Paraoxonase activity and phenotype distribution in patients with chronic obstructive pulmonary disease

dc.authorid0000-0001-7092-8857en_US
dc.authorid0000-0002-1123-6196en_US
dc.authorid0000-0002-5180-9649en_US
dc.authorid0000-0001-7092-8857en_US
dc.contributor.authorSarıoğlu, Nurhan
dc.contributor.authorBilen, Çiğdem
dc.contributor.authorÇevik, Celalettin
dc.contributor.authorGencer, Nahit
dc.date.accessioned2021-03-24T08:23:43Z
dc.date.available2021-03-24T08:23:43Z
dc.date.issued2020en_US
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.departmentFakülteler, Sağlık Bilimleri Fakültesi, Hemşirelik Bölümüen_US
dc.description.abstractObjective: Paraoxonase 1 (PON1) and arylesterase (ARE) enzymes have an important role in the prevention of oxidative stress which is related to the pathogenesis of chronic obstructive pulmonary disease (COPD). PON1 levels vary widely among individuals and ethnic groups, which is in part associated with polymorphisms. Materials and Methods: We investigated PON1 and ARE activity and phenotype distribution in COPD patients and healthy individuals. Sixty six COPD patients and 59 control subjects were involved in the study. Serum PON1 and ARE activities were detected by spectrophotometric method. The ratio of salt-induced PON1 to ARE activity was used to determine phenotypes as QQ, QR, and RR. Results: COPD patients exhibited higher PON1 activity (199.1 vs 129.2, p=0.002) but lower ARE activity compared to control (21.3 vs 33.5, p=0.021). There was a significant difference between COPD and control group with respect to PON1 phenotype characteristics. RR phenotypic distribution was more common in the COPD group than in control (60.6% [95% CI: 48.8 - 72.3] versus 22.0 % [95% CI: 12.0 - 31.9], p=0.001). We also found that smoking (95.0% CI: 0.001-0.036, p<0.001) and RR phenotype (95.0% CI: 0.006 - 0.59, p=0.016) are independent determinants in COPD. Conclusion: We found that RR phenotype was more common in COPD patients compared to control. Smoking and RR phenotype may be defined as independent factors associated with COPD.en_US
dc.identifier.doi10.5152/eurasianjmed.2019.19122
dc.identifier.endpage165en_US
dc.identifier.issn1308-8742
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-85087045373
dc.identifier.scopusqualityQ2
dc.identifier.startpage161en_US
dc.identifier.trdizinid382865
dc.identifier.urihttps://doi.org/10.5152/eurasianjmed.2019.19122
dc.identifier.urihttps://hdl.handle.net/20.500.12462/11295
dc.identifier.volume52en_US
dc.identifier.wosWOS:000542299000012
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherAVESen_US
dc.relation.ispartofEurasian Journal of Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectCOPDen_US
dc.subjectParaoxonase 1en_US
dc.subjectPhenotypeen_US
dc.titleParaoxonase activity and phenotype distribution in patients with chronic obstructive pulmonary diseaseen_US
dc.typeArticleen_US

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