Tumor necrosis factor-alpha gene −308G>A polymorphism is associated with ST-elevation myocardial infarction and with high plasma levels of biochemical ischemia markers

OBJECTIVESAs is well known, acute myocardial infarction presents two electrocardiogram (EKG) patterns, ST-elevation (STEMI) and no ST-elevation (NSTEMI), characterized by different coronary artery thrombotic occlusion. Growing evidence shows that inflammation plays a central role in the pathogenesis...

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Veröffentlicht in:Coronary artery disease 2005-12, Vol.16 (8), p.489-493
Hauptverfasser: Antonicelli, Roberto, Olivieri, Fabiola, Cavallone, Luca, Spazzafumo, Liana, Bonafè, Massimiliano, Marchegiani, Francesca, Cardelli, Maurizio, Galeazzi, Roberta, Giovagnetti, Simona, Perna, Gian Piero, Franceschi, Claudio
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Sprache:eng
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Zusammenfassung:OBJECTIVESAs is well known, acute myocardial infarction presents two electrocardiogram (EKG) patterns, ST-elevation (STEMI) and no ST-elevation (NSTEMI), characterized by different coronary artery thrombotic occlusion. Growing evidence shows that inflammation plays a central role in the pathogenesis of acute myocardial infarction. Among the factors that promote inflammation and arterial thrombosis, one of the most important is the proinflammatory cytokine tumor necrosis factor-α. The expression of this cytokine is modulated by a polymorphism located at nucleotide −308 of tumor necrosis factor-α promoter gene. The objective of our study is to verify whether tumor necrosis factor-α −308 polymorphism is associated with risk of acute myocardial infarction (STEMI and NSTEMI) or with biochemical myocardial ischemia markers, such as troponin I, creatine kinase-MB, lactate dehydrogenase and myoglobin. METHODSWe analyzed tumor necrosis factor-α −308 polymorphism in a total of 603 study participants293 elderly patients affected by acute myocardial infarction (STEMI and NSTEMI) and 310 healthy controls. RESULTSWe found that individuals carrying the tumor necrosis factor-α −308 AG+AA genotypes are significantly more represented among acute myocardial infarction patients affected by STEMI than among NSTEMI patients (OR=1.86, 95% CI 1.08–3.21, p=0.027) and healthy controls (OR=1.64, 95% CI 1.03–2.64, p=0.046). Furthermore, the patients carrying tumor necrosis factor-α −308 AG+AA genotypes displayed significant increased levels of biochemical myocardial ischemia markers. CONCLUSIONSOur study shows a significant association between the tumor necrosis factor-α −308 polymorphism and the occurrence of STEMI, and suggests that the tumor necrosis factor-α −308 polymorphism could play a role in the pathogenesis of cardiac ischemic damage, AA+AG genotype carrier individuals being likely to be affected by more severe ischemic damage than the rest of the population.
ISSN:0954-6928
1473-5830
DOI:10.1097/00019501-200512000-00006