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Canagliflozin for Japanese patients with chronic heart failure and type II diabetes
Akira Sezai1, Hisakuni Sekino2, Satoshi Unosawa3
1Department of Cardiovascular Surgery, Nihon University School of Medicine, 30-1 Oyaguchi-kamimachi, Itabashi-ku, Tokyo, 173-8610, Japan. asezai.med@gmail.com.
Insights
Canagliflozin significantly reduced fat areas, improved cardiac and renal function, and enhanced endothelial function in patients with type II diabetes and chronic heart failure.
Area of Science:
- Cardiology
- Endocrinology
- Metabolic Diseases
Background:
- Sodium glucose cotransporter 2 inhibitors (SGLT2i) show cardiovascular benefits in diabetic patients.
- Canagliflozin is an SGLT2 inhibitor studied for its effects in heart failure.
Purpose of the Study:
- To evaluate the effects of canagliflozin in Japanese patients with chronic heart failure and type II diabetes.
- To assess changes in fat areas, cardiac and renal markers, and endothelial function.
Main Methods:
- A 12-month study involving 35 Japanese patients with chronic heart failure and type II diabetes treated with canagliflozin.
- Primary endpoint: changes in fat areas (subcutaneous, visceral, total) via computed tomography.
- Secondary endpoints: glycemic control, renal function, oxidative stress, lipids, natriuretic peptides (ANP, BNP), flow-mediated dilation (FMD), and echocardiographic function.
Main Results:
- Significant reductions in all measured fat areas were observed at 12 months.
- Significant decreases in ANP and BNP levels, improvements in renal function, oxidized LDL, and diastolic function (E/e') were noted.
- Significant improvement in flow-mediated dilation (FMD) indicated enhanced endothelial function.
Conclusions:
- Canagliflozin demonstrated cardiac and renal protective effects in patients with type II diabetes and chronic heart failure.
- The drug improved oxidative stress, diastolic function, and endothelial function.
- Canagliflozin may be a potential first-line therapy for patients with diabetes and heart failure with preserved ejection fraction.
Background:
Reports that sodium glucose cotransporter 2 inhibitors decrease cardiovascular death and events in patients with diabetes have attracted attention in the cardiology field. We conducted a study of canagliflozin in patients with chronic heart failure and type II diabetes.
Methods:
Thirty-five Japanese patients with chronic heart failure and type II diabetes were treated with canagliflozin for 12 months. The primary endpoints were the changes of subcutaneous, visceral, and total fat areas at 12 months determined by computed tomography. Secondary endpoints included markers of glycemic control, renal function, and oxidative stress, as well as lipid parameters, atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), flow-mediated dilation (FMD), and echocardiographic left ventricular function.
Results:
All fat areas (subcutaneous, visceral, and total) showed a significant decrease at 12 months. ANP and BNP also decreased significantly, along with improvement of renal function, oxidized LDL, and E/e', FMD increased significantly after canagliflozin treatment.
Conclusion:
Canagliflozin demonstrated cardiac and renal protective effects as well as improving oxidative stress, diastolic function, and endothelial function. This drug was effective in patients who had heart failure with preserved ejection fraction and could become first-line therapy for such patients with diabetes. Trial registration UMIN ( http://www.umin.ac.jp/ ), Study ID: UMIN000021239.
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