- Open Access
Canagliflozin reduces epicardial fat in patients with type 2 diabetes mellitus
Diabetology & Metabolic Syndromevolume 9, Article number: 78 (2017)
It is unknown whether canagliflozin, a selective sodium glucose co-transporter 2 inhibitor, reduces epicardial adipose tissue (EAT) thickness, which is associated with insulin resistance and is a risk factor for coronary artery disease.
Methods and results
We administered 100 mg of canagliflozin for 6 months to 13 patients with type 2 diabetes mellitus. We evaluated glycemic control, visceral adipose tissue (VAT) area and subcutaneous adipose tissue (SAT) area, and skeletal muscle mass by using impedance methods, and EAT thickness by using echocardiography. Canagliflozin treatment for 6 months decreased hemoglobin A1c level from 7.1 ± 0.5% to 6.7 ± 0.6% (P < 0.05) and decreased EAT thickness from 9.3 ± 2.5 to 7.3 ± 2.0 mm (P < 0.001), along with a trend of decreasing VAT and SAT area. No association was found between any of these changes.
Canagliflozin reduced EAT thickness in patients with type 2 diabetes mellitus independent of its effect on lowering blood glucose, suggesting that canagliflozin may have an effect in preventing cardiovascular events in these patients (UMIN000021327).
Epicardial adipose tissue (EAT) is associated with various cardiovascular risk factors such as body mass index and area of visceral adipose tissue, as well as with the severity of coronary artery disease (CAD) [1,2,3,4]. Insulin resistance is closely associated with the physiology of adipose tissue [5,6,7]. In addition, it has been reported that various interventions that improve insulin resistance such as diet therapy and exercise also reduce EAT, which implies that insulin resistance is a potential target in reducing EAT and preventing CAD .
Selective sodium glucose co-transporter 2 (SGLT2) inhibitors improve glucose metabolism by inhibiting SGLT2 in the early proximal tubule, which leads to increased urinary glucose excretion by the kidneys, and thus reduce the plasma glucose levels in an insulin-independent manner. Selective sodium glucose co-transporter 2 inhibitors also reduce weight and the amount of visceral adipose tissue (VAT) by caloric elimination, and improve insulin resistance [9,10,11]. Therefore, SGLT2 inhibitors might be capable of reducing EAT.
Previous pilot studies show that the SGLT2 inhibitors luseogliflozin and ipragliflozin reduce the EAT volume, based on magnetic resonance imaging evaluation [12, 13]. However, it has not been elucidated whether the SGLT2 inhibitor canagliflozin reduces EAT thickness in patients with type 2 diabetes or whether the change in EAT thickness through canagliflozin treatment can be detected with echocardiography. The aim of this study was to clarify whether canagliflozin reduces EAT thickness, based on echocardiography evaluation, in patients with type 2 diabetes.
We enrolled 15 patients with type 2 diabetes mellitus and treated them with 100 mg canagliflozin once a day, as a monotherapy or as add-on/combination therapy with existing antidiabetic treatment between May 2016 and December 2016. One meta-analysis showed that the adverse effects of canagliflozin were not influenced by its dosage ; however, the effect of canagliflozin on glycated hemoglobin (HbA1c) is dose-dependent . Thus, we fixed the dosage of canagliflozin at 100 mg to exclude the dosage effects of canagliflozin. During the study period, the patients did not alter their use of antidiabetic drugs such as dipeptidyl peptidase-4 inhibitors, α-glucosidase inhibitors, sulfonylureas, biguanides, glinides, thiazolidinediones, and insulin, or other drugs that can affect glucose metabolism such as angiotensin-converting enzyme inhibitors/angiotensin II receptor blockers, statins, diuretics, or β-blockers.
