The Effect of Aerobic Exercise Training on Oxidized LDL Cholesterol (Ox-LDL) Levels and Some Cardiovascular Risk Factors in Women with Obesity

authors:

avatar Mahtab Sadeghi 1 , avatar Amin Mohammadi ORCID 1 , * , avatar Ali Khajehlandi 1

Department of Physical Education, Gachsaran Branch, Islamic Azad University, Gachsaran, Iran

How To Cite Sadeghi M, Mohammadi A, Khajehlandi A. The Effect of Aerobic Exercise Training on Oxidized LDL Cholesterol (Ox-LDL) Levels and Some Cardiovascular Risk Factors in Women with Obesity. Jundishapur J Health Sci. 2019;11(2):e87511. https://doi.org/10.5812/jjhs.87511.

Abstract

Background:

Today, the prevalence of obesity is seen as a major social challenge, affecting the general health of societies, which creates irreversible psychological, social, and economic consequences. In this regard, exercise training is one of the most important interventions in preventing and controlling obesity and the associated metabolic factors, which can be an appropriate and low-cost option for promoting community health and to some extent, managing metabolic diseases.

Objectives:

The present study was aimed at evaluating the impact of eight weeks of aerobic exercises on the levels of oxidized LDL cholesterol (Ox-LDL) and cardiovascular risk factors among obese and overweight females.

Methods:

This study was conducted in Gachsaran, Iran in 2018. Following a public call for inclusion as part of this quasi-experimental study, 22 obese women who met the inclusion criteria that was set for the study were chosen and were then divided into experimental (exercise training) (n = 11) and control (n = 11) groups. The subjects in the experimental group ran for eight weeks, three sessions per week for 45 minutes at an intensity of 55% to 65% of maximal oxygen consumption (Vo2max). Independent and paired sample t-test were used to account for the variations. For statistical analysis SPSS-21 software was used, and the significance level was set to be less than P < 0.05.

Results:

The findings indicated that the participants’ body mass indices in the experimental group significantly decreased (P < 0.001). In addition, it was found that insulin resistance (HOMA-IR), insulin, glucose and lipoproteins (LDL-TC-TG), and C-reactive protein (CRP) were significantly diminished (P < 0.001), whereas the high-density lipoprotein (HDL) level went up (P < 0.001) following the treatment. No significant changes in Ox-LDL were found after eight weeks of aerobic exercise training (P = 0.07).

Conclusions:

It seems that eight weeks of exercise training with decreasing anthropometric indices, CRP levels, and insulin resistance, even without changing the levels of Ox-LDL, can prevent obesity and metabolic complications.

1. Background

Today, the prevalence of obesity is seen as a major social challenge in various areas of health, especially in the public health sector (1). Obesity is one of the key risk factors in a number of diseases, such as cardiovascular disease, diabetes, high blood pressure, metabolic disorders, and various types of cancer (2). Obese people are more susceptible to risk as well as chronic and endemic diseases, and ultimately these people face a reduction in life expectancy and early death. Sedentary lifestyle, unhealthy diet, obesity, overweight, and unknown genetic factors are factors associated with metabolic syndrome (3). In this vein, metabolic syndrome is one of the most common and rising diseases in the world and its basic causes can be attributed to obesity, genetic factors, and physical inactivity. The metabolic syndrome is closely related to the metabolic disorder of insulin resistance, in which the sensitivity of the tissues of the body to the normal functioning of insulin is impaired. Insulin resistance is a path physiologic disorder that occurs due to a defect in the pathways through which insulin stimulates glucose uptake (4).

