Figures
Abstract
Background
Fatty acid-binding protein 4 (FABP4/A-FABP/aP2) is secreted from adipocytes in association with catecholamine-induced lipolysis, and elevated serum FABP4 level is associated with obesity, insulin resistance and atherosclerosis. Secreted FABP4 as a novel adipokine leads to insulin resistance via increased hepatic glucose production (HGP). Sodium-glucose cotransporter 2 (SGLT2) inhibitors decrease blood glucose level via increased urinary glucose excretion, though HGP is enhanced. Here we investigated whether canagliflozin, an SGLT2 inhibitor, modulates serum FABP4 level.
Methods
Canagliflozin (100 mg/day) was administered to type 2 diabetic patients (n = 39) for 12 weeks. Serum FABP4 level was measured before and after treatment.
Results
At baseline, serum FABP4 level was correlated with adiposity, renal dysfunction and noradrenaline level. Treatment with canagliflozin significantly decreased adiposity and levels of fasting glucose and HbA1c but increased average serum FABP4 level by 10.3% (18.0 ± 1.0 vs. 19.8 ± 1.2 ng/ml, P = 0.008), though elevation of FABP4 level after treatment was observed in 26 (66.7%) out of 39 patients. Change in FABP4 level was positively correlated with change in levels of fasting glucose (r = 0.329, P = 0.044), HbA1c (r = 0.329, P = 0.044) and noradrenaline (r = 0.329, P = 0.041) but was not significantly correlated with change in adiposity or other variables.
Conclusions
Canagliflozin paradoxically increases serum FABP4 level in some diabetic patients despite amelioration of glucose metabolism and adiposity reduction, possibly via induction of catecholamine-induced lipolysis in adipocytes. Increased FABP4 level by canagliflozin may undermine the improvement of glucose metabolism and might be a possible mechanism of increased HGP by inhibition of SGLT2.
Citation: Furuhashi M, Matsumoto M, Hiramitsu S, Omori A, Tanaka M, Moniwa N, et al. (2016) Possible Increase in Serum FABP4 Level Despite Adiposity Reduction by Canagliflozin, an SGLT2 Inhibitor. PLoS ONE 11(4): e0154482. https://doi.org/10.1371/journal.pone.0154482
Editor: Ichiro Manabe, Chiba University Graduate School of Medicine, JAPAN
Received: February 13, 2016; Accepted: April 13, 2016; Published: April 28, 2016
Copyright: © 2016 Furuhashi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: M.F. has been supported by grants from JSPS KAKENHI, MEXT Translational Research Network Program, Uehara Memorial Foundation, SENSHIN Medical Research Foundation, Japan Diabetes Foundation, Takeda Medical Research Foundation, Ono Medical Research Foundation, Takeda Science Foundation, Akiyama Life Science Foundation, Yamaguchi Endocrine Research Foundation, Naito Foundation Natural Science Scholarship, Suhara Memorial Foundation and Kondou Kinen Medical Foundation.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Fatty acid-binding proteins (FABPs), a family of intracellular lipid chaperones, are about 14-15-kDa predominantly cytosolic proteins that can reversibly bind hydrophobic ligands, such as saturated and unsaturated long-chain fatty acids [1–3]. FABPs have been proposed to facilitate the transport of lipids to specific compartments in the cell [1]. Among FABPs, fatty acid-binding protein 4 (FABP4), also referred to as adipocyte FABP (A-FABP) or aP2, is mainly expressed in both adipocytes and macrophages and plays an important role in the development of obesity, insulin resistance, type 2 diabetes mellitus and atherosclerosis [4–6]. We previously demonstrated that the use of a small molecule FABP4-specific inhibitor might be a novel therapeutic strategy against insulin resistance, type 2 diabetes mellitus and atherosclerosis [7].
