Please use this identifier to cite or link to this item:
http://hdl.handle.net/11452/30402
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ceylan, Esma | - |
dc.contributor.author | Karkucak, Mutlu | - |
dc.contributor.author | Çoban, Hikmet | - |
dc.date.accessioned | 2023-01-11T12:33:18Z | - |
dc.date.available | 2023-01-11T12:33:18Z | - |
dc.date.issued | 2016-11-18 | - |
dc.identifier.citation | Ceylan, E. vd. (2017). ''Evaluation of TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms in Turkish patients with tuberculosis''. Journal of Infection and Public Health, 10(6), 774-777. | en_US |
dc.identifier.issn | 1876-0341 | - |
dc.identifier.uri | https://doi.org/10.1016/j.jiph.2016.11.003 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S1876034117300151 | - |
dc.identifier.uri | 1876-035X | - |
dc.identifier.uri | http://hdl.handle.net/11452/30402 | - |
dc.description.abstract | Objective: MBL acts as a binding protein that enables uptake of mycobacteria into macrophages. And, TNF-alpha is an important cytokine that is involved in control of mycobacterial infections both in-vivo and in-vitro. A large number of genetic factors exerting susceptibility to tuberculosis has been identified, among which mannose-binding lectin and tumor necrosis factor-alpha call attention. The objective of this study is to compare the frequency of TNF-alpha and MBL gene polymorphisms between patients diagnosed with tuberculosis and healthy volunteers in Turkey, and determine the association between tuberculosis and TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms. Material and methods: The study included 69 patients who were diagnosed with tuberculosis and 70 control subjects. The polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method was used to detect TNF-alpha (G308A) gene and MBL2 gene codon 54 polymorphisms. For statistical analysis, the significance level was determined as p < 0.05. Results: A comparison between patient and control groups in TNF-alpha (G308A) gene and MBL2 gene codon 54 polymorphisms showed no statistically significant difference (p > 0.05). However, a comparison of mean body mass index (BMI) and smoking status showed a statistically significant difference between the tuberculosis and control groups (p = 0.01 and p = 0.009, respectively). Conclusion: Our results suggest that the MBL2 gene Codon 54 and TNF-alpha gene G308A polymorphisms are not associated with an increased risk for development of tuberculosis in our patients. Further studies are required including more cases of tuberculosis patients and other potentially relevant gene polymorphisms. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Public, environmental & occupational health | en_US |
dc.subject | Infectious diseases | en_US |
dc.subject | Gene polymorphism | en_US |
dc.subject | Mannose-binding lectin | en_US |
dc.subject | Tuberculosis | en_US |
dc.subject | Tumor necrosis factor-alpha | en_US |
dc.subject | Mannose-binding lectin | en_US |
dc.subject | Confers protection | en_US |
dc.subject | Hepatitis-B | en_US |
dc.subject | Association | en_US |
dc.subject | Susceptibility | en_US |
dc.subject | Children | en_US |
dc.subject | Il-10 | en_US |
dc.subject | Interleukin-10 | en_US |
dc.subject | Metaanalysis | en_US |
dc.subject | Meningitis | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Genetic association studies | en_US |
dc.subject.mesh | Genetic predisposition to disease | en_US |
dc.subject.mesh | Genotyping techniques | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Mannose-binding lectin | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Polymerase chain reaction | en_US |
dc.subject.mesh | Polymorphism, restriction fragment length | en_US |
dc.subject.mesh | Polymorphism, single nucleotide | en_US |
dc.subject.mesh | Tuberculosis | en_US |
dc.subject.mesh | Tumor necrosis factor-alpha | en_US |
dc.subject.mesh | Turkey | en_US |
dc.title | Evaluation of TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms in Turkish patients with tuberculosis | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000414231900016 | tr_TR |
dc.identifier.scopus | 2-s2.0-85011903723 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Göğüs Hastalıkları Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı. | tr_TR |
dc.contributor.orcid | 0000-0002-9027-1132 | tr_TR |
dc.identifier.startpage | 774 | tr_TR |
dc.identifier.endpage | 777 | tr_TR |
dc.identifier.volume | 10 | tr_TR |
dc.identifier.issue | 6 | tr_TR |
dc.relation.journal | Journal of Infection and Public Health | en_US |
dc.contributor.buuauthor | Karadağ, Mehmet | - |
dc.contributor.buuauthor | Yakut, Tahsin | - |
dc.contributor.researcherid | AAG-8744-2021 | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.identifier.pubmed | 28189510 | tr_TR |
dc.subject.wos | Public, environmental & occupational health | en_US |
dc.subject.wos | Infectious diseases | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q3 (Infectious diseases) | en_US |
dc.wos.quartile | Q2 (Public, environmental & occupational Health) | en_US |
dc.contributor.scopusid | 6601970351 | tr_TR |
dc.contributor.scopusid | 6602802424 | tr_TR |
dc.subject.scopus | Mannose-Binding Lectins; Ficolin; Collectins | en_US |
dc.subject.emtree | Mannose binding lectin 2 | en_US |
dc.subject.emtree | Tumor necrosis factor | en_US |
dc.subject.emtree | Mannose binding lectin | en_US |
dc.subject.emtree | MBL2 protein, human | en_US |
dc.subject.emtree | Tumor necrosis factor | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Body mass | en_US |
dc.subject.emtree | Codon | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Disease predisposition | en_US |
dc.subject.emtree | DNA isolation | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Gene frequency | en_US |
dc.subject.emtree | Genetic association | en_US |
dc.subject.emtree | Genotype | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Restriction fragment length polymorphism | en_US |
dc.subject.emtree | Smoking | en_US |
dc.subject.emtree | Statistical analysis | en_US |
dc.subject.emtree | Tuberculosis | en_US |
dc.subject.emtree | Genetic association study | en_US |
dc.subject.emtree | Genetic predisposition | en_US |
dc.subject.emtree | Genetics | en_US |
dc.subject.emtree | Genotyping technique | en_US |
dc.subject.emtree | Immunology | en_US |
dc.subject.emtree | Middle aged | en_US |
dc.subject.emtree | Polymerase chain reaction | en_US |
dc.subject.emtree | Restriction fragment length polymorphism | en_US |
dc.subject.emtree | Single nucleotide polymorphism | en_US |
dc.subject.emtree | Tuberculosis | en_US |
Appears in Collections: | Scopus Web of Science |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
Karadağ_vd_2017.pdf | 478.81 kB | Adobe PDF | View/Open |
This item is licensed under a Creative Commons License