- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Recently Accepted Articles ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
Journal of Diabetes Research
Volume 2013 (2013), Article ID 143515, 5 pages
Impact of Serum Retinol-Binding Protein 4 Levels on Regulation of Remnant-Like Particles Triglyceride in Type 2 Diabetes Mellitus
1Department of Internal Medicine, Graduate School of Medical Science, Kanazawa University, 13-1 Takaramachi, Kanazawa 920-8640, Japan
2Department of General Medicine, Kanazawa Medical University, 1-1 Daigaku, Uchinada, Kahoku 920-0293, Japan
Received 25 December 2012; Accepted 12 February 2013
Academic Editor: Aristidis Veves
Copyright © 2013 Naoto Yamaaki et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background. Although retinol-binding protein 4 (RBP4) associates with insulin resistance and remnant-like particles triglyceride (RLP-TG) elevated in the insulin resistant state, few data exist regarding the relationship between RBP4 and RLP-TG. Subjects and Methods. The study included 92 Japanese type 2 diabetic mellitus (T2DM) male patients (age years, body mass index (BMI) kg/m2, waist circumference (WC) cm, and HbA1c (NGSP) %). Patients on medications affecting insulin sensitivity, including fibrates, biguanides, and thiazolidinedione, were excluded. Visceral fat area (VFA) and subcutaneous fat area (SFA) were measured by computed tomography. Results. RBP4 levels showed a significant positive correlation with RLP-TG ( and ), TG ( and ), RLP-TG/TG ( and ), and age ( and ), although there was no significant correlation with VFA, SFA, adiponectin levels, or homeostasis model of assessment insulin resistance (HOMA-R). Multiple regression analysis revealed that RBP4 was an independent determinant of RLP-TG () but was not a determinant of TG. Conclusions. RBP4 correlates positively with serum RLP-TG independent of fat accumulation in T2DM. RBP4 may regulate remnant metabolism independent of glycemic control in T2DM.
Retinol-binding protein 4 (RBP4) was originally identified as a signal molecule, which transfers the intercellular signals for insulin resistance . Previous clinical studies have reported that RBP4 is associated with the extent of systemic insulin resistance and obesity [2, 3]. RBP4 has been shown to significantly correlate with clinical features relating to insulin resistance and metabolic syndrome, including hyperlipidemia and hypertriglyceridemia . Furthermore, recent studies have shown that RBP4 mainly correlates with dyslipidemic profiles in type 2 diabetes, especially in terms of hypertriglyceridemia.
The retention of remnant lipoproteins is known to frequently occur in the insulin resistant state and in metabolic syndrome. Impaired remnant metabolism is one of the “residual cardiovascular risk factor” for atherosclerosis . Remnant clearance is retarded in insulin resistant type 2 diabetics resulting in cardiovascular damage . Even though the cardiovascular risk associated with metabolic syndrome has been well established, few data exist concerning the relationship between RBP4 and lipoprotein remnants such as remnant-like particles triglyceride (RLP-TG). Therefore, we are investigating the relationship between RBP4 and serum lipoprotein levels, including RLP-TG, in Japanese diabetic patients.
2. Patients and Methods
This study was approved by the ethical committee of Kanazawa University. Informed consents were obtained from all subjects. All patients were recruited from Kanazawa University Hospital and its satellite hospital. Of 860 outpatients with type 2 diabetes mellitus, a total of 92 Japanese diabetic men (age 60.5 ± 13.6 years) with their agreement of the computed tomography were included in this study.
Patients on medications affecting the individual insulin sensitivity, including fibrates, biguanides, and thiazolidinedione, were excluded from this study [7, 8]. Patients with other endocrine diseases or significant renal or hepatic disease were also excluded. Obesity was defined as body mass index kg/m2, based on the criteria of the Japan Society for the Study of Obesity . Diabetes mellitus was diagnosed according to World Health Organization criteria  and/or receiving medications for diabetes mellitus.
2.2. Laboratory Measurements
BMI was calculated as weight (kg) divided by height (m) squared. Waist circumference (WC) at the umbilical level was measured in the exhalation phase of respiration while standing.
