Key result
Higher baseline angiopoietin-2 linked to ~27% greater cardiorenal risk in diabetic kidney disease.
Why the study?
Angiopoietin 2 regulates endothelial function partially mediated by VEGF-A and may play a role in diabetic kidney disease, but its associations with cardiorenal outcomes and the effect of canagliflozin were unclear.
Is angiopoietin 2 associated with cardiorenal outcomes in diabetic kidney disease, and does canagliflozin reduce its concentrations?
Cohort (n=2,565)
Double-blind
Yes
Is angiopoietin 2 associated with cardiorenal outcomes in diabetic kidney disease, and does canagliflozin reduce its concentrations?
Angiopoietin 2 is an independent predictor of cardiorenal risk in diabetic kidney disease, and its reduction by canagliflozin partially explains the drug's cardiorenal benefits.
May identify higher-risk patients with diabetic kidney disease; leaves open angiopoietin-2 as a therapeutic target.
BACKGROUND: Angiopoietin 2 regulates endothelial function partially mediated by vascular endothelial growth factor-A (VEGF-A) and may play a role in diabetic kidney disease (DKD). We assessed the association of angiopoietin 2 and VEGF-A with cardiorenal outcomes and investigated the effect of canagliflozin on angiopoietin 2 and VEGF-A concentrations. METHODS: Two thousand five hundred sixty-five study participants with DKD and available plasma samples treated with canagliflozin or placebo in the Canagliflozin and Kidney Events in Diabetes with Established Nephropathy Clinical Evaluation (CREDENCE) trial were included. Angiopoietin 2 and VEGF-A concentrations were measured at baseline, year 1, and year 3. The primary composite end point of the trial was a composite of kidney failure, doubling of the serum creatinine level, and kidney or cardiovascular death. RESULTS: Patients with the highest baseline quartile of angiopoietin 2, but not VEGF-A, concentration had the highest risk clinical profile. Treatment with canagliflozin significantly lowered concentrations of angiopoietin 2 (adjusted geometric mean ratio: 0.94; 95% confidence interval, 0.92 to 0.95; P < 0.001), but not VEGF-A. In multivariable-adjusted modeling, each 50% increment in log baseline angiopoietin 2 concentrations was associated with a higher risk of primary composite outcome (hazard ratio, 1.27; 95% confidence interval, 1.13 to 1.43). Angiopoietin 2 change at year 1 compared with baseline explained 10% of the effect of canagliflozin on the primary composite outcome. VEGF-A concentrations were not associated with outcomes, alone or in combination with angiopoietin 2. CONCLUSIONS: Higher angiopoietin 2 levels were associated with cardiorenal risk among individuals with DKD independent of VEGF-A. Canagliflozin lowered angiopoietin 2 concentrations. CLINICAL TRIAL REGISTRY NAME AND REGISTRATION NUMBER: Evaluation of the Effects of Canagliflozin on Renal and Cardiovascular Outcomes in Participants With Diabetic Nephropathy, NCT02065791 .
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Mohebi et al. (2023) conducted a cohort in Diabetic Kidney Disease (DKD) (n=2,565). Elevated baseline angiopoietin 2 concentration vs. Lower baseline angiopoietin 2 concentration was evaluated on Primary composite outcome (end stage kidney failure, doubling of serum creatinine, and kidney or cardiovascular death) (HR 1.27, 95% CI 1.13 to 1.43). Each 50% increment in log baseline angiopoietin 2 concentration was associated with a 27% higher risk of the primary composite cardiorenal outcome (HR 1.27) in patients with diabetic kidney disease.
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