Clinical measurements were performed before initiating the treatment and at 3 and 6 months after initiating treatment. Epicardial adipose tissue thickness was evaluated with echocardiography . Echocardiography was performed using commercially available ultrasound machines (Vivid E9, GE Healthcare, Milwaukee, WI, USA or Aplio 500, Toshiba Medical Systems, Tochigi, Japan) with a sector transducer. A high-frequency linear probe (7.5–11 MHz) was used to measure the EAT thickness at the end of systole in the anterior interventricular groove. While assessing EAT thickness, the distal portion of the left anterior descending coronary artery was identified and the probe was carefully rotated until a longitudinal section of the artery was obtained. The EAT thickness was measured as the distance between the outer wall of the myocardium and the visceral layer of the epicardium, perpendicular to the pericardium. Measurements were performed during three cardiac cycles for each parameter, and the mean for each parameter was used for statistical analysis. Interobserver and intraobserver variability were 1.1 ± 1.1 and 0.5 ± 0.5 mm, respectively . All measurements were obtained by a single sonographer who was blinded to the metabolic status of the study participants. A representative echocardiographic image is shown in Fig. 1.
The areas of VAT and subcutaneous adipose tissue (SAT) at the level of the umbilicus were measured using the bioelectrical impedance method with a fat area analyzer (Dual Scan HDS-2000®; Omron, Japan). Previous studies have shown a strong correlation between the visceral fat area measured with the fat area analyzer and the visceral fat area measured with computed tomography [16, 17].
Whole body skeletal muscle mass was measured using multifrequency bioelectrical impedance method with a body composition analyzer (Inbody720; Biospace, Seoul, Korea) .
The glucose-lowering efficacy of SGLT2 inhibitors was assessed by measuring the HbA1c level before initiating therapy and at 3 and 6 months after initiating therapy, in addition to assessment by using other laboratory data.
The exclusion criteria included active malignancy and current therapy with drugs that affect glucose metabolism, if they were to be altered during the study period.
Informed consent was obtained from all individuals before enrollment. This study was carried out in conformance with the declaration of Helsinki and the study protocol was approved by the Tokushima University Hospital Ethics Committee (Tokushima, Japan; Approval Number, 2549). In accordance with the Japanese governmental ethical guidelines and the Study Protocol (UMIN000021327), monitoring was performed by members of the Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital (Tokushima, Japan).
For continuous variables, the average was estimated and each value was expressed as the mean ± the standard deviation and categorical parameters were expressed in percentages. Clinical data before initiating therapy with canagliflozin and at 3 months and at 6 months after initiating it were compared using the paired t-test. All statistical analyses were performed using JMP software (version 11; SAS Institute, Cary, NC, USA). Statistical significance was defined as P < 0.05.
Clinical characteristics of study patients
Characteristics of the patients enrolled in this study are shown in Table 1. Overall, these patients had moderate diabetes, an HbA1c level of 7.1 ± 0.5%, and a body mass index of 27 ± 5 kg/m2.
Over the 6-month period, none of them experienced severe side effects such as hypoglycemic episodes, which would have resulted in a hospital visit or hospitalization. However, two patients were excluded from the analysis because one patient stopped taking canagliflozin owing to generalized fatigue and the other patient was found to have stage IV gastric cancer and discontinued this therapy.
Effects of SGLT2 inhibitors on blood glucose and HbA1c levels
At 6 months of therapy, canagliflozin had significantly decreased the HbA1c level from 7.1 ± 0.5% to 6.7 ± 0.6% (P < 0.05) (Fig. 2).
Effect of SGLT2 inhibitors on EAT, VAT, SAT, and skeletal muscle weight
Canagliflozin significantly decreased the EAT thickness from 9.3 ± 2.5 to 8.1 ± 2.3 mm at 3 months (P < 0.01) and to 7.3 ± 2.0 mm at 6 months (P < 0.001) (Fig. 2). The VAT significantly decreased from 109 ± 44 to 97 ± 46 cm2 at 3 months of therapy (P < 0.05), but was not different at 6 months of therapy. The SAT significantly decreased from 193 ± 71 to 177 ± 81 cm2 at 3 months of therapy (P < 0.05), but was not different at 6 months of therapy (Table 2). Canagliflozin therapy did not affect the skeletal muscle weight (Table 2).
