Associations of Angiopoietin 2 and Vascular Endothelial Growth Factor-A Concentrations with Clinical End Points

Author:

Mohebi Reza1ORCID,Liu Yuxi1,Hansen Michael K.2ORCID,Yavin Yshai2,Sattar Naveed3ORCID,Pollock Carol A.4,Butler Javed56,Jardine Meg789ORCID,Masson Serge10,Heerspink Hiddo J.L.11ORCID,Januzzi James L.112ORCID

Affiliation:

1. Cardiology Division, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts

2. Janssen Research & Development, LLC, Spring House, Pennsylvania

3. BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, United Kingdom

4. Kolling Institute, Royal North Shore Hospital University of Sydney, Sydney, New South Wales, Australia

5. Department of Medicine, University of Mississippi Medical Center, Jackson, Mississippi

6. Baylor Scott & White Institute, Dallas, Texas

7. The George Institute for Global Health, UNSW Sydney, Sydney, New South Wales, Australia

8. NHMRC Clinical Trials Centre, University of Sydney, Sydney, New South Wales, Australia

9. Concord Repatriation General Hospital, Sydney, New South Wales, Australia

10. Roche Diagnostics International, Rotkreuz, Switzerland

11. Department Clinical Pharmacy and Pharmacology, University of Groningen, Groningen, The Netherlands

12. Heart Failure and Biomarker Trials, Baim Institute for Clinical Research, Boston, Massachusetts

Abstract

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.

Funder

Janssen Research and Development

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

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