Recently, FABP4 has been reported to be secreted from adipocytes in association with lipolysis via a non-classical secretion pathway [8–11], though there are no typical secretory signal peptides in the sequence of FABP4 [1]. Previous studies using in vitro and in vivo experiments showed that FABP4 acts as an adipokine leading to the development of hepatic insulin resistance through increased hepatic glucose production [9] and atherosclerosis [12]. It has also been reported that elevated serum FABP4 concentration is associated with obesity, insulin resistance, type 2 diabetes mellitus, hypertension, cardiac dysfunction, renal dysfunction, dyslipidemia, atherosclerosis and cardiovascular events [8, 13–23]. However, little is known about the modulation of serum FABP4 level by anti-diabetic agents except for thiazolidinedione [24] and a dipeptidyl peptidase-4 (DPP-4) inhibitor [25].
For treatment of type 2 diabetes mellitus, sodium-glucose cotransporter 2 (SGLT2) inhibitors have recently become available. SGLT2 inhibitors decrease blood glucose level through increased glucose excretion in urine [26]. On the other hand, SGLT2 inhibitors have been reported to enhance hepatic glucose production [27, 28] by an unknown molecular mechanism. In the present study, we investigated the impact of SGLT2 inhibitor therapy on serum FABP4 level in patients with type 2 diabetes mellitus.
Materials and Methods
This study registered in UMIN-CTR Clinical Trial (UMIN000018151) conformed to the principles outlined in the Declaration of Helsinki and was performed with the approval of the Ethical Committee of Fujita Health University. Written informed consent was received from all of the study subjects. The protocol for this trial and supporting TREND checklist are available as S1 checklist and S2 protocol.
Study subjects
Patients with type 2 diabetes mellitus were consecutively recruited from outpatient clinics affiliated with Fujita Health University from October 2014 through March 2015. Exclusion criteria were findings of serious co-morbidities such as hepatic, cerebrovascular, cardiovascular or renal disease. Patients treated with thiazolidinediones, peroxisome proliferator-activated receptor γ (PPARγ) agonists, were also excluded since expression and serum level of FABP4 as a target gene has been reported to be directly regulated by PPARγ activation [1, 24]. The primary endpoint was assessment of change in level of Hemoglobin A1c (HbA1c). The secondary endpoint was assessment of changes in several glucose metabolism-related parameters, including adiposity and levels of fasting glucose, insulin and FABP4. Samples of blood and urine were collected before and after treatment with canagliflozin (100 mg/day), an SGLT2 inhibitor, for 12 weeks. For blood sampling, patients were kept in the supine position for 20 min after an overnight fast. Samples of plasma, serum and urine were analyzed immediately or stored at -80°C until biochemical analyses.
Measurements
The serum concentration of FABP4 was measured using a commercially available enzyme-linked immunosorbent assay kit (Biovendor R&D, Modrice, Czech Republic). The accuracy, precision and reproducibility of the kit have been described previously [8]. The intra- and inter-assay coefficient variances in the kits were < 5%. Serum high molecular weight (HMW)-adiponectin level was measured using a commercially available enzyme-linked immunosorbent assay kit (Fujirebio Inc., Tokyo, Japan). Fasting plasma glucose was determined by the glucose oxidase method. Fasting plasma insulin was measured by a chemiluminescent enzyme immunoassay method. HbA1c was determined by a latex coagulation method and was expressed in National Glycohemoglobin Standardization Program (NGSP) scale. Creatinine (Cr), blood urea nitrogen (BUN), uric acid, aspartate transaminase (AST), alanine aminotransferase (ALT), γ-glutamyl transpeptidase (γ-GTP) and lipid profiles, including total cholesterol, high-density lipoprotein (HDL) cholesterol and triglycerides, were determined by enzymatic methods. Low-density lipoprotein (LDL) cholesterol level was calculated by the Friedewald equation. Cystatin C (Cys-C) was determined by a latex coagulation method. Brain natriuretic peptide (BNP) was measured using an assay kit (Shionogi & Co., Osaka, Japan). High-sensitivity C-reactive protein (hsCRP) was measured by a nephelometry method. Plasma levels of adrenaline and noradrenaline were measured by high-performance liquid chromatography. Homeostasis model assessment of insulin resistance (HOMA-R) was calculated by the previously reported formula: HOMA-R = insulin (μU/ml) × glucose (mg/dl) / 405. As an index of renal function, estimated glomerular filtration rate (eGFR) was calculated by an equation for Japanese [29]: eGFR (ml/min/1.73m2) = 194 × Cr(-1.094) × age(-0.287) × 0.739 (if female). Urinary albumin-to-creatinine ratio (UACR; mg/gCr) was used as a marker of microalbuminuria. Body mass index (BMI) was calculated as body weight (in kilograms) divided by the square of body height (in meters).
