Table 1

Summary of case control studies linking inflammatory gene polymorphisms to myocardial infarction

Investigated geneNumber of patientsMain findingsAuthors, year
IL 1ra, interleukin 1 receptor antagonist; MI, myocardial infarction; OR, odds ratio; PECAM, platelet endothelial cell adhesion molecule; TGF, transforming growth factor; TNF, tumour necrosis factor; VNTR, variable number of tandem repeats.
*Healthy control subjects not included. †Prospective study.
TNF α641 menVarious polymorphisms not associated with MIHerrmann et al, 19984
TNF α and β148Various polymorphisms not associated with MIPadovani et al, 20005
TGF β1563 menPro25 associated with MI (p<0.05) but with regional variationsCambien et al, 19966
234 menLeu10 associated with MI in Japanese patients (OR=3.5, p<0.0001)Yokota et al, 20007
IL-1ra74Intron 2 VNTR alleles not associated with MIManzoli et al, 19998
148Intron 2 VNTR alleles not associated with MIIacoviello et al, 20009
CD14178 men–260T associated with first MI (OR=1.8, p=0.0005)Hubaceck et al, 199910
81 men–260T associated with first MI in Japanese (OR=3.8, p=0.004)Shimada et al, 200011
173*–260T associated with MI in “low risk” patients undergoing angiography (OR=1.6, p<0.05)Unckelbach et al, 199912
387† men–260T not associated with incident MIZee et al, 200113
P selectin650 menPro715 protective against MI (OR=0.7, p<0.02)Herrmann et al, 199814
E selectin650 menArg128 not associated with MIHerrmann et al, 199814
PECAM 11170*Val125 not associated with MIGardemann et al, 200015