On the other hand, fat mass gain in obese people is accompanied by a change in the secretion of adipokines (5). It is now believed that macrophages absorbed from the bloodstream into adipose tissue are the main source of inflammation in obesity. Minor chronic inflammation is associated with higher than normal levels of several cytokines, including alpha tumor necrotizing factor (TNF-α), interleukin 6 (IL-6), and C-reactive protein (CRP) (6). Evidence suggests that levels of inflammatory markers are high in obesity, and a high correlation exists between these inflammatory markers and metabolic-heart problems. The information suggests that inflammation could play a key function in the pathogenesis of metabolic syndrome (5). In recent years, C-reactive protein, as an inflammatory agent, can directly contribute to the pathogenesis of atherosclerosis. Although this substance is produced in the liver, new research has shown that it can be built in the intimal layer of the artery with atherosclerosis as well. Apart from the role of the inflammatory marker, CRP can cause vasodilatation by various mechanisms, such as decreasing nitric oxide production (NO), increasing molecular adhesion, and altering low-density lipoprotein (LDL) adsorption by macrophages. Increasing this protein as the most sensitive inflammatory marker and independent anticipatory indicator of cardiovascular risk rises the risk of cardiovascular events by two to five times (7). It may also be part of the inflammation caused by the accumulation of fat mass and lipid profiles due to undesirable oxidative stress and peroxidation of lipids, especially as it affects the fat deposits in the arteries. Oxidized LDL cholesterol (Ox-LDL) is considered as one of the most important factors in initiating and accelerating vascular fat accumulation and sedimentation (8). Studies have shown that Ox-LDL’s atherogenic property is greater than low-density lipoprotein cholesterol (LDL-C). Low-density lipoprotein oxidation stimulates monocytes, followed by accumulation of vascular macrophages, which are afflicted with arterial cramps (9, 10). In fact, the formation of Ox-LDL from LDL indicates a rise in oxidative stress that ultimately results in the destruction of endothelium tissue with the participation of free radicals, and, together with the progression of atherosclerotic lesions, in particular, the precipitation of cholesterol, and the creation of plaque reduces the vascular function against inflammation. Given the prevalence of obesity and the rapid progression of this complication in the population, research has focused on regulating and balancing body weight, therefore, it is necessary to pay more attention to this problem and provide cost-effective and affordable ways for it to be identified and presented. In this regard, encouraging participation in sports activities is an appropriate and cost-effective option, playing a pivotal role in enhancing the health of the community and, to some extent, managing metabolic diseases. Therefore, exercise and sport exercises are one of the important interventions in preventing and controlling obesity and associated metabolic factors.

Research reports reveal contradictory findings, in which some researchers find that regular physical activity is effective in reducing oxidative stress, especially Ox-LDL levels, and consequently effective prevention of atherosclerosis (11). However, it has been reported that high-intensity short-term exercising maximizes oxidative stress, which interferes with the equilibrium between reactive oxygen species (ROS) and antioxidant defense, which can affect the entire body (12). By contrast, regular aerobic exercise and moderate-intensity exercise increases production and release of antioxidants (13). With regard to the above points, the researcher is addressing the question of how much exercise protocol (aerobic practice) can reduce Ox-LDL and changes in blood lipoproteins. Thus, this study was aimed at investigating the impact of eight-week aerobic exercises on Ox-LDL levels and cardiovascular risk factors among obese and overweight women.

2. Objectives

Obesity and being overweight has become a public health problem over the past 20 years. It has been attributed to many social and environmental determinants. Several studies have linked in this regard; therefore one of the best strategies for preventing obesity and its associated inflammation is participation in regular physical activity. This study was aimed at evaluating the impact of eight weeks of aerobic exercises on the levels of Ox-LDL and cardiovascular risk factors among obese and overweight females.

3. Methods

This study comprised a quasi-experimental design involving a pretest-posttest with the control group. The statistical population of this study included obese and overweight women in 2018 in Gachsaran city. Following a public announcement for participation in this study, those who fulfilled the inclusion criteria, namely not participating in regular sports activities during the past six months, lack of metabolic diseases, lack of alcohol and cigarettes use, and absence of chronic diseases such as cardiovascular and joint diseases, were selected. Then, 22 eligible obese and overweight women aged 35 to 45 years were selected randomly and placed in two groups of experimental (exercise) and control (11). After completing the consent form and physical activities readiness questionnaire (PAR-Q), subjects were evaluated for physical composition measurements.