Statistical analysis
The sample size was calculated on the basis of assumption that the difference between HbA1c levels before and after treatment with canagliflozin for 12 weeks would be 0.7% and that the standard deviations in HbA1c level at baseline and 12 weeks would be 1.2% and 1.2%, respectively. Correlation coefficient of HbA1c levels at baseline and 12 weeks would be 0.50. To detect such a significant difference before and after treatment in the statistical situation of a power greater than 90% with a two-sided type 1 error rate of 0.05, at least 33 patients were required.
Numeric variables are expressed as means ± SEM. The distribution of each parameter was tested for its normality using the Shapiro-Wilk W test, and non-normally distributed parameters were logarithmically transformed for regression analyses. The correlation between two variables was evaluated using Pearson’s correlation coefficient. Comparison between two groups was done with the chi-square test, Wilcoxon signed-rank test for paired samples and Mann-Whitney's U test for unpaired samples. Stepwise regression analysis was performed to identify independent determinants of FABP4 concentration using age, gender and the variables with a significant correlation in simple regression analysis as independent predictors in a forward direction with F value ≥ 4 for the entry, and a subsequent multiple regression analysis was done to show the t-ratio calculated as the ratio of regression coefficient and standard error of regression coefficient and the percentage of variance in the FABP4 concentration that the selected independent predictors explained (R2). A p value of less than 0.05 was considered statistically significant. All data were analyzed by using JMP 9 for Macintosh (SAS Institute, Cary, NC).
Results
A patient flow diagram in the present study is shown in Fig 1. A total of 44 patients with type 2 diabetes mellitus were consecutively recruited for the present study. Two patients met the exclusion criteria prior to this study. Hence, 42 patients were enrolled for canagliflozin treatment. Three patients were excluded because of lost to follow-up (n = 1) and discontinued intervention (n = 2). Finally, a total of 39 type 2 diabetic patients (male/female: 28/11) were analyzed in the present study.
A total of 44 patients with type 2 diabetes mellitus were recruited, and 39 patients were finally analyzed in the present study.
Characteristics of the patients are shown in Table 1. Mean age, BMI and waist circumference of the recruited patients were 63.0 ± 1.5 years, 27.9 ± 0.7 kg/m2 and 94.4 ± 1.5 cm, respectively. More than 90% of the patients had hypertension and dyslipidemia, and most of the patients had received pharmacological agents for hypertension and dyslipidemia including statins, ezetimibe and fibrates. Medication for type 2 diabetes mellitus included biguanides (17.9%), DPP-4 inhibitors (46.2%) and sulfonylureas (5.1%).
At baseline, serum FABP4 level was positively correlated with BMI, waist circumference, pulse rate and levels of Cys-C and noradrenaline and was negatively correlated with levels of eGFR and hematocrit (Table 2). Stepwise regression analysis using age, gender and the correlated parameters revealed that gender (F = 7.97), BMI (F = 11.94) and Cys-C (F = 15.55) were independent predictors of FABP4 concentration. A subsequent multiple regression analysis showed that gender (male; t = -2.86, P = 0.007), BMI (t = 3.65, P = 0.001) and Cys-C (t = 4.01, P < 0.001) were independently correlated with FABP4 level, explaining a total of 54.9% of the variance in this measure (R2 = 0.549) (Table 3), as previously reported [15, 21].
