Effects of a Physical Activity Program on Markers of Endothelial Dysfunction, Oxidative Stress, and Metabolic Status in Adolescents with Metabolic Syndrome

Camarillo-Romero, Eneida; Dominguez-Garcia, Ma Victoria; Amaya-Chavez, Araceli; Camarillo-Romero, Maria del Socorro; Talavera-Piña, Juan; Huitron-Bravo, Gerardo; Majluf-Cruz, Abraham

doi:https://doi.org/10.5402/2012/970629

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Volume 2012 | Article ID 970629 | https://doi.org/10.5402/2012/970629

Effects of a Physical Activity Program on Markers of Endothelial Dysfunction, Oxidative Stress, and Metabolic Status in Adolescents with Metabolic Syndrome

Eneida Camarillo-Romero,¹Ma Victoria Dominguez-Garcia,¹Araceli Amaya-Chavez,²Maria del Socorro Camarillo-Romero,¹Juan Talavera-Piña,^1,3Gerardo Huitron-Bravo,¹and Abraham Majluf-Cruz⁴

Academic Editor: C.-F. Kwok, P. Balagopal

Received11 Apr 2012

Accepted15 May 2012

Published25 Jul 2012

Abstract

The metabolic syndrome (MetS) is a precursor of diabetes. Physical activity (PA) improves endothelial dysfunction and may benefit patients with MetS. Aims. To evaluate the effect of a physical activity (PA) program on markers of endothelial dysfunction and oxidative stress in adolescents with (MetS). Methods. We carried out a cohort study of 38 adolescents with and without MetS (18 females and 20 males). All participants completed a 3-month PA program. All variables of the MetS as well as markers of endothelial dysfunction and oxidative stress tests were evaluated. Results. Females with and without MetS showed significant differences for almost all components of the MetS, whereas males were significantly different in half of the components. After the PA program, components of the MetS were not different from baseline values except for HDL-C levels. Some baseline endothelial dysfunction markers were significantly different among adolescents with and without MetS; however, after the PA program, most of these markers significantly improved in subjects with and without MetS. Conclusion. PA improves the markers of endothelial dysfunction in adolescents with MetS although other changes in the components of the MetS were not observed. Perhaps the benefits of PA on all components of MetS would appear after a PA program with a longer duration.

1. Introduction

Metabolic syndrome (MetS) is a cluster of several atherothrombotic risk factors and is considered to be a precursor of atherothrombotic diseases and diabetes mellitus [1]. Several criteria have been proposed for diagnosis of MetS. The importance of establishing the diagnosis of MetS is that these individuals have a 1.5- to 2.0-fold increase in risk for atherothrombotic events [2], a predictive effect that is similar to that of the Framingham Score [3].

The prevalence of MetS in adolescents according to the Adult Treatment Panel III (ATP-III) definition varies significantly. For example, the prevalence of MetS is higher in Mexico than in the US (19.6% versus 8.6%, resp.) [4, 5]. However, when the criteria of the International Diabetes Federation (IDF) are used, the prevalence of MetS in Mexico and the U.S. does not differ greatly (8.2% versus 4.5%, resp.) [6, 7]. In overweight or obese adolescents, the incidence of MetS increases to 38% and 50%, respectively [6, 8].

Children older than 10 years with overweight or obesity have a high risk for the development of dyslipidemia, arterial hypertension, abnormalities in carbohydrate metabolism, and prothrombotic and proinflammatory states [9]. One necropsy study in adolescents and young adults demonstrated that all the above-mentioned atherogenic conditions begin very early in life [10]. Obese children without other risk factors have markers of endothelial cell (EC) dysfunction [11, 12]. In obese adolescents, markers of EC dysfunction such as high-sensitivity C-reactive protein (hsCRP) and soluble cell adhesion molecules (CAMs) have been described in association with the early stages of the atherosclerotic process. These facts strongly suggest that endothelial dysfunction is one of the seminal pathophysiological abnormalities in atherosclerosis and that its detection may possibly be used as an early marker of atherothrombotic disease [11].

