Evaluation of IFN-γ polymorphism in visceral leishmaniasis
dc.contributor.author | Maghsood, AH | |
dc.contributor.author | Jadideslam, G | |
dc.contributor.author | Fallah, M | |
dc.contributor.author | Bazmani, A | |
dc.date.accessioned | 2018-08-26T08:54:32Z | |
dc.date.available | 2018-08-26T08:54:32Z | |
dc.date.issued | 2014 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54156 | |
dc.description.abstract | Background: Leishmaniasis is a tropical disease that is endemic in some areas of Iran, includ-ing East Azerbaijan. IFN-? is one of the cytokines that triggers cell-mediated immunity, thus initi-ating elimination of the infection. This case-control study was performed to investigate the asso-ciation between the polymorphism of the IFN-? gene at the +874A/T locus and visceral leishman-iasis (VL). Methods: In this study conducted during 2012-2013, 267 participants were selected from indi-viduals living in an endemic area of VL. Subjects were divided into three groups; 86 patients with VL, 82 seropositive individuals without any history of leishmaniasis, and 99 seronegative healthy controls. Genotyping of the IFN-? +874A/T polymorphism was carried out using an Amplification Refractory Mutation System-PCR (ARMS-PCR). Results: The frequency of the +874A allele in the patient group (75.5%) was higher than in the seropositive individuals (54%). The highest frequency of the +874T/T genotype was observed in seropositive individuals, while the patient group had the lowest frequency (34.1% vs. 24.5%). However, these differences were not significant. Conclusion: There was no significant association between IFN-? +874A/T polymorphism and VL. | |
dc.language.iso | English | |
dc.relation.ispartof | Journal of Research in Health Sciences | |
dc.subject | gamma interferon | |
dc.subject | gamma interferon | |
dc.subject | article | |
dc.subject | case control study | |
dc.subject | child | |
dc.subject | child health | |
dc.subject | clinical evaluation | |
dc.subject | controlled study | |
dc.subject | endemic disease | |
dc.subject | female | |
dc.subject | gene frequency | |
dc.subject | gene locus | |
dc.subject | genetic association | |
dc.subject | genetic polymorphism | |
dc.subject | heterozygote | |
dc.subject | human | |
dc.subject | IFN gamma gene | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | polymerase chain reaction | |
dc.subject | preschool child | |
dc.subject | school child | |
dc.subject | sex ratio | |
dc.subject | visceral leishmaniasis | |
dc.subject | adolescent | |
dc.subject | allele | |
dc.subject | Azerbaijan | |
dc.subject | cellular immunity | |
dc.subject | gene frequency | |
dc.subject | genetic predisposition | |
dc.subject | genetics | |
dc.subject | genotype | |
dc.subject | infant | |
dc.subject | Iran | |
dc.subject | single nucleotide polymorphism | |
dc.subject | visceral leishmaniasis | |
dc.subject | Adolescent | |
dc.subject | Alleles | |
dc.subject | Azerbaijan | |
dc.subject | Case-Control Studies | |
dc.subject | Child | |
dc.subject | Child, Preschool | |
dc.subject | Endemic Diseases | |
dc.subject | Gene Frequency | |
dc.subject | Genetic Predisposition to Disease | |
dc.subject | Genotype | |
dc.subject | Humans | |
dc.subject | Immunity, Cellular | |
dc.subject | Infant | |
dc.subject | Interferon-gamma | |
dc.subject | Iran | |
dc.subject | Leishmaniasis, Visceral | |
dc.subject | Polymorphism, Single Nucleotide | |
dc.title | Evaluation of IFN-γ polymorphism in visceral leishmaniasis | |
dc.type | Article | |
dc.citation.volume | 14 | |
dc.citation.issue | 2 | |
dc.citation.spage | 136 | |
dc.citation.epage | 139 | |
dc.citation.index | Scopus |