The role of glutation-s-transferase mu1 and teta1 polymorphisms in chronic obstructive pulmonary disease

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dc.contributor.authorHayat, Buket
dc.contributor.authorYavuz, Muhsin Selçuk
dc.contributor.authorSahin, Engin
dc.contributor.authorDirican, Onur
dc.contributor.authorSarialtin, Sezen Yilmaz
dc.contributor.authorYilmaz, Can
dc.contributor.authorYildirim, Isil
dc.date.accessioned2025-01-21T16:28:58Z
dc.date.available2025-01-21T16:28:58Z
dc.date.issued2021
dc.departmentKırıkkale Üniversitesi
dc.description.abstractObjective: The aim of this study the investigation of "null" alleles in GSTM1 and GSTT1 gene regions in the development of COPD disease. Material and Method: There are 36 patients with COPD and 14 control cases, who received the Ethics Committee permission from Polatli Duatepe State Hospital Chest Diseases Department. DNA isolations were made from blood samples from the end of 2019 and the control group. Deletions in GSTM1 and GSTT1 gene regions were examined by qPCR method in COPD patient and control groups. The results of the study were evaluated comparatively by distributing the gene dose according to the Hardy-Weinberg. Result and Discussion: When seen from 36 COPD patients after qPCR analysis, it was found that deletion expressions due to gene doses in all patient groups; 23 individuals (63.8%) in the (+/-) genotype for GST-M1, 13 individuals (26.2%) in the (-/-) genotype. For GST-T1, 14 (%) in the (+/+) genotype 38.8), while deletion was observed with the highest rate, 4 individuals (11.1%) in the (+/-) genotype and 18 individuals (50.1%) in the (-/-) genotype were found. For GST-M1, deletion was observed in 19 individuals (63.3%) in the genotype (+/-) in male individuals, while it was observed in 4 individuals (66.6%) with the same genotype in women. While deletion was not observed in 11 (36.6%) male patients, this rate was observed as 2 (33.4%) in women. In the GST-T1 gene region, there were 10 (33.3%) males in male patients and 4 (66.6%) individuals in female patients with deletion occurring and the frequency of the "null allele" was high (+/+). In the (+/-) genotype, 3 (10%) in males and 1 (16.7%) in females were found. In the genotype where deletion was not observed and the gene was conserved (-/-), 17 (56.7%) individuals were observed in male patients and 1 (16.7%) in female patients. In the case that the gene "null" allele status in the GST-M1 gene region is slightly higher than the GST-T1 gene communication, this situation is thought to be a factor in obstructive pulmonary disease. © 2021 University of Ankara. All rights reserved.
dc.identifier.doi10.33483/jfpau.839530
dc.identifier.endpage56
dc.identifier.issn2564-6524
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85102646688
dc.identifier.scopusqualityQ3
dc.identifier.startpage41
dc.identifier.trdizinid1118105
dc.identifier.urihttps://doi.org/10.33483/jfpau.839530
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1118105
dc.identifier.urihttps://hdl.handle.net/20.500.12587/23664
dc.identifier.volume45
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.language.isotr
dc.publisherUniversity of Ankara
dc.relation.ispartofAnkara Universitesi Eczacilik Fakultesi Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_20241229
dc.subjectCOPD; Deletion; Gst isozymes; Qpcr
dc.titleThe role of glutation-s-transferase mu1 and teta1 polymorphisms in chronic obstructive pulmonary disease
dc.title.alternativeKronik obstrüktif akciger hastaliginda glutatyon-s-transferaz mu1 ve teta1 polimorfizmlerinin rol
dc.typeArticle

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