Table 1.
Parameter | Sacubitril and Valsartan | Sacubitril | Valsartan |
---|---|---|---|
Driven by drug combination | |||
Proteinuria | ↓, P = 0.061 | ↔ | ↔ |
Renal medullary fibrosis | ↓, P = 0.013* | ↔ | ↓, P = 0.08 |
Primarily sacubitril driven | |||
Atrial natriuretic peptide level in heart tissue | ↑, P = 0.012* | ↑, P = 0.000003* | ↔ |
Glomerular filtration rate | ↑, P = 0.002* | ↑, P = 0.017* | ↔ |
Primarily valsartan driven | |||
Urinary kidney injury molecule-1 excretion | ↓, P = 0.08 | ↔ | ↓, P = 0.02* |
Systolic blood pressure | ↔ | ↔ | ↓, P = 0.008* |
Renal protein casts | ↓, P = 0.003* | ↔ | ↓, P = 0.009* |
Both sacubitril and valsartan driven | |||
Urinary neutrophil gelatinase-associated lipocalin excretion | ↓, P = 0.00003* | ↓, P = 0.002* | ↓, P = 0.0002* |
Creatinine excretion | ↑, P = 0.001* | ↑, P = 0.0004* | ↑, P = 0.000073* |
Shown is a summary of significant outcomes of the study driven by sacubitril only, valsartan only, both sacubitril and valsartan, and their combination. Outcomes with P < 0.05 and important outcomes with P > 0.05 (due to lower power) are shown. An increase, decrease, and no change (vs. the vehicle-treated group) are denoted as ↑, ↓, and ↔, respectively.
P < 0.05, outcome vs. vehicle (end point, on high-salt diet).