HDL-cholesterol is associated with systemic inflammation in cardiac syndrome X
dc.authorid | Yontar, Osman Can/0000-0002-0099-8654 | |
dc.authorid | Aydin, Ufuk/0000-0002-4083-6211 | |
dc.authorid | TENEKECIOGLU, ERHAN/0000-0003-4376-2833 | |
dc.contributor.author | Tenekecioglu, E. | |
dc.contributor.author | Yilmaz, M. | |
dc.contributor.author | Demir, S. | |
dc.contributor.author | Bekler, A. | |
dc.contributor.author | Ozluk, O. A. | |
dc.contributor.author | Aydin, U. | |
dc.contributor.author | Goncu, T. | |
dc.date.accessioned | 2025-01-27T20:35:13Z | |
dc.date.available | 2025-01-27T20:35:13Z | |
dc.date.issued | 2015 | |
dc.department | Çanakkale Onsekiz Mart Üniversitesi | |
dc.description.abstract | Aim. Microvascular inflammation is associated with cardiac syndrome X (CSX). High-density lipoprotein cholesterol (HDL-C) reveals antiatherogenic features with stimulating endothelial NO production, inhibiting oxidative stress and vascular inflammation. We investigated relationship between HDL-C and inflammatory markers in CSX. Methods. Hundred patients with CSX and control group of 80 subjects were evaluated. Hematologic indices, lipid levels and C-reactive protein (CRP) levels were studied in patients underwent coronary angiography. Results. CRP levels were higher in CSX group than control group (4.59 +/- 3.82 mg/dL vs. 2.48 +/- 1.32 mg/dL, P<0.001). HDL-C was significantly lower in CSX group compared to control group (36.5 +/- 4.0 mg/dL vs. 47.5 +/- 12.7 mg/dL, P=0.008). White blood cell (WBC) count was higher in CSX group than in control group. Neutrophil-lymphocyte ratio (NLR) was found significantly increased in CSX group as compared to control group. On multivariate linear regression, lower HDL-C was found to be a significant predictor of higher NLR in patients with CSX independent from other clinical and biochemical variables. Conclusion. Lower HDL-C is associated with systemic inflammation in CSX. In patients with typical angina and normal epicardial coronaries,HDL-C and inflammatory markers should be investigated; one of the goals of treatment should be raising HDL-C. | |
dc.identifier.endpage | 141 | |
dc.identifier.issn | 0026-4806 | |
dc.identifier.issn | 1827-1669 | |
dc.identifier.issue | 3 | |
dc.identifier.pmid | 25028863 | |
dc.identifier.scopus | 2-s2.0-84970998785 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 133 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12428/23600 | |
dc.identifier.volume | 106 | |
dc.identifier.wos | WOS:000360186800002 | |
dc.identifier.wosquality | Q3 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | |
dc.publisher | Edizioni Minerva Medica | |
dc.relation.ispartof | Minerva Medica | |
dc.relation.publicationcategory | info:eu-repo/semantics/openAccess | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.snmz | KA_WoS_20250125 | |
dc.subject | Microvascular angina | |
dc.subject | Inflammation | |
dc.subject | Dyslipidemias | |
dc.title | HDL-cholesterol is associated with systemic inflammation in cardiac syndrome X | |
dc.type | Article |