3.1. Body Composition and Blood Measurements

The height of the subjects was measured without shoes using a height gauge. Measuring people’s weight was made with light clothing, no shoes, and a digital scale of the Seca model (made in Germany). Body mass index (BMI) was measured by dividing the weight (in kilograms) to the square of height (in meters).

Fasting and resting morning blood samples (10 mL) were obtained at the same time preceding and following eight-week treatment. The participants were required to fast at least for half a day, and the fasting blood samples were collected by venipuncture. The Ox-LDL level was determined in duplicate by utilizing enzyme-linked immunosorbent assay (ELISA) kits (Mercodia, Uppsala, Sweden). High-sensitivity C-reactive protein (Hs-CRP) levels were measured in duplicate using enzyme-linked immunosorbent assay (ELISA) kits (Diagnostics Brochem Canada, Inc with a sensitivity 10 ng/mL). Plasma glucose level was measured through the enzymatic (GOD-PAP, Glucose Oxidase-Amino Antipyrine) colorimetric method (Pars Azmoun, Tehran, Iran). The intra and inter-assay coefficients of variation of glucose were found to be < 1.3% with a sensitivity of 1 mg/dl. The serum insulin level was calculated via radioimmunoassay (RIA), and the insulin resistance index was gauged based on the homeostasis model assessment (HOMA-IR). The findings were well consistent with the hyperinsulinemic-euglycemic clamp in diabetic people (5). Automated techniques were used to assay serum cholesterol triglycerides, high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C).

3.2. Exercise Training

The subjects receiving aerobic training attended four exercise training sessions for a period of eight weeks on a weekly basis. The training included a five to 10 minute warm-up followed by muscle stretches. Moreover, it constituted slow-pace jogging and walking at 50% - 55% of the maximal heart rate (HRmax) for 30 - 45 min each day for three days per week and lasted eight weeks. The training involved 30 minutes of walking at the initial sessions and was increased to 45 minutes each session until the end of training. Every exercising session closed with some cooling down activities. The intensity of the exercises were curbed by the researchers via a heart rate monitor in order to ascertain that the heart rate was maintained at the range of 50% and 60% of HRmax during the experiment.

3.3. Statistical Analysis

All data were analyzed through SPSS (version 21). Mean ± and standard deviation (SD) were identified. Independent samples t-test and paired t-test were employed to evaluate shifts among the variables of the study. P values less than 0.05 were considered statistically significant.

4. Results

The results demonstrated that eight weeks of aerobic exercise resulted in a significant reduction in body mass index (t = 5.24 and P = 0.012) in the experimental group. However, these changes were insignificant in the case of the control group. The mean and standard deviation of the variables in the pre-test and post-test are presented in Table 1. The results of independent samples t-test indicated a significant discrepancy in the pre-test and post-test of the experimental group for the main variables including insulin resistance, Hs-CRP. Nonetheless, no significant difference was found in the rate of Ox-LDL after eight weeks of aerobic training. The results of independent t-test on insulin resistance (t = 3.48 and P = 0.002) and Hs-CRP (t = 17.204 and P = 0.001) index variables showed a significant difference between the experimental and control groups after eight weeks of exercise training, however, there was no significant difference in Ox-LDL index (t = 9.27 and P = 0.07).

Table 1.

Anthropometric and Metabolic Characteristics of the Subjects Prior to and Following the Interventiona,b

