Skip to main content
Download PDF
Download ePub
  • Original investigation
  • Open access
  • Published:

Impact of glycemic control on circulating endothelial progenitor cells and arterial stiffness in patients with type 2 diabetes mellitus

Cardiovascular Diabetology volume 10, Article number: 113 (2011) Cite this article

Abstract

Background

Patients with type 2 diabetes mellitus (DM) have increased risk of endothelial dysfunction and arterial stiffness. Levels of circulating endothelial progenitor cells (EPCs) are also reduced in hyperglycemic states. However, the relationships between glycemic control, levels of EPCs and arterial stiffness are unknown.

Methods

We measured circulating EPCs and brachial-ankle pulse wave velocity (baPWV) in 234 patients with type 2 DM and compared them with 121 age- and sex-matched controls.

Results

Patients with DM had significantly lower circulating Log CD34/KDR+ and Log CD133/KDR+ EPC counts, and higher Log baPWV compared with controls (all P < 0.05). Among those 120/234 (51%) of DM patients with satisfactory glycemic control (defined by Hemoglobin A1c, HbA1c < 6.5%), they had significantly higher circulating Log CD34/KDR+ and Log CD133/KDR+ EPC counts, and lower Log baPWV compared with patients with poor glycemic control (all P < 0.05). The circulating levels of Log CD34/KDR+ EPC (r = -0.46, P < 0.001) and Log CD133/KDR+ EPC counts (r = -0.45, P < 0.001) were negatively correlated with Log baPWV. Whilst the level of HbA1c positively correlated with Log baPWV (r = 0.20, P < 0.05) and negatively correlated with circulating levels of Log CD34/KDR+ EPC (r = -0.40, P < 0.001) and Log CD133/KDR+ EPC (r = -0.41, P < 0.001). Multivariate analysis revealed that HbA1c, Log CD34/KDR+ and Log CD133/KDR+ EPC counts were independent predictors of Log baPWV (P < 0.05).

Conclusions

In patients with type 2 DM, the level of circulating EPCs and arterial stiffness were closely related to their glycemic control. Furthermore, DM patients with satisfactory glycemic control had higher levels of circulating EPCs and were associated with lower arterial stiffness.

Background

It is well recognized that patients with type 2 diabetes mellitus (DM) have accelerated stiffening of the elastic arteries beyond that explained by normal aging [1]. Such increase in arterial stiffness, as measured by pulse wave velocity (PWV) may represent a useful integrated index of vascular status, and has been identified as an independent predictor for cardiovascular related mortality in patients with DM [2]. In patients with DM, one of the postulated mechanisms of increased arterial stiffness is hyperglycemia-induced depletion of endothelial nitric oxide (NO), subsequently leading to endothelial dysfunction [3]. Dysregulation of the NO system has also been shown to be responsible for the depletion and dysfunction of endothelial progenitor cells (EPCs) in patients with type 2 DM [4]. Interestingly, studies also showed that plasma glucose and hemogloblin A1c (HbA1c) levels inversely correlates with the bioavailability of NO in EPCs [5]. Therefore, we hypothesized that poor glycemic control in patients with type 2 DM is associated with depletion of circulating EPC and thus increased arterial stiffness. The purpose of this study was to investigate the relationships between glycemic control with circulating EPCs and arterial stiffness in patients with type 2 DM.

Methods

Study population

Consecutive patients with type 2 DM, as defined by the WHO criteria [6] and treated with stable oral hypoglycemic agents and insulin, and cardiovascular medications for at least 6 months were recruited from the medical outpatient clinic. Patients with poorly controlled DM (HbA1c ≥11%), dilated cardiomyopathy, significant valvular heart disease, chronic atrial fibrillation, New York Heart Association class III/IV heart failure, a history of prior atherothrombotic events (including unstable angina, myocardial infarction, stroke and peripheral vascular disease) or stable angina; creatinine level >220 μmol/L, acute infectious disease, chronic obstructive pulmonary disease, hepatic insufficiency and connective tissue disease were excluded. As a result, a total of 234 patients with type 2 DM were eligible for this study.