Several studies have fully demonstrated the beneficial effects of physical activity (PA) in different groups in healthy controls and in patients with several pathological states [13–18], including MetS [19]. This body of evidence also shows that, in adults, PA induces beneficial local and systemic changes in the fibrinolytic system as well as in the vascular metabolism and muscles that may protect against atherothrombotic events.

Due to the very well-known beneficial effects of PA in adult patients with MetS, the aim of this study was to evaluate the effects of a PA program on metabolic parameters and markers of endothelial cell dysfunction and oxidative stress in adolescents with MetS.

2. Materials and Methods

2.1. Study Design

A cohort study including 1200 healthy adolescents between 14 and 16 years of age was carried out between February 2011 and May 2011. A search for MetS was performed. Finally, 575 adolescents accepted to participate (207 males and 368 females) (Figure 1). According to the IDF criteria, 47 participants (8.2%) had MetS. Because waist circumference was higher than the 90th percentile, which was above the cut-off level according to the IDF definition, we used the criteria for adults (males ≥90 cm; females ≥80 cm). Measurement of waist circumference was standardized and strictly evaluated according to the recommendation of the World Health Organization (WHO) [20]. Blood pressure was evaluated twice with a mercury sphygmomanometer with the subjects in a seated position after a resting period [21].

2.2. Interventions

For this study we included 38 age- and gender-matched adolescents (18 females and 20 males): 19 with MetS and 19 without MetS. Exclusion criteria included smoking and presence of infectious disease at the time of evaluation or during the 15 days prior to enrollment or taking anti-inflammatory or antihistamine drugs during the same time period. Alcohol intake during the study was highly discouraged. Pregnancy was always considered as an exclusion criterion. Both groups participated in a 3-month PA program. The program was designed to exercise 45 min/day for 5 days/week with an intermediate intensity (cardiac rate = 60% to 70%, 3 to 6 METs/min) as monitored with a heart rate monitor. This program was designed and supervised by an international certificated instructor. Importantly, although some dietary advice was offered, no specific changes in dietary habits or meal characteristics were indicated to the study participants.

Before and after the PA program, fasting blood samples (10 mL) were obtained using a vacuum system. Blood was drawn in vacuum tubes containing either sodium citrate 3.8% (vol : vol, 1 : 9), heparin, EDTA, and in another tube without anticoagulant. All tubes were centrifuged for 10 min at 500 g in order to obtain platelet-poor plasma and serum. Triglycerides (TGs), high-density lipoprotein cholesterol (HDL-C), and fasting glucose measurements were performed on the same day of the collection using an enzymatic assay (RX Daytona Randox Laboratories Ltd., County Antrim, UK). We measured soluble vascular cell adhesion molecule (VCAM-1) and P-selectin (Invitrogen, Carlsbad, CA, USA). Also, plasma von Willebrand factor (vWF) was evaluated using a commercially available kit (Asserachrome vWF : Ag, Stago, Asnieres, France). hsCRP was assayed using a commercially available kit (CRPH High Sensitivity C-Reactive Protein Reagent; Beckman Coulter; Mervue, Galway, Ireland) in an automated equipment system (IMMAGER Immunochemistry System; Beckman Coulter). Several fibrinolytic variables were evaluated, namely, plasminogen activator inhibitor (PAI-1) (Asserachom PAI-1, Stago), tissue plasminogen activator (tPA) (Asserachrom tPA, Stago), factor VIII (FVIII) (STA Factor VIII, Stago), and fibrinogen (Fibrinogen Reagent, Stago). Hemoglobin was evaluated in the blood collected in EDTA tubes using an AcT Diff Hematology Analyzer (Beckman Coulter, Fullerton, CA, USA). Heparinized blood was used for assays evaluating oxidative stress. Lipoperoxidation, enzymatic activity of superoxide dismutase, catalase activity, and glutathione peroxidase activity were evaluated according to previously described and validated methods [22–25].

