Table 5.
Association of omentin rs2274907A>T gene variation with CAD.
| Genotypes | Healthy Controls | CAD Cases | OR (95% CI) | Risk Ratio (RR) | P-Value |
|---|---|---|---|---|---|
| (N = 100) | (N = 100) | ||||
| Codominant | |||||
| ITLN1-AA | 49 | 24 | 1 (ref.) | 1 (ref.) | |
| ITLN1-AT | 51 | 75 | 3.0 (1.64 to 5.49) | 1.65 (1.27 to 2.163) | 0.002 |
| ITLN1-TT | 0 | 1 | 6.0 (0.23 to 154.31) | 2.67 (0.24 to 29.66) | 0.422 |
| Dominant | |||||
| ITLN1-AA | 49 | 24 | 1 (ref.) | 1 (ref.) | |
| ITLN1-(AT + TT) | 51 | 76 | 3.0 (1.66 to 5.56) | 1.67 (1.28 to 2.18) | 0.003 |
| Recessive | |||||
| ITLN1-(AA + AT) | 100 | 99 | 1 (ref.) | 1 (ref.) | |
| ITLN1-TT | 0 | 1 | 3.03 (0.12 to 75.28) | 2.0 (0.181 to 22.255) | 0.49 |
| Allele | |||||
| ITLN1-A | 149 | 123 | 1 (ref.) | 1 (ref.) | |
| ITLN1-T | 51 | 77 | 1.82 (1.193 to 2.80) | 1.37 (1.08 to 1.74) | 0.005 |