VariablesControl GroupTraining GrouptP Value
Pre TestPost TestPre TestPost Test
Body weight, kg78.25 ± 4.4778.92 ± 4.6478.08 ± 4.5276.01 ± 4.6512.460.001
BMI, kg/m230.24 ± 3.5430.45 ± 3.6230.42 ± 2.3628.68 ± 1.85.240.012
CRP, mg/dL1.84 ± 0.231.87 ± 0.241.85 ± .251.53 ± .2317.2040.001
Ox ldl, IU/L5.68 ± 0.385.71 ± 0.415.75 ± 0.315.68 ± 0.279.270.07
Glucoses, mg/dL101.41 ± 3.06102.11 ± 3.75100.70 ± 6.497.81 ± 5.438.360.001
Insulin, μU/mL12.51 ± 1.1212.80.1.3412.43 ± 1.1711.90 ± 1.316.230.001
HOMA-IR3.08 ± 0.353.19 ± 0.363.09 ± 0.392.87 ± 0.323.480.002
LDL-c, mg/dL125.66 ± 8.27126.11 ± 9.58126.2 ± 8.4119.40 ± 8.217.300.001
HDL-c, mg/dL55.24 ± 3.4154.86 ± 3.2854.73 ± 2.8357.266 ± 2.71-4.470.001
Triglyceride, mg/dL207.20 ± 11.56209.21 ± 12.68206.95 ± 10.47191.86 ± 8.629.220.001
Cholesterol, mg/dL198.64 ± 11.25200.23 ± 12.68198.60 ± 12.54186.06 ± 10.689.440.001

5. Discussion

In the present study, the effects of aerobic exercises on blood levels of Ox-LDL and insulin resistance, CRP and blood lipoprotein were evaluated in obese and overweight women. Based on the findings, Ox-LDL levels did not change significantly after eight weeks of aerobic exercises. It seems that this type of exercise does not have enough stimulation for effective mechanisms to reduce Ox-LDL in obese women. The findings of some researchers showed that the Ox-LDL after a period of aerobic exercise combined with diet had a significant reduction in coronary heart disease (14). On the other hand, Rahimi and Jalili (15), showed that Ox-LDL concentration immediately decreased after resistance training with green tea consumption. Zahabi et al. (16), in their research showed that four weeks of combined exercise leads to inhibition of oxidation of LDL and consequently prevents cardiovascular disease. Fathei et el. (17), demonstrated that eight weeks of aerobic training, green tea consumption, and their composition reduce the cardiovascular risk factors in inactive obese women in a relatively similar manner. The research evidence showed the association between Ox-LDL and obesity (18, 19), which contradicts the findings of this study. Perhaps the main reasons for this discrepancy between the findings may be the manner and nature of the different exercises in these studies (in this study, the intensity of training was moderate). On the other hand, the findings of the study conducted by Afzalpour et al. (20), showed that Ox-LDL levels did not change significantly after eight weeks of aerobic training, which is consistent with this study. It has been shown that obesity is associated with increased oxidative stress and antioxidant defense in resting conditions. Therefore, since obese people have lower antioxidant defense than normal people, they are more exposed to free radicals.

Due to exercise activity, the amount of antioxidants increases and prevents the processes leading to the production of Ox-LDL, so the body’s immune system improves due to increased antioxidants due to exercise activity (21). In obese people, there are also higher levels of lipid peroxidation (such as cholesterol and triglyceride). Higher fat levels in obese individuals stimulate the production of free radicals in cells more than normal (22), which may lead to damage to the protein, lipid, and DNA of the cell. Sport exercises prevent the accumulation of fatty acids in muscle cells by increasing the oxidation of fatty acids. Hence, lifestyle changes focusing on weight loss and increased physical activity are the main strategies for coping with the development of obesity (23). Based on the findings of this study, after eight weeks of aerobic exercises, blood CRP showed a significant decrease compared to baseline. CRP is known as the independent marker of cardiovascular complications, whose levels rapidly increase in response to inflammation in blood circulation and contribute to the pathogenesis of chronic inflammatory diseases such as cardiovascular disease, diabetes, and cancer (24); and one of the most important drivers of its production is obesity (25). Research reports reveal contradictory results regardin the effect of regular physical exercises on blood pressure levels in CRP. Eizadi et al. (26), observed significant reductions in CRP values after three months of aerobic exercise. On the other hand, in Wong et al. (27), despite a significant reduction in body mass index and an increase in fat-free mass, CRP concentration did not significantly decrease.

Previous studies on the effect of exercise on CRP have given different results. Lakka et al. (28), reported a significant reduction in serum CRP levels of inactive people after the 20-week cycling exercise (30 to 50 minutes per week). In addition, Olson et al. (29), reported improvement in hs-CRP levels after 12 months of exercise in obese women, while Wang et al. (27), did not see any significant change in CRP levels after three months of regular exercise in obese subjects.

