The Role of Glutation-S Mu1 and Teta1 Polymorphisms in Chronic Obstructive Pulmonary Disease

dc.contributor.author Hayat, B.
dc.contributor.author Yavuz, M.S.
dc.contributor.author Sahin, E.
dc.contributor.author Dirican, O.
dc.contributor.author Sarialtin, S.Y.
dc.contributor.author Yilmaz, C.
dc.contributor.author Oguztüzün, S.
dc.date.accessioned 2025-05-10T17:03:18Z
dc.date.available 2025-05-10T17:03:18Z
dc.date.issued 2021
dc.description.abstract Objective: 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. en_US
dc.identifier.doi 10.33483/jfpau.839530
dc.identifier.issn 2564-6524
dc.identifier.scopus 2-s2.0-85102646688
dc.identifier.uri https://doi.org/10.33483/jfpau.839530
dc.identifier.uri https://hdl.handle.net/20.500.14720/5677
dc.language.iso tr en_US
dc.publisher University of Ankara en_US
dc.relation.ispartof Ankara Universitesi Eczacilik Fakultesi Dergisi en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Copd en_US
dc.subject Deletion en_US
dc.subject Gst Isozymes en_US
dc.subject Qpcr en_US
dc.title The Role of Glutation-S Mu1 and Teta1 Polymorphisms in Chronic Obstructive Pulmonary Disease en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.scopusid 57222401737
gdc.author.scopusid 57222400749
gdc.author.scopusid 57222407542
gdc.author.scopusid 57194340152
gdc.author.scopusid 57146469600
gdc.author.scopusid 57221517895
gdc.author.scopusid 59662797300
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp Hayat B., Biyoloji Bölümü, Kirikkale ÜNiversitesi, Kirikkale, 71450, Turkey; Yavuz M.S., Duatepe Polatli Devlet Hastanesi, Anestezi Ve Reanimasyon Klinigi, Ankara, 06900, Turkey; Sahin E., Ankara Atatürk Gögüs Hastaliklari Egitim Ve Arastirma Hastanesi, Gögüs Hastaliklari Klinigi, Ankara, 06280, Turkey; Dirican O., Biyoloji Bölümü, Kirikkale ÜNiversitesi, Kirikkale, 71450, Turkey; Sarialtin S.Y., Eczacilik Fakültesi, Ankara ÜNiversitesi, Farmasötik Toksikoloji Anabilim Dali, Ankara, 06560, Turkey; Yilmaz C., Moleküler Biyoloji Ve Genetik Bölümü, Fen Fakültesi, Van Yüzüncuÿil ÜNiversitesi, Van, 65090, Turkey; Yildirim I., Eczane Hizmetleri Programi, Beykent ÜNiversitesi, Meslek Yüksekokulu, Biyokimya Alani, Istanbul, 34500, Turkey; Çoban T., Eczacilik Fakültesi, Ankara ÜNiversitesi, Farmasötik Toksikoloji Anabilim Dali, Ankara, 06560, Turkey; Simsek G.G., Saglik Bilimleri ÜNiversitesi, Keçiören Egitim Ve Arastirma Hastanesi, Ankara, 06000, Turkey; Oguztüzün S., Biyoloji Bölümü, Kirikkale ÜNiversitesi, Kirikkale, 71450, Turkey en_US
gdc.description.endpage 56 en_US
gdc.description.issue 1 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q4
gdc.description.startpage 41 en_US
gdc.description.volume 45 en_US
gdc.description.wosquality N/A
gdc.identifier.trdizinid 1118105
gdc.index.type Scopus
gdc.index.type TR-Dizin

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