Correlation of oxidative stress parameters and inflammatory markers in coronary artery disease patients
Authorized Users Only
2007
Authors
Kotur-Stevuljević, Jelena
Memon, Lidija

Stefanović, Aleksandra

Spasić, Slavica
Spasojević-Kalimanovska, Vesna

Bogavac-Stanojević, Nataša

Kalimanovska-Oštrić, Dimitra
Jelić-Ivanović, Zorana

Zunić, Gordana
Article (Published version)

Metadata
Show full item recordAbstract
Objectives: In addition to many traditional risk factors for coronary artery disease (CAD) development, enhanced oxidative stress and inflammation are serious conditions that may also be classified as novel risk factors. In the present study, we assessed the relationship between several parameters of oxidative stress status [malonaldehyde (MDA), superoxide anion (O-2(center dot)-) and plasma and erythrocyte superoxide dismutase (SOD) activities] with high sensitivity C-reactive protein (hsCRP) and fibrinogen as inflammation markers. Design and methods: Oxidative stress status parameters, inflammation markers and lipid status parameters were measured in 385 subjects [188 coronary heart disease (CHD) patients with angiographically diagnosed coronary artery disease (CAD), 141 patients with occlusion > 50% in at least one major coronary artery (CAD+) and 47 patients with occlusion less than 50% (CAD-), and 197 CHD-free middle-aged subjects (the control group)]. Results: The plasma MDA conc...entration and the level of O-2(center dot)- in plasma were significantly higher in combination with significantly lower SOD activity in the CAD+ group vs. the control group. By using multiple stepwise regression analysis, fibrinogen and hsCRP showed independent correlation with MDA. Binary logistic regression analysis indicated that both MDA and O-2(center dot)- were significantly associated with CAD development and adjustment for inflammatory markers weakened this association in the case of MDA. Conclusions: The relationship between oxidative stress parameters and inflammatory species suggest their strong mutual involvement in atherosclerosis development that leads to CAD progression.
Keywords:
oxidative stress / coronary artery disease / inflammationSource:
Clinical Biochemistry, 2007, 40, 3-4, 181-187Publisher:
- Pergamon-Elsevier Science Ltd, Oxford
Funding / projects:
DOI: 10.1016/j.clinbiochem.2006.09.007
ISSN: 0009-9120
PubMed: 17070511
WoS: 000244193000007
Scopus: 2-s2.0-33846287199
Collections
Institution/Community
PharmacyTY - JOUR AU - Kotur-Stevuljević, Jelena AU - Memon, Lidija AU - Stefanović, Aleksandra AU - Spasić, Slavica AU - Spasojević-Kalimanovska, Vesna AU - Bogavac-Stanojević, Nataša AU - Kalimanovska-Oštrić, Dimitra AU - Jelić-Ivanović, Zorana AU - Zunić, Gordana PY - 2007 UR - https://farfar.pharmacy.bg.ac.rs/handle/123456789/947 AB - Objectives: In addition to many traditional risk factors for coronary artery disease (CAD) development, enhanced oxidative stress and inflammation are serious conditions that may also be classified as novel risk factors. In the present study, we assessed the relationship between several parameters of oxidative stress status [malonaldehyde (MDA), superoxide anion (O-2(center dot)-) and plasma and erythrocyte superoxide dismutase (SOD) activities] with high sensitivity C-reactive protein (hsCRP) and fibrinogen as inflammation markers. Design and methods: Oxidative stress status parameters, inflammation markers and lipid status parameters were measured in 385 subjects [188 coronary heart disease (CHD) patients with angiographically diagnosed coronary artery disease (CAD), 141 patients with occlusion > 50% in at least one major coronary artery (CAD+) and 47 patients with occlusion less than 50% (CAD-), and 197 CHD-free middle-aged subjects (the control group)]. Results: The plasma MDA concentration and the level of O-2(center dot)- in plasma were significantly higher in combination with significantly lower SOD activity in the CAD+ group vs. the control group. By using multiple stepwise regression analysis, fibrinogen and hsCRP showed independent correlation with MDA. Binary logistic regression