Canagliflozin and Cardiovascular and Renal Events in Type 2 Diabetes

Bruce Neal1, Vlado Perkovic1, Kenneth W Mahaffey1

  • 1From the George Institute for Global Health, Faculty of Medicine, UNSW Sydney (B.N., V.P.), the Charles Perkins Centre (B.N.), and the Royal North Shore Hospital (V.P., G.F.), University of Sydney, and the Faculty of Medicine, University of New South Wales (B.N.) - all in Sydney; Imperial College London, London (B.N.), and the Oxford Centre for Diabetes, Endocrinology, and Metabolism and Harris Manchester College, University of Oxford, Oxford (D.R.M.) - both in the United Kingdom; the Stanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine, Stanford, CA (K.W.M.); the University Medical Center Groningen, University of Groningen, Groningen, the Netherlands (D.Z.); and Janssen Research and Development, Raritan, NJ (N.E., W.S., G.L., M.D.).

Insights

Canagliflozin reduced cardiovascular events in type 2 diabetes patients. However, it increased the risk of amputation, mainly of the toe or metatarsal, requiring careful consideration of benefits and risks.

Area of Science:

  • Cardiology
  • Nephrology
  • Endocrinology

Background:

  • Canagliflozin, a sodium-glucose cotransporter 2 inhibitor, is known to lower glucose, blood pressure, body weight, and albuminuria in diabetic patients.
  • The CANVAS Program integrated data from two large trials to assess canagliflozin's impact on cardiovascular, renal, and safety outcomes.

Purpose of the Study:

  • To evaluate the efficacy and safety of canagliflozin compared to placebo in patients with type 2 diabetes and high cardiovascular risk.
  • To analyze the effects of canagliflozin on primary composite cardiovascular outcomes, renal outcomes, and adverse events.

Main Methods:

  • The CANVAS Program included 10,142 participants with type 2 diabetes and high cardiovascular risk, randomized to canagliflozin or placebo.
  • Participants were followed for a mean of 188.2 weeks, with the primary outcome being a composite of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke.

Main Results:

  • Canagliflozin significantly reduced the primary composite cardiovascular outcome (hazard ratio, 0.86; P=0.02 for superiority).
  • While not statistically significant per prespecified testing, canagliflozin showed potential benefits in reducing albuminuria progression and composite renal outcomes.
  • An increased risk of amputation, primarily of the toe or metatarsal, was observed with canagliflozin (hazard ratio, 1.97).

Conclusions:

  • Canagliflozin treatment led to a lower risk of major adverse cardiovascular events in patients with type 2 diabetes and high cardiovascular risk.
  • Despite cardiovascular benefits, canagliflozin use was associated with an increased risk of lower-extremity amputations.
  • The findings highlight a need to balance the cardiovascular advantages of canagliflozin against its safety concerns, particularly regarding amputation risk.

Related Concept Videos

Oral Hypoglycemic Agents: Biguanides and Glitazones01:26

Oral Hypoglycemic Agents: Biguanides and Glitazones

Biguanides, particularly metformin (Glucophage), are insulin sensitizers that enhance glucose uptake, thereby reducing insulin resistance. Unlike sulfonylureas, metformin doesn't prompt insulin secretion, which helps to curb hypoglycemia risk. Metformin is beneficial in treating conditions like polycystic ovary syndrome due to its insulin-resistance reduction capability. The drug's primary action involves curtailing hepatic gluconeogenesis, a significant contributor to high blood...
739
Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
787
Diabetes Mellitus: Type 2 and Gestational01:22

Diabetes Mellitus: Type 2 and Gestational

Type 2 diabetes, characterized by insulin resistance, arises when the insulin receptors on cells lose responsiveness to insulin, diminishing the cell's capacity to take up glucose, resulting in elevated blood glucose levels. To receive a diagnosis of Type 2 diabetes, a series of blood glucose tests are necessary to assess whether the blood glucose falls within normal parameters. If the result is out of the normal range, a patient may be diagnosed as prediabetic or diabetic, depending on the...
5.2K
Oral Hypoglycemic Agents: Glinides01:06

Oral Hypoglycemic Agents: Glinides

Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively...
760
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors01:19

Oral Hypoglycemic Agents: α-Glucosidase Inhibitors

α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are...
684
Insulin: Dosing Regimen and Adverse Effects01:16

Insulin: Dosing Regimen and Adverse Effects

Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
952