Treatment with canagliflozin for 12 weeks significantly decreased BMI, waist circumference, systolic and diastolic blood pressures, pulse rate and levels of fasting glucose, insulin, HOMA-R, HbA1c, uric acid, ALT, γ-GPT and hsCRP, while it oppositely increased levels of BUN, Cys-C, hematocrit and HMW-adiponectin (Table 4). No significant change after canagliflozin treatment was found in levels of total cholesterol, HDL cholesterol, LDL cholesterol, triglycerides, Cr, eGFR, UACR, AST, BNP, adrenaline and noradrenaline. Interestingly, treatment with canagliflozin significantly increased the mean value of serum FABP4 concentration by 10.3% (18.0 ± 1.0 vs. 19.8 ± 1.2 ng/ml, P = 0.008) (Fig 2A) despite reduction of adiposity. However, the direction and magnitude of change in FABP4 level were different on a patient-to-patient basis, and FABP4 level was increased and decreased in 66.7% (26/39) and 33.3% (13/39) of the patients, respectively. There was no significant difference in baseline clinical parameters between the two groups of patients showing different responses of FABP4 level to canagliflozin treatment (Table 5). Reduction of HOMA-R by canagliflozin was significantly smaller in patients with increased FABP4 after canagliflozin treatment than in those with decreased FABP4 (-0.53 ± 0.28 vs. -2.02 ± 0.43, P = 0.009).
A. Treatment with canagliflozin (100 mg/day) for 12 weeks significantly increased FABP4 level in patients with type 2 diabetes mellitus (n = 39; male/female: 28/11). Open circles: males, closed circles: females. *P = 0.008. B-E. Change in FABP4 level was positively correlated with changes in levels of fasting glucose (B), HbA1c (C) and noradrenaline (D) but was not significantly correlated with change in waist circumference (E).
Change (Post—Pre) in FABP4 level after canagliflozin treatment was positively correlated with changes in levels of fasting glucose (r = 0.329, P = 0.044) (Fig 2B) and HbA1c (r = 0.329, P = 0.044) (Fig 2C), indicating that improvement in fasting glucose and HbA1c by canagliflozin was less in patients with greater increase in FABP4 level. Furthermore, change in FABP4 level was positively correlated with change in level of noradrenaline (r = 0.329, P = 0.041) (Fig 2D) but was not significantly correlated with change in BMI (r = -0.021, P = 0.901), waist circumference (r = 0.135, P = 0.425) (Fig 2E) or other variables.
Discussion
The present study showed for the first time that canagliflozin, an SGLT2 inhibitor, increased the average serum FABP4 concentration in patients with type 2 diabetes mellitus despite amelioration of glucose metabolism and reduction of adiposity (Fig 2A, Table 4). However, the direction and magnitude of change in FABP4 level after canagliflozin treatment were different between patients. Compared to patients with decreased FABP4 level by canagliflozin (33.3%), patients with increased FABP4 (66.7%) had significantly smaller improvement of insulin resistance assessed by change in HOMA-R. Furthermore, change in FABP4 level caused by canagliflozin was positively correlated with change in levels of fasting glucose and HbA1c but was not significantly correlated with change in adiposity (Fig 2B, 2C and 2E). These findings suggest that the paradoxical increase in FABP4 concentration by inhibition of SGLT2 is independent of alteration of adiposity and undermines the improvement of glucose metabolism since circulating FABP4 leads to hepatic insulin resistance [9].