2.3. Statistical Analysis

We described baseline value and values after the PA program (mean and standard deviation) of the components of the MetS as well as markers of inflammation, EC dysfunction, and oxidative stress. Differences of these variables between cases and controls were established using Student’s t-test. We then described the mean and standard deviation of the same variables in males and females after application of the PA program. Before and after results were compared using a paired t-test, significant differences were considered when . All statistical analyses were performed using a Statistical Package for the Social Sciences (SPSS) software (v.16; SPSS Inc., Chicago, IL, USA).

2.4. Ethical Considerations

Before entering the study, all participants and their parents were informed about the characteristics and objectives of the investigation. Signed informed consent was obtained from the parents and from each adolescent. The study was conducted according to all the principles of the Declaration of Helsinki. The protocol was approved by the ethics committee of our research center.

3. Results

As previously mentioned, 19 adolescents (9 females and 10 males) with MetS were included and compared with a paired control group without MetS. Baseline general characteristics of the adolescents in both groups are shown in Table 1. Females with and without MetS showed differences for all the components of the MetS, except for diastolic blood pressure. On the contrary, males with and without MetS were significantly different in only half of the components of the MetS. After completing the PA program, most of the components of the MetS were not significantly different from baseline levels in adolescent females and males, with and without MetS (Table 2). Only levels of HDL-C significantly increased after the PA program in females and males in both groups. Also, in females and males with MetS, a significant reduction in fasting glucose levels was observed after the PA program.

Table 3 shows baseline levels of markers of EC dysfunction. As shown, only some variables were different in males and females with and without MetS. However, when we compared the data in regard to the same markers after completing the PA program, most inflammatory and EC dysfunction markers decreased in all study participants with and without MetS (Table 4). As depicted in Table 4, results of the analysis of oxidative stress were contradictory.

4. Discussion

4.1. Metabolic Syndrome and Endothelial Cell Dysfunction

MetS is caused by a combination of genetic factors, poor dietary habits, and sedentary lifestyle. It is a major risk factor for atherothrombotic diseases [26]. According to some cohorts of adolescents from several countries, the prevalence of MetS ranges from 8.2 to 12.6% [6].

Upon appropriate stimulation with inflammatory mediators the endothelium may become dysfunctional. Endothelial dysfunction is defined as impairment in any of the normal functions of the ECs leading to vasoconstriction, thrombosis, upregulation of CAMs, increased cytokine and chemokine secretion, and leukocyte adherence, among others. EC dysfunction is regarded as a precursor for atherogenesis, and it is associated with a high risk of atherothrombotic events [27, 28]. Therefore, EC dysfunction seems to be the common link between risk factors and atherosclerosis. Thus, restoration of normal EC function is a highly desirable therapeutic goal.

4.2. Endothelial Cell Dysfunction and Atherosclerosis

ECs have other functions in addition to the regulation of vascular tone. Today it is possible to measure plasma or serum constituents as alternative markers of endothelial function. For example, CAMs are expressed on the surface of ECs in response to endothelial dysfunction, and their circulating levels are considered as surrogate markers of dysfunction, or damage [29]. Elevated soluble CAMs are found in patients with vascular risk factors and early or established atherosclerosis and may predict future atherothrombotic events [29]. On the other hand, thrombus is central to the progression of atherosclerosis. Several blood coagulation factors are proposed as markers of EC dysfunction, namely, increased vWF, fibrinogen, tPA, and PAI-1 [30]. Also, hsCRP are a predictor of atherothrombotic disease [31]. Because atherosclerosis is an inflammatory process, markers of inflammation such as hsCRP is an indirect marker of EC dysfunction and may be useful for global assessment of atherothrombotic risk, especially among individuals without known atherothrombotic disease [29]. Finally, because oxidoreduction is important for the regulation of EC function, oxidative stress contributes to EC dysfunction and may be central in atherogenesis due to increased lipoperoxidation and free radical production [32]. Reactive oxygen species may interact with proteins, lipids, and DNA, and their excessive production is implicated in atherogenesis [33].

