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. 2020 May 28;319(1):F63–F75. doi: 10.1152/ajprenal.00125.2020

Table 1.

Summary of the experimental outcomes

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).