Majithia A, Bhatt DL, Friedman AN, et al.
Benefits of Icosapent Ethyl Across a Range of Baseline Renal Function
in Patients with Established Cardiovascular Disease or Diabetes:
Results of REDUCE-IT RENAL
ASN Annual Meeting 2020 -- Digital Meeting
J Am Soc Nephrol
(Oct) 31:21A 2020

BACKGROUND
Chronic kidney disease is associated with adverse
outcomes among patients with established cardiovascular disease (CVD) or
diabetes. Medications for treatment of CVD among patients with low estimated
glomerular filtration rate (eGFR) may be
ineffective.
METHODS
The Reduction of Cardiovascular Events
with Icosapent Ethyl-Intervention Trial (REDUCE-IT) randomized patients with
CVD or diabetes and one additional risk factor to treatment with icosapent
ethyl or placebo. Patients from REDUCE-IT were categorized by prespecified
eGFR categories for analysis of the effect of icosapent ethyl (IPE) on the
primary endpoint (composite of cardiovascular (CV) death, nonfatal myocardial
infarction (MI), nonfatal stroke, coronary revascularization, or unstable
angina) and key secondary endpoint (a composite of CV death, nonfatal MI, or
nonfatal stroke). In post hoc analysis, patients were categorized by
additional eGFR cutoffs consistent with current medical
guidelines.
RESULTS
Among the 8179 REDUCE-IT patients, median
baseline eGFR was 75 mL/min/1.73m2 (range: 17 to 123
mL/min/1.73m2). There were no meaningful changes in median eGFR
for IPE versus placebo across study visits. IPE benefit was consistent across
baseline eGFR for the primary (Figure) and key secondary endpoints. The
numerical reduction in CV death was greatest in the eGFR <60
mL/min/1.73m2 group (IPE: 7.6%; placebo: 10.6%; HR 0.70,
95%CI 0.51, 0.95, p=0.02). The rate of microalbuminuria in adverse event
reporting was lower among IPE-treated patients (0.1% versus 0.3%,
p=0.01).
CONCLUSION
In REDUCE-IT, icosapent ethyl reduced fatal
and nonfatal ischemic events across the broad range of baseline eGFR
categories.


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