<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JBM</journal-id><journal-title-group><journal-title>Journal of Biosciences and Medicines</journal-title></journal-title-group><issn pub-type="epub">2327-5081</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jbm.2019.77005</article-id><article-id pub-id-type="publisher-id">JBM-93672</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Comparative Evaluation of Antioxidant Enzymes and Serum Selenium Levels in Libyan Atherosclerotic Patients
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rabia</surname><given-names>Alghazeer</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Eenas</surname><given-names>Aboulmeedah</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Sana</surname><given-names>Elgahmasi</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Nadia</surname><given-names>Alghazir</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Zohra</surname><given-names>Almukthar</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Maryouma</surname><given-names>Enaami</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Abdurrahman</surname><given-names>Rhuma</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Chemistry, Faculty of Sciences, University of Tripoli, Tripoli, Libya</addr-line></aff><aff id="aff2"><addr-line>Pediatric Department, Faculty of Medicine, University of Tripoli, Tripoli, Libya</addr-line></aff><aff id="aff4"><addr-line>Department of Statistics, Faculty of Science, University of Tripoli, Tripoli, Libya</addr-line></aff><aff id="aff3"><addr-line>Tajoura National Heart Center, Tripoli, Libya</addr-line></aff><pub-date pub-type="epub"><day>05</day><month>07</month><year>2019</year></pub-date><volume>07</volume><issue>07</issue><fpage>51</fpage><lpage>69</lpage><history><date date-type="received"><day>5,</day>	<month>June</month>	<year>2019</year></date><date date-type="rev-recd"><day>12,</day>	<month>July</month>	<year>2019</year>	</date><date date-type="accepted"><day>15,</day>	<month>July</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Introduction: Atherosclerosis is the major source of morbidity and mortality in the developed countries like Libya. Oxidative stress represents a risk factor and plays a key role at several steps of atherosclerosis. Formation of atherosclerotic plaques is the main reason for coronary artery disease. 
  Aim: This study is aimed to assess the impact of the imbalance between body oxidants and antioxidants (oxidative stress) and its involvement in developing and severity of atherosclerosis in atherosclerotic with and without diabetes Libyan patients. 
  Methods: The study sample comprised of atherosclerosis with and without diabetes patients (n = 73), as well as healthy controls (n = 27). Blood samples were collected to determine the levels of malonaldehyde (MDA) as oxidative biomarker, serum selenium level, total antioxidant status (TAS) level and some antioxidant enzymes including glutathione peroxidase (GPx), Catalase (Cat) and superoxide dismutase (SOD). Additionally, oxidant/antioxidant status was compared between atherosclerotic patients with and without diabetes in comparison to controls. 
  Results: The results indicated a significant increase in MDA level among atherosclerotic patients compared to healthy subjects (P &lt; 0.05). While the level of TAS, Cat, SOD and GPx was significantly decreased among patients compared to the controls (P &lt; 0.05). For the atherosclerotic diabetic patients, the study was found a rise in the level of MDA as well as a marked decrease in TAS and the activity of tested antioxidant enzymes (P &lt; 0.05). A good correlation was obtained between elevated MDA and decreased TAS, Cat, SOD and GPx. 
  Conclusion: Determination of antioxidative defense markers contributes to understanding the effect of oxidative stress on the development and the prevention of cardiovascular disease.
 
</p></abstract><kwd-group><kwd>Atherosclerosis</kwd><kwd> Free Radicals</kwd><kwd> Oxidative Stress</kwd><kwd> Antioxidants</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Atherosclerosis is the major source of morbidity and mortality in many African countries including Libya [<xref ref-type="bibr" rid="scirp.93672-ref1">1</xref>] . It is characterized by the accumulation of cholesterol deposits in macrophages, which lead to a proliferation of certain cell types within the arterial wall (foam cells) that gradually impinges on the vessel lumen and impedes blood flow. Reduced blood flow to target organs like heart and brain can cause attack and stroke.</p><p>Oxidative stress is the result of imbalance between the reactive oxygen species (ROS) and antioxidants in the body. Oxidative modifications within the arterial wall that may initiate and/or contribute to atherogenesis are likely to occur, which result in imbalance between the reactive oxygen species and antioxidants in the body. Therefore, it is important to consider the sources of oxidants in the context of available antioxidants [<xref ref-type="bibr" rid="scirp.93672-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref3">3</xref>] . Oxidative stress, particularly the oxidation of low density lipoprotein (LDL), represents a risk factor and plays a key role at several steps of atherosclerosis, according to the oxidative-modification hypothesis of atherosclerosis [<xref ref-type="bibr" rid="scirp.93672-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref5">5</xref>] . The oxidative modification hypothesis, antioxidant protection of LDL in the extracellular space deserves focus, as oxidized LDL has many potential proatherogenic activities [<xref ref-type="bibr" rid="scirp.93672-ref6">6</xref>] , and the cellular accumulation of oxidized LDL is considered a hallmark of atherosclerosis [<xref ref-type="bibr" rid="scirp.93672-ref7">7</xref>] .</p><p>The possible sources of oxidative stress in atherosclerosis results from endothelial production of ROS, especially superoxide ( O 2 − ), with the subsequent reaction with nitric oxide (NO) are an important mechanism of vascular dysfunction in atherosclerosis. O 2 − and NO rapidly interact to generate peroxynitrite (ONOO<sup>−</sup>), a potent oxidant and a mediator of vascular tissue injury [<xref ref-type="bibr" rid="scirp.93672-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref9">9</xref>] . Excess generation of ROS has been demonstrated in atherosclerosis and peroxynitrite formation has been shown to occur in atherosclerotic human [<xref ref-type="bibr" rid="scirp.93672-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref11">11</xref>] .</p><p>Diabetes mellitus (DM) has also been shown to play a crucial role in progress of cardiovascular diseases [<xref ref-type="bibr" rid="scirp.93672-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref13">13</xref>] . Recently, it has been found that significant indicators for rising risk of coronary heart disease, stroke or death are associated with higher levels of baseline HbA1c [<xref ref-type="bibr" rid="scirp.93672-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref15">15</xref>] . Actually, interest has developed in alternative markers, such as plasma markers of oxidative stress, which have a role to predict CVD risk [<xref ref-type="bibr" rid="scirp.93672-ref16">16</xref>] .