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. 2017 Dec 13;7:17517. doi: 10.1038/s41598-017-17537-1

Table 3.

Association analysis of 5 genotyped SNPs of the MMP9, ALOX5AP, MTHFR, FGB, and eNOS genes with CES.

Gene SNP Genotype AF patients with CES (n=479) AF patients without CES (n=580) P P HWE
No Frequency No Frequency
MMP9 C1562T CC 293 61.5% 357 61.8% 0.963 0.921
CT 160 33.5% 194 33.5%
TT 24 5.0% 27 4.7%
C:T 0.78:0.22 0.79:0.21 0.846
ALOX5AP SG13S114A/T AA 147 30.7.2% 205 35.3% 0.116 0.500
AT 256 53.4% 273 47.1%
TT 76 15.9% 102 17.6%
A:T 0.57:0.43 0.59:0.41 0.495
MTHFR 677 C/T CC 285 59.5% 321 55.5% 0.425 0.298
CT 162 33.8% 213 36.9%
TT 32 6.7% 44 7.6%
C:T 0.76:0.24 0.74:0.26 0.195
FGB 455 G/A GG 271 56.6% 382 65.9% 0.001 0.929
GA 172 35.9% 177 30.5%
AA 36 7.5% 21 3.6%
G:A 0.75:0.25 0.81:0.19  < 0.001
eNOS G894T GG 338 70.6% 418 72.3% 0.437 0.058
GT 129 26.9% 140 24.2%
TT 12 2.5% 20 3.5%
G:T 0.84:0.16 0.84:0.16 0.802

AF: atrial fibrillation; CES: cardioembolic stroke; SNP: single nucleotide polymorphism; MMP-9: matrix metallopeptidas-9 gene; ALOX5AP: arachidonate 5-lipoxygenase-activating protein gene; MTHFR: methylene tetrahydrofolate reductase gene; FGB: the β-fibrinogen gene; and eNOS: endothelial nitric oxide synthase gene.