The change in EAT thickness at 6 months was not associated with a change in HbA1c, which indicated that the effect of canagliflozin on reducing EAT is independent of its glucose-lowering effect (Additional file 1: Figure S1). In addition, the change in EAT thickness was not associated with the change in the surface area of VAT or SAT or the change in body weight at 6 months (Additional file 1: Figure S2).
Effect of SGLT2 inhibitors on laboratory data
There was a significant increase in the hematocrit from 42 ± 5% to 43 ± 5% at 3 months (P < 0.05) and to 45 ± 6% at 6 months (P < 0.01). There was also a significant decrease in the serum uric acid level from 4.9 ± 1.3 to 4.2 ± 1.1 mg/dL at 3 months (P < 0.01), and to 4.2 ± 1.0 mg/dL (P < 0.01) at 6 months of therapy with canagliflozin. However, no effects were observed on the levels of low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, triglycerides, serum creatinine, estimated glomerular filtration rate, and urinary albumin (Table 2).
We demonstrated that canagliflozin reduces EAT at 3 and 6 months without affecting VAT, SAT, and muscle weight. Epicardial adipose tissue, a lipid storage depot, covers the surface of the heart and surrounds the coronary arteries while also functioning as an endocrine organ secreting hormones and inflammatory cytokines . Epicardial adipose tissue releases proinflammatory and proatherogenic cytokines, including tumor necrosis factor-α, monocyte chemoattractant protein-1, interleukin-6, nerve growth factor, resistin, visfatin, omentin, leptin, plasminogen activator inhibitor-1, and angiotensinogen . These cytokines influence coronary atherogenesis and myocardial function because there is no fibrous fascial layer to impede the diffusion of free fatty acids and adipokines between EAT and the underlying vessel wall, as well as the myocardium . Thus, reducing EAT can help in preventing CAD.
It has been reported that weight loss , bariatric surgery , exercise , or atorvastatin therapy [22, 23] lead to a regression of EAT. A meta-analysis has shown that exercise has little effect on reducing EAT and body weight . On the contrary, diet therapy reduces EAT and body weight, which indicates that caloric elimination has more preferable effects, compared to caloric consumption. Therefore, SGLT2 inhibitors can be good candidates to reduce EAT effectively. Recent studies have shown that luseogliflozin and ipragliflozin treatment for 12 weeks reduced EAT volume, which was evaluated by magnetic resonance imaging evaluation [12, 13].
It has been reported that canagliflozin reduces VAT in 52 weeks . However, the effect of canagliflozin on EAT has not been investigated. In our study, canagliflozin treatment demonstrated a tendency to reduce VAT, but it was not statistically significant in 6 months because of the heterogeneity of the participants. However, canagliflozin treatment reduced EAT by 3 months, which was earlier than we expected. Precise mechanisms underlying these results are unknown. However, EAT has a higher rate of fatty acid intake and secretin than VAT, and functions as a local energy source during times of energy demand. The high metabolic turnover might explain why EAT was more sensitive to SGLT2 treatment, compared to VAT .
Epicardial adipose tissue has been evaluated with magnetic resonance imaging or computed tomography (CT) to quantify its thickness and volume [25, 26]. Magnetic resonance imaging and CT are superior to echocardiography for measuring overall EAT volume. Echocardiography is advantageous because it is noninvasive, costs less, does not expose the patient to radiation, and is easier to perform, although it provides only measurements of the regional thickness of EAT. Recent evidence has shown that echocardiographic epicardial fat thickness reflects visceral adiposity rather than general obesity, which is correlated with metabolic syndrome, insulin resistance, CAD, and subclinical atherosclerosis. Thus EAT evaluation with echocardiography is a simple tool for estimating cardiometabolic risk [27–29]. We previously demonstrated that the reliability of our method of evaluating EAT thickness in the anterior interventricular groove to predict the presence of CAD is similar to that of CT scan . A meta-analysis demonstrated that EAT thickness in the anterior interventricular groove is associated with CAD . In addition, we used a linear probe with high frequency (7.5–11 MHz) with high special resolution of 0.1–0.2 mm, which is used clinically to measure the intima-media thickness of the carotid artery. The sector probe that is used for usual cardiac scanning is a lower frequency probe (2–3 MHz) with a low special resolution of 0.5 mm, which might be insufficient to evaluate EAT thickness. Thus, by using this noninvasive and highly sensitive method, we monitored EAT periodically during the therapy and detected the fine change in EAT thickness after canagliflozin treatment.
