Insulin-Like Growth Factor Binding Protein 7 Predicts Renal and Cardiovascular Outcomes in the Canagliflozin Cardiovascular Assessment Study

Author:

Januzzi James L.1,Butler Javed2ORCID,Sattar Naveed3,Xu Jialin4ORCID,Shaw Wayne5,Rosenthal Norman5,Pfeifer Michael6,Mahaffey Kenneth W.7,Neal Bruce89ORCID,Hansen Michael K.4

Affiliation:

1. Cardiology Division, Massachusetts General Hospital and Baim Institute for Clinical Research, Boston, MA

2. University of Mississippi, Jackson, MS

3. Glasgow Cardiovascular Research, Glasgow, U.K.

4. Janssen Research & Development, LLC, Spring House, PA

5. Janssen Research & Development, LLC, Raritan, NJ

6. Janssen Scientific Affairs, LLC, Titusville, NJ

7. Stanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine, Stanford, CA

8. The George Institute for Global Health and Charles Perkins Centre, University of Sydney, Sydney, Australia

9. Imperial College London, London, U.K.

Abstract

OBJECTIVE To analyze the association between concentrations of plasma insulin-like growth factor binding protein 7 (IGFBP7) with renal and cardiac outcomes among participants with type 2 diabetes and high cardiovascular risk. RESEARCH DESIGN AND METHODS Associations between IGFBP7 levels and clinical outcomes were assessed among participants in the Canagliflozin Cardiovascular Assessment Study (CANVAS) with type 2 diabetes and high cardiovascular risk. RESULTS Among CANVAS participants, 3,577 and 2,898 had IGFBP7 measured at baseline and 1 year, respectively. Per log-unit higher concentration, baseline IGFBP7 was significantly associated with the composite renal end point of sustained 40% reduction in estimated glomerular filtration rate, need for renal replacement therapy, or renal death (hazard ratio [HR] 3.51; P < 0.001) and the composite renal end point plus cardiovascular death (HR 4.90; P < 0.001). Other outcomes, including development or progression of albuminuria, were also predicted by baseline IGFBP7. Most outcomes were improved by canagliflozin regardless of baseline IGFBP7; however, those with baseline concentrations ≥96.5 ng/mL appeared to benefit more from canagliflozin relative to the first progression of albuminuria compared with those with lower baseline IGFBP7 (HR 0.64 vs. 0.95; Pinteraction = 0.003). Canagliflozin did not lower IGFBP7 concentrations by 1 year; however, at 1 year, higher IGFBP7 concentrations more strongly predicted the composite renal end point (HR 15.7; P < 0.001). Patients with rising IGFBP7 between baseline and 1 year had the highest number of composite renal events. CONCLUSIONS Plasma IGFBP7 concentrations predicted renal and cardiac events among participants with type 2 diabetes and high cardiovascular risk. More data are needed regarding circulating IGFBP7 and progression of diabetic kidney disease and its complications.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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