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Association of white blood cell count with metabolic syndrome in patients undergoing peritoneal dialysis

DC Field Value Language
dc.contributor.author강신욱-
dc.contributor.author박정탁-
dc.contributor.author유태현-
dc.contributor.author이정은-
dc.contributor.author장태익-
dc.contributor.author최훈영-
dc.date.accessioned2015-04-24T17:03:08Z-
dc.date.available2015-04-24T17:03:08Z-
dc.date.issued2009-
dc.identifier.issn0026-0495-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/104668-
dc.description.abstractMetabolic syndrome is associated with an increased risk of diabetes and cardiovascular disease. Although some data suggest that the prevalence of metabolic syndrome is higher in patients undergoing peritoneal dialysis (PD), the factors related to this increased risk are not well elucidated. We therefore examined whether peripheral white blood cell (WBC) count is correlated with the risk of metabolic syndrome in nondiabetic PD patients. We enrolled 104 nondiabetic PD patients without current infections or chronic inflammatory diseases. Complete blood cell count, anthropometry, blood pressure, fasting glucose, insulin, and lipid profiles were measured. Metabolic syndrome was defined in accordance with the National Cholesterol Education Program (Adult Treatment Panel III) criteria. Metabolic syndrome was present in 49 patients (47.1%). Patients with metabolic syndrome had a higher WBC count and high-sensitivity C-reactive protein level. As the number of metabolic syndrome components increased, WBC count increased significantly. White blood cell count was significantly positively correlated with body mass index, insulin, homeostasis model assessment of insulin resistance, and triglyceride and negatively correlated with high-density lipoprotein cholesterol. The risk of metabolic syndrome increased significantly with a higher WBC count, resulting in an adjusted odds ratio of 1.65 (per 10(3)/muL increase, P = .002). These findings demonstrate that metabolic syndrome is prevalent among nondiabetic PD patients and that WBC count is strongly associated with metabolic syndrome and its components-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfMETABOLISM-CLINICAL AND EXPERIMENTAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHBlood Glucose/metabolism-
dc.subject.MESHBody Mass Index-
dc.subject.MESHCross-Sectional Studies-
dc.subject.MESHDialysis Solutions/metabolism-
dc.subject.MESHFemale-
dc.subject.MESHGlucose/metabolism-
dc.subject.MESHHumans-
dc.subject.MESHInsulin/blood-
dc.subject.MESHInsulin Resistance-
dc.subject.MESHKidney Failure, Chronic/blood*-
dc.subject.MESHKidney Failure, Chronic/complications-
dc.subject.MESHKidney Failure, Chronic/therapy-
dc.subject.MESHLeukocyte Count*-
dc.subject.MESHLeukocytes/physiology*-
dc.subject.MESHMale-
dc.subject.MESHMetabolic Syndrome/blood*-
dc.subject.MESHMetabolic Syndrome/complications-
dc.subject.MESHPeritoneal Dialysis*-
dc.subject.MESHROC Curve-
dc.titleAssociation of white blood cell count with metabolic syndrome in patients undergoing peritoneal dialysis-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorJung Tak Park-
dc.contributor.googleauthorTae Ik Chang-
dc.contributor.googleauthorDong Ki Kim-
dc.contributor.googleauthorHoon Young Choi-
dc.contributor.googleauthorJung Eun Lee-
dc.contributor.googleauthorHyun Wook Kim-
dc.contributor.googleauthorJae Hyun Chang-
dc.contributor.googleauthorSun Young Park-
dc.contributor.googleauthorEunyoung Kim-
dc.contributor.googleauthorTae-Hyun Yoo-
dc.contributor.googleauthorDae-Suk Han-
dc.contributor.googleauthorShin-Wook Kang-
dc.identifier.doi10.1016/j.metabol.2009.05.002-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00053-
dc.contributor.localIdA01654-
dc.contributor.localIdA02526-
dc.contributor.localIdA03486-
dc.contributor.localIdA04226-
dc.contributor.localIdA00811-
dc.contributor.localIdA03119-
dc.relation.journalcodeJ02223-
dc.identifier.eissn1532-8600-
dc.identifier.pmid19501862-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0026049509001644-
dc.contributor.alternativeNameKang, Shin Wook-
dc.contributor.alternativeNameKim, Eun Young-
dc.contributor.alternativeNamePark, Jung Tak-
dc.contributor.alternativeNameYoo, Tae Hyun-
dc.contributor.alternativeNameLee, Jung Eun-
dc.contributor.alternativeNameChang, Tae Ik-
dc.contributor.alternativeNameChoi, Hoon Young-
dc.contributor.affiliatedAuthorKang, Shin Wook-
dc.contributor.affiliatedAuthorPark, Jung Tak-
dc.contributor.affiliatedAuthorYoo, Tae Hyun-
dc.contributor.affiliatedAuthorChang, Tae Ik-
dc.contributor.affiliatedAuthorChoi, Hoon Young-
dc.contributor.affiliatedAuthorKim, Eun Young-
dc.contributor.affiliatedAuthorLee, Jung Eun-
dc.citation.volume58-
dc.citation.number10-
dc.citation.startPage1379-
dc.citation.endPage1385-
dc.identifier.bibliographicCitationMETABOLISM-CLINICAL AND EXPERIMENTAL, Vol.58(10) : 1379-1385, 2009-
dc.identifier.rimsid52847-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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