4.3. Effects of PA on Markers of Endothelial Cell Dysfunction and Metabolic Variables

We attempted to determine the pattern of markers of EC dysfunction before and after a PA program in adolescents with and without MetS. We measured several markers of endothelial dysfunction which are widely used and accepted in the literature [12, 15, 17–19, 34–36]. As expected, we found significant differences for the components of the MetS between male and female adolescents with and without this syndrome. These differences were found for most of the components, a fact that suggests that, indeed, we had two significantly different populations from a metabolic perspective. Although there was a trend towards lower levels of most of the markers of EC dysfunction, results were not significant between adolescents with MetS versus those without MetS. An explanation for this finding may be that some adolescents of the control group had one or more of the components of the MetS, although they did not fulfill the criteria to be considered carriers of the syndrome. However, as previously shown, some of the clinical criteria of the MetS may directly induce EC dysfunction. As a consequence, some control individuals may have markers of EC dysfunction, although they did not fulfill the criteria to be considered as carriers of MetS, a fact that impeded us to find significant differences between groups.

Our most important findings appeared after the PA program. We found significant changes in HDL-C levels in all groups; however, no changes were found for TG as previously shown [37]. An explanation for this finding may be that we did not include a dietary intervention; thus, some adolescents may increase their intake of carbohydrates. Glucose improved only in the groups of adolescents with MetS, and blood pressure did not change and may be explained because this was the most infrequent component of the MetS in our study population. Regarding analysis of markers of EC dysfunction, we found a significant effect in most of these markers after the completion of the PA program. In terms of inflammatory markers, only hsCRP was not modified, and a similar nonbeneficial effect was observed for the majority of the oxidative stress tests. Only lipoperoxidation levels were significantly lower in male and female adolescents with MetS. On the contrary, the most important findings in our research derived from the changes in the EC dysfunction markers in adolescents with MetS as well as in the controls without MetS, as previously described in healthy populations [13]. Except for vWF levels, almost all markers of EC dysfunction significantly improved after exercising, even for P-selectin levels in male adolescents with MetS. These did not reach significant differences but there is a clear trend towards improvement after PA.

The effects observed after the PA program are not that surprising. Indeed, many atherothrombotic risk factors associated with MetS can be reduced or eliminated through weight control, diet, and, most importantly, regular exercise [38]. PA induces beneficial effects in patients with chronic heart failure, coronary artery disease, arterial hypertension, and hypercholesterolemia [14, 39]. Moderate-vigorous daily PA prevents both the incidence of chronic diseases and premature death [40]. The positive effects of PA include increased expression of nitric oxide synthase and EC-derived superoxide dismutase, improvement in vascular structure and local and systemic fibrinolysis, and improvement of coronary EC function [41–43]. Regular PA helps in achieving appropriate weight loss and improves insulin sensitivity and EC function in insulin-resistant individuals [44]. Also, there is a significant association between PA and a reduction of inflammatory cytokine levels, an effect that is associated with improvement of the EC function [45]. Finally, it has been shown that PA improves EC function by increasing the bioavailability of nitric oxide although its beneficial effect is lost within weeks after the end of training [46]. This body of evidence suggests that EC function is modulated by the extent of daily PA.

4.4. Study Limitations

In this study we found a beneficial effect of PA on markers of EC dysfunction, namely, CAMs and blood coagulation markers; however, we could not demonstrate a positive consequence for other variables such as hsCRP and oxidative stress tests. We can hypothesize that this lack of effect may be due to a PA program of insufficient length to induce the desired changes. Perhaps each marker of EC dysfunction requires a specific time in order to be reversed with PA, and such timing possibly was not fully achieved in our study for all variables analyzed.

