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dc.contributor.authorDemir, Nalan
dc.contributor.authorErçen Diken, Özlem
dc.contributor.authorKarabulut, Halil Gürhan
dc.contributor.authorKarnak, Demet
dc.contributor.authorKayacan, Oya
dc.date.accessioned2019-05-13T09:02:45Z
dc.date.available2019-05-13T09:02:45Z
dc.date.issued2017
dc.identifier.citationDemir, N., Erçen Diken, Ö., Karabulut, H. G., Karnak, D., Kayacan, O. (2017). Alpha-1 antitrypsin levels and polymorphisms in interstitial lung diseases. Turkish Journal of Medical Sciences, 47(2), 476-482.en_US
dc.identifier.issn1300-0144
dc.identifier.urihttps://doi.org/10.3906/sag-1508-76
dc.identifier.urihttps://hdl.handle.net/11491/1321
dc.description.abstractBackground/aim: Alpha-1 antitrypsin deficiency may be a potential predisposing factor for interstitial lung fibrosis. We investigated alpha-1 antitrypsin levels and its polymorphisms in patients with interstitial lung disease. Materials and methods: A total of 103 interstitial lung disease patients were compared. Results: The mean alpha-1 antitrypsin level in idiopathic interstitial pneumonia patients was 1.67 ± 0.33 g/L, and it was 1.54 ± 0.37 g/L in patients with nonidiopathic interstitial pneumonia (P = 0.13). Low alpha-1 antitrypsin levels were more frequently observed in nonidiopathic interstitial pneumonia patients compared with idiopathic interstitial pneumonia, but the difference was not statistically significant (8.9% vs. 0%, respectively, P = 0.4). In 100 patients, the normal PiMM genotype was detected, while abnormal ones (PiMZ, n = 2, 1.9%; PiMS, n = 1, 0.97%) were determined in three cases. When the frequency of alpha-1 antitrypsin polymorphism in interstitial lung disease patients was compared with the data of the healthy population, no significant difference was detected for the PiMZ and PiMS variants (P = 0.15 and P = 0.44, respectively). Conclusion: Lower levels of serum alpha-1 antitrypsin were more frequent in nonidiopathic interstitial pneumonia patients than idiopathic interstitial pneumonia without an increase in genetic polymorphism. The difference was not statistically significant. © TÜBİTAK.en_US
dc.language.isoeng
dc.publisherTurkiye Klinikleri Journal of Medical Sciencesen_US
dc.relation.isversionof10.3906/sag-1508-76en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAlpha-1 Antitrypsin Deficiencyen_US
dc.subjectIdiopathic Interstitial Pneumoniasen_US
dc.subjectInterstitial Lung Diseaseen_US
dc.titleAlpha-1 antitrypsin levels and polymorphisms in interstitial lung diseasesen_US
dc.typearticleen_US
dc.relation.journalTurkish Journal of Medical Sciencesen_US
dc.departmentHitit Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.identifier.volume47en_US
dc.identifier.issue2en_US
dc.identifier.startpage476en_US
dc.identifier.endpage482en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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