Venous blood samples were performed after a 12-hour overnight fast. Total cholesterol (TC) and triglyceride (TG) were determined by enzymatic methods, and high-density lipoprotein cholesterol (HDL-C) levels were measured by a polyanion-polymer/detergent method. RLP isolation was based on the removal of apo A-I-containing particles and most apo B-containing particles, using an immunoseparation technique, which has been shown to leave remnants of both intestinal and hepatic origin in the unbound fraction. Briefly, monoclonal antibodies to apo A-I and specific monoclonal antibodies to apo B, which do not recognize partially hydrolyzed, apo E-enriched lipoprotein remnants, were immobilized on agarose gel. RLP-TG concentrations were measured in the FHS plasma aliquots that had been frozen at −80°C until the time of analysis. Plasma was incubated with the gel for 2 hours, after which the gel, containing the bound (non-RLP) lipoproteins, was precipitated by low-speed centrifugation. Triglyceride concentrations were then measured in the unbound supinates. Blood glucose was measured with the glucose oxidase method and HbA1c by high-pressure liquid chromatography. Plasma adiponectin levels were measured with an enzyme-linked immunosorbent assay kit (Otsuka Pharmaceutical Co., Tokushima, Japan), and serum RBP4 was measured with Human RBP4 Competitive ELISA kit (Adipogen, Seoul, Republic of Korea).
It is well known that RLP-TG has strongly correlated with TG, which represents both overproduction and catabolism of VLDL. This suggests that RLP-TG levels can reflect VLDL overproduction. Therefore, we examined RLP-TG/TG ratio as the focused index for remnant catabolism. Homeostasis model of assessment insulin resistance (HOMA-R) is calculated using the following formula: fasting glucose (mg/dl) × fasting insulin (μU/mL)/405.
2.3. Body Fat Distribution
All subjects underwent computed tomography (CT) at the umbilical level to measure cross-sectional visceral fat area (VFA) and abdominal subcutaneous fat area (SFA) using Fat Scan (N2 System Corp, Osaka, Japan) . VFA/SFA ratio was calculated as VFA divided by SFA.
2.4. Statistical Analysis
All data are shown as mean ± SD. Continuous variables were compared by ANOVA after being adjusted for age, BMI, and sex. All statistical analyses were conducted with JMP ver. 10.0.2 for Macintosh OSX (SAS institute, NC, USA). A P value of less than 0.05 was considered statistically significant.
Baseline clinical characteristics of the patients are shown in Table 1. Our previous report showed that poorly controlled type 2 diabetic men had more unfavorable lipid profiles than women, thus resulting in decreased lipolysis of plasma TG-rich lipoproteins . Therefore, only type 2 diabetic men were enrolled in this study.
Relationships between RBP4 and other clinical parameters were shown in Table 2. RBP4 showed significant positive correlation with TG ( and ) (Figure 1(a)), RLP-TG ( and ) (Figure 1(b)), WC ( and ), and negatively correlated with age ( and ). RBP4 also showed good correlation with RLP-TG/TG ( and ) (Figure 1(c)). Importantly, there was no significant correlation between RBP4 and HOMA-R.
RLP-TG showed positive correlation with TC ( and ), TG ( and ), HbA1c ( and ), HOMA-R ( and ), RBP4 and negative correlation with age ( and ), and HDL-C ( and ).
TG showed positive correlation with TC ( and ), RLP-TG, HbA1c ( and ), negative relationships with age ( and ), and HDL-C ( and ). Unlike RLP-TG, TG did not have a significant correlation with HOMA-R.
To investigate which factors independently determined RLP-TG and TG, we performed multiple regression analysis. Multiple regression analysis with RLP-TG (log) (Table 3(a)) as an objective variable revealed that RBP4 and age had independent relationships with RLP-TG. Multiple regression analysis with TG as an objective variable showed that VFA and age had independent relationships with TG, but RBP4 had no independent relationships with TG (Table 3(b)).
In the present study, we showed for the first time that serum RBP4 levels correlated with RLP-TG. Univariate analyses showed that RBP4 was significantly associated with RLP-TG and TG. There was no correlation of RBP4 with most of the insulin-resistance-associated factors (adiponectin, VFA, BMI, and HOMA-R) except for a weak correlation with WC, even though most of these factors were significantly correlated with RLP-TG. Furthermore, multiple regression analysis revealed that RBP4 had an independent association with RLP-TG, although RBP4 did not have an independent association with TG levels. These results suggested that RBP4 could regulate TG metabolism especially at the remnant lipoprotein level.