Most studies on EC dysfunction have been performed in adults with specific pathological states and only a few have addressed children and adolescents [47]. In adolescents, a 45 min/day moderate PA significantly reduces the risk of MetS, prevents overweight, effectively reduces weight, and improves the oxidative and cytokine profile [48, 49]. However, most of these studies are cross-sectional, and, to our knowledge, none of the previous studies has shown the beneficial effects of PA on markers of EC dysfunction.

5. Conclusions

We have shown that a PA program effectively reduces the levels of several markers of EC dysfunction in adolescents with MetS, although these beneficial changes are not associated with the expected changes in the clinical components of the MetS. Perhaps these benefits on EC dysfunction markers may be increased or extended either to inflammation markers, to oxidative stress tests, or to the clinical components of MetS with a PA program beyond 3 months.

Conflict of Interests

The authors declare that they have no conflict of interests.

Acknowledgments

This work was carried out with a grant from the Programa Nacional de Posgrado CONACYT and from the Universidad Autonoma del Estado de Mexico (2571/2007U). A. Majluf-Cruz is the recipient of a grant from Fundacion IMSS.

References

Expert Panel on Detection, Evaluation and Treatment of High Blood Cholesterol in Adults, “Executive summary of the third report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III),” Journal of the American Medical Association, vol. 285, no. 19, pp. 2486–2497, 2001.
View at: Google Scholar
A. M. McNeill, W. D. Rosamond, C. J. Girman et al., “The metabolic syndrome and 11-year risk of incident cardiovascular disease in the atherosclerosis risk in communities study,” Diabetes Care, vol. 28, no. 2, pp. 385–390, 2005.
View at: Publisher Site | Google Scholar
J. M. Baena-Diez, M. Grau, R. Sanchez-Perez, E. Altes-Vaques, and L. Salas-Gaetjens, “La función calibrada REGICOR mejora la clasificación de los pacientes de alto riesgo tratados con estatinas respecto a Framingham y SCORE en la población española,” Revista Española de Cardiolologia, vol. 62, no. 10, pp. 1134–1140, 2009.
View at: Publisher Site | Google Scholar
E. H. Castillo, G. Borges, J. O. Talavera et al., “Body mass index and the prevalence of metabolic syndrome among children and adolescents in two mexican populations,” Journal of Adolescent Health, vol. 40, no. 6, pp. 521–526, 2007.
View at: Publisher Site | Google Scholar
W. D. Johnson, J. J. M. Kroon, F. L. Greenway, C. Bouchard, D. Ryan, and P. T. Katzmarzyk, “Prevalence of risk factors for metabolic syndrome in adolescents: national health and nutrition examination survey (NHANES), 2001–2006,” Archives of Pediatrics and Adolescent Medicine, vol. 163, no. 4, pp. 371–377, 2009.
View at: Publisher Site | Google Scholar
E. Camarillo-Romero, M. V. Domínguez Garcia, A. Amaya-Chavez, G. Huitron-Bravo, and A. Majluf-Cruz, “Dificultades en la clasificación del síndrome metabólico. El ejemplo de los adolescentes mexicanos,” Salud Publica de Mexico, vol. 52, no. 6, pp. 524–527, 2010.
View at: Google Scholar
E. S. Ford, C. Li, G. Zhao, W. S. Pearson, and A. H. Mokdad, “Prevalence of the metabolic syndrome among U.S. adolescents using the definition from the international diabetes federation,” Diabetes Care, vol. 31, no. 3, pp. 587–589, 2008.
View at: Publisher Site | Google Scholar
R. Weiss, J. Dziura, T. S. Burgert et al., “Obesity and the metabolic syndrome in children and adolescents,” The New England Journal of Medicine, vol. 350, no. 23, pp. 2362–2374, 2004.
