIVE: The MEDCOR trial is a double-blind, randomized study aiming at demonstrating the superiority of molsidomine (direct NO donor) over placebo, used as add-on treatments, on improving endothelial function (EF) after 12 months, in stable angina patients undergoing percutaneous coronary intervention. METHODS: EF was assessed by peripheral vasodilator response (i.e. Endoscore) using arterial tonometry and by several biomarkers, in terms of changes versus baseline after a one-year treatment. RESULTS: The change in Endoscore was +75 ± 130% in placebo group and +39 ± 145% in molsidomine group (p = 0.143). There was a decrease in sICAM-1 with molsidomine (-6%) and an increase with placebo (+6%). The MPO activity/antigen ratio slightly increased with placebo (+9%) and strongly decreased with molsidomine (-42%) (p = 0.020). CONCLUSION: The MEDCOR trial was not able to demonstrate significant differences between molsidomine and placebo for all parameters, except the MPO activity/antigen ratio which significantly decreased with molsidomine (p = 0.020 versus placebo).


Asunto(s)
Angina Estable/terapia , Enfermedad de la Arteria Coronaria/terapia , Endotelio Vascular/efectos de los fármacos , Molsidomina/uso terapéutico , Donantes de Óxido Nítrico/uso terapéutico , Intervención Coronaria Percutánea , Vasodilatación/efectos de los fármacos , Vasodilatadores/uso terapéutico , Anciano , Angina Estable/sangre , Angina Estable/diagnóstico , Angina Estable/fisiopatología , Bélgica , Biomarcadores/sangre , Terapia Combinada , Enfermedad de la Arteria Coronaria/sangre , Enfermedad de la Arteria Coronaria/diagnóstico , Enfermedad de la Arteria Coronaria/fisiopatología , Método Doble Ciego , Endotelio Vascular/metabolismo , Endotelio Vascular/fisiopatología , Femenino , Humanos , Molécula 1 de Adhesión Intercelular/sangre , Masculino , Manometría , Persona de Mediana Edad , Molsidomina/efectos adversos , Donantes de Óxido Nítrico/efectos adversos , Intervención Coronaria Percutánea/efectos adversos , Peroxidasa/sangre , Factores de Tiempo , Resultado del Tratamiento , Vasodilatadores/efectos adversos
3.
J Cardiovasc Transl Res ; 7(2): 226-31, 2014 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-24142804

RESUMEN

The effects of molsidomine (a direct nitric oxide donor) on the endothelial dysfunction have never been evaluated using reactive hyperemia peripheral arterial tonometry (RH-PAT). The objective of the MEDCOR double-blind trial will be to demonstrate the superiority of molsidomine (Coruno® 16 mg, once daily) over placebo, on improving the endothelial function (Endoscore by RH-PAT) after 12 months of treatment in stable angina patients undergoing elective percutaneous coronary intervention (PCI). Study design will take care of the real-life situation, in which patients are being offered PCI and stent placement (drug-eluting or bare metal), but also gold standard medical therapy (beta-blockers, statins, angiotensin-converting enzyme inhibitors (ACEIs), and/or calcium antagonists). Demonstrating clinical and statistical superiority of the study drug over placebo will be a real challenge. Therefore, a sequential approach has been designed with a pilot phase aiming at recruiting 50 patients. Upon evaluation of the results by an independent data steering committee, a larger sample size phase will eventually be considered.


Asunto(s)
Angina Estable/terapia , Vasos Coronarios/efectos de los fármacos , Endotelio Vascular/efectos de los fármacos , Molsidomina/uso terapéutico , Donantes de Óxido Nítrico/uso terapéutico , Intervención Coronaria Percutánea , Proyectos de Investigación , Angina Estable/diagnóstico , Angina Estable/fisiopatología , Bélgica , Protocolos Clínicos , Vasos Coronarios/fisiopatología , Método Doble Ciego , Quimioterapia Combinada , Endotelio Vascular/fisiopatología , Humanos , Intervención Coronaria Percutánea/efectos adversos , Intervención Coronaria Percutánea/instrumentación , Proyectos Piloto , Stents , Factores de Tiempo , Resultado del Tratamiento
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