From: Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population
Study group | Integrated discrimination improvement | Net reclassification improvement | ||
---|---|---|---|---|
%Δ (95 % CI) | P | %Δ (95 % CI) | P | |
All (n = 2027) | 0.81 (−0.02 to 1.65) | 0.056 | 21.7 (2.5 to 40.8) | 0.026 |
Free of CHD at entry (n = 1986) | 1.15 (0.17 to 2.12) | 0.021 | 24.9 (4.7 to 45.3) | 0.016 |