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Clinics ; 70(3): 169-172, 03/2015. tab
Article Dans Anglais | LILACS | ID: lil-747107

Résumé

BACKGROUND: To evaluate the macrophage migration inhibitory factor and E-selectin levels in patients with acute coronary syndrome. MATERIALS/METHODS: We examined the plasma migration inhibitory factor and E-selectin levels in 87 patients who presented with chest pain at our hospital. The patients were classified into two groups according to their cardiac status. Sixty-five patients had acute myocardial infarction, and 22 patients had non-cardiac chest pain (non-coronary disease). We designated the latter group of patients as the control group. The patients who presented with acute myocardial infarction were further divided into two subgroups: ST-elevated myocardial infarction (n = 30) and non-ST elevated myocardial infarction (n = 35). RESULTS: We found higher plasma migration inhibitory factor levels in both acute myocardial infarction subgroups than in the control group. However, the E-selectin levels were similar between the acute myocardial infarction and control patients. In addition, we did not find a significant difference in the plasma migration inhibitory factor levels between the ST elevated myocardial infarction and NST-elevated myocardial infarction subgroups. DISCUSSION: The circulating concentrations of migration inhibitory factor were significantly increased in acute myocardial infarction patients, whereas the soluble E-selectin levels were similar between acute myocardial infarction patients and control subjects. Our results suggest that migration inhibitory factor may play a role in the atherosclerotic process. .


Sujets)
Animaux , Femelle , Souris , /métabolisme , Interféron gamma/métabolisme , Tumeurs mammaires de l'animal/immunologie , Sphéroïdes de cellules/immunologie , Lymphocytes T cytotoxiques/métabolisme , Lymphocytes T auxiliaires/métabolisme , Alginates , Antigènes néoplasiques/immunologie , Antigènes néoplasiques/métabolisme , Lignée cellulaire tumorale , Mouvement cellulaire , Chitosane , /génétique , /immunologie , Acide glucuronique , Granzymes/métabolisme , Acides hexuroniques , Immunité cellulaire , Interféron gamma/génétique , Interféron gamma/immunologie , Tumeurs mammaires de l'animal/génétique , Tumeurs mammaires de l'animal/métabolisme , Tumeurs mammaires de l'animal/anatomopathologie , Sphéroïdes de cellules/métabolisme , Sphéroïdes de cellules/anatomopathologie , Lymphocytes T cytotoxiques/immunologie , Lymphocytes T auxiliaires/immunologie , Microenvironnement tumoral
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