Table 3.
Associations of polygenic and genetic risk scores of coronary artery disease with primary incident CAD in the UK Biobank
Genetic predisposition* | All HR (95% CI) | Men HR (95% CI) | Women HR (95% CI) | Interaction P-value | |
---|---|---|---|---|---|
CAD-GRS | Per SD increase | 1.34 (1.31, 1.36) | 1.38 (1.34, 1.41) | 1.25 (1.21, 1.30) | 5×10−5 |
High | 2.20 (2.06, 2.35) | 2.39 (2.21, 2.59) | 1.82 (1.62, 2.05) | ||
GRSCAD-BP | Per SD increase | 1.14 (1.12, 1.16) | 1.17 (1.14, 1.20) | 1.08 (1.04, 1.12) | 4×10−4 |
High | 1.42 (1.34, 1.51) | 1.54 (1.43, 1.66) | 1.19 (1.06, 1.33) | ||
GRSCAD-lipids | Per SD increase | 1.18 (1.16, 1.21) | 1.19 (1.17, 1.22) | 1.16 (1.12, 1.20) | 0.17 |
High | 1.57 (1.47, 1.67) | 1.60 (1.48, 1.73) | 1.49 (1.34, 1.67) | ||
GRSCAD-BMI | Per SD increase | 1.08 (1.06, 1.10) | 1.07 (1.05, 1.10) | 1.08 (1.05, 1.12) | 0.47 |
High | 1.25 (1.17, 1.33) | 1.25 (1.16, 1.35) | 1.24 (1.10, 1.38) | ||
CAD-LDpred | Per SD increase | 1.36 (1.33, 1.39) | 1.39 (1.36, 1.43) | 1.29 (1.24, 1.33) | 3×10−3 |
Intermediate | 1.51 (1.42, 1.60) | 1.59 (1.47, 1.71) | 1.33 (1.20, 1.49) | 7×10−3 | |
High | 2.35 (2.20, 2.51) | 2.55 (2.35, 2.77) | 1.95 (1.73, 2.19) |
When scores were categorized, participants with low genetic risk (quintile 1) for each score were used as the reference group