The control group was recruited from a local health exhibition and consisted of 121 age- and sex-matched healthy subjects with fasting blood glucose level < 6.1mmol/L and no history of diabetes or cardiovascular diseases. A written informed consent was obtained from each subject and the study was approved by the local institutional review board.

Study Design

Cardiovascular risk factors including: tobacco smoking, hypercholesterolemia, hypertension and family history of cardiovascular disease diagnosed in first-degree relatives before 55 years of age were assessed. Baseline demographic data and cardiovascular medications were recorded in all subjects [7]. Hypertension was defined as either resting systolic or diastolic blood pressure >140 or >90mmHg, at two different clinical visits or the prescription of anti-hypertensive medications. Hypercholesterolemia was defined as fasting total plasma cholesterol of ≥4.9mmol/L or the prescription of lipid-lowering medications. Smoking status was recorded as ever-smoker (past or current) or non-smoker.

Anthropometric measurements including body weight and waist-hip circumference ratio (WHR) were performed. Body-mass index (BMI) was calculated as kg/m2. Systolic and diastolic blood pressures were measured. Fasting blood samples were obtained to measure serum levels of glucose, HbA1c, total cholesterol, triglyceride, low-density lipoprotein-cholesterol (LDL-C), high-density lipoprotein-cholesterol (HDL-C), creatinine and number of circulating EPCs. Glomerular filtration rate (GFR) was calculated using the Modification of Diet in Renal Disease Study equation.

Arterial stiffness

Arterial stiffness was measured non-invasively, by a single experienced operator, with the VP-2000 System (Colin Corp., USA) and represented as brachial to ankle pulse wave velocity (baPWV). Previous studies have validated that baPWV was closely correlated with aortic PWV as a measurement of arterial stiffness [8]. Patients were allowed to rest for 5 minutes and the sites of maximum arterial pulsation were determined by physical examination. Sequential recordings of pressure waveforms at the brachial and posterior tibial arteries were made using hand-held manometer probes with simultaneous electrocardiogram gating. Measurements were taken after achieving coherent reproduction of signals with maximum amplitudes.

Transmission time (TBA) was defined as the time interval between the initial increase in brachial and posterior tibial waveforms. Transmission distance from the suprasternal notch to the brachium (DB) and ankle (DA) were determined by direct superficial measurement. The value baPWV was automatically calculated as the transmission distance divided by the transmission time: baPWV = (DA - DB)/TBA. After obtaining bilateral baPWV values, the mean value of the two was used for subsequent analysis. Intra-observer variability testing revealed an intra-class correlation coefficient of 0.89 (P < 0.001).

Circulating endothelial progenitor cells

Circulating EPCs were measured by fluorescence-activated cell analysis of a peripheral blood sample and defined by the expression of surface markers: CD34/KDR+ and CD133/KDR+ [7]. In brief, 100 μl of peripheral blood was incubated with a phycoerythrin-conjugated monoclonal antibody against human KDR (Sigma, St Louis, Missouri, USA), followed by a fluorescein isothiocyanate (FITC)-conjugated CD34 and CD133 antibodies (Beckman Coulter, Fullerton, California, USA). FITC-labeled anti-human CD45 antibody was used for differential gating during flow analysis. FITC-labeled IgG1a (Beckman Coulter) and phycoerythrin-labeled IgG2b (Becton Dickinson, Franklin Lakes, New Jersey, USA) served as the isotypic control for color compensation. Analysis was performed with an automated fluorescence-activated cell counter (Elite; Beckman Coulter) in which 1,000,000 events were counted. The percentages of all the measured components defined as the absolute cell counts divided by the lymphocyte counts were calculated. Intra-observer variability testing revealed an intra-class correlation coefficient of 0.90 (P < 0.001).

Statistical analysis

Data were expressed as mean ± standard deviation for continuous variables and proportions for categorical variables. Baseline characteristics were compared between groups using independent samples t-test or Fisher's exact test, as appropriate. Patients with type 2 DM were divided into those with satisfactory glycemic control (HbA1c < 6.5%) and those with poor glycemic control (HbA1c ≥6.5%).