We showed that canagliflozin decreased the level of uric acid. The mechanism by which SGLT2 inhibitors reduce the level of uric acid has not been fully established. However, the facilitative glucose transporter 9 isoform 2 (SLC2A9b) may be involved: it is expressed at the apical membrane of the renal tubular cells and exchanges glucose for uric acid . Higher glucose concentrations in urine, which are attributable to canagliflozin treatment, could increase the exchange of uric acid in the apical membrane of tubular cells through the transporter, increase the release of uric acid from blood into the urine, and thereby reduce the serum uric acid levels. This potential mechanism has been supported by the evidence of trans-stimulation of uric acid efflux with high glucose concentrations in Xenopus oocytes expressing SLC2A9b .
The present study had several limitations. First, the study is a single-arm observational study with a small sample size. Thus, the study contains a patient selection bias and less statistical power due to the patients’ heterogeneity. Second, the observational period was relatively short. Hence, the long-term effects of SGLT2 inhibitors could not be analyzed. Third, we could not exclude the effects of concomitant drugs that can affect glucose metabolism, even though the patients’ drugs were not changed during the study period. Fourth, because of a methodological issue, we evaluated only EAT thickness and did not study the effect of canagliflozin on EAT volume. Randomized, large, clinical cohort studies with a longer observation period are needed to evaluate further the findings of this study.
Canagliflozin treatment for 6 months reduced EAT thickness, as evaluated by echocardiography, in patients with type 2 diabetes mellitus, independent of its effect on lowering blood glucose, which suggests that canagliflozin may have an effect in preventing cardiovascular events in these patients.
epicardial adipose tissue
coronary artery disease
- A1c HDL:
selective sodium glucose co-transporter 2
subcutaneous adipose tissue
visceral adipose tissue
Rosito GA, Massaro JM, Hoffmann U, Ruberg FL, Mahabadi AA, Vasan RS, et al. Pericardial fat, visceral abdominal fat, cardiovascular disease risk factors, and vascular calcification in a community-based sample: the Framingham Heart Study. Circulation. 2008;117:605–13.
Mahabadi AA, Massaro JM, Rosito GA, Levy D, Murabito JM, Wolf PA, et al. Association of pericardial fat, intrathoracic fat, and visceral abdominal fat with cardiovascular disease burden: the Framingham Heart Study. Eur Heart J. 2009;30:850–6.
Mahabadi AA, Lehmann N, Kalsch H, Robens T, Bauer M, Dykun I, et al. Association of epicardial adipose tissue with progression of coronary artery calcification is more pronounced in the early phase of atherosclerosis: results from the Heinz Nixdorf recall study. JACC Cardiovasc Imaging. 2014;7:909–16.
Shimabukuro M, Hirata Y, Tabata M, Dagvasumberel M, Sato H, Kurobe H, et al. Epicardial adipose tissue volume and adipocytokine imbalance are strongly linked to human coronary atherosclerosis. Arterioscler Thromb Vasc Biol. 2013;33:1077–84.
Akoumianakis I, Tarun A, Antoniades C. Perivascular adipose tissue as a regulator of vascular disease pathogenesis: identifying novel therapeutic targets. Br J Pharmacol. 2016;174:3411–24.
Narumi T, Watanabe T, Kadowaki S, Otaki Y, Takahashi H, Arimoto T, et al. Increased epicardial adipose tissue volume predicts presence of insulin resistance and coronary artery disease in non-obese subjects without metabolic syndrome. IJC Metabolic and Endocrine. 2014;3:14–9.
Iacobellis G, Leonetti F. Epicardial adipose tissue and insulin resistance in obese subjects. J Clin Endocr Metab. 2005;90:6300–2.
