dc.contributorLaboratory of Immunogenetics
dc.contributorUniversidade Estadual Paulista (UNESP)
dc.contributorHospital de Base of the Regional Medical Faculty Foundation (HB-FUNFARME)
dc.contributorVisum Clinic
dc.date.accessioned2022-04-29T08:45:55Z
dc.date.accessioned2022-12-20T03:16:54Z
dc.date.available2022-04-29T08:45:55Z
dc.date.available2022-12-20T03:16:54Z
dc.date.created2022-04-29T08:45:55Z
dc.date.issued2021-01-01
dc.identifierMolecular Biology Reports.
dc.identifier1573-4978
dc.identifier0301-4851
dc.identifierhttp://hdl.handle.net/11449/231514
dc.identifier10.1007/s11033-021-06708-z
dc.identifier2-s2.0-85115372217
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5411648
dc.description.abstractBackground: Until a few years ago, keratoconus was defined as a noninflammatory degenerative disease. However, recent studies have shown that the altered balance between inflammatory cytokines, proteases, and protease inhibitors, as well as free radicals and oxidants, have a crucial role in the pathogenesis of this disease. The aim of this study is to investigate whether interleukin 17 A G197A (rs2275913) and interleukin 17 F T7488C (rs763780) polymorphisms are associated with keratoconus in patients from a population of the northwestern region of the State of São Paulo, Brazil. Methods and Results: 35 patients and 61 controls were enrolled. Genotyping of interleukin 17 A G197A and interleukin 17 F T7488C polymorphisms was carried out using the polymerase chain reaction-restriction fragment length polymorphism technique. Statistical analyses were conducted using the chi-square test, and an odds ratio with a 95% confidence interval was also calculated to evaluate the association between polymorphisms and disease. Evaluating interleukin 17 F T7488C, we found that the TT genotype is associated as a risk factor for keratoconus (P = 0.04; OR = 3.01; CI 1.11–8.14). As for evaluating interleukin 17 A G197A, the allele and genotype frequencies between patients and controls were compared and no statistically significant differences were found. Conclusions: Our data showed that the interleukin 17 F T7488C polymorphisms may exert an influence in keratoconus.
dc.languageeng
dc.relationMolecular Biology Reports
dc.sourceScopus
dc.subjectCytokines
dc.subjectEctasia
dc.subjectGenetic polymorphisms
dc.subjectIL17 genotypes
dc.subjectInterleukins
dc.subjectKeratoconus
dc.titleInfluence of interleukin 17 A and 17 F polymorphisms in keratoconus
dc.typeArtículos de revistas


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