Since the distribution pattern of baPWV and the number of circulating EPCs were highly skewed, these variables were log-transformed to normalize their distribution before analysis. Correlation coefficients were calculated to assess the association between the circulating EPCs and baPWV. Stepwise backward linear regression analysis was used to identify independent predictors for circulating EPCs and baPWV. Only parameters with P < 0.1 in uni-variate analysis were subsequently entered into a multi-variate model. All statistical analyses were performed using the statistical package SPSS for Windows (Version 15.0, SPSS, Chicago, USA). A P value < 0.05 was considered as statistically significant.

Results

Clinical characteristics

As shown in Table 1, there were no significant differences in age or sex between patients with type 2 DM and controls (all P>0.05). Patients with type 2 DM had significantly higher prevalence of hypertension, hypercholesterolemia and smokers, greater BMI and WHR, and more likely to be prescribed with anti-hypertensive medications, statins and aspirin (Table 1, P < 0.01). Furthermore, the serum fasting glucose, HbA1c, triglyceride and creatinine levels were higher and the GFR was lower in DM patients as compared with controls (Table 1, P < 0.01). In contrast, DM patients had significantly lower serum total cholesterol and LDL-C than controls which were likely due to an increased use of statins in DM patients.

Table 1 Clinical characteristics of patients with DM and Controls
Full size table

Among those patients with DM, 120/234 (51%) of them had satisfactory glycemic control with HbA1c < 6.5%. As expected, DM patients with satisfactory glycemic control had a significantly lower serum fasting glucose and HbA1c levels compared with those with poor glycemic control (Table 2, P < 0.01). Furthermore, DM patients with satisfactory glycemic control had a lower prevalence of hypertension, hyperlipidemia, smoking history and were less frequently prescribed with insulin than those with poor glycemic control (Table 2, P < 0.05). However, there were no significant differences in the serum lipid profile, GFR and use of cardiovascular medications between the two groups (Table 2, P>0.05).

Table 2 Clinical characteristics of DM patients with satisfactory (HbA1c < 6.5%) or poor (HbA1c≥6.5%) glycemic control
Full size table

Circulating endothelial progenitor cells and arterial stiffness

Compared with controls, patients with type 2 DM had significantly lower circulating Log CD34/KDR+ EPCs (0.96 ± 0.31 10-3/ml vs. 1.23 ± 0.36 10-3/ml, P < 0.01) and Log CD133/KDR+ EPCs (0.70 ± 0.26 10-3/ml vs. 1.13 ± 0.38 10-3/ml, P < 0.01). Among patients with DM, those with satisfactory glycemic control had significantly higher levels of circulating Log CD34/KDR+ EPCs (1.05 ± 0.27 10-3/ml vs. 0.88 ± 0.32 10-3/ml, P < 0.01) and Log CD133/KDR+ EPCs (0.78 ± 0.28 10-3/ml vs. 0.61 ± 0.21 10-3/ml, P < 0.01) than those with poor glycemic control.

Arterial stiffness as measured by Log baPWV, was significantly greater in patients with type 2 DM as compared with controls (3.24 ± 0.08 cm/s vs. 3.18 ± 0.09 cm/s, P < 0.01). Among patients with DM, those with satisfactory glycemic control had significantly lower Log baPWV than those with poor glycemic control (3.23 ± 0.08 cm/s vs. 3.27 ± 0.09 cm/s, P < 0.05).

The circulating levels of Log CD34/KDR+ EPCs (r = -0.46, P < 0.001, Figure 1) and Log CD133/KDR+ EPCs (r = -0.45, P < 0.001, Figure 2) were negatively correlated with Log baPWV. Whilst the level of HbA1c positively correlated with Log baPWV (r = 0.20, P < 0.05) and negatively correlated with circulating levels of Log CD34/KDR+ EPCs (r = -0.40, P < 0.001, Figure 3) and Log CD133/KDR+ EPCs (r = -0.41, P < 0.001, Figure 4).

