Efficacy and Safety of Canagliflozin, an Inhibitor of Sodium-Glucose Cotransporter 2, When Used in Conjunction With Insulin Therapy in Patients With Type 2 Diabetes

被引:217
作者
Neal, Bruce [1 ,2 ]
Perkovic, Vlado [1 ,2 ]
de Zeeuw, Dick [3 ]
Mahaffey, Kenneth W. [4 ]
Fulcher, Greg [5 ,6 ]
Ways, Kirk [7 ]
Desai, Mehul [7 ]
Shaw, Wayne [7 ]
Capuano, George [7 ]
Alba, Maria [7 ]
Jiang, Joel [7 ]
Vercruysse, Frank [7 ]
Meininger, Gary [7 ]
Matthews, David [8 ]
机构
[1] Univ Sydney, George Inst Global Hlth, Sydney, NSW 2006, Australia
[2] Royal Prince Alfred Hosp, Sydney, NSW, Australia
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Groningen, Netherlands
[4] Stanford Univ, Dept Med, Sch Med, Stanford, CA 94305 USA
[5] Royal N Shore Hosp, Sydney, NSW, Australia
[6] Univ Sydney, Sydney, NSW 2006, Australia
[7] Janssen Res & Dev LLC, Raritan, NJ USA
[8] Univ Oxford, Oxford, England
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
GLYCEMIC CONTROL; POOLED ANALYSIS; DOUBLE-BLIND; METFORMIN; MELLITUS; MONOTHERAPY; PLACEBO; SULFONYLUREA; SITAGLIPTIN; PHASE-3;
D O I
10.2337/dc14-1237
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE There are limited data about the effects of sodium-glucose cotransporter 2 inhibitors when used with insulin. We report the efficacy and safety of canagliflozin in patients with type 2 diabetes using insulin. RESEARCH DESIGN AND METHODS The CANagliflozin CardioVascular Assessment Study is a double-blind, placebo-controlled study that randomized participants to placebo, canagliflozin 100 mg, or canagliflozin 300 mg once daily, added to a range of therapies. The primary end point of this substudy was the change in HbA(1c) from baseline at 18 weeks among patients using insulin; 52-week effects were also examined. RESULTS Individuals receiving insulin at baseline were randomized to receive placebo (n 5 690), canagliflozin 100 mg (n 5 692), or canagliflozin 300 mg (n 5 690). These individuals were 66% male and had a median age of 63 years, mean HbA(1c) of 8.3% (67 mmol/mol), BMI of 33.1 kg/m(2), estimated glomerular filtration rate of 75 mL/min/1.73 m(2), fasting plasma glucose of 9.2 mmol/L, and a median daily insulin dose of 60 IU. Most individuals were using basal/bolus insulin. Reductions in HbA1c with canagliflozin 100 and 300 mg versus placebo were -0.62% (95% CI -0.69, -0.54; -6.8 mmol/mol [95% CI -7.5, -5.9]; P < 0.001) and -0.73% (95% CI -0.81,-0.65; -8.0mmol/mol [95% CI -8.9, -7.1]; P < 0.001) at 18 weeks and -0.58% (95% CI -0.68, -0.48; -6.3 mmol/mol [95% CI -7.4, -5.2]) and -0.73% (95% CI -0.83, -0.63; -8.0 mmol/mol [95% CI -9.1, -6.9]) at 52 weeks. There were significant falls in fasting plasma glucose, body weight, and blood pressure at both time points and there was a greater incidence of hypoglycemia, genital mycotic infections, and hypovolemia with both canagliflozin doses. CONCLUSIONS Canagliflozin added to insulin therapy improved glycemic control and decreased body weight. There was a greater frequency of several anticipated side effects, although few led to discontinuation of treatment.
引用
收藏
页码:403 / 411
页数:9
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