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http://hdl.handle.net/11452/28667
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DC Field | Value | Language |
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dc.date.accessioned | 2022-09-13T08:45:30Z | - |
dc.date.available | 2022-09-13T08:45:30Z | - |
dc.date.issued | 2007-04 | - |
dc.identifier.citation | Şentürk, T. vd. (2007). "Procalcitonin in patients with acute coronary syndrome: Correlation with high-sensitive C-reactive protein, prognosis and severity of coronary artery disease". Acta Cardiologica, 62(2), 135-141. | en_US |
dc.identifier.issn | 0001-5385 | - |
dc.identifier.issn | 1784-973X | - |
dc.identifier.uri | https://doi.org/10.2143/AC.62.2.2020233 | - |
dc.identifier.uri | https://poj.peeters-leuven.be/content.php?url=article&id=2020233&journal_code=AC | - |
dc.identifier.uri | http://hdl.handle.net/11452/28667 | - |
dc.description.abstract | Objectives - The aim of this study is to determine the relation of high-sensitive serum C-reactive protein (hsCRP) and procalcitonin with presence and severity of coronary artery disease and early prognosis in patients with acute coronary syndrome (ACS). Methods and results - Procalcitonin and hsCRP levels were measured at admission and after 48 hours in 50 patients (41 men, 9 women) with ACS. The patients were assigned to three groups according to their clinical diagnosis: unstable angina pectoris (UAP) (Braunwald III-B), non-ST-segment elevation myocardial infarction (NSTEMI) and ST-segment elevation myocardial infarction (STEMI). Incidences of adverse cardiac events were recorded in a 3-month follow-up. Coronary angiography was performed to evaluate presence and severity of coronary artery disease. In the groups of STEMI, NSTEMI and UAP, procalcitonin (P = 0.013, P = 0.045 and P = 0.0001, respectively) and hsCRP (P = 0.0001, P = 0.01 and P = 0.001, respectively) levels were significantly increased. No significant correlation was found between these markers and the presence and severity of coronary artery disease. There was no correlation between procalcitonin and hsCRP levels at admission and after 48 hours and primary end points after 3 months except in the group of UAP with revascularization procedure. In the group of UAP, hsCRP levels at 48 hours were found higher in the patients with a revascularization procedure (P = 0.04). Conclusions - In conclusion, levels of hsCRP and procalcitonin are increased in patients with ACS but failed to correlate with severity of coronary disease and early prognosis. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Acta Cardiologica | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Acute coronary syndrome | en_US |
dc.subject | hsCRP | en_US |
dc.subject | Procalcitonin | en_US |
dc.subject | Prognosis | en_US |
dc.subject | Acute myocardial-infarction | en_US |
dc.subject | Practice guidelines committee | en_US |
dc.subject | Association task-force | en_US |
dc.subject | Unstable angina | en_US |
dc.subject | Cardiovascular-disease | en_US |
dc.subject | Acc/Aha guidelines | en_US |
dc.subject | American-college | en_US |
dc.subject | Inflammation | en_US |
dc.subject | Atherosclerosis | en_US |
dc.subject | Management | en_US |
dc.subject.mesh | Analysis of variance | en_US |
dc.subject.mesh | Acute disease | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | C-Reactive protein | en_US |
dc.subject.mesh | Research design | en_US |
dc.subject.mesh | Angina, unstable | en_US |
dc.subject.mesh | Angioplasty, transluminal, percutaneous coronary | en_US |
dc.subject.mesh | Coronary artery bypass | en_US |
dc.subject.mesh | Calcitonin | en_US |
dc.subject.mesh | Coronary angiography | en_US |
dc.subject.mesh | Coronary arteriosclerosis | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Creatine kinase, MB form | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Follow-up studies | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Inflammation mediators | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Myocardial infarction | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Syndrome | en_US |
dc.subject.mesh | Protein precursors | en_US |
dc.subject.mesh | Severity of illness index | en_US |
dc.subject.mesh | Treatment outcome | en_US |
dc.subject.mesh | Troponin I | en_US |
dc.subject.mesh | Turkey | en_US |
dc.title | Procalcitonin in patients with acute coronary syndrome: correlation with high-sensitive C-reactive protein, prognosis and severity of coronary artery disease | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000246063200004 | tr_TR |
dc.identifier.scopus | 2-s2.0-34247468445 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Kardiyoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Mikrobiyoloji Bölümü. | tr_TR |
dc.contributor.orcid | 0000-0002-8974-8837 | tr_TR |
dc.identifier.startpage | 135 | tr_TR |
dc.identifier.endpage | 141 | tr_TR |
dc.identifier.volume | 62 | tr_TR |
dc.identifier.issue | 2 | tr_TR |
dc.relation.journal | Acta Cardiologica | en_US |
dc.contributor.buuauthor | Şentürk, Tunay | - |
dc.contributor.buuauthor | Cordan, Jale | - |
dc.contributor.buuauthor | Baran, İbrahim | - |
dc.contributor.buuauthor | Özdemir, Bülent | - |
dc.contributor.buuauthor | Güllülü, Sümeyye | - |
dc.contributor.buuauthor | Aydınlar, Ali | - |
dc.contributor.buuauthor | Göral, Guher | - |
dc.contributor.researcherid | C-1517-2017 | tr_TR |
dc.contributor.researcherid | AAI-6632-2021 | tr_TR |
dc.identifier.pubmed | 17536601 | tr_TR |
dc.subject.wos | Cardiac & cardiovascular systems | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q4 | en_US |
dc.contributor.scopusid | 8342098300 | tr_TR |
dc.contributor.scopusid | 6602518666 | tr_TR |
dc.contributor.scopusid | 35572557400 | tr_TR |
dc.contributor.scopusid | 7004168959 | tr_TR |
dc.contributor.scopusid | 57204660708 | tr_TR |
dc.contributor.scopusid | 6603131517 | tr_TR |
dc.contributor.scopusid | 6603453166 | tr_TR |
dc.subject.scopus | Procalcitonin; Sepsis; C Reactive Protein | en_US |
dc.subject.emtree | CD8+ T lymphocyte | en_US |
dc.subject.emtree | C reactive protein | en_US |
dc.subject.emtree | Immunoglobulin A | en_US |
dc.subject.emtree | Placebo | en_US |
dc.subject.emtree | Probiotic agent | en_US |
dc.subject.emtree | Reflor | en_US |
dc.subject.emtree | Unclassified drug | en_US |
dc.subject.emtree | Acute diarrhea | en_US |
dc.subject.emtree | Acute gastroenteritis | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Child | en_US |
dc.subject.emtree | Clinical trial | en_US |
dc.subject.emtree | Controlled clinical trial | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Double blind procedure | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Follow up | en_US |
dc.subject.emtree | Immune response | en_US |
dc.subject.emtree | Protein blood level | en_US |
dc.subject.emtree | Immunoglobulin blood level | en_US |
dc.subject.emtree | Infant | en_US |
dc.subject.emtree | Lymphocyte count | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Nonhuman | en_US |
dc.subject.emtree | Oral rehydration therapy | en_US |
dc.subject.emtree | Randomized controlled trial | en_US |
dc.subject.emtree | Saccharomyces boulardii | en_US |
Appears in Collections: | PubMed Scopus Web of Science |
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