On the other hand, the findings of this study showed that there was a significant relationship between training practices and insulin resistance. Although insulin is one of the most important components that are effective in insulin resistance, insulin response to exercise may be different. Eizadi et al. (26), reported that short-term exercise training does not improve insulin sensitivity or may worsen it. Other researchers found that long-term endurance (aerobic) exercises reduced insulin sensitivity (30), which is consistent with the findings of the present study. The causes of insulin resistance are reversible with weight loss, diet, and physical activity. Therefore, sports exercises can increase the body’s response to insulin through increased glucose transport to muscle cells (GLUT-4) and insulin receptor substrates (IRS), as well as muscle mass increase (more than 75% glucose uptake is due to insulin-induced muscle tissue stimulation) (31). The findings of this study showed that aerobic exercises improved blood lipoproteins including decreased total glycerides (TG), total cholesterol (TC), LDL, and increased HDL-C. Therefore, due to the fact that LDL oxidation, by creating fatty plaques in the endothelial wall, is an important event in atherogenesis, improving HDL-C can have a protective effect against LDL oxidation. Researchers have found that continuous physical training can lead to an increase in HDL-C over many years of life. It is worth mentioning that lipoprotein lipase enzyme is activated by physical activity, and the more it is activated, the more amount of HDL-C is formed. On the other hand, increased production of HDL-C, due to physical activity, has been reported in addition to the activation of lipoprotein lipase due to the activation of lecithin-cholesterol-acyl transferase and decreased liver lipase activity. It has been argued that HDL acts as an antioxidant in addition to reversing the transfusion of cholesterol from tissue to the liver and preventing the accumulation of cholesterol in the tissue. In addition, by having the paraoxonase enzyme, it prevents further oxidation of LDL, and in this regard, physical activity plays a strong protective role for the body (32).

5.1. Conclusions

The results of this study showed that eight weeks of aerobic exercise improved cardiovascular risk factors and inflammatory factors, which result in the improvement in insulin resistance and blood lipoprotein resistance. Therefore, it seems that this practice can be recommended for adult women who are obese and overweight. So far, many studies have not been done regarding the effects of aerobic exercise on the Ox-LDL index. Meanwhile, the findings of this study should be interpreted with some caution owing to lack of control over some factors such as the participants’ genetic tendencies regarding cellular modifications and adaptation, motivation level, psychological stress, and even lifestyle. Therefore, other studies are warranted to probe further into varying intensities of exercising with longer intervention periods to provide a precise understanding of the appropriate intensity of exercise for weight gain or loss.

Acknowledgements

References

  • 1.

    Forsythe LK, Wallace JM, Livingstone MB. Obesity and inflammation: The effects of weight loss. Nutr Res Rev. 2008;21(2):117-33. [PubMed ID: 19087366]. https://doi.org/10.1017/S0954422408138732.

  • 2.

    Zarghami N, Mohammadzadeh G, Zahedi Asl S, Hosseinpanah F. [Changes of serum leptin levels in healthy women with different grades of obesity and its correlation with hormonal and anthropometric factors]. Iran J Endocrinol Metab. 2008;10(3):227-34. Persian.

  • 3.

    Shavandi N, Saremi A, Shahrjerdi S, Pooryamanesh L. [Effect of ten-week aerobic training with flax seed supplementation on blood lipids profile and C- reactive protein in obese women]. J Gorgan Univ Med Sci. 2016;18(2):19-26. Persian.

  • 4.

    Ebrahim K, Basami M, Kolahdozi S, Karimnia SV. [The impact of resistance exercise on metabolism of fats and carbohydrates circle during endurance exercise in overweight men]. Iran J Endocrinol Metab. 2012;14(3):257-66. Persian.

  • 5.

    Sell H, Eckel J. Chemotactic cytokines, obesity and type 2 diabetes: In vivo and in vitro evidence for a possible causal correlation? Proc Nutr Soc. 2009;68(4):378-84. [PubMed ID: 19698204]. https://doi.org/10.1017/S0029665109990218.

