Publication:
Evaluation of TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms in Turkish patients with tuberculosis

dc.contributor.authorCeylan, Esma
dc.contributor.authorKarkucak, Mutlu
dc.contributor.authorÇoban, Hikmet
dc.contributor.buuauthorKaradağ, Mehmet
dc.contributor.buuauthorYakut, Tahsin
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentGöğüs Hastalıkları Ana Bilim Dalı
dc.contributor.departmentTıbbi Genetik Ana Bilim Dalı
dc.contributor.orcid0000-0002-9027-1132
dc.contributor.researcheridAAG-8744-2021
dc.contributor.scopusid6601970351
dc.contributor.scopusid6602802424
dc.date.accessioned2023-01-11T12:33:18Z
dc.date.available2023-01-11T12:33:18Z
dc.date.issued2016-11-18
dc.description.abstractObjective: 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.
dc.identifier.citationCeylan, 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.
dc.identifier.endpage777
dc.identifier.issn1876-0341
dc.identifier.issue6
dc.identifier.pubmed28189510
dc.identifier.scopus2-s2.0-85011903723
dc.identifier.startpage774
dc.identifier.urihttps://doi.org/10.1016/j.jiph.2016.11.003
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1876034117300151
dc.identifier.uri1876-035X
dc.identifier.urihttp://hdl.handle.net/11452/30402
dc.identifier.volume10
dc.identifier.wos000414231900016
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherElsevier
dc.relation.collaborationYurt içi
dc.relation.collaborationSanayi
dc.relation.journalJournal of Infection and Public Health
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectPublic, environmental & occupational health
dc.subjectInfectious diseases
dc.subjectGene polymorphism
dc.subjectMannose-binding lectin
dc.subjectTuberculosis
dc.subjectTumor necrosis factor-alpha
dc.subjectMannose-binding lectin
dc.subjectConfers protection
dc.subjectHepatitis-B
dc.subjectAssociation
dc.subjectSusceptibility
dc.subjectChildren
dc.subjectIl-10
dc.subjectInterleukin-10
dc.subjectMetaanalysis
dc.subjectMeningitis
dc.subject.emtreeMannose binding lectin 2
dc.subject.emtreeTumor necrosis factor
dc.subject.emtreeMannose binding lectin
dc.subject.emtreeMBL2 protein, human
dc.subject.emtreeTumor necrosis factor
dc.subject.emtreeAdult
dc.subject.emtreeArticle
dc.subject.emtreeBody mass
dc.subject.emtreeCodon
dc.subject.emtreeControlled study
dc.subject.emtreeDisease predisposition
dc.subject.emtreeDNA isolation
dc.subject.emtreeFemale
dc.subject.emtreeGene frequency
dc.subject.emtreeGenetic association
dc.subject.emtreeGenotype
dc.subject.emtreeHuman
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreePriority journal
dc.subject.emtreeRestriction fragment length polymorphism
dc.subject.emtreeSmoking
dc.subject.emtreeStatistical analysis
dc.subject.emtreeTuberculosis
dc.subject.emtreeGenetic association study
dc.subject.emtreeGenetic predisposition
dc.subject.emtreeGenetics
dc.subject.emtreeGenotyping technique
dc.subject.emtreeImmunology
dc.subject.emtreeMiddle aged
dc.subject.emtreePolymerase chain reaction
dc.subject.emtreeRestriction fragment length polymorphism
dc.subject.emtreeSingle nucleotide polymorphism
dc.subject.emtreeTuberculosis
dc.subject.meshAdult
dc.subject.meshFemale
dc.subject.meshGenetic association studies
dc.subject.meshGenetic predisposition to disease
dc.subject.meshGenotyping techniques
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMannose-binding lectin
dc.subject.meshMiddle aged
dc.subject.meshPolymerase chain reaction
dc.subject.meshPolymorphism, restriction fragment length
dc.subject.meshPolymorphism, single nucleotide
dc.subject.meshTuberculosis
dc.subject.meshTumor necrosis factor-alpha
dc.subject.meshTurkey
dc.subject.scopusMannose-Binding Lectins; Ficolin; Collectins
dc.subject.wosPublic, environmental & occupational health
dc.subject.wosInfectious diseases
dc.titleEvaluation of TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms in Turkish patients with tuberculosis
dc.typeArticle
dc.wos.quartileQ3 (Infectious diseases)
dc.wos.quartileQ2 (Public, environmental & occupational Health)
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Göğüs Hastalıkları Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS

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