It has been reported that SGLT2 inhibitors increase hepatic glucose production [27, 28], though the molecular mechanism has not been completely elucidated. Involvement of various factors has been postulated for the rise in hepatic glucose production: compensatory response by change in glucose level and decrease in insulin secretion [26], increase in glucagon secretion from pancreatic α cells [30] and influx of free fatty acids via lipolysis from adipocytes by attenuated anti-lipolytic action of insulin [31]. It has been shown that FABP4 is secreted from adipocytes in association with lipolysis [9–11]. In the present study, FABP4 concentration at baseline was positively correlated with level of noradrenaline, an index of activation of the sympathetic nerve system (Table 2). Furthermore, change in FABP4 concentration by canagliflozin was positively correlated with change in noradrenaline level (Fig 2D), though there was no significant difference between noradrenalin level before and after treatment with canagliflozin (Table 4). These findings support the notion that enhancement of catecholamine-induced lipolysis in adipocytes by canagliflozin in some patients with type 2 diabetes mellitus contributes to elevation of FABP4 level. Increased FABP4 level by canagliflozin might be a possible mechanism of increased hepatic glucose production by inhibition of SGLT2. To prove this hypothesis, animal experiments in which FABP4-deficient mice are treated with SGLT2 inhibitors will be necessary.
Serum FABP4 level has been reported to predict long-term cardiovascular events [21–23]. The association of cardiovascular events and serum FABP4 level has been explained by a significant role of FABP4 in insulin resistance and atherosclerosis [4–6]. The present study showed that an SGLT2 inhibitor, canagliflozin, increased the average FABP4 level by 10.3% in patients with type 2 diabetes mellitus, though FABP4 level was reduced in 33.3% of the studied patients. The findings suggest that SGLT2 inhibitors might have an adverse effect on cardiovascular events in some diabetic patients. Recently, a large-scale randomized controlled trial study, EMPA-REG OUTCOME [32], showed that empagliflozin, an SGLT2 inhibitor, decreased composite cardiovascular events, mainly due to reduction of heart failure by a hemodynamic effect including osmotic diuresis rather than reduction of blood pressure [33]. However, the incidence of acute myocardial infarction or stroke was not significantly reduced by empagliflozin in the EMPA-REG OUTCOME study [32]. Hence, there is the possibility that the benefit of glycemic control by an SGLT2 inhibitor for atherosclerotic events is partly offset by increased serum FABP4 level. This possibility needs to be further investigated by large-scale clinical studies.
The present study has several limitations. First, the number of patients enrolled was small, and the possibility of type 1 or type 2 errors in statistical tests cannot be excluded. Second, most of the study subjects had been treated at baseline with several drugs, including angiotensin II receptor blockers [34, 35], antidyslipidemic drugs [36, 37] and DPP-4 inhibitors [25], that have been reported to affect circulating FABP4 concentration. Therefore, such drugs might have modulated the change in FABP4 level. Third, adiposity was assessed by BMI and waist circumference but not by computer technologies. Fourth, levels of free fatty acid and glucagon, which are related to lipolysis and hepatic glucose production, were not measured in the present study due to a lack of remaining blood samples. Lastly, the present study lacked a placebo control group. Hence, the difference in FABP4 level before and after canagliflozin treatment may not be totally attributable to this SGLT2 inhibitor. A prospective and placebo-controlled study with larger numbers of subjects is necessary for confirming the impact of SGLT2 inhibitor treatment on circulating FABP4 level and for determining the clinical outcome of treatment with an SGLT2 inhibitor.
In conclusion, treatment with canagliflozin paradoxically increases serum FABP4 level in some patients with type 2 diabetes mellitus despite amelioration of glucose metabolism and reduction of adiposity, and this effect is possibly mediated by catecholamine-induced lipolysis in adipocytes. Increased FABP4 level by canagliflozin may partly offset the benefit of improvement in glucose metabolism and might be a possible mechanism of increased hepatic glucose production by inhibition of SGLT2. A further understanding of the mechanisms of FABP4 expression in and secretion from adipocytes and their pharmacological modulation may enable development of new therapeutic strategies for cardiovascular and metabolic diseases.