View at: Publisher Site | Google Scholar
N. Mauras, C. DelGiorno, C. Kollman et al., “Obesity without established comorbidities of the metabolic syndrome is associated with a proinflammatory and prothrombotic state, even before the onset of puberty in children,” Journal of Clinical Endocrinology and Metabolism, vol. 95, no. 3, pp. 1060–1068, 2010.
View at: Publisher Site | Google Scholar
H. C. McGill Jr., C. A. McMahan, A. W. Zieske et al., “Association of coronary heart disease risk factors with microscopic qualities of coronary atherosclerosis in youth,” Circulation, vol. 102, no. 4, pp. 374–379, 2000.
View at: Google Scholar
S. Kapiotis, G. Holzer, G. Schaller et al., “A proinflammatory state is detectable in obese children and is accompanied by functional and morphological vascular changes,” Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 26, no. 11, pp. 2541–2546, 2006.
View at: Publisher Site | Google Scholar
O. J. MacEneaney, M. Harrison, D. J. O'Gorman, E. V. Pankratieva, P. L. O'Connor, and N. M. Moyna, “Effect of prior exercise on postprandial lipemia and markers of inflammation and endothelial activation in normal weight and overweight adolescent boys,” European Journal of Applied Physiology, vol. 106, no. 5, pp. 721–729, 2009.
View at: Publisher Site | Google Scholar
L. Jungersten, A. Ambring, B. Wall, and A. Wennmalm, “Both physical fitness and acute exercise regulate nitric oxide formation in healthy humans,” Journal of Applied Physiology, vol. 82, no. 3, pp. 760–764, 1997.
View at: Google Scholar
Y. Higashi, S. Sasaki, S. Kurisu et al., “Regular aerobic exercise augments endothelium-dependent vascular relaxation in normotensive as well as hypertensive subjects: role of endothelium-derived nitric oxide,” Circulation, vol. 100, no. 11, pp. 1194–1202, 1999.
View at: Google Scholar
T. Saetre, E. Enoksen, T. Lyberg et al., “Supervised exercise training reduces plasma levels of the endothelial inflammatory markers E-selectin and ICAM-1 in patients with peripheral arterial disease,” Angiology, vol. 62, no. 4, pp. 301–305, 2011.
View at: Publisher Site | Google Scholar
A. Pinto, D. Di Raimondo, and A. Tuttolomondo, “Effects of physical exercise on inflammatory markers of atherosclerosis,” Current Pharmaceutical Design. In press.
View at: Google Scholar
E. Hopps, B. Canino, and G. Caimi, “Effects of exercise on inflammation markers in type 2 diabetic subjects,” Acta Diabetologica, vol. 48, no. 3, pp. 183–189, 2011.
View at: Publisher Site | Google Scholar
G. Zoppini, G. Targher, C. Zamboni et al., “Effects of moderate-intensity exercise training on plasma biomarkers of inflammation and endothelial dysfunction in older patients with type 2 diabetes,” Nutrition, Metabolism and Cardiovascular Diseases, vol. 16, no. 8, pp. 543–549, 2006.
View at: Publisher Site | Google Scholar
K. Aizawa, J. K. Shoemaker, T. J. Overend, and R. J. Petrella, “Metabolic syndrome, endothelial function and lifestyle modification,” Diabetes and Vascular Disease Research, vol. 6, no. 3, pp. 181–189, 2009.
View at: Google Scholar
World Health Organization, Technical Report Series WHO, Geneva, Switzerland, 1993.
A. V. Chobanian, G. L. Bakris, H. R. Black et al., “Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure,” Hypertension, vol. 42, no. 6, pp. 1206–1252, 2003.
View at: Publisher Site | Google Scholar
J. A. Buege and S. D. Aust, “Microsomal lipid peroxidation,” Methods in Enzymology, vol. 52, no. 8, pp. 302–310, 1978.
View at: Publisher Site | Google Scholar