RBP4 was identified as a signal transferring protein for insulin resistance. Therefore, we focused mainly on its relationship with insulin-resistant states in this study, although some reports have shown that RBP4 could play a more important role in lipid metabolism than in insulin resistance . RBP4 correlates with serum TG levels in type 2 diabetic patients independent from liver fat content [14, 15]. Furthermore, some reports have shown that RBP4 correlates with hypertriglyceridemia independent of insulin resistance [4, 13, 16]. In this study, serum RBP4 levels significantly correlated with parameters relating to RLP-TG and TG. Among the generally accepted markers for insulin resistance, no significant relationships were observed between RBP4 and BMI, VFA, HOMA-R, or adiponectin. WC showed a relatively weak relationship with RBP4. The correlation with WC is indirect and is usually considered as a surrogate marker reflecting the extent of insulin resistance. Actually, the appropriate cutoff value of WC to detect metabolic syndrome is still under discussion . However, it is still unclear why RBP4 correlated only with WC instead of VFA which is closely related to insulin resistance. Imbalance of fat distribution in the study group may explain this dissociation. Even under these conditions, RBP4 can regulate TG metabolism especially at the remnant level, but visceral fat accumulation and factors associated with insulin resistance may not be the main pathway for RBP4 to regulate TG metabolism.
Two possible mechanisms explaining the increased level of RLP-TG could be presented, one is the decreased metabolism of TG caused by decreased LPL activity induced by insulin resistance  and another is the overproduction of TG. Decreased LPL activity accounts for a great deal of the elevation of serum TG in insulin-deficient diabetes patients [19, 20]. As the RLP-TG to TG ratio has been reported to correlate with LPL activity , the result of a significant and positive relationship between RBP4 and the RLP-TG to TG ratio in this study suggests that decreased LPL activity would have contributed much to the elevation of RLP-TG. In addition, RBP4 carries ligands of retinoid X receptor (RXR), and RXR modulates the expression of several genes including apoC-III, which is an inhibitor of the lipoprotein lipase [22, 23]. Based on the present findings and previous reports, RBP4 is thought to increase RLP-TG through the activation of RXR, inducing the overexpression of apoC-III and decreasing LPL activity in type 2 diabetic patients.
This study has several limitations. First, we did not measured LPL activity. As the RLP-TG to TG ratio has been reported to correlate with LPL activity , we used a surrogate marker of RLP-TG to TG ratios for LPL activity. Although direct measurement would be ideal, our current results seemed to justify using a surrogate marker to represent LPL activity. Second, some patients were treated with insulin or sulphonylureas, which might affect RBP4 metabolism. However, these medicines were discontinued the day prior to the examination, so the effect on remnant metabolism would be minimized.
In conclusion, RBP4 correlates positively with serum RLP-TG independent of markers reflecting insulin resistance including visceral fat accumulation in patients with type 2 diabetes mellitus. These results suggest that RBP4 may have a negative effect on remnant metabolism independent of visceral fat accumulation, glycemic control, or factors associated with insulin resistance.
- Q. Yang, T. E. Graham, N. Mody et al., “Serum retinol binding protein 4 contributes to insulin resistance in obesity and type 2 diabetes,” Nature, vol. 436, no. 7049, pp. 356–362, 2005.
- N. Klöting, T. E. Graham, J. Berndt et al., “Serum retinol-binding protein is more highly expressed in visceral than in subcutaneous adipose tissue and is a marker of intra-abdominal fat mass,” Cell Metabolism, vol. 6, no. 1, pp. 79–87, 2007.
- T. E. Graham, Q. Yang, M. Blüher et al., “Retinol-binding protein 4 and insulin resistance in lean, obese, and diabetic subjects,” New England Journal of Medicine, vol. 354, no. 24, pp. 2552–2563, 2006.
- K. Takebayashi, M. Suetsugu, S. Wakabayashi, Y. Aso, and T. Inukai, “Retinol binding protein-4 levels and clinical features of type 2 diabetes patients,” Journal of Clinical Endocrinology and Metabolism, vol. 92, no. 7, pp. 2712–2719, 2007.
- T. Nakamura, J. E. Obata, M. Hirano, et al., “Predictive value of remnant lipoprotein for cardiovascular events in patients with coronary artery disease after achievement of LDL-cholesterol goals,” Atherosclerosis, vol. 218, no. 1, pp. 163–167, 2011.
- J. Pang, D. C. Chan, P. H. Barrett, and G. F. Watts, “Postprandial dyslipidaemia and diabetes: mechanistic and therapeutic aspects,” Current Opinion in Lipidology, vol. 23, no. 4, pp. 303–309, 2012.
- M. Ohira, Y. Miyashita, M. Ebisuno et al., “Effect of metformin on serum lipoprotein lipase mass levels and LDL particle size in type 2 diabetes mellitus patients,” Diabetes Research and Clinical Practice, vol. 78, no. 1, pp. 34–41, 2007.