</p><p>Intracellular antioxidant defense is primarily provided by antioxidant enzymes which catalyze decomposition of reactive oxygen species. The three major antioxidant enzymes, superoxide dismutase (SOD), glutathione peroxidase (GPx), and catalase (Cat), differ from each other in structure, tissue distribution, and cofactor requirement. In addition, Selenium is a powerful antioxidant regulating the activity of the glutathione peroxidase enzymes which catalyze the detoxification of hydrogen peroxide and organic hydroperoxides [<xref ref-type="bibr" rid="scirp.93672-ref17">17</xref>] . Therefore, it is worthy to know whether the change in the level of antioxidants has an impact in the progressed of atherosclerosis.</p></sec><sec id="s2"><title>2. Patients and Methods</title><sec id="s2_1"><title>2.1. Study Design</title><p>This study was conducted which recruited males with atherosclerosis and volunteers healthy subjects. A cross-sectional study was conducted on 73 atherosclerotic patients aged 45 - 65 years who attended the Tajora Central Heart Hospital. The control group (27 males) encompassed blood donors from the hospital staff with no known pathology that can be classified as their cases, their age was within the same age range as the other patients. A detailed medical history was taken and a physical examination was performed upon all participants. The Ethics committee of Biotechnology Research Center (Tripoli, Libya) approved the study (BEC-BTRC 03-2016). All patients provided a written informed consent prior to start of the study procedures.</p></sec><sec id="s2_2"><title>2.2. Selection Criteria</title><p>Subjects included in the current study were selected according to the following criteria: first, they were newly diagnosed as atherosclerotic patient. Hemolytic anemia, hemoglobin variants, hepatic disease and infectious diseases like tuberculosis, sarcoidosis, etc., were excluded from this study. In addition, subjects under treatment with drugs such as chelating agents, ethambutol, and D-penicillamine were also excluded.</p></sec><sec id="s2_3"><title>2.3. Blood Sample Collection</title><p>Blood samples were collected into commercial tubes after overnight fasting for analysis of laboratory parameters. Venous blood samples were obtained from the capital vein of each participant using sterile disposable plastic syringes. Specimens were collected at the same standardized time to minimize any effect of diurnal variation. After centrifugation, the clear, non-hemolyzed supernatant sera were separated using clean dry disposable plastic syringes. Samples were stored at −80˚C and used within 1 month for the analysis of oxidative and non-oxidative parameters.</p></sec><sec id="s2_4"><title>2.4. Determination of Biochemical Parameters</title><p>Various biochemical parameters in blood were measured according to standard methods including Glucose, Glycosylated hemoglobin A1c (HbA1c), total protein, alanine amino transaminase (ALT), aspartate amino transaminase (AST). Triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), and Low-density lipoprotein cholesterol (LDL-C). All parameters measured according to standard protocols in all subjects using Pre-modular analytics by using a kit with Cobas Integra&#174; 400 plus in the Biochemistry Laboratory, at the Tajora Central Heart Hospital, Tripoli, Libya.</p></sec><sec id="s2_5"><title>2.5. Oxidative Stress Parameter</title><p>Thiobarbituric acid reacting substances (TBARS) content, a measure of lipid peroxidation was determined spectrophotometrically in serum according to the method of Zhang, [<xref ref-type="bibr" rid="scirp.93672-ref18">18</xref>] .</p></sec><sec id="s2_6"><title>2.6. Antioxidative Parameters</title><p>The catalase activity was assayed by the spectrophotometric method, based on the ability of hydrogen peroxide to form a stable stained complex with dichromate/acetic acid reagent [<xref ref-type="bibr" rid="scirp.93672-ref19">19</xref>] . Glutathione peroxidase activity was determined according to the method of Hafeman et al. [<xref ref-type="bibr" rid="scirp.93672-ref20">20</xref>] . Estimation of SOD activity was performed using a SOD Assay kit-WST (Sigma Aldrich, USA) according to the manufacturer’s protocol (Dojindo, Gaithersburg, MD, USA). Total antioxidant activity was preformed using commercial tests manufactured by kit (Antioxidant assay kit, cat. No. CS0790; Sigma-Aldrich, St. Louis, MO, USA). The level of selenium was determined by using Inductively Coupled Plasma Optical Emission Spectrometer (ICP-OES) technique.</p></sec><sec id="s2_7"><title>2.7. Statistical Analysis</title><p>Statistical analysis was done using the SPSS program version 11.0 statistic software package. The results were expressed as mean &#177; standard deviation. Statistical significance was assessed using the analysis of variance (ANOVA), Tukey HSD and Pearson’s correlation coefficient. P values of &lt;0.05 were considered statistically significant.</p></sec></sec><sec id="s3"><title>3. Results</title><p><xref ref-type="fig" rid="fig1">Figure 1</xref> shows demographic data of atherosclerotic patients and control group. The clinical and biochemical data for the population studied are summarized in <xref ref-type="table" rid="table1">Table 1</xref>. Among 73 atherosclerotic male subjects, 43.84% were diabetic and 57.53%</p><p>were hypertensive while 53.42% were smokers. Body mass indexes (BMI) of patients were found significantly increased from control (P &lt; 0.009). 57.53% of patients were on antihypertensive treatment and their blood pressure was significantly higher compared to control <xref ref-type="table" rid="table1">Table 1</xref>.</p><p>Serum cholesterol and LDL concentrations in atherosclerotic subjects were significantly raised (P &lt; 0.01, P &lt; 0.05) as compared to control. Serum total cholesterol (TC) concentration in-group with atherosclerosis was no significantly higher (P &gt; 0.05) as compared to control (<xref ref-type="table" rid="table2">Table 2</xref>). However, no significant change was observed in group with atherosclerosis in comparison with control (P &gt; 0.05) (<xref ref-type="table" rid="table1">Table 1</xref>).</p><sec id="s3_1"><title>3.1. Patient Characteristics</title><p>BMI, Body mass index, TC: Total cholesterol; TG: Triglyceride; LDL-C: Lowdensity lipoprotein cholesterol; HDL-C: High-density lipoprotein cholesterol, HbA<sub>1C</sub>: Glycosylated hemoglobin; SOD: Superoxide dismutase; GPx: Glutathione peroxidase; MDA: Malondialdehyde; TAS: Total Antioxidants.</p><p>The mean percentage changes of the oxidant and antioxidant parameters in patients as compared to the controls are shown in (<xref ref-type="fig" rid="fig2">Figure 2</xref>). In comparison with control group, the level of MDA was increased significantly (P &lt; 0.001) from 0.066 &#177; 0.048 to 0.52 &#177; 0.32 nmol/mgP by 213% and a significant increase in HbA1c levels (P &lt; 0.001) from 5.27% &#177; 0.40% to 6.88 &#177; 1.74% by 30.55% was observed in atheroserotic patients with respect to normal healthy control subjects (<xref ref-type="table" rid="table1">Table 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>). A significant decrease in Cat activity (P &lt; 0.002) by 3.98% (from 1.885 &#177; 0.84 U/mgP to 1.81 &#177; 0.90 U/mg P) was found in patients as compared with control groups (<xref ref-type="table" rid="table1">Table 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>).</p><p><xref ref-type="table" rid="table1">Table 1</xref> shows the distribution of serum selenium concentration in patients and controls. The mean concentration of serum selenium was marked decrease</p><p>(P &lt; 0.00) by 56.91% (from 0.094 &#177; 0.0114 to 0.0405 &#177; 0.0039 ppm for controls and atherosclerotic subjects) (<xref ref-type="table" rid="table1">Table 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>).