BACKGROUND
In the EMPA-REG OUTCOME trial, empagliflozin (10 or 25mg once daily) reduced the risk
of hospitalization for heart failure (HHF) as well as kidney events in patients with
type 2 diabetes (T2D) and established cardiovascular (CV) disease by 35-39%. We aimed
to evaluate the yet ill-defined bi-directional relationship between kidney and CV
outcomes in this population.
METHODS AND RESULTS
Of the 2,061 patients on placebo in our analysis, 388 (18.8%) experienced a kidney
event (progression to macroalbuminuria with UACR >300mg/g, doubling of serum creatinine
with eGFR ≤45 ml/min/1.73 m², initiation of renal-replacement therapy or renal death).
Low baseline eGFR, albuminuria ≥30mg/g, high uric acid and LDL-C were among the factors
significantly associated with the risk of experiencing a kidney event, also prior
HF but no coronary artery disease. Associations of kidney events and subsequent CV
events and vice versa were explored using Cox regression with time-varying covariates
and adjustment for various baseline factors. In the placebo arm, the occurrence of
a non-fatal kidney event (excluding renal death) increased the risk of subsequent
HHF (HR 2.40, 95% CI 1.42, 4.05) but not 3P-MACE (HR 1.30, 95% CI 0.89, 1.91) (panel
A). Also, seemingly vice versa, HHF (HR 2.03, 95% CI 1.22, 3.39) but not myocardial
infarction (MI) or stroke (HR 0.94, 95% CI 0.56, 1.56) increased the risk of subsequent
kidney event in the placebo arm (panel B). The associations for kidney event following
MI/Stroke were consistent in the pooled empagliflozin arm and in the overall population
(panel B). For 3-P MACE following kidney event, the risk was significantly increased
in the empagliflozin and overall groups although to a lesser extent and not significant
from placebo (panel A).
CONCLUSION
Our results demonstrate strong and bidirectional inter-relationship between HHF and
kidney events. Strategies to optimize the use of therapies such as empagliflozin,
reducing both kidney and HF outcomes, are warranted, as their benefits may be thereby
compounded.
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© 2021 Published by Elsevier Inc.