- K. Shirai, Y. Itoh, H. Sasaki et al., “The effect of insulin sensitizer, troglitazone, on lipoprotein lipase mass in preheparin serum,” Diabetes Research and Clinical Practice, vol. 46, no. 1, pp. 35–41, 1999.
- Examination Committee of Criteria for ‘Obesity Disease’ in Japan and Japan Society for the Study of Obesity, “New criteria for ‘obesity disease’ in Japan,” Circulation Journal, vol. 66, no. 11, pp. 987–992, 2002.
- R. Kahn, “Report of the expert committee on the diagnosis and classification of diabetes mellitus,” Diabetes Care, vol. 20, no. 7, pp. 1183–1197, 1997.
- T. Yoshizumi, T. Nakamura, M. Yamane et al., “Abdominal fat: standardized technique for measurement at CT,” Radiology, vol. 211, no. 1, pp. 283–286, 1999.
- J. Kobayashi, T. Maruyama, H. Watanabe et al., “Gender differences in the effect of type 2 diabetes on serum lipids, pre-heparin plasma lipoprotein lipase mass and other metabolic parameters in Japanese population,” Diabetes Research and Clinical Practice, vol. 62, no. 1, pp. 39–45, 2003.
- M. von Eynatten, P. M. Lepper, D. Liu et al., “Retinol-binding protein 4 is associated with components of the metabolic syndrome, but not with insulin resistance, in men with type 2 diabetes or coronary artery disease,” Diabetologia, vol. 50, no. 9, pp. 1930–1937, 2007.
- B. Verges, B. Guiu, J. P. Cercueil, et al., “Retinol-binding protein 4 is an independent factor associated with triglycerides and a determinant of very low-density lipoprotein-apolipoprotein b100 catabolism in type 2 diabetes mellitus,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 32, no. 12, pp. 3050–3057, 2012.
- S. C. Huang and Y. J. Yang, “Serum retinol-binding protein 4 is independently associated with pediatric NAFLD and fasting triglyceride level,” Journal of Pediatric Gastroenterology and Nutrition, vol. 56, no. 2, pp. 145–150, 2013.
- Q. Qi, Z. Yu, X. Ye et al., “Elevated retinol-binding protein 4 levels are associated with metabolic syndrome in Chinese people,” Journal of Clinical Endocrinology and Metabolism, vol. 92, no. 12, pp. 4827–4834, 2007.
- R. Oka, J. Kobayashi, K. Yagi et al., “Reassessment of the cutoff values of waist circumference and visceral fat area for identifying Japanese subjects at risk for the metabolic syndrome,” Diabetes Research and Clinical Practice, vol. 79, no. 3, pp. 474–481, 2008.
- J. Kobayashi, K. Saito, I. Fukamachi et al., “Pre-heparin plasma lipoprotein lipase mass: correlation with intra-abdominal visceral fat accumulation,” Hormone and Metabolic Research, vol. 33, no. 7, pp. 412–416, 2001.
- E. A. Nikkila, J. K. Huttunen, and C. Ehnholm, “Postheparin plasma lipoprotein lipase and hepatic lipase in diabetes mellitus. Relationship to plasma triglyceride metabolism,” Diabetes, vol. 26, no. 1, pp. 11–21, 1977.
- J. Kobayashi, K. Nakajima, A. Nohara et al., “The relationship of serum lipoprotein lipase mass with fasting serum apolipoprotein B-48 and remnant-like particle triglycerides in type 2 diabetic patients,” Hormone and Metabolic Research, vol. 39, no. 8, pp. 612–616, 2007.
- T. Nakano, Y. Tokita, T. Nagamine et al., “Measurement of serum remnant-like lipoprotein particle-triglyceride (RLP-TG) and RLP-TG/total TG ratio using highly sensitive triglyceride assay reagent,” Clinica Chimica Acta, vol. 412, no. 1-2, pp. 71–78, 2011.
- N. Noy, “Retinoid-binding proteins: mediators of retinoid action,” Biochemical Journal, vol. 348, no. 3, pp. 481–495, 2000.
- N. Vu-Dac, P. Gervois, I. P. Torra et al., “Retinoids increase human apo C-III expression at the transcriptional level via the retinoid X receptor: contribution to the hypertriglyceridemic action of retinoids,” Journal of Clinical Investigation, vol. 102, no. 3, pp. 625–632, 1998.