Canagliflozin and Cardiovascular and Renal Events in Type 2 Diabetes
Канаглифлозин и сердечно-сосудистые и почечные события при сахарном диабете 2 типа
2017-06-12
SCID: 54.1/2dcn64n3
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Amputation riskCanagliflozinCardiovascular eventsSGLT2 inhibitorType 2 diabetes
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Abstract (AI)
Background Canagliflozin is a sodium-glucose cotransporter 2 inhibitor that reduces glycemia as well as blood pressure, body weight, and albuminuria in people with diabetes. We report the effects of treatment with canagliflozin on cardiovascular, renal, and safety outcomes. Methods The CANVAS Program integrated data from two trials involving a total of 10,142 participants with type 2 diabetes and high cardiovascular risk. Participants in each trial were randomly assigned to receive canagliflozin or placebo and were followed for a mean of 188.2 weeks. The primary outcome was a composite of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke. Results The mean age of the participants was 63.3 years, 35.8% were women, the mean duration of diabetes was 13.5 years, and 65.6% had a history of cardiovascular disease. The rate of the primary outcome was lower with canagliflozin than with placebo (occurring in 26.9 vs. 31.5 participants per 1000 patient-years; hazard ratio, 0.86; 95% confidence interval [CI], 0.75 to 0.97; P<0.001 for noninferiority; P=0.02 for superiority). Although on the basis of the prespecified hypothesis testing sequence the renal outcomes are not viewed as statistically significant, the results showed a possible benefit of canagliflozin with respect to the progression of albuminuria (hazard ratio, 0.73; 95% CI, 0.67 to 0.79) and the composite outcome of a sustained 40% reduction in the estimated glomerular filtration rate, the need for renal-replacement therapy, or death from renal causes (hazard ratio, 0.60; 95% CI, 0.47 to 0.77). Adverse reactions were consistent with the previously reported risks associated with canagliflozin except for an increased risk of amputation (6.3 vs. 3.4 participants per 1000 patient-years; hazard ratio, 1.97; 95% CI, 1.41 to 2.75); amputations were primarily at the level of the toe or metatarsal. Conclusions In two trials involving patients with type 2 diabetes and an elevated risk of cardiovascular disease, patients treated with canagliflozin had a lower risk of cardiovascular events than those who received placebo but a greater risk of amputation, primarily at the level of the toe or metatarsal. (Funded by Janssen Research and Development; CANVAS and CANVAS-R ClinicalTrials.gov numbers, NCT01032629 and NCT01989754 , respectively.).
Key Findings
1
Adverse reactions besides amputation were consistent with previously reported risks of canagliflozin (no novel safety signals beyond the increased amputation risk noted).
2
Canagliflozin showed possible renal benefits: reduced progression of albuminuria (HR 0.73, 95% CI 0.67–0.79) and reduced composite renal outcome (sustained 40% eGFR decline, renal-replacement therapy, or renal death; HR 0.60, 95% CI 0.47–0.77), though these were not considered statistically significant per the prespecified testing sequence.
3
In 10,142 type 2 diabetes patients at high cardiovascular risk, canagliflozin reduced the primary composite cardiovascular outcome (26.9 vs 31.5 events per 1000 patient-years; HR 0.86, 95% CI 0.75–0.97; P=0.02 for superiority).
4
Treatment with canagliflozin was associated with an increased risk of amputations (6.3 vs 3.4 participants per 1000 patient-years; HR 1.97, 95% CI 1.41–2.75), primarily at the toe or metatarsal level.
Research Object
Treatment with canagliflozin in patients with type 2 diabetes at high cardiovascular risk
Research Subject
Effects of canagliflozin on cardiovascular and renal clinical outcomes and safety (including rates of major cardiovascular events, progression of albuminuria and renal decline, and risk of amputation)
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2017-06-12
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