</p><p>Thirty-two atherosclerotic type-II diabetes mellitus and forty-one atherosclerotic non-diabetic age matched normal blood pressure controls were included in the study. Baseline characteristics of both groups are shown in <xref ref-type="table" rid="table2">Table 2</xref>. In type-II diabetes mellitus group, HbA1c was significantly higher than the non-diabetic group (P &lt; 0.000) (<xref ref-type="table" rid="table2">Table 2</xref>). Serum cholesterol, TG and LDL concentrations in diabetic subjects were significantly raised as compared to non-diabetic group (TC: 170.35 &#177; 25.79 mg/dl vs. 162.7 &#177; 35.8 mg/dl, TG: 145.72 &#177; 85.31 mg/dl vs. 134.83 &#177; 50.93 mg/dl, LDL: 98.5 &#177; 26.245 mg/dl vs. 93.625 &#177; 29.71 mg/dl. However, there was no significant change was observed in the level of HDL AST, ALT in diabetic group with respect to the control group (P &gt; 0.05).</p><p><xref ref-type="fig" rid="fig3">Figure 3</xref> shows the values of MDA and anti-oxidative parameters in atherosclerotic diabetic patients and atherosclerotic none diabetic subjects. The results</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Characteristic laboratory variables and the values of anti-oxidative parameters atherosclerotic and control subjects</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Measure Indices (unit)</th><th align="center" valign="middle" ></th><th align="center" valign="middle" >Patients with atherosclerosis (n = 73)</th><th align="center" valign="middle" >Controls (n = 30)</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >(Years, X &#177; δ)</td><td align="center" valign="middle" >54.33 &#177; 6.04</td><td align="center" valign="middle" >48.52 &#177; 5.03</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >BMI</td><td align="center" valign="middle" >(Kg/m<sup>2</sup>, X &#177; δ)</td><td align="center" valign="middle" >19.66 &#177; 2.88</td><td align="center" valign="middle" >16.96 &#177; 2.71</td><td align="center" valign="middle" >0.009</td></tr><tr><td align="center" valign="middle" >Diabetes</td><td align="center" valign="middle" >n (%)</td><td align="center" valign="middle" >43.84%</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Hypertension</td><td align="center" valign="middle" >n (%)</td><td align="center" valign="middle" >57.53%</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Smoking</td><td align="center" valign="middle" >n (%)</td><td align="center" valign="middle" >53.42%</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >AST</td><td align="center" valign="middle" >(U/l, X &#177; δ)</td><td align="center" valign="middle" >25.38 &#177; 10.75</td><td align="center" valign="middle" >24.29 &#177; 4.18</td><td align="center" valign="middle" >0.664</td></tr><tr><td align="center" valign="middle" >ALT</td><td align="center" valign="middle" >(U/l, X &#177; δ)</td><td align="center" valign="middle" >26.77 &#177; 13.44</td><td align="center" valign="middle" >24.74 &#177; 11.83</td><td align="center" valign="middle" >0.632</td></tr><tr><td align="center" valign="middle" >GPx</td><td align="center" valign="middle" >(U/mg P, X &#177; δ)</td><td align="center" valign="middle" >4.02 &#177; 1.95</td><td align="center" valign="middle" >4.9 &#177; 2.73</td><td align="center" valign="middle" >0.137</td></tr><tr><td align="center" valign="middle" >SOD</td><td align="center" valign="middle" >(U/mg P, X &#177; δ)</td><td align="center" valign="middle" >12.09 &#177; 5.5</td><td align="center" valign="middle" >13.32 &#177; 6.18</td><td align="center" valign="middle" >0.537</td></tr><tr><td align="center" valign="middle" >Cat</td><td align="center" valign="middle" >(U/mg P, X &#177; δ)</td><td align="center" valign="middle" >1.18 &#177; 0.90</td><td align="center" valign="middle" >1.885 &#177; 0.84</td><td align="center" valign="middle" >0.002</td></tr><tr><td align="center" valign="middle" >HbA1c</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >6.88 &#177; 1.74</td><td align="center" valign="middle" >5.27 &#177; 0.40</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >TC</td><td align="center" valign="middle" >(mg/dl, X &#177; δ)</td><td align="center" valign="middle" >170.21 &#177; 45.01</td><td align="center" valign="middle" >159.6 &#177; 27.37</td><td align="center" valign="middle" >0.015</td></tr><tr><td align="center" valign="middle" >HDL-C</td><td align="center" valign="middle" >(mg/dl, X &#177; δ)</td><td align="center" valign="middle" >40.30 &#177; 9.7</td><td align="center" valign="middle" >49.59 &#177; 10.33</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >LDL-C</td><td align="center" valign="middle" >(mg/dl, X &#177; δ)</td><td align="center" valign="middle" >108.7 &#177; 28.65</td><td align="center" valign="middle" >91.75 &#177; 24.24</td><td align="center" valign="middle" >0.047</td></tr><tr><td align="center" valign="middle" >TG</td><td align="center" valign="middle" >(mg/dl, X &#177; δ)</td><td align="center" valign="middle" >158.15 &#177; 97.14</td><td align="center" valign="middle" >122 &#177; 52.2</td><td align="center" valign="middle" >0.111</td></tr><tr><td align="center" valign="middle" >TAS</td><td align="center" valign="middle" >(nmol/mgP, X &#177; δ)</td><td align="center" valign="middle" >0.34 &#177; 0.22</td><td align="center" valign="middle" >0.39 &#177; 0.20</td><td align="center" valign="middle" >0.597</td></tr><tr><td align="center" valign="middle" >MDA</td><td align="center" valign="middle" >(nmol/mgP, X &#177; δ)</td><td align="center" valign="middle" >0.52 &#177; 0.32</td><td align="center" valign="middle" >0.166 &#177; 0.048</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >Se</td><td align="center" valign="middle" >(ppm, X &#177; δ)</td><td align="center" valign="middle" >0.0405 &#177; 0.0039</td><td align="center" valign="middle" >0.094 &#177; 0.0114</td><td align="center" valign="middle" >0.000</td></tr></tbody></table></table-wrap><p>Values are expressed as mean &#177; SD for n subjects, BMI, Body mass index, TC: Total cholesterol; TG: Triglyceride; LDL-C: Low-density lipoprotein cholesterol; HDL-C: High-density lipoprotein cholesterol, HbA1<sub>C</sub>: Glycated haemoglobin A1<sub>C</sub>; SOD: Superoxide dismutase; GPx: Glutathione peroxidase; MDA: Malondialdehyde; TAS: Total Antioxidant status. One-way ANOVA followed by Tuceky test, n = 3. Non-significant groups: P ≥ 0.05; *P &lt; 0.05; **P &lt; 0.001 considered statistically significant as compared to atherosclerotic non-diabetic group.