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Association between hypoadiponectinemia and cardiovascular risk factors in nonobese healthy adults

DC Field Value Language
dc.contributor.author심재용-
dc.contributor.author이덕철-
dc.contributor.author이지원-
dc.contributor.author이혜리-
dc.date.accessioned2015-06-10T12:05:13Z-
dc.date.available2015-06-10T12:05:13Z-
dc.date.issued2006-
dc.identifier.issn0026-0495-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/109165-
dc.description.abstractAdiponectin levels are significantly lower in obeseadultpatients with type 2 diabetes mellitus, essential hypertension, dyslipidemia, andcardiovasculardisease. However, the role ofhypoadiponectinemiainnonobesehealthyadultshas not been fully elucidated. In this study, we examined theassociationbetweenhypoadiponectinemiaandcardiovascularrisk factorsand estimated plasma adiponectin values innonobese, apparentlyhealthyadults. A total of 204 male and 214 femalehealthyindividuals aged 20 to 80 years, with a body mass index (BMI) of less than 25 kg/m2, were included in this study. We measured patients' plasma adiponectin levels, serum lipid profiles, high-sensitivity C-reactive protein (hs-CRP) levels, fasting glucose levels, and fasting insulin levels. Mean values of plasma adiponectin were 5.45 +/- 3.3 microg/mL in male and 8.16 +/- 4.6 microg/mL in female subjects. Thehypoadiponectinemiagroup (< 4.0 microg/mL) had significantly higher levels (P < .01) of BMI, fasting glucose, fasting insulin, homeostasis model assessment of insulin resistance (HOMA-IR), and triglycerides, but lower levels of high-density lipoprotein cholesterol (HDL-C). In males, plasma adiponectin levels were inversely correlated with BMI (r = -0.32, P < .01), HOMA-IR (r = -0.14, P < .05), triglyceride levels (r = -0.17, P < .05), and hs-CRP levels (r = -0.15, P < .05), and positively correlated with HDL-C (r = 0.24, P < .01). In females, plasma adiponectin levels were negatively correlated with BMI (r = -0.31, P < .01), fasting glucose (r = -0.18, P < .01), fasting insulin (r = -0.23, P < .01), HOMA-IR (r = -0.24, P < .01), and triglyceride (r = -0.18, P < .01) levels, and positively correlated with HDL-C (r = 0.37, P < .01). Sex, age, BMI, and HDL-C (P < .01 for each) were found to be independentfactorsassociated with plasma adiponectin levels in multivariate analysis.Hypoadiponectinemiais significantly associated withcardiovascularrisk factorssuch as insulin resistance and atherogenic lipid profiles innonobese, apparentlyhealthysubjects.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1546~1550-
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.MESHAdiponectin/blood-
dc.subject.MESHAdult-
dc.subject.MESHAge Factors-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHBlood Glucose/analysis-
dc.subject.MESHBody Mass Index-
dc.subject.MESHC-Reactive Protein/metabolism-
dc.subject.MESHCardiovascular Diseases/blood*-
dc.subject.MESHCholesterol/blood-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHInsulin/blood-
dc.subject.MESHInsulin Resistance/physiology-
dc.subject.MESHLinear Models-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHRisk Factors-
dc.subject.MESHSex Factors-
dc.subject.MESHTriglycerides/blood-
dc.titleAssociation between hypoadiponectinemia and cardiovascular risk factors in nonobese healthy adults-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Family Medicine (가정의학)-
dc.contributor.googleauthorJee-Aee Im-
dc.contributor.googleauthorSang-Hwan Kim-
dc.contributor.googleauthorJi-Won Lee-
dc.contributor.googleauthorJae-Yong Shim-
dc.contributor.googleauthorHye-Ree Lee-
dc.contributor.googleauthorDuk-Chul Lee-
dc.identifier.doi10.1016/j.metabol.2006.06.027-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA02207-
dc.contributor.localIdA02716-
dc.contributor.localIdA03310-
dc.contributor.localIdA03203-
dc.relation.journalcodeJ02223-
dc.identifier.eissn1532-8600-
dc.identifier.pmid17046559-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0026049506002472-
dc.contributor.alternativeNameShim, Jae Yong-
dc.contributor.alternativeNameLee, Duk Chul-
dc.contributor.alternativeNameLee, Ji Won-
dc.contributor.alternativeNameLee, Hye Ree-
dc.contributor.affiliatedAuthorShim, Jae Yong-
dc.contributor.affiliatedAuthorLee, Duk Chul-
dc.contributor.affiliatedAuthorLee, Hye Ree-
dc.contributor.affiliatedAuthorLee, Ji Won-
dc.rights.accessRightsnot free-
dc.citation.volume55-
dc.citation.number11-
dc.citation.startPage1546-
dc.citation.endPage1550-
dc.identifier.bibliographicCitationMETABOLISM-CLINICAL AND EXPERIMENTAL, Vol.55(11) : 1546-1550, 2006-
dc.identifier.rimsid50632-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Family Medicine (가정의학교실) > 1. Journal Papers

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