  • 6.

    Robinson LE, Graham TE. Metabolic syndrome, a cardiovascular disease risk factor: Role of adipocytokines and impact of diet and physical activity. Can J Appl Physiol. 2004;29(6):808-29. [PubMed ID: 15630152].

  • 7.

    Pedersen BK. The anti-inflammatory effect of exercise: Its role in diabetes and cardiovascular disease control. Essays Biochem. 2006;42:105-17. [PubMed ID: 17144883]. https://doi.org/10.1042/bse0420105.

  • 8.

    Eftekhari M, Mozafari KH. [Effect of soybeans on homocysteine and serum lipoproteins in hyperlipidemic postmenopausal women]. Iran J Endocrinol Metab. 2008:31-9. Persian.

  • 9.

    Cornelissen VA, Fagard RH. Effects of endurance training on blood pressure, blood pressure-regulating mechanisms, and cardiovascular risk factors. Hypertension. 2005;46(4):667-75. [PubMed ID: 16157788]. https://doi.org/10.1161/01.HYP.0000184225.05629.51.

  • 10.

    Haghighi AH, Mahmoudi M, Delgosha H. [Hormonal responses to two programs of exhaustive resistance training of different intensities in male body builders]. Iran J Endocrinol Metab. 2012;14(3):267-74. Persian.

  • 11.

    Mehrabani J, Azimi B, Khosravi A, Mehrabani F. [The effect of 19 weeks of physical training on insulin resistance and high-sensitivity C-reactive protein in obese and non-obese]. Iran J Endocrinol Metab. 2011;14(5):437-44. Persian.

  • 12.

    Urso ML, Clarkson PM. Oxidative stress, exercise, and antioxidant supplementation. Toxicology. 2003;189(1-2):41-54. [PubMed ID: 12821281].

  • 13.

    Wang JS, Lin CC, Chen JK, Wong MK. Role of chronic exercise in decreasing oxidized LDL-potentiated platelet activation by enhancing platelet-derived no release and bioactivity in rats. Life Sci. 2000;66(20):1937-48. [PubMed ID: 10821118].

  • 14.

    Srimahachota S, Wunsuwan R, Siritantikorn A, Boonla C, Chaiwongkarjohn S, Tosukhowong P. Effects of lifestyle modification on oxidized LDL, reactive oxygen species production and endothelial cell viability in patients with coronary artery disease. Clin Biochem. 2010;43(10-11):858-62. [PubMed ID: 20416290]. https://doi.org/10.1016/j.clinbiochem.2010.04.056.

  • 15.

    Rahimi R, Jalili A. [Effect of green tea extract on serum concentration of homocysteine and Ox-LDL after resistance exercise in untrained men]. Metab Exercise Bioannual J. 2016;6(2). Persian.

  • 16.

    Zahabi GH, Barari AR, Ahmadi M. [Effect of concurrent on paraoxonase activity levels and some of the lipid plasma maekers in blood of women without exercise activity]. J Paramed Sci Rehabil. Persian.

  • 17.

    Fathei M, Khairabadi S, Ramezani F, Hejazi K. [The effects of 8-week aerobic trainings and green tea supplementation on some of the cardio-vascular risk factors in inactive overweight women]. J Q Horizon Med Sci. 2016;22(4):283-9. Persian.

  • 18.

    Weinbrenner T, Schroder H, Escurriol V, Fito M, Elosua R, Vila J, et al. Circulating oxidized LDL is associated with increased waist circumference independent of body mass index in men and women. Am J Clin Nutr. 2006;83(1):30-5. quiz 181-2. [PubMed ID: 16400046]. https://doi.org/10.1093/ajcn/83.1.30.

  • 19.

    Njajou OT, Kanaya AM, Holvoet P, Connelly S, Strotmeyer ES, Harris TB, et al. Association between oxidized LDL, obesity and type 2 diabetes in a population-based cohort, the health, aging and body composition study. Diabetes Metab Res Rev. 2009;25(8):733-9. [PubMed ID: 19780064]. [PubMed Central ID: PMC3269343]. https://doi.org/10.1002/dmrr.1011.

