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Severity of Mitral Valve Stenosis ― Possible Relationships With Blood Oxidant Markers and Antioxidants ―

dc.authorscopusid 56957205400
dc.authorscopusid 57217683541
dc.authorwosid Çibuk, Salih/Kyq-7768-2024
dc.contributor.author Duz, Ramazan
dc.contributor.author Cibuk, Salih
dc.date.accessioned 2025-05-10T17:23:57Z
dc.date.available 2025-05-10T17:23:57Z
dc.date.issued 2024
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Duz, Ramazan] Yuzuncu Yil Univ, Dept Cardiol, Fac Med, Van, Turkiye; [Cibuk, Salih] Van Yuzuncu Yil Univ, Van Vocat Higher Sch Healthcare Studies, Van, Turkiye; [Duz, Ramazan] Yuzuncu Yil Univ, Dept Cardiol, Fac Med, TR-65090 Van, Turkiye en_US
dc.description.abstract Background: This study examined whether the severity of mitral valve stenosis (MVS) is associated with oxidative stress (OS) markers in the blood, and other hematological and clinicodemographic parameters. Methods and Results: This prospective study was conducted between March and May 2022. Seventy-five patients with newly diagnosed MVS (25 mild, 25 moderate, 25 severe) were included. Mild, moderate, and severe MVS was defined as MV area >2, 1.5-2, and <1.5 cm(2), respectively. Various OS markers and laboratory parameters were determined in venous blood samples. For predictive analyses, 2 different analyses were performed to detect patients with severe MVS and those with moderate or severe (moderate/severe) MVS. Age (P=0.388) and sex (P=0.372) distribution were similar in the 3 groups. Multiple logistic regression analysis revealed that a high white blood cell (WBC) count (P=0.023) and high malondialdehyde (P=0.010), superoxide dismutase (SOD; P=0.008), and advanced oxidation protein products (AOPP; P=0.007) levels were independently associated with severe MVS. A low platelet count (P=0.030) and high malondialdehyde (P=0.018), SOD (P=0.008), and AOPP (P=0.001) levels were independently associated with having moderate/severe MVS. The best discriminatory factors for severe MVS were SOD (cut-off >315.5 ng/mL) and glutathione (cut-off >4.7 mu mol/L). Conclusions: MVS severity seems to be affected by oxidant markers (malondialdehyde and AOPP), antioxidant enzymes (SOD), and inflammation-related cells (WBC and platelets). Future studies are needed to examine these relationships in larger populations. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1253/circj.CJ-22-0750
dc.identifier.endpage 605 en_US
dc.identifier.issn 1346-9843
dc.identifier.issn 1347-4820
dc.identifier.issue 4 en_US
dc.identifier.pmid 36858609
dc.identifier.scopus 2-s2.0-85189051937
dc.identifier.scopusquality Q1
dc.identifier.startpage 597 en_US
dc.identifier.uri https://doi.org/10.1253/circj.CJ-22-0750
dc.identifier.uri https://hdl.handle.net/20.500.14720/11054
dc.identifier.volume 88 en_US
dc.identifier.wos WOS:001189927100010
dc.identifier.wosquality Q2
dc.language.iso en en_US
dc.publisher Japanese Circulation Soc en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Advanced Oxidation Protein Products en_US
dc.subject Catalase Activity en_US
dc.subject Glutathione en_US
dc.subject Malondialdehyde en_US
dc.subject Mitral Valve Stenosis Severity en_US
dc.title Severity of Mitral Valve Stenosis ― Possible Relationships With Blood Oxidant Markers and Antioxidants ― en_US
dc.type Article en_US

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