Rabkin SW, Campbell H. Comparison of reducing epicardial fat by exercise, diet or bariatric surgery weight loss strategies: a systematic review and meta-analysis. Obes Rev. 2015;16:406–15.
Zinman B, Wanner C, Lachin JM, Fitchett D, Bluhmki E, Hantel S, et al. Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes. NEng J Med. 2015;373:2117–28.
Cefalu WT, Leiter LA, Yoon KH, Arias P, Niskanen L, Xie J, et al. Efficacy and safety of canagliflozin versus glimepiride in patients with type 2 diabetes inadequately controlled with metformin (CANTATA-SU): 52 week results from a randomised, double-blind, phase 3 non-inferiority trial. Lancet. 2013;382:941–50.
Merovci A, Solis-Herrera C, Daniele G, Eldor R, Fiorentino TV, Tripathy D, et al. Dapagliflozin improves muscle insulin sensitivity but enhances endogenous glucose production. J Clin Investig. 2014;124:509–14.
Bouchi R, Terashima M, Sasahara Y, Asakawa M, Fukuda T, Takeuchi T, et al. Luseogliflozin reduces epicardial fat accumulation in patients with type 2 diabetes: a pilot study. Cardiovasc Diabetol. 2017;16:32.
Fukuda T, Bouchi R, Terashima M, Sasahara Y, Asakawa M, Takeuchi T, et al. Ipragliflozin reduces epicardial fat accumulation in non-obese type 2 diabetic patients with visceral obesity: a pilot study. Diabetes Ther. 2017;8:851–61.
Bundhun PK, Janoo G, Huang F. Adverse drug events observed in patients with type 2 diabetes mellitus treated with 100 mg versus 300 mg canagliflozin: a systematic review and meta-analysis of published randomized controlled trials. BMC Pharmacol Toxicol. 2017;18:19.
Hirata Y, Yamada H, Kusunose K, Iwase T, Nishio S, Hayashi S, et al. Clinical utility of measuring epicardial adipose tissue thickness with echocardiography using a high-frequency linear probe in patients with coronary artery disease. J Am Soc Echocardiog. 2015;28:1240–6.
Yagi S, Kadota M, Aihara K, Nishikawa K, Hara T, Ise T, et al. Association of lower limb muscle mass and energy expenditure with visceral fat mass in healthy men. Diabetol Metabol Syndr. 2014;6:27.
Park KS, Lee DH, Lee J, Kim YJ, Jung KY, Kim KM, et al. Comparison between two methods of bioelectrical impedance analyses for accuracy in measuring abdominal visceral fat area. J Diabetes Complicat. 2016;30:343–9.
Jensky-Squires NE, Dieli-Conwright CM, Rossuello A, Erceg DN, McCauley S, Schroeder ET. Validity and reliability of body composition analysers in children and adults. Brit J Nutr. 2008;100:859–65.
Sacks HS, Fain JN. Human epicardial adipose tissue: a review. Am Heart J. 2007;153:907–17.
Iacobellis G, Singh N, Wharton S, Sharma AM. Substantial changes in epicardial fat thickness after weight loss in severely obese subjects. Obesity. 2008;16:1693–7.
Kim MK, Tomita T, Kim MJ, Sasai H, Maeda S, Tanaka K. Aerobic exercise training reduces epicardial fat in obese men. J Appl Physiol. 2009;106:5–11.
Park JH, Park YS, Kim YJ, Lee IS, Kim JH, Lee JH, et al. Effects of statins on the epicardial fat thickness in patients with coronary artery stenosis underwent percutaneous coronary intervention: comparison of atorvastatin with simvastatin/ezetimibe. J Cardiovasc Ultrasound. 2010;18:121–6.
Takase H, Dohi Y, Okado T, Hashimoto T, Goto Y, Kimura G. Effects of ezetimibe on visceral fat in the metabolic syndrome: a randomised controlled study. Eur J Clin Invest. 2012;42:1287–94.
Marchington JM, Pond CM. Site-specific properties of pericardial and epicardial adipose tissue: the effects of insulin and high-fat feeding on lipogenesis and the incorporation of fatty acids in vitro. Int J Obes. 1990;14:1013–22.
