Does Neutrophil / Lymphocyte Ratio Contribute To Diagnostics in Patients With Fascioliasis

dc.contributor.author Cicek, Mutalip
dc.contributor.author Deveci, Ozcan
dc.contributor.author Cengiz, ZeynepTas
dc.contributor.author Bilden, Alican
dc.contributor.author Bilik, Ozge Alkan
dc.date.accessioned 2025-05-10T17:59:35Z
dc.date.available 2025-05-10T17:59:35Z
dc.date.issued 2018
dc.description.abstract Introduction: Fasciolia sp. is a trematode causes infection by settling in the liver bile ducts of domestic animal and human liver. Fascioliasis is a parasite disease that might have changes in liver parenchyma and in bile ducts. Many inflammatory reactions occur during the settlement of larvae and mature parasites into the liver. The neutrophil/lymphocyte ratio (NLR) has become a prominent marker of underlying inflammation. The objective of the present study is to investigate the relationship between the hematological parameters in patients with fascioliasis. Materials and methods: The diagnosis of fascioliasis was based on patient history, clinical and laboratory findings, radiological imaging (ultrasound), stool examination and IgG antibody titer determination by ELISA. Clinical and laboratory data were collected for 56 patients with fascioliasis, and diagnosed with serological and radiological imaging. 56 healthy volunteers were selected for the control group. Stool and blood samples were collected from patients with fascioliasis for serologic, biochemical, hematologic tests and ova examination. Total leukocyte, neutrophil, eosinophil and lymphocyte counts were recorded and NLR was calculated. ELISA antibody cut off titer value of patients with fascioliasis was 10> positive. Results: We compared neutrophil/lymphocyte ratio, eosinophil/lymphocyte ratio, the relation of eosinophilia and IgG antibody titers between two groups (patient and control groups). There was no statistically significant difference between patients and healthy controls neither based on age and gender nor NLR. According to these findings, NLR can not be considered as a diagnostic marker in fascioliasis. Conclusion: As a result, it was determined that NLR is not a crucial indicator of inflammation in parasitic fascioliasis. Extensive studies are need to be done to clarify the correlation between NLR and progression of other parasitic diseases. en_US
dc.identifier.doi 10.19193/0393-6384_2018_4_145
dc.identifier.issn 0393-6384
dc.identifier.issn 2283-9720
dc.identifier.scopus 2-s2.0-85061457339
dc.identifier.uri https://doi.org/10.19193/0393-6384_2018_4_145
dc.identifier.uri https://hdl.handle.net/20.500.14720/20585
dc.language.iso en en_US
dc.publisher Carbone Editore en_US
dc.relation.ispartof Acta Medica Mediterranea en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Fascioliasis en_US
dc.subject Neutrophil/Lymphocyte Ratio en_US
dc.subject Contribution To Diagnosis en_US
dc.title Does Neutrophil / Lymphocyte Ratio Contribute To Diagnostics in Patients With Fascioliasis en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 8524442500
gdc.author.scopusid 55676015400
gdc.author.scopusid 6504565816
gdc.author.scopusid 57205754559
gdc.author.scopusid 57205752558
gdc.author.wosid Tas Cengiz, Zeynep/Hjh-3466-2023
gdc.author.wosid Deveci, Ozcan/A-2031-2017
gdc.author.wosid Alkan Bi̇li̇k, Özge/Gro-6059-2022
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Cicek, Mutalip] Ahi Evran Univ, Fac Med, Dept Med Microbiol, Kirsehir, Turkey; [Deveci, Ozcan] Elazig Med Pk Hosp, Dept Clin Microbiol & Infect Dis, Elazig, Turkey; [Cengiz, ZeynepTas] Yuzuncu Yil Univ, Fac Med, Dept Med Parasitol, Van, Turkey; [Bilden, Alican; Bilik, Ozge Alkan] Dicle Univ, Fac Med, Dept Med Microbiol, Diyarbakir, Turkey en_US
gdc.description.endpage 958 en_US
gdc.description.issue 4 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality N/A
gdc.description.startpage 955 en_US
gdc.description.volume 34 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q4
gdc.identifier.wos WOS:000434986500008
gdc.index.type WoS
gdc.index.type Scopus

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