» Articles » PMID: 29941478

Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function

Abstract

Background: Canagliflozin is approved for glucose lowering in type 2 diabetes and confers cardiovascular and renal benefits. We sought to assess whether it had benefits in people with chronic kidney disease, including those with an estimated glomerular filtration rate (eGFR) between 30 and 45 mL/min/1.73 m in whom the drug is not currently approved for use.

Methods: The CANVAS Program randomized 10 142 participants with type 2 diabetes and eGFR >30 mL/min/1.73 m to canagliflozin or placebo. The primary outcome was a composite of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke, with other cardiovascular, renal, and safety outcomes. This secondary analysis describes outcomes in participants with and without chronic kidney disease, defined as eGFR <60 and ≥60 mL/min/1.73 m, and according to baseline kidney function (eGFR <45, 45 to <60, 60 to <90, and ≥90 mL/min/1.73 m).

Results: At baseline, 2039 (20.1%) participants had an eGFR <60 mL/min/1.73 m, 71.6% of whom had a history of cardiovascular disease. The effect of canagliflozin on the primary outcome was similar in people with chronic kidney disease (hazard ratio, 0.70; 95% CI, 0.55-0.90) and those with preserved kidney function (hazard ratio, 0.92; 95% CI, 0.79-1.07; P heterogeneity = 0.08). Relative effects on most cardiovascular and renal outcomes were similar across eGFR subgroups, with possible heterogeneity suggested only for the outcome of fatal/nonfatal stroke ( P heterogeneity = 0.01), as were results for almost all safety outcomes.

Conclusions: The effects of canagliflozin on cardiovascular and renal outcomes were not modified by baseline level of kidney function in people with type 2 diabetes and a history or high risk of cardiovascular disease down to eGFR levels of 30 mL/min/1.73 m. Reassessing current limitations on the use of canagliflozin in chronic kidney disease may allow additional individuals to benefit from this therapy.

Clinical Trial Registration: URL: https://www.clinicaltrials.gov . Unique identifiers: NCT01032629, NCT01989754.

Citing Articles

Comparative Efficacy and Safety of Cardio-Renoprotective Pharmacological Interventions in Chronic Kidney Disease: An Umbrella Review of Network Meta-Analyses and a Multicriteria Decision Analysis.

Bellos I, Marinaki S, Lagiou P, Benetou V Biomolecules. 2025; 15(1).

PMID: 39858434 PMC: 11764242. DOI: 10.3390/biom15010039.


11. Chronic Kidney Disease and Risk Management: Standards of Care in Diabetes-2025.

Diabetes Care. 2024; 48(Supplement_1):S239-S251.

PMID: 39651975 PMC: 11635029. DOI: 10.2337/dc25-S011.


Effects of canagliflozin on brain natriuretic peptide levels in patients with type 2 diabetes on peritoneal dialysis in Japan: protocol for a multicentre, prospective, randomised controlled trial (CARD-PD trial).

Matsuoka N, Nakazawa D, Nishio S, Cho K, Maoka T, Kaneshima N BMJ Open. 2024; 14(11):e084846.

PMID: 39592158 PMC: 11590846. DOI: 10.1136/bmjopen-2024-084846.


Single Center Experience With Sodium-Glucose Co-Transporter-2 Inhibitors (SGLT2i) in Kidney Transplant Recipients With Diabetes.

Angjeli A, Montada-Atin T, Nisenbaum R, Dacouris N, Nash M, Prasad G Can J Kidney Health Dis. 2024; 11:20543581241293202.

PMID: 39534785 PMC: 11555736. DOI: 10.1177/20543581241293202.


Inhibition of SGLT2 protects podocytes in diabetic kidney disease by rebalancing mitochondria-associated endoplasmic reticulum membranes.

Li X, Li Q, Jiang X, Song S, Zou W, Yang Q Cell Commun Signal. 2024; 22(1):534.

PMID: 39511548 PMC: 11542362. DOI: 10.1186/s12964-024-01914-1.


References
1.
Sha S, Devineni D, Ghosh A, Polidori D, Chien S, Wexler D . Canagliflozin, a novel inhibitor of sodium glucose co-transporter 2, dose dependently reduces calculated renal threshold for glucose excretion and increases urinary glucose excretion in healthy subjects. Diabetes Obes Metab. 2011; 13(7):669-72. DOI: 10.1111/j.1463-1326.2011.01406.x. View

2.
Cherney D, Cooper M, Tikkanen I, Pfarr E, Johansen O, Woerle H . Pooled analysis of Phase III trials indicate contrasting influences of renal function on blood pressure, body weight, and HbA1c reductions with empagliflozin. Kidney Int. 2017; 93(1):231-244. DOI: 10.1016/j.kint.2017.06.017. View

3.
Sarwar N, Gao P, Kondapally Seshasai S, Gobin R, Kaptoge S, Di Angelantonio E . Diabetes mellitus, fasting blood glucose concentration, and risk of vascular disease: a collaborative meta-analysis of 102 prospective studies. Lancet. 2010; 375(9733):2215-22. PMC: 2904878. DOI: 10.1016/S0140-6736(10)60484-9. View

4.
Ferrannini E, Mark M, Mayoux E . CV Protection in the EMPA-REG OUTCOME Trial: A "Thrifty Substrate" Hypothesis. Diabetes Care. 2016; 39(7):1108-14. DOI: 10.2337/dc16-0330. View

5.
Afkarian M, Sachs M, Kestenbaum B, Hirsch I, Tuttle K, Himmelfarb J . Kidney disease and increased mortality risk in type 2 diabetes. J Am Soc Nephrol. 2013; 24(2):302-8. PMC: 3559486. DOI: 10.1681/ASN.2012070718. View