analysis indicated that both MDA and O-2(center dot)- were significantly associated with CAD development and adjustment for inflammatory markers weakened this association in the case of MDA. Conclusions: The relationship between oxidative stress parameters and inflammatory species suggest their strong mutual involvement in atherosclerosis development that leads to CAD progression. PB - Pergamon-Elsevier Science Ltd, Oxford T2 - Clinical Biochemistry T1 - Correlation of oxidative stress parameters and inflammatory markers in coronary artery disease patients VL - 40 IS - 3-4 SP - 181 EP - 187 DO - 10.1016/j.clinbiochem.2006.09.007 ER -
@article{ author = "Kotur-Stevuljević, Jelena and Memon, Lidija and Stefanović, Aleksandra and Spasić, Slavica and Spasojević-Kalimanovska, Vesna and Bogavac-Stanojević, Nataša and Kalimanovska-Oštrić, Dimitra and Jelić-Ivanović, Zorana and Zunić, Gordana", year = "2007", abstract = "Objectives: In addition to many traditional risk factors for coronary artery disease (CAD) development, enhanced oxidative stress and inflammation are serious conditions that may also be classified as novel risk factors. In the present study, we assessed the relationship between several parameters of oxidative stress status [malonaldehyde (MDA), superoxide anion (O-2(center dot)-) and plasma and erythrocyte superoxide dismutase (SOD) activities] with high sensitivity C-reactive protein (hsCRP) and fibrinogen as inflammation markers. Design and methods: Oxidative stress status parameters, inflammation markers and lipid status parameters were measured in 385 subjects [188 coronary heart disease (CHD) patients with angiographically diagnosed coronary artery disease (CAD), 141 patients with occlusion > 50% in at least one major coronary artery (CAD+) and 47 patients with occlusion less than 50% (CAD-), and 197 CHD-free middle-aged subjects (the control group)]. Results: The plasma MDA concentration and the level of O-2(center dot)- in plasma were significantly higher in combination with significantly lower SOD activity in the CAD+ group vs. the control group. By using multiple stepwise regression analysis, fibrinogen and hsCRP showed independent correlation with MDA. Binary logistic regression analysis indicated that both MDA and O-2(center dot)- were significantly associated with CAD development and adjustment for inflammatory markers weakened this association in the case of MDA. Conclusions: The relationship between oxidative stress parameters and inflammatory species suggest their strong mutual involvement in atherosclerosis development that leads to CAD progression.", publisher = "Pergamon-Elsevier Science Ltd, Oxford", journal = "Clinical Biochemistry", title = "Correlation of oxidative stress parameters and inflammatory markers in coronary artery disease patients", volume = "40", number = "3-4", pages = "181-187", doi = "10.1016/j.clinbiochem.2006.09.007" }
Kotur-Stevuljević, J., Memon, L., Stefanović, A., Spasić, S., Spasojević-Kalimanovska, V., Bogavac-Stanojević, N., Kalimanovska-Oštrić, D., Jelić-Ivanović, Z.,& Zunić, G.. (2007). Correlation of oxidative stress parameters and inflammatory markers in coronary artery disease patients. in Clinical Biochemistry Pergamon-Elsevier Science Ltd, Oxford., 40(3-4), 181-187. https://doi.org/10.1016/j.clinbiochem.2006.09.007
Kotur-Stevuljević J, Memon L, Stefanović A, Spasić S, Spasojević-Kalimanovska V, Bogavac-Stanojević N, Kalimanovska-Oštrić D, Jelić-Ivanović Z, Zunić G. Correlation of oxidative stress parameters and inflammatory markers in coronary artery disease patients. in Clinical Biochemistry. 2007;40(3-4):181-187. doi:10.1016/j.clinbiochem.2006.09.007 .
Kotur-Stevuljević, Jelena, Memon, Lidija, Stefanović, Aleksandra, Spasić, Slavica, Spasojević-Kalimanovska, Vesna, Bogavac-Stanojević, Nataša, Kalimanovska-Oštrić, Dimitra, Jelić-Ivanović, Zorana, Zunić, Gordana, "Correlation of oxidative stress parameters and inflammatory markers in coronary artery disease patients" in Clinical Biochemistry, 40, no. 3-4 (2007):181-187, https://doi.org/10.1016/j.clinbiochem.2006.09.007 . .