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dc.contributor.authorEmir, Seyfi
dc.contributor.authorAydın, M.
dc.contributor.authorCan, G.
dc.contributor.authorBali, İlhan
dc.contributor.authorYıldırım, Oğuzhan
dc.contributor.authorÖznur, Meltem
dc.contributor.authorGürel, A.
dc.date.accessioned2022-05-11T14:07:40Z
dc.date.available2022-05-11T14:07:40Z
dc.date.issued2015
dc.identifier.issn1128-3602
dc.identifier.urihttps://hdl.handle.net/20.500.11776/5170
dc.description.abstractOBJECTIVE: Cancer-related inflammation affects many aspects of malignancy, including proliferation and survival of malignant cells, angiogenesis, and therapeutic response. Some biomarkers representing the degree of systemic inflammation, such as the Glasgow prognostic score, NLR and PLR, have been shown to have prognostic value in many kinds of cancer patients. Aim of this study to investigate to compare neutrophil/leukocyte (NLR) and platelet/lymphocyte (PLR) ratios of the patients with colorectal neoplastic polyps and colorectal cancer (CRC) and tried to determine whether this could be used as a biomarker in follow up of the patients with neoplastic polyps. PATIENTS AND METHODS: A total of 100 colorectal polyps, 113 colorectal cancers and 124 healthy controls were included in the study. Exculusion criteria were endocrinologic or metabolic diseases, acute or chronic diseases, hypertension and atherosclerotic heart diseases, renal diseases. Blood count parameters of the patients were measured. The NLR was calculated as a simple ratio between the absolute neutrophil and the absolute lymphocyte counts. The PLR was defined as the platelet counts to lymphocyte ratio. RESULTS: A statistically significant difference was not detected between Group A and C with regard to NLR and PLR. NLR and PLR were found statistically significantly high in Group B (CRC), Group A (colorectal polyp) and Group C (healthy individuals) (p < 0.001 and p < 0.001). Our study showed that the optimum NLR cutoff point for neoplastic polyps was 2.28 (sensitivity: 68.7%, specificity: 42.3%). When the sensitivity and specificity levels of the PLR were assessed, they were 68.7% and 46.5% for neoplastic polyps, 80% and 68.9% for colorectal cancer. CONCLUSIONS: NLR and PLR may be used for follow up conversion of colonic and rectal neoplastic polyps to invasive tumor.en_US
dc.language.isoengen_US
dc.publisherVerduci Publisheren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiomarkeren_US
dc.subjectColorectal canceren_US
dc.subjectNeutrophil lymphocyte ratioen_US
dc.subjectPlatelet lymphocyte ratioen_US
dc.subjectNeutrophil-Lymphocyte Ratioen_US
dc.subjectColony-Stimulating Factoren_US
dc.subjectElevated Preoperative Neutrophilen_US
dc.subjectIn-Vivoen_US
dc.subjectPrognostic Markeren_US
dc.subjectIschemic-Strokeen_US
dc.subjectCancer Patientsen_US
dc.subjectOvarian-Canceren_US
dc.subjectPlateleten_US
dc.subjectInflammationen_US
dc.titleComparison of colorectal neoplastic polyps and adenocarcinoma with regard to NLR and PLRen_US
dc.typearticleen_US
dc.relation.ispartofEuropean Review For Medical and Pharmacological Sciencesen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Genel Cerrahi Ana Bilim Dalıen_US
dc.departmentFakülteler, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyokimya Ana Bilim Dalıen_US
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalıen_US
dc.departmentFakülteler, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Tıbbi Patoloji Ana Bilim Dalıen_US
dc.authorid0000-0003-2006-9198
dc.authorid0000-0003-1584-2510
dc.identifier.volume19en_US
dc.identifier.issue19en_US
dc.identifier.startpage3613en_US
dc.identifier.endpage3618en_US
dc.institutionauthorEmir, Seyfi
dc.institutionauthorAydın, M.
dc.institutionauthorCan, G.
dc.institutionauthorBali, İlhan
dc.institutionauthorYıldırım, Oğuzhan
dc.institutionauthorÖznur, Meltem
dc.institutionauthorGürel, A.
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.authorscopusid17433815200
dc.authorscopusid7102765266
dc.authorscopusid57189216901
dc.authorscopusid55624501100
dc.authorscopusid55445082300
dc.authorscopusid15844109600
dc.authorscopusid25625782200
dc.authorwosidYildirim, Oguzhan/ABI-8174-2020
dc.authorwosidSözen, Selim/ABA-6337-2020
dc.identifier.wosWOS:000363789700014en_US
dc.identifier.scopus2-s2.0-84966293247en_US
dc.identifier.pmid26502851en_US


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