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Characteristic laboratory variables and the values of anti-oxidative parameters atherosclerotic patients with and without type 2 diabetes</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" ></th><th align="center" valign="middle" >Diabetic patients (n = 32)*</th><th align="center" valign="middle" >Non diabetic patients (n = 41)</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >(years, X &#177; δ)</td><td align="center" valign="middle" >56.47 &#177; 5.41</td><td align="center" valign="middle" >52.66 &#177; 6.04</td><td align="center" valign="middle" >0.013</td></tr><tr><td align="center" valign="middle" >BMI</td><td align="center" valign="middle" >(Kg/m<sup>2</sup>, X &#177; δ)</td><td align="center" valign="middle" >20.11 &#177; 2.58</td><td align="center" valign="middle" >&#177; 3.08 19.32</td><td align="center" valign="middle" >0.981</td></tr><tr><td align="center" valign="middle" >Diabetes duration</td><td align="center" valign="middle" >Years</td><td align="center" valign="middle" >1.5 &#177; 0.51</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Hypertension</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >50%</td><td align="center" valign="middle" >63.41%</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >Smoking</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >56.25%</td><td align="center" valign="middle" >51.22%</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >HbA1c</td><td align="center" valign="middle" >%</td><td align="center" valign="middle" >8.25 &#177; 1.64**</td><td align="center" valign="middle" >5.84 &#177; 0.88</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >AST</td><td align="center" valign="middle" >U/L</td><td align="center" valign="middle" >24.35 &#177; 8.72</td><td align="center" valign="middle" >26.19 &#177; 12.15</td><td align="center" valign="middle" >0.632</td></tr><tr><td align="center" valign="middle" >ALT</td><td align="center" valign="middle" >U/L</td><td align="center" valign="middle" >25.76 &#177; 11.25</td><td align="center" valign="middle" >27.57 &#177; 15.014</td><td align="center" valign="middle" >0.664</td></tr><tr><td align="center" valign="middle" >TC</td><td align="center" valign="middle" >(mg/dl, X &#177; δ)</td><td align="center" valign="middle" >170.35 &#177; 25.79*</td><td align="center" valign="middle" >162.7 &#177; 35.8</td><td align="center" valign="middle" >0.026</td></tr><tr><td align="center" valign="middle" >HDL-C</td><td align="center" valign="middle" >(mg/dl, X &#177; δ)</td><td align="center" valign="middle" >40.16 &#177; 8.65</td><td align="center" valign="middle" >40.41 &#177; 10.51</td><td align="center" valign="middle" >0.993</td></tr><tr><td align="center" valign="middle" >LDL-C</td><td align="center" valign="middle" >(mg/dl, X &#177; δ)</td><td align="center" valign="middle" >98.5 &#177; 26.245*</td><td align="center" valign="middle" >93.625 &#177; 29.71</td><td align="center" valign="middle" >0.052</td></tr><tr><td align="center" valign="middle" >TG</td><td align="center" valign="middle" >(mg/dl, X &#177; δ)</td><td align="center" valign="middle" >145.72 &#177; 85.31*</td><td align="center" valign="middle" >134.83 &#177; 50.93</td><td align="center" valign="middle" >0.033</td></tr></tbody></table></table-wrap><p>Values are expressed as mean &#177; SD for n subjects, BMI, Body mass index, *: non-insulin dependent (Type-2) diabetes mellitus, TC: Total cholesterol; TG: Triglyceride; LDL-C: Low-density lipoprotein cholesterol; HDL C: High density lipoprotein cholesterol; HbA<sub>1C</sub>: Glycosylated hemoglobin. One-way ANOVA followed by Tuckey test, n = 3. Non-significant groups: P ≥ 0.05; *P &lt; 0.05; **P &lt; 0.001 considered statistically significant as compared to atherosclerotic non-diabetic group.</p><p>revealed that the lipid peroxidation level as an indicator of oxidative stress was significantly increased (P &lt; 0.001) in diabetic patients compared to non-diabetic subjects (0.53 &#177; 0.31 nmol/mgP vs. 0.33 &#177; 0.23 nmol/mgP). In addition, diabetic patients had significantly lower values of TAS, GPX, SOD and Cat with respect to the non-diabetics group (TAS: 0.35 &#177; 0.22 mmol/l vs. 0.33 &#177; 0.23 mmol/l, GPx: U/mgP 4.27 &#177; 1.76 vs. 3.81 &#177; 2.08 U/mgP, SOD: 11.64 &#177; 4.61 U/mgP vs. 12.433 &#177; 6.11 U/mgP, Cat: 1.089 &#177; 0.79 U/mgP vs. 1.25 &#177; 0.99 U/mgP). Atherosclerotic patients with type II diabetes had slightly higher values of Se in relation to its level in non-diabetic patients (0.039 &#177; 0.0032 ppm vs. 0.042 &#177; 0.0042 ppm) (<xref ref-type="fig" rid="fig4">Figure 4</xref>).</p></sec><sec id="s3_2"><title>3.2. Correlations</title><p><xref ref-type="table" rid="table3">Table 3</xref> shows the correlations between TAS activity and some clinical and laboratory variables in atherosclerotic diabetic patients as well as atherosclerotic none diabetic subjects. Pearson’s correlation coefficient in atherosclerotic diabetic patients was observed a significant positive correlation between TAS and HbA1c (r = 0.134, P &lt; 0.049) while a negative correlation was found between TAS and MDA (r = −0.061, P &lt; 0.039) (<xref ref-type="table" rid="table3">Table 3</xref>). In atherosclerotic non-diabetic patients, TAS showed significant negative correlation with the TG (r = −0.423, P &lt; 0.006), MDA (r = −0.200, P &lt; 0.02) (<xref ref-type="table" rid="table3">Table 3</xref>).</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Correlations of Total Antioxidants (TAS) activity with some clinical and laboratory variables in atherosclerotic patients with and without type 2 diabetes</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Parameters</th><th align="center" valign="middle"  colspan="2"  >Diabetic patients (n = 32)</th><th align="center" valign="middle"  colspan="2"  >Non diabetic patients (n = 41)</th></tr></thead><tr><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >−0.220</td><td align="center" valign="middle" >0.227</td><td align="center" valign="middle" >0.089</td><td align="center" valign="middle" >0.584</td></tr><tr><td align="center" valign="middle" >BMI</td><td align="center" valign="middle" >−0.172</td><td align="center" valign="middle" >0.354</td><td align="center" valign="middle" >−0.215</td><td align="center" valign="middle" >0.182</td></tr><tr><td align="center" valign="middle" >HbA1C</td><td align="center" valign="middle" >0.134</td><td align="center" valign="middle" >0.049</td><td align="center" valign="middle" >−0.143</td><td align="center" valign="middle" >0.419</td></tr><tr><td align="center" valign="middle" >GPX</td><td align="center" valign="middle" >0.068</td><td align="center" valign="middle" >0.711</td><td align="center" valign="middle" >0.004</td><td align="center" valign="middle" >0.983</td></tr><tr><td align="center" valign="middle" >SOD</td><td align="center" valign="middle" >−0.065</td><td align="center" valign="middle" >0.729</td><td align="center" valign="middle" >0.176</td><td align="center" valign="middle" >0.278</td></tr><tr><td align="center" valign="middle" >Cat</td><td align="center" valign="middle" >−0.014</td><td align="center" valign="middle" >0.937</td><td align="center" valign="middle" >−0.042</td><td align="center" valign="middle" >0.797</td></tr><tr><td align="center" valign="middle" >HbA1c</td><td align="center" valign="middle" >−0.052</td><td align="center" valign="middle" >0.793</td><td align="center" valign="middle" >−0.010</td><td align="center" valign="middle" >0.956</td></tr><tr><td align="center" valign="middle" >HDL-C</td><td align="center" valign="middle" >0.042</td><td align="center" valign="middle" >0.820</td><td align="center" valign="middle" >0.051</td><td align="center" valign="middle" >0.753</td></tr><tr><td align="center" valign="middle" >LDL-C</td><td align="center" valign="middle" >−0.090</td><td align="center" valign="middle" >0.626</td><td align="center" valign="middle" >−0.197</td><td align="center" valign="middle" >0.224</td></tr><tr><td align="center" valign="middle" >TG</td><td align="center" valign="middle" >0.074</td><td align="center" valign="middle" >0.686</td><td align="center" valign="middle" >−0.423**</td><td align="center" valign="middle" >0.006</td></tr><tr><td align="center" valign="middle" >TC</td><td align="center" valign="middle" >−0.025</td><td align="center" valign="middle" >−0.891</td><td align="center" valign="middle" >−0.261</td><td align="center" valign="middle" >0.108</td></tr><tr><td align="center" valign="middle" >MDA</td><td align="center" valign="middle" >−0.061</td><td align="center" valign="middle" >0.039</td><td align="center" valign="middle" >−0.200</td><td align="center" valign="middle" >0.021</td></tr><tr><td align="center" valign="middle" >Se</td><td align="center" valign="middle" >0.468</td><td align="center" valign="middle" >0.172</td><td align="center" valign="middle" >0.230</td><td align="center" valign="middle" >0.522</td></tr></tbody></table></table-wrap><p>r = correlation coefficient. BMI, Body mass index, *: non-insulin dependent (Type-2) diabetes mellitus, TC: Total cholesterol; TG: Triglyceride; LDL-C: Low-density lipoprotein cholesterol; HDL-C: High-density lipoprotein cholesterol, HbA<sub>1C</sub>: Glycosylated hemoglobin, SOD: Superoxide dismutase; GPx: Glutathione peroxidase; Cat: Catalase; MDA: Malondialdehyde. Non-significant groups: P ≥ 0.05; *P &lt; 0.05; **P &lt; 0.001 considered statistically significant as compared to atherosclerotic non-diabetic group.