Figure 1
figure 1

Relationship between levels of circulating Log CD34/KDR+ EPCs with Log baPWV in patients with DM.

Full size image
Figure 2
figure 2

Relationship between levels of circulating Log CD133/KDR+ EPCs with Log baPWV in patients with DM.

Full size image
Figure 3
figure 3

Relationship between levels of circulating Log CD34/KDR+ EPCs and HbA1c in patients with DM.

Full size image
Figure 4
figure 4

Relationship between levels of circulating Log CD133/KDR+ EPCs and HbA1c in patients with DM.

Full size image

Multivariate regression analysis revealed that in patients with diabetes, HbA1c, diabetes duration, Log CD34/KDR+ EPCs and Log CD133/KDR+ EPCs were independent predictors of Log baPWV (Table 3).

Table 3 Clinical predictors for arterial stiffness in patients with DM
Full size table

Discussion

Our results demonstrate a close inter-relationship between glycemic control, circulating EPCs and arterial stiffness in patients with type 2 DM. Patients with type 2 DM had a lower level of circulating EPCs and increased arterial stiffness compared with normal controls. Amongst those with diabetes, a poor glycemic control correlated with a lower number of EPCs as well as increased arterial stiffness, whilst better glycemic control correlated with a relatively greater number of EPCs as well as a lesser degree of arterial stiffness. Furthermore, after adjusting for other cardiovascular risk factors and medications, glycemic control and EPC counts were identified as independent risk predictors for arterial stiffness.

The mechanisms by which hyperglycemia leads to an increase in arterial stiffness remain unclear but is likely related to an imbalance between the protective versus detrimental pathways. Vascular endothelial cells secrete large amounts of chemical mediators and biologically active substances that actively regulate vascular tone and permeability [9]. Among those protective substances secreted, NO is one of the main factor which has vasodilatory, anti-platelet, anti-inflammatory and anti-oxidant properties for maintenance of endothelial function [10]. However, in the presence of chronic hyperglycemia, polyol, protein kinase C and pentose phosphate pathways are enhanced. These pathways are detrimental to the vascular endothelium and results in an increased oxidative stress and accelerated endothelial cell apoptosis [11, 12]. Furthermore, the availability and biological activity of NO are also reduced in hyperglycemic states, resulting in worsening endothelial dysfunction [13–16]. In addition, hyperglycemia induces vascular smooth muscle cell proliferation as well as promotes their conversion from the contractile phenotype to the synthentic phenotype, thus promoting the development of arterial stiffness [17].

On the other hand, circulating EPCs may play an important role in repairing damaged vascular endothelium [18]. Prior studies have shown that the number of circulating EPCs was positively correlated to endothelial function [19]. However, in hyperglycemic states, EPCs exhibit impaired proliferation, adhesion, and incorporation into vascular structures [20]. An impairment of vascular NO system has also been shown to result in the dysfunction and depletion of EPCs [4]. Indeed, the levels of circulating EPCs were reduced in patients with type 2 DM as compared with normal subjects, and have been shown to have a significant inverse correlation with serum glucose and HbA1c levels [21]. EPCs have also been found to be reduced in pre-diabetic states (impaired fasting glucose and impaired glucose tolerance) with further significant reductions in number at the clinical onset of diabetes and after ~20 years of disease [22]. Moreover, recent interesting studies noted reduced numbers and functions of EPCs in subjects who are predisposed to having DM (e.g. polycystic ovarian syndrome), indicating that reduced EPCs may even be a risk factor of DM [23].

