Deficiency of a New Protein Associated with Cardiac Syndrome X; Called Adropin

dc.contributor.authorCelik, Ahmet
dc.contributor.authorBalin, Mehmet
dc.contributor.authorKobat, Mehmet Ali
dc.contributor.authorErdem, Kenan
dc.contributor.authorBaydas, Adil
dc.contributor.authorBulut, Musa
dc.contributor.authorAydin, Suleyman
dc.date.accessioned2026-08-12T17:31:50Z
dc.date.issued2013
dc.departmentFırat Üniversitesi
dc.description.abstractThe pathophysiology of cardiac syndrome X (CSX) is still unclear, but most patients with CSX have endothelial dysfunction. It has been shown that adropin uniquely effects the regulation of endothelial function. The purpose of the study was to evaluate the role of adropin in CSX. Eighty-six consecutive cardiac syndrome X-diagnosed patients and 86 age-sex matched healthy subjects were enrolled into the study. Serum adropin levels, nitrite/nitrate levels were measured in each subject. The adropin levels were significantly lower in patients with CSX than healthy subjects (1.7 +/- 0.8ng/mL and 3.4 +/- 1.8ng/mL, respectively; P<0.001). The BMI values of patients with CSX were significantly higher than control subjects (28.1 +/- 2.4kg/m2 and 26.0 +/- 3.7kg/m2, respectively; P<0.001). Plasma nitrite/nitrate levels were lower in patients with CSX than control subjects (15.9 +/- 1.6mol/L vs. 25.4 +/- 2.8mol/L, respectively; P<0.001), and they have a significantly positive correlation with plasma adropin levels (r=0.463, P<0.001). In the multiple linear regression analysis, nitrite/nitrate levels, BMI, and adropin were found to be independent risk factors for CSX. A ROC curve is used to identify the ability of adropin levels to predict the cardiac syndrome X. The area under the ROC curve was 0.854 for adropin levels (P=0.0001). The sensitivity and specificity values of adropin levels were 90.7 and 70.9%, respectively (cut-off value 2.73). In conclusion, lower serum adropin levels were associated with CSX. Adropin is an independent risk factor for CSX.
dc.identifier.doi10.1111/1755-5922.12025
dc.identifier.endpage178
dc.identifier.issn1755-5914
dc.identifier.issue3
dc.identifier.orcid0000-0002-9417-7610
dc.identifier.pmid23356444
dc.identifier.scopus2-s2.0-84876471358
dc.identifier.scopusqualityQ1
dc.identifier.startpage174
dc.identifier.urihttps://doi.org/10.1111/1755-5922.12025
dc.identifier.urihttps://hdl.handle.net/11508/56412
dc.identifier.volume31
dc.identifier.wosWOS:000318039100009
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley-Blackwell
dc.relation.ispartofCardiovascular Therapeutics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectadropin
dc.subjectcardiac syndrome X
dc.subjectendothelial dysfunction
dc.titleDeficiency of a New Protein Associated with Cardiac Syndrome X; Called Adropin
dc.typeArticle

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