</p><p>There was a correlation of GPx activity with some clinical and laboratory variables in atherosclerotic diabetic patients as well as atherosclerotic none diabetic subjects (<xref ref-type="table" rid="table4">Table 4</xref>). A significant correlation was found between GPx and SOD (r = 0.359, P &lt; 0.047), GPx and Cat (r = 0.488, P &lt; 0.005), GPx and MDA (r = 0.575, P &lt; 0.001) in atherosclerotic diabetic patients.</p><p>Atherosclerotic diabetic group, atherosclerotic non-diabetic group showed highly significant correlations between GPx and SOD (r = 0.684, P &lt; 0.000), GPx and Cat (r = 0.488, P &lt; 0.001) (<xref ref-type="table" rid="table4">Table 4</xref>).</p><p>In addition, Pearson’s correlation reveals a positive significant correlation between MDA and GPx (r = 0.575, P &lt; 0.001), MDA and Cat (r = 0.673, P &lt; 0.00), MDA and SOD (r = 0.449, P &lt; 0.011) in atherosclerotic diabetic groups and in atherosclerotic non-diabetic patients, a highly significant positive correlation between MDA and Cat (r = −0.604, P &lt; 0.00) was obtained (<xref ref-type="table" rid="table5">Table 5</xref>).</p><p>Moreover, a significant positive correlations was obtained between SOD-GPx (r = 0.359, P &lt; 0.047), and SOD-MDA (r = 0.449, P &lt; 0.011) in atherosclerotic diabetics while in atherosclerotic non-diabetics as marked positive correlations were observed between SOD-GPx (r = 0.684, P &lt; 0.00), and GPx-Cat (r = 0.421, P &lt; 0.006) (<xref ref-type="table" rid="table6">Table 6</xref>).</p><p>Furthermore, <xref ref-type="table" rid="table7">Table 7</xref> shows the correlations between Cat activity and some</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Correlations of Glutathione peroxidase (GPx) activity with some clinical and laboratory variables in atherosclerotic patients with and without type 2 diabetes</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Parameters</th><th align="center" valign="middle"  colspan="2"  >Diabetic patients (n = 32)</th><th align="center" valign="middle"  colspan="2"  >Non diabetic patients (n = 41)</th></tr></thead><tr><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >−0.321</td><td align="center" valign="middle" >0.073</td><td align="center" valign="middle" >−0.089</td><td align="center" valign="middle" >0.579</td></tr><tr><td align="center" valign="middle" >BMI</td><td align="center" valign="middle" >−0.321</td><td align="center" valign="middle" >0.078</td><td align="center" valign="middle" >0.040</td><td align="center" valign="middle" >0.802</td></tr><tr><td align="center" valign="middle" >CBC</td><td align="center" valign="middle" >0.194</td><td align="center" valign="middle" >0.323</td><td align="center" valign="middle" >−0.221</td><td align="center" valign="middle" >0.201</td></tr><tr><td align="center" valign="middle" >TAS</td><td align="center" valign="middle" >0.068</td><td align="center" valign="middle" >0.711</td><td align="center" valign="middle" >0.004</td><td align="center" valign="middle" >0.983</td></tr><tr><td align="center" valign="middle" >SOD</td><td align="center" valign="middle" >0.359*</td><td align="center" valign="middle" >0.047</td><td align="center" valign="middle" >0.684**</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >Cat</td><td align="center" valign="middle" >0.488**</td><td align="center" valign="middle" >0.005</td><td align="center" valign="middle" >0.489**</td><td align="center" valign="middle" >0.001</td></tr><tr><td align="center" valign="middle" >HbA1c</td><td align="center" valign="middle" >−0.047</td><td align="center" valign="middle" >0.814</td><td align="center" valign="middle" >−0.021</td><td align="center" valign="middle" >0.901</td></tr><tr><td align="center" valign="middle" >HDL-C</td><td align="center" valign="middle" >−0.030</td><td align="center" valign="middle" >0.870</td><td align="center" valign="middle" >−0.168</td><td align="center" valign="middle" >0.294</td></tr><tr><td align="center" valign="middle" >LDL-C</td><td align="center" valign="middle" >−0.028</td><td align="center" valign="middle" >0.879</td><td align="center" valign="middle" >−0.127</td><td align="center" valign="middle" >0.430</td></tr><tr><td align="center" valign="middle" >TG</td><td align="center" valign="middle" >0.163</td><td align="center" valign="middle" >0.374</td><td align="center" valign="middle" >−0.074</td><td align="center" valign="middle" >0.644</td></tr><tr><td align="center" valign="middle" >TC</td><td align="center" valign="middle" >0.011</td><td align="center" valign="middle" >0.952</td><td align="center" valign="middle" >0.004</td><td align="center" valign="middle" >0.983</td></tr><tr><td align="center" valign="middle" >MDA</td><td align="center" valign="middle" >0.575**</td><td align="center" valign="middle" >0.001</td><td align="center" valign="middle" >0.275</td><td align="center" valign="middle" >0.086</td></tr><tr><td align="center" valign="middle" >Se</td><td align="center" valign="middle" >0.412</td><td align="center" valign="middle" >0.236</td><td align="center" valign="middle" >0.430</td><td align="center" valign="middle" >0.215</td></tr></tbody></table></table-wrap><p>r = correlation coefficient. BMI, Body mass index, *: non-insulin dependent (Type-2) diabetes mellitus, TC: Total cholesterol; TG: Triglyceride; LDL-C: Low-density lipoprotein cholesterol; HDL-C: High-density lipoprotein cholesterol, HbA<sub>1C</sub>: Glycosylated hemoglobin, SOD: Superoxide dismutase; Cat: Catalase; MDA: Malondialdehyde; TAS: Total Antioxidants. Non-significant groups: P ≥ 0.05; *P &lt; 0.05; **P &lt; 0.001 considered statistically significant as compared to atherosclerotic non-diabetic group.