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dc.contributor.authorSağlam, Hayrettin
dc.contributor.authorKaya, Eser
dc.contributor.authorCemek, Mustafa
dc.contributor.authorÇiçek, Yüksel
dc.contributor.authorKulaç, Mustafa
dc.contributor.authorKaraca, Şemsettin
dc.date.accessioned2022-05-11T14:37:18Z
dc.date.available2022-05-11T14:37:18Z
dc.date.issued2010
dc.identifier.issn1386-0291
dc.identifier.issn1875-8622
dc.identifier.urihttps://doi.org/10.3233/CH-2010-1278
dc.identifier.urihttps://hdl.handle.net/20.500.11776/8651
dc.description.abstractBehcet's disease (BD) is a chronic, progressive and inflammatory multisystemic disease, that significantly affects the cardiovascular system. Oxidative stress (OS) is a disturbance in oxidant/antioxidant balance in favor of oxidants. The OS that increases acutely and chronically due to the inflammatory process plays an important role in the pathogenesis of the cardiovascular system effects of the disease by causing endothelial dysfunction in vascular structures. The aim of our study was to investigate the relationship between OS and myocardial perfusion, which is based on microvascular dysfunction, in BD. Material and method: Twenty-seven patients with BD (16 M, 11 F, mean age: 38.7 +/- 9.4 years) and 22 healthy volunteers (12 M, 10 F, mean age: 35.8 +/- 6.5 years) participated in our study. Technetium-99m methoxyisobutylisonitrile single photon emission computed tomography (Tc-99m MIBI SPECT) stress-rest test was performed with two-day protocol. Myocardial perfusion scores (summed stress score, summed rest score, summed difference score, fix defect score) and perfusion defect prevalence (stress, rest, ischemic and fixed) were determined as the percentage of left ventricle. Coronary angiography was performed in patients with abnormal myocardial perfusion scintigraphy. For OS analysis, the blood samples were taken immediately before the first imaging procedure and were studied for malondialdehyde, glutathione, nitrite, nitrate, vitamin C, retinol, and carotene. Results: In the BD group, a total of 9 patients had abnormal findings in their stress and rest electrocardiography. Perfusion defect in myocardial perfusion scintigraphy was observed in 14 patients (51.8%). Twelve patients accepted coronary angiography, and their results were normal. In the comparison of myocardial perfusion scores, perfusion defect prevalence and OS parameters, there was a significant difference between the BD and control groups. In the BD group, no correlation was observed between myocardial perfusion scores, perfusion defect prevalence and OS parameters. Conclusion: Defects in myocardial perfusion and increase in OS were observed in BD; however, there was no correlation between the two findings in the inactive period. In other words, the prevalence and intensity of myocardial perfusion defects can vary at different OS levels.en_US
dc.language.isoengen_US
dc.publisherIos Pressen_US
dc.identifier.doi10.3233/CH-2010-1278
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBehcet's diseaseen_US
dc.subjectmyocardial perfusion scintigraphyen_US
dc.subjectoxidative stressen_US
dc.subjectMyocardial-Perfusionen_US
dc.subjectVascular Involvementen_US
dc.subjectLipid-Peroxidationen_US
dc.subjectGated Specten_US
dc.subjectDysfunctionen_US
dc.titleNo apparent correlation between Behcet's disease and oxidative stress disturbanceen_US
dc.typearticleen_US
dc.relation.ispartofClinical Hemorheology and Microcirculationen_US
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Deri ve Zührevi Hastalıkları Ana Bilim Dalıen_US
dc.identifier.volume44en_US
dc.identifier.issue4en_US
dc.identifier.startpage287en_US
dc.identifier.endpage296en_US
dc.institutionauthorKulaç, Mustafa
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid16835779300
dc.authorscopusid15076694100
dc.authorscopusid55970945900
dc.authorscopusid6701325407
dc.authorscopusid10639223100
dc.authorscopusid10640274000
dc.authorwosidkaya, eser/F-1949-2018
dc.identifier.wosWOS:000279013700006en_US
dc.identifier.scopus2-s2.0-77954099762en_US
dc.identifier.pmid20571243en_US


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