Skip to main content
. 2017 Feb 9;101(6):791–802. doi: 10.1002/cpt.589

Table 4.

Association of genetic polymorphisms with the occurrence of major adverse cardiac event in 299 patients with coronary heart disease

SNP Gene symbol Genotype With MACE Without MACE OR per variant allele (95% CI) P value FDR
No. (%) No. (%)
rs74460025 GABRB2 TT 64 (71.91) 160 (77.29) 1.487 (0.9–2.457) 0.1216 0.4726
TC 21 (23.60) 46 (22.22)
CC 4 (4.49) 1 (0.48)
rs17145154 DNAH11 TT 51 (59.3) 104 (51.23) 1.272 (0.859–1.884) 0.2299 0.6292
TG 28 (32.56) 78 (38.42)
GG 7 (8.14) 21 (10.34)
rs4741806 Intergenic AA 72 (80.9) 158 (76.33) 0.718 (0.402–1.282) 0.2623 0.6292
AC 17 (19.1) 45 (21.74)
CC 0 (0) 4 (1.93)
rs1048196 HELLS CC 41 (46.07) 92 (45.1) 0.942 (0.638–1.393) 0.7661 0.9422
CT 41 (46.07) 93 (45.59)
TT 7 (7.78) 19 (9.31)
rs1926711 CYP2C18 GG 33 (37.5) 74 (36.63) 1.022 (0.693–1.505) 0.9143 0.9463
GA 45 (51.14) 105 (51.98)
AA 10 (11.36) 23 (11.39)
rs4244285 CYP2C19 GG 42 (46.67) 98 (47.34) 0.987 (0.666–1.461) 0.9463 0.9463
GA 42 (46.67) 90 (43.48)
AA 6 (6.67) 19 (9.18)
rs2852213 GRIK4 CC 13 (14.61) 62 (30.10) 1.302 (0.918–1.847) 0.139 0.4726
CT 54 (60.67) 89 (43.20)
TT 22 (24.72) 55 (26.70)
rs774392 GRIP1 CC 3 (3.33) 3 (1.44) 0.904 (0.548–1.49) 0.6913 0.9422
CA 20 (22.22) 49 (23.56)
AA 67 (74.44) 156 (75.00)
rs12913988a ATP10A CC 7 (7.78) 43 (20.77) 1.876 (1.285–2.740)a 0.0011a 0.0187a
CT 40 (44.44) 99 (47.83)
TT 43 (47.78) 65 (31.4)
rs12456693a SLC14A2 CC 66 (74.16) 141 (67.46) 0.654 (0.398–1.077)a 0.0953a 0.4726a
CT 23 (25.84) 58 (27.75)
TT 0 (0) 10 (4.78)
rs2254638a N6AMT1 TT 13 (14.77) 42 (20.59) 1.428 (0.978–2.086)a 0.0653a 0.4726a
TC 45 (51.14) 113 (55.39)
CC 30 (34.09) 49 (24.02)
rs17209532 Intergenic GG 33 (36.67) 92 (45.10) 0.822 (0.57–1.187) 0.2961 0.6292
GA 46 (51.11) 88 (43.14)
AA 11 (12.22) 24 (11.76)
rs7292279 Intergenic GG 31 (34.44) 82 (39.42) 0.974 (0.68–1.396) 0.8876 0.9463
GA 48 (53.33) 94 (44.98)
AA 11 (12.22) 33 (15.79)
rs13123057 UGT2B11 GG 41 (45.56) 98 (47.34) 1.162 (0.771–1.751) 0.4725 0.7302
GT 28 (31.11) 72 (34.78)
AG 7 (7.78) 16 (7.73)
TT 9 (10.00) 12 (5.80)
AT 5 (5.56) 7 (3.38)
AA 0 (0) 2 (0.97)
rs12369968 MGST1 AA 32 (33.71) 73 (34.93) 1.16 (0.814–1.655) 0.4114 0.7052
AG 40 (44.94) 104 (49.76)
GG 19 (21.35) 32 (15.31)
rs2487032 ABCA1 GG 36 (40.91) 83 (40.1) 0.954 (0.688–1.322) 0.7759 0.9422
GA 31 (35.23) 82 (39.61)
AA 21 (23.86) 42 (20.29)
rs4147820 ABCA4 GG 44 (48.89) 120 (57.42) 1.177 (0.796–1.739) 0.4148 0.7052
GA 41 (45.56) 73 (34.93)
AA 5 (5.56) 16 (7.66)

CI, confidence interval; FDR, false discovery rate; MACE, major adverse cardiac event; OR, odds ratio; SNP, single‐nucleotide polymorphism.

FDR control was used to correct for multiple comparisons.

a

Indicates the associations of genetic polymorphisms with the occurrence of MACE are significant.