</p><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Correlations of Malondialdehyde (MDA) activity with some clinical and laboratory variables in atherosclerotic patients with and without type 2 diabetes</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Parameters</th><th align="center" valign="middle"  colspan="2"  >Diabetic patients (n = 32)</th><th align="center" valign="middle"  colspan="2"  >Non diabetic patients (n = 41)</th></tr></thead><tr><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >−0.320</td><td align="center" valign="middle" >0.074</td><td align="center" valign="middle" >0.206</td><td align="center" valign="middle" >0.202</td></tr><tr><td align="center" valign="middle" >BMI</td><td align="center" valign="middle" >−0.235</td><td align="center" valign="middle" >0.203</td><td align="center" valign="middle" >−0.015</td><td align="center" valign="middle" >0.928</td></tr><tr><td align="center" valign="middle" >GPx</td><td align="center" valign="middle" >0.575**</td><td align="center" valign="middle" >0.001</td><td align="center" valign="middle" >0.275</td><td align="center" valign="middle" >0.086</td></tr><tr><td align="center" valign="middle" >TAS</td><td align="center" valign="middle" >−0.061</td><td align="center" valign="middle" >0.739</td><td align="center" valign="middle" >−0.200</td><td align="center" valign="middle" >0.216</td></tr><tr><td align="center" valign="middle" >SOD</td><td align="center" valign="middle" >0.449*</td><td align="center" valign="middle" >0.011</td><td align="center" valign="middle" >0.155</td><td align="center" valign="middle" >0.341</td></tr><tr><td align="center" valign="middle" >Cat</td><td align="center" valign="middle" >0.673**</td><td align="center" valign="middle" >0.000</td><td align="center" valign="middle" >0.604**</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >HbA1c</td><td align="center" valign="middle" >0.027</td><td align="center" valign="middle" >0.894</td><td align="center" valign="middle" >0.043</td><td align="center" valign="middle" >0.805</td></tr><tr><td align="center" valign="middle" >HDL-C</td><td align="center" valign="middle" >−0.070</td><td align="center" valign="middle" >0.704</td><td align="center" valign="middle" >−0.204</td><td align="center" valign="middle" >0.207</td></tr><tr><td align="center" valign="middle" >LDL-C</td><td align="center" valign="middle" >−0.077</td><td align="center" valign="middle" >0.677</td><td align="center" valign="middle" >−0.056</td><td align="center" valign="middle" >0.733</td></tr><tr><td align="center" valign="middle" >TG</td><td align="center" valign="middle" >−0.107</td><td align="center" valign="middle" >0.561</td><td align="center" valign="middle" >0.000</td><td align="center" valign="middle" >0.999</td></tr><tr><td align="center" valign="middle" >TC</td><td align="center" valign="middle" >−0.126</td><td align="center" valign="middle" >0.493</td><td align="center" valign="middle" >−0.143</td><td align="center" valign="middle" >0.385</td></tr><tr><td align="center" valign="middle" >Se</td><td align="center" valign="middle" >0.309</td><td align="center" valign="middle" >0.385</td><td align="center" valign="middle" >−0.174</td><td align="center" valign="middle" >0.630</td></tr></tbody></table></table-wrap><p>r = correlation coefficient. BMI, Body mass index, *: non-insulin dependent (Type-II) diabetes mellitus, TC: Total cholesterol; TG: Triglyceride; LDL-C: Low-density lipoprotein cholesterol; HDL-C: High-density lipoprotein cholesterol, HbA1<sub>C</sub>: Glycated haemoglobin A1<sub>C</sub>; GPx: Glutathione peroxidase; Cat: Catalase; TAS: Total Antioxidant status. Non-significant groups: P ≥ 0.05; *P &lt; 0.05; **P &lt; 0.001 considered statistically significant as compared to atherosclerotic non-diabetic group.</p><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> Correlations of Superoxide dismutase (SOD) activity with some clinical and laboratory variables in atherosclerotic patients with and without type 2 diabetes</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Parameters</th><th align="center" valign="middle"  colspan="2"  >Diabetic patients (n = 32)</th><th align="center" valign="middle"  colspan="2"  >Non diabetic patients (n = 41)</th></tr></thead><tr><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >−0.099</td><td align="center" valign="middle" >0.598</td><td align="center" valign="middle" >−0.147</td><td align="center" valign="middle" >0.360</td></tr><tr><td align="center" valign="middle" >BMI</td><td align="center" valign="middle" >−0.043</td><td align="center" valign="middle" >0.822</td><td align="center" valign="middle" >−0.197</td><td align="center" valign="middle" >0.218</td></tr><tr><td align="center" valign="middle" >CBC</td><td align="center" valign="middle" >−0.114</td><td align="center" valign="middle" >0.564</td><td align="center" valign="middle" >−0.242</td><td align="center" valign="middle" >0.162</td></tr><tr><td align="center" valign="middle" >GPx</td><td align="center" valign="middle" >0.359*</td><td align="center" valign="middle" >0.047</td><td align="center" valign="middle" >0.684**</td><td align="center" valign="middle" >.000</td></tr><tr><td align="center" valign="middle" >TAS</td><td align="center" valign="middle" >−0.065</td><td align="center" valign="middle" >0.729</td><td align="center" valign="middle" >0.176</td><td align="center" valign="middle" >0.278</td></tr><tr><td align="center" valign="middle" >MDA</td><td align="center" valign="middle" >0.449*</td><td align="center" valign="middle" >0.011</td><td align="center" valign="middle" >0.155</td><td align="center" valign="middle" >0.341</td></tr><tr><td align="center" valign="middle" >Cat</td><td align="center" valign="middle" >0.066</td><td align="center" valign="middle" >0.726</td><td align="center" valign="middle" >0.421**</td><td align="center" valign="middle" >0.006</td></tr><tr><td align="center" valign="middle" >HbA1c</td><td align="center" valign="middle" >−0.020</td><td align="center" valign="middle" >0.918</td><td align="center" valign="middle" >−0.050</td><td align="center" valign="middle" >0.771</td></tr><tr><td align="center" valign="middle" >HDL-C</td><td align="center" valign="middle" >0.082</td><td align="center" valign="middle" >0.659</td><td align="center" valign="middle" >0.061</td><td align="center" valign="middle" >0.706</td></tr><tr><td align="center" valign="middle" >LDL-C</td><td align="center" valign="middle" >−0.230</td><td align="center" valign="middle" >0.213</td><td align="center" valign="middle" >−0.101</td><td align="center" valign="middle" >0.529</td></tr><tr><td align="center" valign="middle" >TG</td><td align="center" valign="middle" >−0.153</td><td align="center" valign="middle" >0.410</td><td align="center" valign="middle" >−0.077</td><td align="center" valign="middle" >0.632</td></tr><tr><td align="center" valign="middle" >TC</td><td align="center" valign="middle" >−0.236</td><td align="center" valign="middle" >0.202</td><td align="center" valign="middle" >−0.106</td><td align="center" valign="middle" >0.514</td></tr><tr><td align="center" valign="middle" >Se</td><td align="center" valign="middle" >0.623</td><td align="center" valign="middle" >0.054</td><td align="center" valign="middle" >0.314</td><td align="center" valign="middle" >0.378</td></tr></tbody></table></table-wrap><p>r = correlation coefficient. BMI, Body mass index, *: non-insulin dependent (Type-2) diabetes mellitus, TC: Total cholesterol; TG: Triglyceride; LDL-C: Low-density lipoprotein cholesterol; HDL-C: High-density lipoprotein cholesterol; HbA<sub>1C</sub>: Glycosylated hemoglobin; GPx: Glutathione peroxidase; Cat: Catalase; MDA: Malondialdehyde; TAS: Total Antioxidants. Non-significant groups: P ≥ 0.05; *P &lt; 0.05; **P &lt; 0.001 considered statistically significant as compared to atherosclerotic non-diabetic group.</p><p>clinical and laboratory variables in atherosclerotic diabetics as well as atherosclerotic non-diabetics. In atherosclerotic diabetic patients, Pearson’s correlation coefficient shows significant positive correlation between Cat and GPx (r = 0.488, P &lt; 0.005) and Cat-MDA (r = 0.673, P &lt; 0.00). In atherosclerotic non-diabetic patients Pearson’s correlation observes a significant positive correlation between Cat-GPx (r = 0.489, P &lt; 0.001), Cat-MDA (r = 0.604, P &lt; 0.00) and Cat-SOD (r = 0.421, P &lt; 0.000) (<xref ref-type="table" rid="table7">Table 7</xref>).