Consistent with previous studies [24, 25], the present study confirmed that patients with DM have a blunted endothelium regenerating capacity as reflected by a decrease in number of circulating EPCs and was associated with large artery atherosclerosis as measured by PWV. Importantly, our results further demonstrated that the degree of hyperglycemia control in those patients with type 2 DM was closely related to the levels of circulating EPCs as well as the arterial stiffness. In this study, DM patients who could achieve satisfactory hyperglycemia had significantly higher circulating level of EPCs and lower arterial stiffness. This might be one of the mechanisms in which satisfactory glycemic control in type 2 DM patients (HbA1c < 6.5%) had reduced cardiovascular events [26]. On the other hand, recent studies have also shown that an over vigorous lowering of HbA1c to < 6.0% has been associated with increased all-cause mortality [27]. The mechanism of such observations has yet to be determined but is less likely to be related to a change in PWV and EPC number according to our findings.

This study has several limitations. First, this was only a modest size cross-sectional study of approximately 350 subjects and the result needs further confirmation in other cohorts. Second, the causal relationship between reduced circulating EPC and arterial stiffness could not be confirmed. Whether improved glycemic control in DM patients can increase circulating EPCs and decrease arterial stiffness needs to be confirmed in future prospective studies. Third, the effect of hyperinsulinemia and insulin resistance on circulating EPCs counts, endothelial function and arterial stiffness were not assessed in the present study. Forth, in addition to the number of circulating EPCs, the function of EPCs might also play an important role in vascular repair. Unfortunately, the function of EPCs was not measured in this study.

Conflicts of interests

None of the authors has a real or perceived conflict of interest or has received any personal or financial support.

References

  1. Stehouwer CDA, Ferreira I: Diabetes, lipids and other cardiovascular risk factors. Arterial stiffness in Hypertension. Edited by: Safar ME and O'Rourke MF. 2006, Amsterdam, The Netherlands: Elsevier, 427-456.

    Google Scholar 

  2. Cruickshank K, Riste L, Anderson SG, Wright JS, Dunn G, Gosling RG: Aortic pulse-wave velocity and its relationship to mortality in diabetes and glucose intolerance: An integrated index of vascular function?. Circulation. 2002, 106: 2085-2090. 10.1161/01.CIR.0000033824.02722.F7.

    Article  PubMed  Google Scholar 

  3. Creager MA, Lüscher TF, Cosentino F, Beckman JA: Diabetes and vascular disease: pathophysiology, clinical consequences, and medical therapy: Part I. Circulation. 2003, 108: 1527-1532. 10.1161/01.CIR.0000091257.27563.32.

    Article  PubMed  Google Scholar 

  4. Hamed S, Brenner B, Roguin A: Nitric oxide: a key factor behind the dysfunctionality of endothelial progenitor cells in diabetes mellitus type-2. Cardiovasc Res. 2011, 91: 9-15. 10.1093/cvr/cvq412.

    Article  CAS  PubMed  Google Scholar 

  5. Hamed S, Brenner B, Aharon A, Daoud D, Roguin A: Nitric oxide and superoxide dismutase modulate endothelial progenitor cell function in type 2 diabetes mellitus. Cardiovasc Diabetol. 2009, 8: 56-10.1186/1475-2840-8-56.

    Article  PubMed Central  PubMed  Google Scholar 

  6. Alberti KG, Zimmet PZ: Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med. 1998, 15: 539-553. 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO;2-S.

    Article  CAS  PubMed  Google Scholar 

  7. Wong CY, Qiuwaxi J, Chen H, Li SW, Chan HT, Tam S, Shu XO, Lau CP, Kwong YL, Tse HF: Daily intake of thiamine correlates with the circulating level of endothelial progenitor cells and the endothelial function in patients with type II diabetes. Mol Nutr Food Res. 2008, 52: 1421-1427. 10.1002/mnfr.200800056.

    Article  CAS  PubMed  Google Scholar 

  8. Tsuchikura S, Shoji T, Kimoto E, Shinohara K, Hatsuda S, Koyama H, Emoto M, Nishizawa Y: Brachial-ankle pulse wave velocity as an index of central arterial stiffness. J Atheroscler Thromb. 2010, 17: 658-665. 10.5551/jat.3616.

