TY - JOUR AU - Li Qiang AU - Jardine Meg AU - Mahaffey Kenneth AU - Fulcher Greg AU - Desai Mehul AU - Rosenthal Norm AU - de Zeeuw Dick AU - Matthews David AU - Deng Hsiaowei AU - Ohkuma Toshiaki AU - Perkovic Vlado AU - Neuen Brendon AU - Bakris George AU - Neal Bruce AB -
: 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 (CKD), 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. : The CANagliflozin cardioVascular Assessment Study Program (CANVAS) randomized 10,142 participants with type 2 diabetes and eGFR greater than 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 CKD, defined as eGFR <60 and ≥60 mL/min/1.73 m, and according to baseline kidney function (eGFR <45, 45-<60, 60-<90, and ≥90 mL/min/1.73 m). : At baseline, 2039 (20.1%) participants had an eGFR <60 mL/min/1.73 m, of whom 71.6% had a history of cardiovascular disease. The effect of canagliflozin on the primary outcome was similar in people with CKD (HR 0.70, 95% CI 0.55-0.90) and those with preserved kidney function (HR 0.92, 95% CI 0.79-1.07, 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 ( heterogeneity = 0.01), as were results for almost all safety outcomes. : The effect of canagliflozin on cardiovascular and renal outcomes was 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 CKD may allow additional individuals to benefit from this therapy. : URL: https://clinicaltrials.gov. Unique identifiers: NCT01032629, NCT01989754.
BT - Circulation C1 - https://www.ncbi.nlm.nih.gov/pubmed/29941478?dopt=Abstract DO - 10.1161/CIRCULATIONAHA.118.035901 J2 - Circulation LA - eng N2 -: 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 (CKD), 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. : The CANagliflozin cardioVascular Assessment Study Program (CANVAS) randomized 10,142 participants with type 2 diabetes and eGFR greater than 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 CKD, defined as eGFR <60 and ≥60 mL/min/1.73 m, and according to baseline kidney function (eGFR <45, 45-<60, 60-<90, and ≥90 mL/min/1.73 m). : At baseline, 2039 (20.1%) participants had an eGFR <60 mL/min/1.73 m, of whom 71.6% had a history of cardiovascular disease. The effect of canagliflozin on the primary outcome was similar in people with CKD (HR 0.70, 95% CI 0.55-0.90) and those with preserved kidney function (HR 0.92, 95% CI 0.79-1.07, 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 ( heterogeneity = 0.01), as were results for almost all safety outcomes. : The effect of canagliflozin on cardiovascular and renal outcomes was 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 CKD may allow additional individuals to benefit from this therapy. : URL: https://clinicaltrials.gov. Unique identifiers: NCT01032629, NCT01989754.
PY - 2018 T2 - Circulation TI - Cardiovascular and Renal Outcomes With Canagliflozin According to Baseline Kidney Function: Data from the CANVAS Program. SN - 1524-4539 ER -