
To investigate the association between 347 single-nucleotide polymorphisms within candidate genes of the tumor necrosis factor, interleukin 1 and interleukin 6 families with neutrophil count.Four hundred cases with heart failure after myocardial infarction (MI) were matched by age, sex, and date of incident MI to 694 controls (MI without post-MI heart failure). Both genotypes and neutrophil count at admission for incident MI were available in 314 cases and 515 controls.We found significant associations between the TNFSF8 poly morphisms rs927374 (P=5.1 x 10(-5)) and rs2295800 (P=1.3 x 10(-4)) and neutrophil count; these single-nucleotide polymorphisms are in high linkage disequilibrium (r(2)=0.97). Associations persisted after controlling for clinical characteristics and were unchanged after adjusting for case-control status. For rs927374, the neutrophil count of GG homozygotes (7.6±5.1) was 16% lower than that of CC homozygotes (9.0±5.2).The TNFSF8 polymorphisms rs927374 and rs2295800 were associated with neutrophil count. This finding suggests that post-MI inflammatory response is genetically modulated.
Aged, 80 and over, Male, Genotype, Interleukin-6, Tumor Necrosis Factor-alpha, Myocardial Infarction, Middle Aged, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Leukocyte Count, Case-Control Studies, Humans, Female, CD30 Ligand, Genetic Association Studies, Aged, Interleukin-1
Aged, 80 and over, Male, Genotype, Interleukin-6, Tumor Necrosis Factor-alpha, Myocardial Infarction, Middle Aged, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Leukocyte Count, Case-Control Studies, Humans, Female, CD30 Ligand, Genetic Association Studies, Aged, Interleukin-1
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