</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>Accumulative evidence shows that oxidative stress plays a crucial role in the initiation and progression of a number of human diseases such as cancer, diabetes mellitus, and atherosclerosis. An imbalance between increased oxidative stress and impaired antioxidants defense may play a role in the progression of atherosclerotic disease. The present study was done to evaluate the oxidative stress parameters in the Libyans atherosclerotic participates and to demonstrate the correlation between oxidative stress, diabetes, and atherosclerosis. Present results concluded that the values of studied anti-oxidative parameters (SOD, GPx, Cat and TAS) were significantly lower in atherosclerotic participates comparatively with controls. In addition, lipid peroxidation level was significantly higher in</p><table-wrap id="table7" ><label><xref ref-type="table" rid="table7">Table 7</xref></label><caption><title> Correlations of Catalase (Cat) activity with some clinical and laboratory variables in atherosclerotic patients with and without type 2 diabetes</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="2"  >Parameters</th><th align="center" valign="middle"  colspan="2"  >Diabetics patients (n = 32)</th><th align="center" valign="middle"  colspan="2"  >Non diabetics patients (n = 41)</th></tr></thead><tr><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td><td align="center" valign="middle" >r</td><td align="center" valign="middle" >P</td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >−0.224</td><td align="center" valign="middle" >0.217</td><td align="center" valign="middle" >−0.058</td><td align="center" valign="middle" >0.720</td></tr><tr><td align="center" valign="middle" >BMI</td><td align="center" valign="middle" >−0.155</td><td align="center" valign="middle" >0.404</td><td align="center" valign="middle" >−0.178</td><td align="center" valign="middle" >0.265</td></tr><tr><td align="center" valign="middle" >GPx</td><td align="center" valign="middle" >0.488**</td><td align="center" valign="middle" >0.005</td><td align="center" valign="middle" >0.489**</td><td align="center" valign="middle" >0.001</td></tr><tr><td align="center" valign="middle" >TAS</td><td align="center" valign="middle" >−0.014</td><td align="center" valign="middle" >0.937</td><td align="center" valign="middle" >−0.042</td><td align="center" valign="middle" >0.797</td></tr><tr><td align="center" valign="middle" >MDA</td><td align="center" valign="middle" >0.673**</td><td align="center" valign="middle" >0.000</td><td align="center" valign="middle" >0.604**</td><td align="center" valign="middle" >0.000</td></tr><tr><td align="center" valign="middle" >SOD</td><td align="center" valign="middle" >0.066</td><td align="center" valign="middle" >0.726</td><td align="center" valign="middle" >0.421**</td><td align="center" valign="middle" >0.006</td></tr><tr><td align="center" valign="middle" >HbA1c</td><td align="center" valign="middle" >−0.132</td><td align="center" valign="middle" >0.502</td><td align="center" valign="middle" >−0.009</td><td align="center" valign="middle" >0.957</td></tr><tr><td align="center" valign="middle" >HDL-C</td><td align="center" valign="middle" >−0.001</td><td align="center" valign="middle" >0.997</td><td align="center" valign="middle" >0.004</td><td align="center" valign="middle" >0.980</td></tr><tr><td align="center" valign="middle" >LDL-C</td><td align="center" valign="middle" >0.063</td><td align="center" valign="middle" >0.732</td><td align="center" valign="middle" >0.006</td><td align="center" valign="middle" >0.968</td></tr><tr><td align="center" valign="middle" >TG</td><td align="center" valign="middle" >0.148</td><td align="center" valign="middle" >0.420</td><td align="center" valign="middle" >0.079</td><td align="center" valign="middle" >0.625</td></tr><tr><td align="center" valign="middle" >TC</td><td align="center" valign="middle" >0.079</td><td align="center" valign="middle" >0.668</td><td align="center" valign="middle" >0.012</td><td align="center" valign="middle" >0.940</td></tr><tr><td align="center" valign="middle" >Se</td><td align="center" valign="middle" >0.197</td><td align="center" valign="middle" >0.586</td><td align="center" valign="middle" >0.029</td><td align="center" valign="middle" >0.937</td></tr></tbody></table></table-wrap><p>r = correlation coefficient. BMI, Body mass index, *: non-insulin dependent (Type-2) diabetes mellitus, TC: Total cholesterol; TG: Triglyceride; LDL-C: Low-density lipoprotein cholesterol; HDL-C: High-density lipoprotein cholesterol, HbA<sub>1C</sub>: Glycosylated hemoglobin, SOD: Superoxide dismutase; GPx: Glutathione peroxidase; MDA: Malondialdehyde; TAS: Total Antioxidants. Non-significant groups: P ≥ 0.05; *P &lt; 0.05; **P &lt; 0.001 considered statistically significant as compared to atherosclerotic non-diabetic group.</p><p>patients in relation to healthy subjects (<xref ref-type="table" rid="table1">Table 1</xref>).</p><p>Various studies have demonstrated that diabetes mellitus, smoking, and hypertension, consider the main risk factors of atherosclerosis, which are correlated with an increased production of ROS by the endothelium [<xref ref-type="bibr" rid="scirp.93672-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref23">23</xref>] . It has been recently found a good correlation between elevated HbA1c values and the atherosclerosis [<xref ref-type="bibr" rid="scirp.93672-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref26">26</xref>] which result from oxidative stress induced by various glucose oxidation, change in antioxidant enzymes status and impaired glutathione metabolism [<xref ref-type="bibr" rid="scirp.93672-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref28">28</xref>] .</p><p>Reactive oxygen species (ROS) especially free oxygen radicals and peroxides may have both physiological and pathological roles in atherosclerosis. ROS are important regulators of vascular homeostasis [<xref ref-type="bibr" rid="scirp.93672-ref29">29</xref>] , they are key mediators of signaling pathways that cause vascular inflammation in atherogenesis, starting from the initiation of fatty streak development through lesion progression to ultimate plaque rupture. Animal studies found that ROS are involved in atherosclerosis by the accumulation of lipid peroxidation products and induction of inflammatory genes and activation of matrix metalloproteinases [<xref ref-type="bibr" rid="scirp.93672-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref30">30</xref>] . The findings that show TAS levels are lower and MDA levels are higher in atherosclerotic patients (diabetic and non-diabetic) as compared to the healthy group. An explanation for the observed reduction in TAS among atherosclerotic patients could be due to the presence of high amount of free radicals and other oxygen derived (superoxide) species, which ultimately activate the depletion of plasma antioxidants and increases lipid peroxidation [<xref ref-type="bibr" rid="scirp.93672-ref8">8</xref>] .