H. P. Misra and I. Fridovich, “The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase.,” Journal of Biological Chemistry, vol. 247, no. 10, pp. 3170–3175, 1972.
View at: Google Scholar
R. Radi, J. F. Turrens, L. Y. Chang, K. M. Bush, J. D. Crapo, and B. A. Freeman, “Detection of catalase in rat heart mitochondria,” Journal of Biological Chemistry, vol. 266, no. 32, pp. 22028–22034, 1991.
View at: Google Scholar
D. E. Paglia and W. N. Valentine, “Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase,” The Journal of Laboratory and Clinical Medicine, vol. 70, no. 1, pp. 158–169, 1967.
View at: Google Scholar
R. H. Eckel, S. M. Grundy, and P. Z. Zimmet, “The metabolic syndrome,” The Lancet, vol. 365, no. 9468, pp. 1415–1428, 2005.
View at: Publisher Site | Google Scholar
P. Libby, “Current concepts of the pathogenesis of the acute coronary syndromes,” Circulation, vol. 104, no. 3, pp. 365–372, 2001.
View at: Google Scholar
J. A. Suwaidi, S. Hamasaki, S. T. Higano, R. A. Nishimura, D. R. Holmes, and A. Lerman, “Long-term follow-up of patients with mild coronary artery disease and endothelial dysfunction,” Circulation, vol. 101, no. 9, pp. 948–954, 2000.
View at: Google Scholar
H. M. O. Farouque and I. T. Meredith, “The assessment of endothelial function in humans,” Coronary Artery Disease, vol. 12, no. 6, pp. 445–454, 2001.
View at: Publisher Site | Google Scholar
P. Welsh, M. Woodward, A. Rumley, and G. Lowe, “Associations of plasma pro-inflammatory cytokines, fibrinogen, viscosity and C-reactive protein with cardiovascular risk factors and social deprivation: the fourth Glasgow MONICA study,” British Journal of Haematology, vol. 141, no. 6, pp. 852–861, 2008.
View at: Publisher Site | Google Scholar
P. M. Ridker, M. J. Stampfer, and N. Rifai, “Novel risk factors for systemic atherosclerosis: a comparison of C-reactive protein, fibrinogen, homocysteine, lipoprotein(a), and standard cholesterol screening as predictors of peripheral arterial disease,” Journal of the American Medical Association, vol. 285, no. 19, pp. 2481–2485, 2001.
View at: Google Scholar
G. Kojda and D. Harrison, “Interactions between NO and reactive oxygen species: pathophysiological importance in atherosclerosis, hypertension, diabetes and heart failure,” Cardiovascular Research, vol. 43, no. 3, pp. 562–571, 1999.
View at: Publisher Site | Google Scholar
A. S. Kelly, J. Steinberger, D. R. Kaiser, T. P. Olson, A. J. Bank, and D. R. Dengel, “Oxidative stress and adverse adipokine profile characterize the metabolic syndrome in children,” Journal of the cardiometabolic syndrome, vol. 1, no. 4, pp. 248–252, 2006.
View at: Publisher Site | Google Scholar
C. Hoppe, F. Kuypers, S. Larkin, W. Hagar, E. Vichinsky, and L. Styles, “A pilot study of the short-term use of simvastatin in sickle cell disease: effects on markers of vascular dysfunction,” British Journal of Haematology, vol. 153, no. 5, pp. 655–663, 2011.
View at: Publisher Site | Google Scholar
E. Fidan, H. Onder Ersoz, M. Yilmaz et al., “The effects of rosiglitazone and metformin on inflammation and endothelial dysfunction in patients with type 2 diabetes mellitus,” Acta Diabetologica, vol. 48, no. 4, pp. 297–302, 2011.
View at: Publisher Site | Google Scholar
V. J. Karthikeyan, A. D. Blann, S. Baghdadi, D. A. Lane, D. Gareth Beevers, and G. Y. H. Lip, “Endothelial dysfunction in hypertension in pregnancy: associations between circulating endothelial cells, circulating progenitor cells and plasma von Willebrand factor,” Clinical Research in Cardiology, vol. 100, no. 6, pp. 531–537, 2011.
