Table 2.
History of HF/LVD | No History of HF/LVD | |||||||
---|---|---|---|---|---|---|---|---|
Variable Label | N events | CIF | N events | CIF | Unadjusted HR (95% CI) | Unadjusted p | Adjusted* HR (95% CI) | Adjusted* p |
Primary outcome | 78 | 22.68 (17.79, 27.95) | 592 | 13.78 (12.67, 14.93) | 1.68 (1.32, 2.12) | <0.001 | 1.43 (1.12, 1.82) | 0.004 |
CV death/MI | 67 | 19.74 (15.11, 24.82) | 523 | 12.26 (11.20, 13.37) | 1.61 (1.25, 2.08) | <0.001 | 1.37 (1.06, 1.78) | 0.016 |
All-cause Death | 40 | 11.60 (8.05, 15.85) | 249 | 6.05 (5.25, 6.92) | 2.00 (1.43, 2.79) | <0.001 | 1.58 (1.13, 2.22) | 0.008 |
CV Death | 33 | 9.51 (6.35, 13.44) | 170 | 4.15 (3.50, 4.88) | 2.42 (1.67, 3.52) | <0.001 | 1.89 (1.30, 2.77) | <0.001 |
Primary Definition of MI | 44 | 13.25 (9.48, 17.65) | 399 | 9.26 (8.35, 10.23) | 1.38 (1.01, 1.89) | 0.041 | 1.22 (0.89, 1.67) | 0.223 |
Unstable Angina | 3 | 0.78 (0.22, 2.14) | 45 | 1.05 (0.77, 1.42) | 0.84 (0.26, 2.70) | 0.771 | 0.83 (0.26, 2.69) | 0.758 |
Hospitalization for Heart Failure | 17 | 4.46 (2.50, 7.25) | 59 | 1.30 (0.96, 1.73) | 3.61 (2.10, 6.20) | <0.001 | 2.73 (1.57, 4.75) | <0.001 |
All-cause death or HF Hosp | 52 | 14.95 (10.91, 19.59) | 287 | 6.88 (6.04, 7.80) | 2.29 (1.70, 3.08) | <0.001 | 1.80 (1.33, 2.43) | <0.001 |
HF death | 4 | 1.22 (0.31, 3.44) | 9 | 0.18 (0.07, 0.40) | 5.61 (1.72, 18.26) | 0.004 | 4.19 (1.25, 14.08) | 0.021 |
NYHA Class II or greater† | 62 | 34.43 (27.10, 41.87) | 984 | 27.77 (26.18, 29.38) | 1.31 (1.01, 1.70) | 0.038 | 1.32 (1.02, 1.70) | 0.038 |
Rose Dyspnea Scale 2 or more‡ | 91 | 40.63 (33.56, 47.58) | 1026 | 33.77 (31.91, 35.64) | 1.28 (1.03, 1.58) | 0.026 | 1.23 (0.99, 1.53) | 0.064 |
CV indicates cardiovascular; CIF, Cumulative incidence function; HF/LVD, heart failure/ left ventricular dysfunction; HR, hazard ratio; MI, myocardial infarction; NYHA, New York Heart Association
Adjusted for age (restricted cubic spline), sex, eGFR (restricted cubic spline), and diabetes.
NYHA Class II or greater outcome assessed at baseline and in each study visit is restricted to 4158 participants without NYHA Class II or greater at baseline.
Rose Dyspnea Scale 2 or more outcome assessed at baseline and in each study visit is restricted to 3566 participants without Rose Dyspnea Scale 2 or more at baseline.