Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/18888
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dc.contributor.authorChristodoulou, Andria-
dc.contributor.authorIerodiakonou, Despo-
dc.contributor.authorAwofala, Awoyemi Abayomi-
dc.contributor.authorPetrou, Michael-
dc.contributor.authorKales, Stefanos N.-
dc.contributor.authorChristiani, David C.-
dc.contributor.authorMantzoros, Christos S.-
dc.contributor.authorChristophi, Costas A.-
dc.date.accessioned2020-09-08T06:38:01Z-
dc.date.available2020-09-08T06:38:01Z-
dc.date.issued2020-01-01-
dc.identifier.citationPLoS ONE, 2020, vol. 15, no. 1, articl. no. e0225662en_US
dc.identifier.issn19326203-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/18888-
dc.descriptionThe article was funded by the “CUT Open Access Author Fund”en_US
dc.description.abstractBackground Obesity is a major risk factor for many chronic diseases, including reduced lung function. The role of polymorphisms of the adiponectin gene, though linked with cardiometabolic consequences of obesity, has not been studied in relation to lung function. Objectives The aim of this study is to examine polymorphisms in the ADIPOQ, ADIPOR1, and ADIPOR2 genes in relation to adiponectin serum levels, BMI, and adiposity in 18-year old Cypriot males, as well as determine whether BMI, adipokines levels and polymorphisms in adipokine related genes are associated with lung function levels. Results From the participants, 8% were classified as obese, 22% as overweight, and the remaining 71% as normal. We found that rs266729 and rs1501299 in ADIPOQ and rs10920531 in ADIPOR1 were significantly associated with serum adiponectin levels, after adjusting for ever smoking. In addition, there was an overall significant increase in FEV1%predicted with increasing BMI (β = 0.53, 95% CI: 0.27, 0.78) and in FVC %predicted (β = 1.02, 95% CI: 0.73, 1.30). There was also a decrease in FEV1/FVC with increasing BMI (β = -0.53, 95% CI: -0.71, -0.35). Finally, rs1501299 was associated with lung function measures. Discussion Functional variants in the ADIPOQ gene were linked with lung function in young males. Further studies should concentrate on the role of adipokines on lung function which may direct novel therapeutic approaches.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofPLoS ONEen_US
dc.rights© 2020 Christodoulou et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAdiponectin Receptorsen_US
dc.subjectAdipoRonen_US
dc.subjectHypoadiponectinemiaen_US
dc.titleVariants in ADIPOQ gene are linked to adiponectin levels and lung function in young males independent of obesityen_US
dc.typeArticleen_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationUniversity of Creteen_US
dc.collaborationTai Solarin University of Educationen_US
dc.collaborationCyprus Anti-doping Authorityen_US
dc.collaborationHarvard Universityen_US
dc.subject.categoryClinical Medicineen_US
dc.journalsOpen Accessen_US
dc.countryCyprusen_US
dc.countryGreeceen_US
dc.countryNigeriaen_US
dc.countryUnited Statesen_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1371/journal.pone.0225662en_US
dc.identifier.pmid31978107-
dc.identifier.scopus2-s2.0-85078244595-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85078244595-
dc.relation.issue1en_US
dc.relation.volume15en_US
cut.common.academicyear2019-2020en_US
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.openairetypearticle-
crisitem.author.deptDepartment of Rehabilitation Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0003-0503-1538-
crisitem.author.parentorgFaculty of Health Sciences-
crisitem.journal.journalissn1932-6203-
crisitem.journal.publisherPloS-
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