View at: Publisher Site | Google Scholar
K. S. Woo, P. Chook, C. W. Yu et al., “Effects of diet and exercise on obesity-related vascular dysfunction in children,” Circulation, vol. 109, no. 16, pp. 1981–1986, 2004.
View at: Publisher Site | Google Scholar
W. E. Kraus, C. E. Torgan, B. D. Duscha et al., “Studies of a targeted risk reduction intervention through defined exercise (STRRIDE),” Medicine and Science in Sports and Exercise, vol. 33, no. 10, pp. 1774–1784, 2001.
View at: Google Scholar
R. Hambrecht, A. Wolf, S. Gielen et al., “Effect of exercise on coronary endothelial function in patients with coronary artery disease,” The New England Journal of Medicine, vol. 342, no. 7, pp. 454–460, 2000.
View at: Publisher Site | Google Scholar
D. E. R. Warburton, C. W. Nicol, and S. S. D. Bredin, “Health benefits of physical activity: the evidence,” Canadian Medical Association Journal, vol. 174, no. 6, pp. 801–809, 2006.
View at: Publisher Site | Google Scholar
T. Fukai, M. R. Siegfried, M. Ushio-Fukai, Y. Cheng, G. Kojda, and D. G. Harrison, “Regulation of the vascular extracellular superoxide dismutase by nitric oxide and exercise training,” Journal of Clinical Investigation, vol. 105, no. 11, pp. 631–1639, 2000.
View at: Google Scholar
M. J. Rieder, R. Carmona, J. E. Krieger, K. A. Pritchard Jr., and A. S. Greene, “Suppression of angiotensin-converting enzyme expression and activity by shear stress,” Circulation Research, vol. 80, no. 3, pp. 312–319, 1997.
View at: Google Scholar
P. Brambilla, G. Pozzobon, and A. Pietrobelli, “Physical activity as the main therapeutic tool for metabolic syndrome in childhood,” International Journal of Obesity, vol. 35, no. 1, pp. 16–28, 2011.
View at: Publisher Site | Google Scholar
A. S. Kelly, R. J. Wetzsteon, D. R. Kaiser, J. Steinberger, A. J. Bank, and D. R. Dengel, “Inflammation, insulin, and endothelial function in overweight children and adolescents: the role of exercise,” Journal of Pediatrics, vol. 145, no. 6, pp. 731–736, 2004.
View at: Publisher Site | Google Scholar
C. K. Roberts, D. Won, S. Pruthi et al., “Effect of a short-term diet and exercise intervention on oxidative stress, inflammation, MMP-9, and monocyte chemotactic activity in men with metabolic syndrome factors,” Journal of Applied Physiology, vol. 100, no. 5, pp. 1657–1665, 2006.
View at: Publisher Site | Google Scholar
B. Hornig, V. Maier, and H. Drexler, “Physical training improves endothelial function in patients with chronic heart failure,” Circulation, vol. 93, no. 2, pp. 210–214, 1996.
View at: Google Scholar
C. K. Roberts and K. K. Sindhu, “Oxidative stress and metabolic syndrome,” Life Sciences, vol. 84, no. 21-22, pp. 705–712, 2009.
View at: Publisher Site | Google Scholar
C. K. Roberts, D. Won, S. Pruthi, S. S. Lin, and R. J. Barnard, “Effect of a diet and exercise intervention on oxidative stress, inflammation and monocyte adhesion in diabetic men,” Diabetes Research and Clinical Practice, vol. 73, no. 3, pp. 249–259, 2006.
View at: Publisher Site | Google Scholar
G. P. Nassis, K. Papantakou, K. Skenderi et al., “Aerobic exercise training improves insulin sensitivity without changes in body weight, body fat, adiponectin, and inflammatory markers in overweight and obese girls,” Metabolism, vol. 54, no. 11, pp. 1472–1479, 2005.
View at: Publisher Site | Google Scholar

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Copyright © 2012 Eneida Camarillo-Romero 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.

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