Dagvasumberel M, Shimabukuro M, Nishiuchi T, Ueno J, Takao S, Fukuda D, et al. Gender disparities in the association between epicardial adipose tissue volume and coronary atherosclerosis: a 3-dimensional cardiac computed tomography imaging study in Japanese subjects. Cardiovasc Diabetol. 2012;11:106.
Maimaituxun G, Shimabukuro M, Salim HM, Tabata M, Yuji D, Morimoto Y, et al. Gender-linked impact of epicardial adipose tissue volume in patients who underwent coronary artery bypass graft surgery or non-coronary valve surgery. PLoS ONE. 2017;12:e0177170.
Iacobellis G, Willens HJ. Echocardiographic epicardial fat: a review of research and clinical applications. J Am Soc Echocardiog. 2009;22:1311–9.
Natale F, Tedesco MA, Mocerino R, de Simone V, Di Marco GM, Aronne L, et al. Visceral adiposity and arterial stiffness: echocardiographic epicardial fat thickness reflects, better than waist circumference, carotid arterial stiffness in a large population of hypertensives. Eur J Echocardiogr. 2009;10:549–55.
Nishio S, Kusunose K, Yamada H, Hirata Y, Ise T, Yamaguchi K, et al. Echocardiographic epicardial adipose tissue thickness is associated with symptomatic coronary vasospasm during provocative testing. J Am Soc Echocardiogr 2017.doi:10.1016/j.echo.2017.06.024.
Wu FZ, Chou KJ, Huang YL, Wu MT. The relation of location-specific epicardial adipose tissue thickness and obstructive coronary artery disease: systemic review and meta-analysis of observational studies. BMC Cardiovasc Disord. 2014;14:62.
Davies MJ, Trujillo A, Vijapurkar U, Damaraju CV, Meininger G. Effect of canagliflozin on serum uric acid in patients with type 2 diabetes mellitus. Diabetes Obes Metab. 2015;17:426–9.
Chino Y, Samukawa Y, Sakai S, Nakai Y, Yamaguchi J, Nakanishi T, et al. SGLT2 inhibitor lowers serum uric acid through alteration of uric acid transport activity in renal tubule by increased glycosuria. Biopharm Drug Dispos. 2014;35:391–404.
SY designed the study, analyzed the data, and wrote the manuscript. YH and SN performed echocardiography and measured EAT thickness. SY, TI, KK, HY, YT, SH, TM, KY, TT, TS, and TW collected the data. DF, HMS, GM, YT, and KA contributed to the intellectual discussion and reviewed and edited the manuscript. MA, MSh, and MSa supervised the study. All authors read and approved the final manuscript.
We would like to thank Editage (http://www.editage.jp) for English language editing.
M. Sata received research funding from Tanabe-Mitsubishi, Takeda, Astellas, Daiichi-Sankyo, MSD, Byer Healthcare, and Ono, and received lecture fees from Tanabe-Mitsubishi, Takeda, Boehringer Ingelheim, Byer Healthcare, Mochida, Astellas, Novartis, AstraZeneca, MSD, and Shionogi. The Department of Cardio-Diabetes Medicine, Tokushima University Graduate School (Tokushima, Japan) is supported in part by unrestricted research grants from Tanabe-Mitsubishi, Boehringer Ingelheim, Kowa, and Actelion. The other authors declare no competing interests.
Ethics approval and consent to participate, and consent for publication
Informed consent was obtained from all patients before enrollment. This study was carried out in conformance with the declaration of Helsinki and the study protocol was approved by the Tokushima University Hospital Ethics Committee (Tokushima, Japan; Approval Number, 2549). In accordance with the Japanese governmental ethical guidelines and the Study Protocol (UMIN000021327), monitoring was performed by members of the Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital (Tokushima, Japan).
The study was funded by Mitsubishi Tanabe Pharma Corporation (Osaka, Japan). This work was partially supported by JSPS Kakenhi Grants (Grant Numbers 17K13037, 16H05299 and 26248050), The Uehara Memorial Foundation, and Takeda Science Foundation.
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