Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/3614
DC FieldValueLanguage
dc.contributor.authorHamnvik, Ole-Petter R.-
dc.contributor.authorLiu, Xiamen-
dc.contributor.authorPetrou, Michael-
dc.contributor.authorGong, Huizhi-
dc.contributor.authorChamberland, John P.-
dc.contributor.authorKim, Esther H.-
dc.contributor.authorKales, Stefanos N.-
dc.contributor.authorChristiani, David C.-
dc.contributor.authorMantzoros, Christos S.-
dc.contributor.authorChristophi, Costas A.-
dc.dateJUL 2011en
dc.date.accessioned2014-07-09T08:06:46Z-
dc.date.accessioned2015-12-08T11:09:10Z-
dc.date.available2014-07-09T08:06:46Z-
dc.date.available2015-12-08T11:09:10Z-
dc.date.issued2011-07-
dc.identifier0026-0495en
dc.identifier.citationMetabolism, 2011, vol. 60, no. 7, pp. 987-993en_US
dc.identifier.issn15328600-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/3614-
dc.description.abstractWe examined the relationship between serum levels of leptin-binding protein (soluble leptin receptor [sOB-R]) and leptin with metabolic parameters at baseline and prospectively at 2-year follow-up in young healthy men. A total of 916 eighteen-year-old men were examined at baseline, with a subgroup of 91 participants examined again 2 years later. Anthropometric and metabolic measurements were performed at baseline and at follow-up. In the cross-sectional study, levels of sOB-R were significantly inversely correlated with all baseline measures of obesity and metabolic risk factors (blood pressure, total and low-density lipoprotein cholesterol, and fasting glucose), and significantly positively correlated with high-density lipoprotein cholesterol. After correcting for age, smoking status, and waist-to-hip ratio, the inverse correlation remained statistically significant for all measures of adiposity, fasting glucose, and the metabolic syndrome score. Correlations for leptin were similar in magnitude but opposite in direction to correlations for sOB-R. In prospective analyses, baseline levels of sOB-R were predictive at 2-year follow-up of fasting glucose, the metabolic syndrome score, and measures of adiposity in both unadjusted and adjusted models. Similarly, leptin was predictive of fasting glucose, the metabolic syndrome score, adiposity, and systolic blood pressure. We confirm correlations of leptin and sOB-R levels with measures of adiposity and metabolic risk factors at baseline, and demonstrate for the first time prospectively the role of sOB-R as an independent, although weak, predictor of metabolic syndrome and fasting glucose in young men. (C) 2011 Elsevier Inc. All rights reserved.en_US
dc.languageEnglishen
dc.language.isoenen_US
dc.relation.ispartofMetabolismen_US
dc.rights© Elsevieren_US
dc.subjectLeptin Receptoren_US
dc.subjectAdiponectinen_US
dc.subjectOvary Polycystic Diseaseen_US
dc.titleSoluble leptin receptor and leptin are associated with baseline adiposity and metabolic risk factors, and predict adiposity, metabolic syndrome, and glucose levels at 2-year follow-up: the Cyprus Metabolism Prospective Cohort Studyen_US
dc.typeArticleen_US
dc.collaborationBrigham and Women's Hospitalen_US
dc.collaborationHarvard Universityen_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationBoston VA Healthcare Systemen_US
dc.subject.categoryBasic Medicineen_US
dc.journalsSubscriptionen_US
dc.reviewPEER-REVIEWED-
dc.countryUnited Statesen_US
dc.countryCyprusen_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1016/j.metabol.2010.09.009en_US
dc.dept.handle123456789/108en
dc.relation.issue7en_US
dc.relation.volume60en_US
cut.common.academicyear2011-2012en_US
dc.identifier.spage987en_US
dc.identifier.epage993en_US
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.journal.journalissn0026-0495-
crisitem.journal.publisherElsevier-
crisitem.author.deptDepartment of Rehabilitation Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0003-0503-1538-
crisitem.author.parentorgFaculty of Health Sciences-
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