Supporting Information
S1 Protocol. This protocol was used in this trial.
https://doi.org/10.1371/journal.pone.0154482.s002
(PDF)
S2 Protocol. English version of this protocol.
https://doi.org/10.1371/journal.pone.0154482.s003
(DOCX)
Acknowledgments
We thank Ms. Shiho Ishikawa and Ms. Yoko Tamura for experimental management and technical help. M.F. has been supported by grants from JSPS KAKENHI, MEXT Translational Research Network Program, Uehara Memorial Foundation, SENSHIN Medical Research Foundation, Japan Diabetes Foundation, Takeda Medical Research Foundation, Ono Medical Research Foundation, Takeda Science Foundation, Akiyama Life Science Foundation, Yamaguchi Endocrine Research Foundation, Naito Foundation Natural Science Scholarship, Suhara Memorial Foundation and Kondou Kinen Medical Foundation.
Author Contributions
Conceived and designed the experiments: MF SH JI. Performed the experiments: MF MM SH AO MT JI. Analyzed the data: MF SH NM HY JI TM. Wrote the paper: MF TM.
References
- 1. Furuhashi M, Hotamisligil GS. Fatty acid-binding proteins: role in metabolic diseases and potential as drug targets. Nat Rev Drug Discov. 2008;7(6):489–503. Epub 2008/05/31. pmid:18511927.
- 2. Furuhashi M, Ishimura S, Ota H, Miura T. Lipid chaperones and metabolic inflammation. Int J Inflam. 2011;2011:642612. Epub 2011/11/29. pmid:22121495.
- 3. Furuhashi M, Saitoh S, Shimamoto K, Miura T. Fatty Acid-Binding Protein 4 (FABP4): Pathophysiological Insights and Potent Clinical Biomarker of Metabolic and Cardiovascular Diseases. Clin Med Insights Cardiol. 2014;8(Suppl 3):23–33. pmid:25674026.
- 4. Hotamisligil GS, Johnson RS, Distel RJ, Ellis R, Papaioannou VE, Spiegelman BM. Uncoupling of obesity from insulin resistance through a targeted mutation in aP2, the adipocyte fatty acid binding protein. Science. 1996;274(5291):1377–9. Epub 1996/11/22. pmid:8910278.
- 5. Makowski L, Boord JB, Maeda K, Babaev VR, Uysal KT, Morgan MA, et al. Lack of macrophage fatty-acid-binding protein aP2 protects mice deficient in apolipoprotein E against atherosclerosis. Nat Med. 2001;7(6):699–705. Epub 2001/06/01. pmid:11385507.
- 6. Furuhashi M, Fucho R, Gorgun CZ, Tuncman G, Cao H, Hotamisligil GS. Adipocyte/macrophage fatty acid-binding proteins contribute to metabolic deterioration through actions in both macrophages and adipocytes in mice. J Clin Invest. 2008;118(7):2640–50. Epub 2008/06/14. pmid:18551191.
- 7. Furuhashi M, Tuncman G, Gorgun CZ, Makowski L, Atsumi G, Vaillancourt E, et al. Treatment of diabetes and atherosclerosis by inhibiting fatty-acid-binding protein aP2. Nature. 2007;447(7147):959–65. Epub 2007/06/08. pmid:17554340.
- 8. Xu A, Wang Y, Xu JY, Stejskal D, Tam S, Zhang J, et al. Adipocyte fatty acid-binding protein is a plasma biomarker closely associated with obesity and metabolic syndrome. Clin Chem. 2006;52(3):405–13. Epub 2006/01/21. pmid:16423904.
- 9. Cao H, Sekiya M, Ertunc ME, Burak MF, Mayers JR, White A, et al. Adipocyte lipid chaperone AP2 is a secreted adipokine regulating hepatic glucose production. Cell Metab. 2013;17(5):768–78. Epub 2013/05/15. pmid:23663740.
- 10. Mita T, Furuhashi M, Hiramitsu S, Ishii J, Hoshina K, Ishimura S, et al. FABP4 is secreted from adipocytes by adenyl cyclase-PKA- and guanylyl cyclase-PKG-dependent lipolytic mechanisms. Obesity (Silver Spring). 2015;23(2):359–67. pmid:25521833.