</p><p>ROS and reactive nitrogen species (RNS) produced by the endothelium promote oxidative modification of LDL (low-density lipoprotein). Oxidized LDL has been implicated in several facets of the inflammatory process, including the invasion of monocytes and macrophages, their differentiation, and the induction of injury to endothelial cells [<xref ref-type="bibr" rid="scirp.93672-ref31">31</xref>] . It has been proven that oxidized LDL involved in plaque formation in atherosclerosis as it is naturally being considered to play the most important role in lipid storage and inflammation [<xref ref-type="bibr" rid="scirp.93672-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref33">33</xref>] . Previous studies have found that atheroscloresis is related to increase in lipid peroxidation [<xref ref-type="bibr" rid="scirp.93672-ref34">34</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref35">35</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref36">36</xref>] . An increase in lipid peroxidation product especially malondialdehyde level (MDA) may also related to the higher level of oxidized LDL. Present results correlate with previous findings [<xref ref-type="bibr" rid="scirp.93672-ref37">37</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref38">38</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref39">39</xref>] which illustrated that elevated levels of MDA indicate increase in the level of production of oxygen free radicals, suggesting their possible role in atherogenesis.</p><p>Antioxidants are a diverse group of compounds within which play important role in inhibiting oxidant formation, intercepting oxidants once they have formed, and repairing oxidant-induced injury. Although It is well documented that exposure to ROS increases the expression of antioxidant enzymes [<xref ref-type="bibr" rid="scirp.93672-ref40">40</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref41">41</xref>] , many studies have revealed that a decrease in the level of antioxidant defense as an expression of increase in free radical production [<xref ref-type="bibr" rid="scirp.93672-ref42">42</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref43">43</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref44">44</xref>] . Various enzyme systems including superoxide dismutase (SOD), glutathione peroxidases (GPx) and catalase (Cat) are involved in regulating ROS production and degradation in vascular cells [<xref ref-type="bibr" rid="scirp.93672-ref45">45</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref46">46</xref>] .</p><p>SOD, Cat and GPx play association role in the elimination of superoxide radicals, in which SOD transforms them to H<sub>2</sub>O<sub>2</sub> while GPx and Cat convert H<sub>2</sub>O<sub>2</sub> to water [<xref ref-type="bibr" rid="scirp.93672-ref47">47</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref48">48</xref>] . Therefore, prevent the formation of hydroxyl radicals, which is considered highly toxic molecule [<xref ref-type="bibr" rid="scirp.93672-ref49">49</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref50">50</xref>] . In this study, results demonstrated lower levels of SOD, GPx, and catalase in serum of atherosclerotic patients with and without diabetes as compared to controls (<xref ref-type="fig" rid="fig3">Figure 3</xref> and <xref ref-type="fig" rid="fig4">Figure 4</xref>), that was in agreement with the outcomes of other studies [<xref ref-type="bibr" rid="scirp.93672-ref51">51</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref52">52</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref53">53</xref>] . In atherosclerotic with diabetes group, there was found a very good positive correlation between elevated MDA and decreased GPx level (r = 0.575., P &lt; 0.001) (<xref ref-type="table" rid="table5">Table 5</xref>). In addition, Significant positive correlations were noted between serum MDA level and SOD activity (r = 0.449, P = 0.011) and serum MDA level and Cat activity (r = 0.673, P = 0.000) (<xref ref-type="table" rid="table5">Table 5</xref>) which was in consistent with previous study [<xref ref-type="bibr" rid="scirp.93672-ref54">54</xref>] . The declined in the activity of SOD was feasibly due to the accumulation of H<sub>2</sub>O<sub>2</sub>, and glycation of these enzymes, which was in concord with previous findings [<xref ref-type="bibr" rid="scirp.93672-ref55">55</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref56">56</xref>] . In addition, [<xref ref-type="bibr" rid="scirp.93672-ref57">57</xref>] were reported that the lower activity of GPx activity in atherosclerotic with diabetes group was related to inactivation of the enzyme because of severe oxidative stress condition.</p><p>Selenium, an essential micronutrient that play a pivotal role in maintaining optimal health by regulating the redox balance. It is involved in the complex system of defense against oxidative stress through selenium-dependent glutathione peroxidases and other selenoproteins. In this investigation results demonstrated that the selenium concentrations were lower in the atherosclerotic patients in relation to its content in controls which was in agreement with the outcomes of other studies [<xref ref-type="bibr" rid="scirp.93672-ref58">58</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref59">59</xref>] . However, the <xref ref-type="fig" rid="fig4">Figure 4</xref> shows that the distribution of patients with and without diabetes was similar at all selenium concentrations, indicating that a serum selenium is not related to the regulation and severity of the disease [<xref ref-type="bibr" rid="scirp.93672-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.93672-ref60">60</xref>] .</p></sec><sec id="s5"><title>5. Conclusion</title><p>An imbalance between increased oxidative stress and impaired antioxidant defense may play a role in the progression of atherosclerotic disease. Aforementioned observations indicate that oxidative stress was increased in atherosclerotic diabetic patients as approved by the significant changes in the levels of oxidative stress parameters. The relationship between oxidative stress parameters and imbalance antioxidants suggests their strong involvement in atherosclerosis. Further investigations with large clinical trials are recommended.</p></sec><sec id="s6"><title>Acknowledgements</title><p>The authors would like to thank the medical record in charge and staff of Tajoura National Heart Center, Tripoli, Libya, for their cooperation and support during the study and patients who participate in this study.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s8"><title>Authors’ Contributions</title><p>This work was carried out in collaboration between all authors. Author RA designed the study, wrote the protocol and wrote the first draft of the manuscript. Authors SE and EA preformed the experiments, ZA collected the data and samples, author NA interpreted the analyses of the study and contributed important intellectual content, author ME performed the statistical analysis, and author AR managed the literature searches and critically revised the manuscript. All authors read and approved the final manuscript.</p></sec><sec id="s9"><title>Ethics Approval and Consent to Participate</title><p>The Ethics committee of Biotechnology Research Center (Tripoli, Libya) approved the study (BEC-BTRC 03-2016). All patients provided a written informed consent prior to start of the study procedures.</p></sec><sec id="s10"><title>Cite this paper</title><p>Alghazeer, R., Aboulmeedah, E., Elgahmasi, S., Alghazir, N., Almukthar, Z., Enaami, M. and Rhuma, A. (2019) Comparative Evaluation of Antioxidant Enzymes and Serum Selenium Levels in Libyan Atherosclerotic Patients. 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