Cited 54 times in
Association between hypoadiponectinemia and cardiovascular risk factors in nonobese healthy adults
DC Field | Value | Language |
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dc.contributor.author | 심재용 | - |
dc.contributor.author | 이덕철 | - |
dc.contributor.author | 이지원 | - |
dc.contributor.author | 이혜리 | - |
dc.date.accessioned | 2015-06-10T12:05:13Z | - |
dc.date.available | 2015-06-10T12:05:13Z | - |
dc.date.issued | 2006 | - |
dc.identifier.issn | 0026-0495 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/109165 | - |
dc.description.abstract | Adiponectin 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.statementOfResponsibility | open | - |
dc.format.extent | 1546~1550 | - |
dc.relation.isPartOf | METABOLISM-CLINICAL AND EXPERIMENTAL | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Adiponectin/blood | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Age Factors | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Aged, 80 and over | - |
dc.subject.MESH | Blood Glucose/analysis | - |
dc.subject.MESH | Body Mass Index | - |
dc.subject.MESH | C-Reactive Protein/metabolism | - |
dc.subject.MESH | Cardiovascular Diseases/blood* | - |
dc.subject.MESH | Cholesterol/blood | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Insulin/blood | - |
dc.subject.MESH | Insulin Resistance/physiology | - |
dc.subject.MESH | Linear Models | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Risk Factors | - |
dc.subject.MESH | Sex Factors | - |
dc.subject.MESH | Triglycerides/blood | - |
dc.title | Association between hypoadiponectinemia and cardiovascular risk factors in nonobese healthy adults | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Family Medicine (가정의학) | - |
dc.contributor.googleauthor | Jee-Aee Im | - |
dc.contributor.googleauthor | Sang-Hwan Kim | - |
dc.contributor.googleauthor | Ji-Won Lee | - |
dc.contributor.googleauthor | Jae-Yong Shim | - |
dc.contributor.googleauthor | Hye-Ree Lee | - |
dc.contributor.googleauthor | Duk-Chul Lee | - |
dc.identifier.doi | 10.1016/j.metabol.2006.06.027 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A02207 | - |
dc.contributor.localId | A02716 | - |
dc.contributor.localId | A03310 | - |
dc.contributor.localId | A03203 | - |
dc.relation.journalcode | J02223 | - |
dc.identifier.eissn | 1532-8600 | - |
dc.identifier.pmid | 17046559 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S0026049506002472 | - |
dc.contributor.alternativeName | Shim, Jae Yong | - |
dc.contributor.alternativeName | Lee, Duk Chul | - |
dc.contributor.alternativeName | Lee, Ji Won | - |
dc.contributor.alternativeName | Lee, Hye Ree | - |
dc.contributor.affiliatedAuthor | Shim, Jae Yong | - |
dc.contributor.affiliatedAuthor | Lee, Duk Chul | - |
dc.contributor.affiliatedAuthor | Lee, Hye Ree | - |
dc.contributor.affiliatedAuthor | Lee, Ji Won | - |
dc.rights.accessRights | not free | - |
dc.citation.volume | 55 | - |
dc.citation.number | 11 | - |
dc.citation.startPage | 1546 | - |
dc.citation.endPage | 1550 | - |
dc.identifier.bibliographicCitation | METABOLISM-CLINICAL AND EXPERIMENTAL, Vol.55(11) : 1546-1550, 2006 | - |
dc.identifier.rimsid | 50632 | - |
dc.type.rims | ART | - |
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