- 11. Ertunc ME, Sikkeland J, Fenaroli F, Griffiths G, Daniels MP, Cao H, et al. Secretion of fatty acid binding protein aP2 from adipocytes through a nonclassical pathway in response to adipocyte lipase activity. J Lipid Res. 2015;56(2):423–34. pmid:25535287.
- 12. Furuhashi M, Fuseya T, Murata M, Hoshina K, Ishimura S, Mita T, et al. Local Production of Fatty Acid-Binding Protein 4 in Epicardial/Perivascular Fat and Macrophages Is Linked to Coronary Atherosclerosis. Arterioscler Thromb Vasc Biol. 2016. pmid:27013610.
- 13. Xu A, Tso AW, Cheung BM, Wang Y, Wat NM, Fong CH, et al. Circulating adipocyte-fatty acid binding protein levels predict the development of the metabolic syndrome: a 5-year prospective study. Circulation. 2007;115(12):1537–43. Epub 2007/03/29. pmid:17389279.
- 14. Tso AW, Xu A, Sham PC, Wat NM, Wang Y, Fong CH, et al. Serum adipocyte fatty acid binding protein as a new biomarker predicting the development of type 2 diabetes: a 10-year prospective study in a Chinese cohort. Diabetes Care. 2007;30(10):2667–72. Epub 2007/07/11. pmid:17620449.
- 15. Ishimura S, Furuhashi M, Watanabe Y, Hoshina K, Fuseya T, Mita T, et al. Circulating levels of fatty acid-binding protein family and metabolic phenotype in the general population. PLoS ONE. 2013;8(11):e81318. Epub 2013/11/28. pmid:24278421.
- 16. Ota H, Furuhashi M, Ishimura S, Koyama M, Okazaki Y, Mita T, et al. Elevation of fatty acid-binding protein 4 is predisposed by family history of hypertension and contributes to blood pressure elevation. Am J Hypertens. 2012;25(10):1124–30. Epub 2012/06/22. pmid:22717543.
- 17. Fuseya T, Furuhashi M, Yuda S, Muranaka A, Kawamukai M, Mita T, et al. Elevation of circulating fatty acid-binding protein 4 is independently associated with left ventricular diastolic dysfunction in a general population. Cardiovasc Diabetol. 2014;13(1):126. pmid:25142635.
- 18. Cabre A, Lazaro I, Girona J, Manzanares JM, Marimon F, Plana N, et al. Plasma fatty acid-binding protein 4 increases with renal dysfunction in type 2 diabetic patients without microalbuminuria. Clin Chem. 2008;54(1):181–7. pmid:18024526.
- 19. Cabre A, Lazaro I, Girona J, Manzanares JM, Marimon F, Plana N, et al. Plasma fatty acid binding protein 4 is associated with atherogenic dyslipidemia in diabetes. J Lipid Res. 2008;49(8):1746–51. pmid:18421072.
- 20. Yeung DC, Xu A, Cheung CW, Wat NM, Yau MH, Fong CH, et al. Serum adipocyte fatty acid-binding protein levels were independently associated with carotid atherosclerosis. Arterioscler Thromb Vasc Biol. 2007;27(8):1796–802. Epub 2007/05/19. pmid:17510463.
- 21. Furuhashi M, Ishimura S, Ota H, Hayashi M, Nishitani T, Tanaka M, et al. Serum fatty acid-binding protein 4 is a predictor of cardiovascular events in end-stage renal disease. PLoS ONE. 2011;6(11):e27356. Epub 2011/11/22. pmid:22102888.
- 22. von Eynatten M, Breitling LP, Roos M, Baumann M, Rothenbacher D, Brenner H. Circulating adipocyte fatty acid-binding protein levels and cardiovascular morbidity and mortality in patients with coronary heart disease: a 10-year prospective study. Arterioscler Thromb Vasc Biol. 2012;32(9):2327–35. Epub 2012/06/09. pmid:22679309.
