Cardiorenal Biomarkers, Canagliflozin, and Outcomes in Diabetic Kidney Disease: The CREDENCE Trial

Author:

Januzzi James L.12ORCID,Mohebi Reza1,Liu Yuxi1,Sattar Naveed3ORCID,Heerspink Hiddo J.L.4ORCID,Tefera Eshetu5,Vaduganathan Muthiah6ORCID,Butler Javed78ORCID,Yavin Yshai5,Li Jingwei91011,Pollock Carol A.12ORCID,Perkovic Vlado111314ORCID,Neal Bruce111516ORCID,Hansen Michael K.5ORCID

Affiliation:

1. Cardiology Division, Massachusetts General Hospital and Harvard Medical School, Boston (J.L.J., R.M., Y.L.).

2. Heart Failure and Biomarker Trials, Baim Institute for Clinical Research, Boston, MA (J.L.J.).

3. BHF Glasgow Cardiovascular Research Centre, University of Glasgow, UK (N.S.).

4. Department Clinical Pharmacy and Pharmacology, University of Groningen, University Medical Center Groningen, the Netherlands (H.J.L.H.).

5. Janssen Research & Development, LLC, Spring House, PA (E.T., Y.Y., M.K.H.).

6. Cardiology Division, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA (M.V.).

7. University of Mississippi Medical Center, Jackson (J.B.).

8. Baylor Scott & White Institute, Dallas, TX (J.B.).

9. Department of Cardiology, People’s Liberation Army General Hospital, Beijing, China (J.L.).

10. Department of Cardiology, Xinqiao Hospital, Army Military Medical University, Chongqing, China (J.L.).

11. The George Institute for Global Health (J.L., V.P., B.N.), UNSW Sydney, Australia.

12. Kolling Institute, Royal North Shore Hospital University of Sydney, NSW, Australia (C.A.P.).

13. Faculty of Medicine (V.P.), UNSW Sydney, Australia.

14. The Royal North Shore Hospital, Sydney, Australia (V.P.).

15. Charles Perkins Centre, University of Sydney, NSW, Australia (B.N.).

16. Imperial College London, UK (B.N.).

Abstract

BACKGROUND: People with type 2 diabetes and albuminuria are at an elevated risk for cardiac and renal events. The optimal biomarkers to aid disease prediction and to understand the benefits of sodium-glucose cotransporter-2 inhibition remain unclear. METHODS: Among 2627 study participants in the CREDENCE trial (Canagliflozin and Renal Events in Diabetes With Established Nephropathy Clinical Evaluation), concentrations of NT-proBNP (N-terminal pro-B-type natriuretic peptide), high-sensitivity cardiac troponin T, growth differentiation factor-15, and IGFBP7 (insulin-like growth factor binding protein 7) were measured. The effect of canagliflozin on biomarker concentrations was evaluated. The prognostic potential of each biomarker on the primary outcome (a composite of end-stage kidney disease [dialysis, transplantation, or a sustained estimated glomerular filtration rate of <15 mL·min −1 ·1.73 m −2 ], doubling of the serum creatinine level, or renal death or cardiovascular death) was assessed. RESULTS: The median (quartiles 1 and 3) concentration of each biomarker was generally elevated: NT-proBNP, 180 ng/L (82, 442 ng/L); high-sensitivity cardiac troponin T, 19 ng/L (12, 29 ng/L); growth differentiation factor-15, 2595 ng/L (1852, 3775 ng/L); and IGFBP7, 121.8 ng/mL (105.4, 141.5 ng/mL). At 1 year, the biomarkers all rose by 6% to 29% in the placebo arm but only by 3% to 10% in the canagliflozin arm (all P <0.01 in multivariable linear mixed-effect models). Baseline concentrations of each biomarker were strongly predictive of cardiac and renal outcomes. When the biomarkers were analyzed together in a multimarker panel, individuals with high risk scores (hazard ratio [HR], 4.01 [95% CI, 2.52–6.35]) and moderate risk scores (HR, 2.39 [95% CI, 1.48–3.87]) showed a higher risk for the primary outcome compared with those with low risk scores. By 1 year, a 50% increase in NT-proBNP (HR, 1.11 [95% CI, 1.08–1.15]), high-sensitivity cardiac troponin T (HR, 1.86 [95% CI, 1.64–2.10]), growth differentiation factor-15 (HR, 1.45 [95% CI, 1.24–1.70]), and IGFBP7 (HR, 3.76 [95% CI, 2.54–5.56]) was associated with risk of the primary outcome. CONCLUSIONS: Multiple cardiorenal stress biomarkers are strongly prognostic in people with type 2 diabetes and albuminuria. Canagliflozin modestly reduced the longitudinal trajectory of rise in each biomarker. Change in the biomarker level in addition to the baseline level augments the primary outcome prediction. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT02065791.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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