    Article  PubMed  Google Scholar 

  9. Quyyumi AA: Endothelial function in health and disease: new insights into the genesis of cardiovascular disease. Am J Med. 1998, 105: 32S-39S. K

    Article  CAS  PubMed  Google Scholar 

  10. Kawashima S: The two faces of endothelial nitric oxide synthase in the pathophysiology of atherosclerosis. Endothelium. 2004, 11: 99-107. 10.1080/10623320490482637.

    Article  CAS  PubMed  Google Scholar 

  11. Gabbay KH: Hyperglycemia, polyol metabolism, and complications of diabetes mellitus. Annu Rev Med. 1975, 26: 521-536. 10.1146/annurev.me.26.020175.002513.

    Article  CAS  PubMed  Google Scholar 

  12. Baumgartner-Parzer SM, Wagner L, Pettermann M, Grillari J, Gessl A, Waldhäusl W: High-glucose-triggered apoptosis in cultured endothelial cells. Diabetes. 1995, 44: 1323-1327. 10.2337/diabetes.44.11.1323.

    Article  CAS  PubMed  Google Scholar 

  13. Chen S, Apostolova MD, Cherian MG, Chakrabarti S: Interaction of endothelin-1 with vasoactive factors in mediating glucose-induced increased permeability in endothelial cells. Lab Invest. 2000, 80: 1311-1321. 10.1038/labinvest.3780139.

    Article  CAS  PubMed  Google Scholar 

  14. van den Oever IA, Raterman HG, Nurmohamed MT, Simsek S: Endothelial dysfunction, inflammation, and apoptosis in diabetes mellitus. Mediators Inflamm. 2010, 2010: 792393.

    PubMed Central  PubMed  Google Scholar 

  15. Dagher Z, Park YS, Asnaghi V, Hoehn T, Gerhardinger C, Lorenzi M: Studies of rat and human retinas predict a role for the polyol pathway in human diabetic retinopathy. Diabetes. 2004, 53: 2404-2411. 10.2337/diabetes.53.9.2404.

    Article  CAS  PubMed  Google Scholar 

  16. Harrison DG: Cellular and molecular mechanisms of endothelial cell dysfunction. J Clin Invest. 1997, 100: 2153-2157. 10.1172/JCI119751.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  17. Watson PA, Nesterova A, Burant CF, Klemm DJ, Reusch JE: Diabetes-related changes in cAMP response element-binding protein content enhance smooth muscle cell proliferation and migration. J Biol Chem. 2001, 276: 46142-46150. 10.1074/jbc.M104770200.

    Article  CAS  PubMed  Google Scholar 

  18. Asahara T, Murohara T, Sullivan A, Silver M, van der Zee R, Li T, Witzenbichler B, Schatteman G, Isner JM: Isolation of putative progenitor endothelial cells for angiogenesis. Science. 1997, 275: 964-967. 10.1126/science.275.5302.964.

    Article  CAS  PubMed  Google Scholar 

  19. Hill JM, Zalos G, Halcox JP, Schenke WH, Waclawiw MA, Quyyumi AA, Finkel T: Circulating endothelial progenitor cells, vascular function, and cardiovascular risk. N Engl J Med. 2003, 348: 593-600. 10.1056/NEJMoa022287.

    Article  PubMed  Google Scholar 

  20. Tepper OM, Galiano RD, Capla JM, Kalka C, Gagne PJ, Jacobowitz GR, Levine JP, Gurtner GC: Human endothelial progenitor cells from type II diabetics exhibit impaired proliferation, adhesion, and incorporation into vascular structures. Circulation. 2002, 106: 2781-2786. 10.1161/01.CIR.0000039526.42991.93.

    Article  PubMed  Google Scholar 

  21. Churdchomjan W, Kheolamai P, Manochantr S, Tapanadechopone P, Tantrawatpan C, U-Pratya Y, Issaragrisil S: Comparison of endothelial progenitor cell function in type 2 diabetes with good and poor glycemic control. BMC Endocr Disord. 2010, 10: 5-10.1186/1472-6823-10-5.