- 23. Chow WS, Tso AW, Xu A, Yuen MM, Fong CH, Lam TH, et al. Elevated circulating adipocyte-fatty acid binding protein levels predict incident cardiovascular events in a community-based cohort: a 12-year prospective study. J Am Heart Assoc. 2013;2(1):e004176. pmid:23525430.
- 24. Cabre A, Lazaro I, Girona J, Manzanares JM, Marimon F, Plana N, et al. Fatty acid binding protein 4 is increased in metabolic syndrome and with thiazolidinedione treatment in diabetic patients. Atherosclerosis. 2007;195(1):e150–8. Epub 2007/06/08. pmid:17553506.
- 25. Furuhashi M, Hiramitsu S, Mita T, Fuseya T, Ishimura S, Omori A, et al. Reduction of serum FABP4 level by sitagliptin, a DPP-4 inhibitor, in patients with type 2 diabetes mellitus. J Lipid Res. 2015;56(12):2372–80. pmid:26467280.
- 26. Rajeev SP, Cuthbertson DJ, Wilding JP. Energy balance and metabolic changes with sodium-glucose co-transporter 2 inhibition. Diabetes Obes Metab. 2016;18(2):125–34. pmid:26403227.
- 27. Ferrannini E, Muscelli E, Frascerra S, Baldi S, Mari A, Heise T, et al. Metabolic response to sodium-glucose cotransporter 2 inhibition in type 2 diabetic patients. J Clin Invest. 2014;124(2):499–508. pmid:24463454.
- 28. 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 Invest. 2014;124(2):509–14. pmid:24463448.
- 29. Matsuo S, Imai E, Horio M, Yasuda Y, Tomita K, Nitta K, et al. Revised equations for estimated GFR from serum creatinine in Japan. Am J Kidney Dis. 2009;53(6):982–92. Epub 2009/04/03. pmid:19339088.
- 30. Bonner C, Kerr-Conte J, Gmyr V, Queniat G, Moerman E, Thevenet J, et al. Inhibition of the glucose transporter SGLT2 with dapagliflozin in pancreatic alpha cells triggers glucagon secretion. Nat Med. 2015;21(5):512–7. pmid:25894829.
- 31. Taylor SI, Blau JE, Rother KI. SGLT2 Inhibitors May Predispose to Ketoacidosis. J Clin Endocrinol Metab. 2015;100(8):2849–52. pmid:26086329.
- 32. Zinman B, Wanner C, Lachin JM, Fitchett D, Bluhmki E, Hantel S, et al. Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes. N Engl J Med. 2015;373(22):2117–28. pmid:26378978.
- 33. Zinman B, Lachin JM, Inzucchi SE. Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes. N Engl J Med. 2016;374(11):1094. pmid:26981940.
- 34. Miyoshi T, Doi M, Hirohata S, Kamikawa S, Usui S, Ogawa H, et al. Olmesartan reduces arterial stiffness and serum adipocyte fatty acid-binding protein in hypertensive patients. Heart Vessels. 2011;26(4):408–13. Epub 2010/11/11. pmid:21063874.
- 35. Furuhashi M, Mita T, Moniwa N, Hoshina K, Ishimura S, Fuseya T, et al. Angiotensin II receptor blockers decrease serum concentration of fatty acid-binding protein 4 in patients with hypertension. Hypertens Res. 2015;38(4):252–9. pmid:25672659.
- 36. Karpisek M, Stejskal D, Kotolova H, Kollar P, Janoutova G, Ochmanova R, et al. Treatment with atorvastatin reduces serum adipocyte-fatty acid binding protein value in patients with hyperlipidaemia. Eur J Clin Invest. 2007;37(8):637–42. Epub 2007/07/20. pmid:17635574.
- 37. Furuhashi M, Hiramitsu S, Mita T, Omori A, Fuseya T, Ishimura S, et al. Reduction of circulating FABP4 level by treatment with omega-3 fatty acid ethyl esters. Lipids Health Dis. 2016;15(1):5. pmid:26754658.