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Lack of association between the Klotho gene and COPD

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dc.contributor.authorKim, Woo Jin-
dc.contributor.authorOh, Yeon-Mok-
dc.contributor.authorKim, Tae-Hyung-
dc.contributor.authorLee, Ji-Hyun-
dc.contributor.authorKim, Eun-Kyung-
dc.contributor.authorLee, Jin Hwa-
dc.contributor.authorLee, Sang-Min-
dc.contributor.authorShin, Tae Rim-
dc.contributor.authorYoon, Ho Il-
dc.contributor.authorLim, Seong-Yong-
dc.contributor.authorLee, Sang Do-
dc.date.accessioned2022-07-16T18:59:31Z-
dc.date.available2022-07-16T18:59:31Z-
dc.date.created2021-05-11-
dc.date.issued2011-10-
dc.identifier.issn1738-3536-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/167542-
dc.description.abstractBackground: Although the aging process and features of chronic obstructive pulmonary disease (COPD) have several similarities, the relationship between aging and COPD pathogenesis remains incompletely understood. The klotho gene was found to be related to premature aging and emphysematous changes in an animal model. We investigated whether klotho gene polymorphisms are related to COPD susceptibility and emphysema severity. Methods: A total of 219 COPD subjects from the Korean Obstructive Lung Disease Cohort and 305 control subjects were genotyped for two single nucleotide polymorphisms (SNPs) of the klotho gene associated with coronary artery disease. Logistic regression was performed to determine the association of these SNPs with COPD susceptibility and linear, regression was performed to investigate their association with emphysema severity in COPD subjects. Results: The mean age of the COPD subjects was 66 years and their mean FEV1 was 1.46 L. There were no associations between either SNP or COPD susceptibility (p=0.6 and 0.2, respectively) and there were no associations with emphysema severity. Conclusion: Genetic polymorphisms of the klotlto gene were not associated with COPD in a Korean population.-
dc.language영어-
dc.language.isoen-
dc.publisher대한결핵및호흡기학회-
dc.titleLack of association between the Klotho gene and COPD-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Tae-Hyung-
dc.identifier.doi10.4046/trd.2011.71.4.254-
dc.identifier.scopusid2-s2.0-81455128946-
dc.identifier.bibliographicCitationTuberculosis and Respiratory Diseases, v.71, no.4, pp.254 - 258-
dc.relation.isPartOfTuberculosis and Respiratory Diseases-
dc.citation.titleTuberculosis and Respiratory Diseases-
dc.citation.volume71-
dc.citation.number4-
dc.citation.startPage254-
dc.citation.endPage258-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001598142-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordPlusKlotho protein-
dc.subject.keywordPlusaged-
dc.subject.keywordPlusarticle-
dc.subject.keywordPluschronic obstructive lung disease-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPluscoronary artery disease-
dc.subject.keywordPlusdisease predisposition-
dc.subject.keywordPlusdisease severity-
dc.subject.keywordPlusemphysema-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusforced expiratory volume-
dc.subject.keywordPlusgenetic association-
dc.subject.keywordPlusgenetic polymorphism-
dc.subject.keywordPlusgenotype-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusKorea-
dc.subject.keywordPluslogistic regression analysis-
dc.subject.keywordPlusmajor clinical study-
dc.subject.keywordPlusmale-
dc.subject.keywordPlussingle nucleotide polymorphism-
dc.subject.keywordAuthorChronic obstructive-
dc.subject.keywordAuthorGenetic-
dc.subject.keywordAuthorPolymorphism-
dc.subject.keywordAuthorPulmonary disease-
dc.identifier.urlhttps://www.e-trd.org/journal/view.php?doi=10.4046/trd.2011.71.4.254-
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