  • 20.

    Afzalpour ME, Gharakhanlou R, Gaeini AA, Mohebbi H, Hedayati M, Khazaei M. The effects of aerobic exercises on the serum oxidized LDL and total antioxidant capacity in non-active men. CDV Prev Control. 2008;3(2):77-82.

  • 21.

    Clarkson PM, Thompson HS. Antioxidants: What role do they play in physical activity and health? Am J Clin Nutr. 2000;72(2 Suppl):637S-46S. [PubMed ID: 10919970]. https://doi.org/10.1093/ajcn/72.2.637S.

  • 22.

    Kallio J, Komi P, Komulainen J, Avela J. Oxidative stress responses following acute exercise: The effect of fatness level. 12th Annual Congress of the European College of Sport Science. 11-14 July 2007; Jyvaskyla, Finland. 2007.

  • 23.

    Thompson PD, Lazarus B, Cullinane E, Henderson LO, Musliner T, Eshleman R, et al. Exercise, diet, or physical characteristics as determinants of HDL-levels in endurance athletes. Atherosclerosis. 1983;46(3):333-9. [PubMed ID: 6405759].

  • 24.

    Bassuk SS, Rifai N, Ridker PM. High-sensitivity C-reactive protein: Clinical importance. Curr Probl Cardiol. 2004;29(8):439-93. [PubMed ID: 15258556].

  • 25.

    Retnakaran R, Hanley AJ, Raif N, Connelly PW, Sermer M, Zinman B. C-reactive protein and gestational diabetes: The central role of maternal obesity. J Clin Endocrinol Metab. 2003;88(8):3507-12. [PubMed ID: 12915627]. https://doi.org/10.1210/jc.2003-030186.

  • 26.

    Eizadi M, Sohaily S, Khorshidi D, Samarikhalaj H. Effect of aerobic training program on serum C-reactive protein levels. Avicenna J Med Biochem. 2016;Inpress(Inpress). https://doi.org/10.17795/ajmb-33294.

  • 27.

    Wong PC, Chia MY, Tsou IY, Wansaicheong GK, Tan B, Wang JC, et al. Effects of a 12-week exercise training programme on aerobic fitness, body composition, blood lipids and C-reactive protein in adolescents with obesity. Ann Acad Med Singapore. 2008;37(4):286-93. [PubMed ID: 18461212].

  • 28.

    Lakka TA, Lakka HM, Rankinen T, Leon AS, Rao DC, Skinner JS, et al. Effect of exercise training on plasma levels of C-reactive protein in healthy adults: The HERITAGE family study. Eur Heart J. 2005;26(19):2018-25. [PubMed ID: 15987707]. https://doi.org/10.1093/eurheartj/ehi394.

  • 29.

    Olson TP, Dengel DR, Leon AS, Schmitz KH. Changes in inflammatory biomarkers following one-year of moderate resistance training in overweight women. Int J Obes (Lond). 2007;31(6):996-1003. [PubMed ID: 17299382]. https://doi.org/10.1038/sj.ijo.0803534.

  • 30.

    Praet SF, Manders RJ, Lieverse AG, Kuipers H, Stehouwer CD, Keizer HA, et al. Influence of acute exercise on hyperglycemia in insulin-treated type 2 diabetes. Med Sci Sports Exerc. 2006;38(12):2037-44. [PubMed ID: 17146308]. https://doi.org/10.1249/01.mss.0000235352.09061.1d.

  • 31.

    Bonen A, Dohm GL, van Loon LJ. Lipid metabolism, exercise and insulin action. Essays Biochem. 2006;42:47-59. [PubMed ID: 17144879]. https://doi.org/10.1042/bse0420047.

  • 32.

    Javadi E, Shafaye A, Irvani A. [Sensitive of oxidized LDL between athletic and non- athletic]. Diabet Lipid J. 2003;2(2):143-6. Persian.