    Article  PubMed Central  PubMed  Google Scholar 

  22. Fadini GP, Boscaro E, de Kreutzenberg S, Agostini C, Seeger F, Dimmeler S, Zeiher A, Tiengo A, Avogaro A: Time course and mechanisms of circulating progenitor cell reduction in the natural history of type 2 diabetes. Diabetes Care. 2010, 33: 1097-1102. 10.2337/dc09-1999.

    Article  PubMed Central  PubMed  Google Scholar 

  23. Dessapt-Baradez C, Reza M, Sivakumar G, Hernandez-Fuentes M, Markakis K, Gnudi L, Karalliedde J: Circulating vascular progenitor cells and central arterial stiffness in polycystic ovary syndrome. PLoS One. 2011, 6: e20317-10.1371/journal.pone.0020317.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  24. Liao YF, Chen LL, Zeng TS, Li YM, Fan Yu, Hu LJ, Ling Yue: Number of circulating endothelial progenitor cells as a marker of vascular endothelial function for type 2 diabetes. Vasc Med. 2010, 15: 279-285. 10.1177/1358863X10367537.

    Article  PubMed  Google Scholar 

  25. Palombo C, Kozakova M, Morizzo C, Gnesi L, Barsotti MC, Spontoni P, Massart F, Salvi P, Balbarini A, Saggese G, Di Stefano R, Federico G: Circulating endothelial progenitor cells and large artery structure and function in young subjects with uncomplicated type 1 diabetes. Cardiovasc Diabetol. 2011, 10: 88-10.1186/1475-2840-10-88.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  26. ADVANCE Collaborative Group, Patel A, MacMahon S, Chalmers J, Neal B, Billot L, Woodward M, Marre M, Cooper M, Glasziou P, Grobbee D, Hamet P, Harrap S, Heller S, Liu L, Mancia G, Mogensen CE, Pan C, Poulter N, Rodgers A, Williams B, Bompoint S, de Galan BE, Joshi R, Travert F: Intensive blood glucose control and vascular outcomes in patients with type 2 diabetes. N Engl J Med. 2008, 358: 2560-2572.

    Article  Google Scholar 

  27. ACCORD Study Group, Gerstein HC, Miller ME, Genuth S, Ismail-Beigi F, Buse JB, Goff DC, Probstfield JL, Cushman WC, Ginsberg HN, Bigger JT, Grimm RH, Byington RP, Rosenberg YD, Friedewald WT: Long-term effects of intensive glucose lowering on cardiovascular outcomes. N Engl J Med. 2011, 364: 818-828.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Cardiology Division, Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China

    Wen-Sheng Yue, Chung-Wah Siu, Mei Wang, Guo-Hui Yan, Kai-Hang Yiu & Hung-Fat Tse

  2. Medical Imaging Key Laboratory of Sichuan Province & Affiliated Hospital of North Sichuan Medical College, Nanchong, China

    Wen-Sheng Yue

  3. Neurology Division, Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China

    Kui-Kai Lau

  4. Research Center of Heart, Brain, Hormone and Healthy Aging, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China

    Kui-Kai Lau, Chung-Wah Siu, Mei Wang, Kai-Hang Yiu & Hung-Fat Tse

Authors
  1. Wen-Sheng Yue
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Kui-Kai Lau
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Chung-Wah Siu
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Mei Wang
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Guo-Hui Yan
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Kai-Hang Yiu
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Hung-Fat Tse
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Hung-Fat Tse.

Additional information

Authors' contributions

WSY planned the study, collected the data, performed the statistical analysis and was involved in the preliminary writing of the manuscript. KKL and CWS was involved in writing of the manuscript. MW, GHY and KHY was involved in data collection. HFT supervised the project and with writing of the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Rights and permissions

Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Yue, WS., Lau, KK., Siu, CW. et al. Impact of glycemic control on circulating endothelial progenitor cells and arterial stiffness in patients with type 2 diabetes mellitus. Cardiovasc Diabetol 10, 113 (2011). https://doi.org/10.1186/1475-2840-10-113

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1475-2840-10-113

Keywords

Cardiovascular Diabetology

ISSN: 1475-2840