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Soluble fms-like tyrosine kinase-1 and the progression of carotid intima-media thickness – 24-month follow-up study –.

DC Field Value Language
dc.contributor.author심원흠-
dc.contributor.author이상학-
dc.contributor.author장양수-
dc.contributor.author정남식-
dc.contributor.author조승연-
dc.contributor.author강석민-
dc.contributor.author박성하-
dc.contributor.author신상훈-
dc.date.accessioned2015-04-23T17:00:36Z-
dc.date.available2015-04-23T17:00:36Z-
dc.date.issued2010-
dc.identifier.issn1346-9843-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/101653-
dc.description.abstractBACKGROUND: The relationship between fms-like tyrosine kinase-1 (sFlt-1), a soluble receptor for vascular endothelial growth factor (VEGF), and vascular disease has not been established, so this study aimed to elucidate the association between sFlt-1 and the progression of carotid intima - media thickness (IMT) in hypertensive patients. METHODS AND RESULTS: The 120 hypertensive patients under medical control were enrolled and 112 completed the study (age 59 ± 9 years, 57 females). Plasma VEGF and sFlt-1 levels were measured at enrollment. At baseline and 24-month visit, carotid IMT was measured and the association between sFlt-1 and IMT progression was assessed by linear regression. At baseline, age (r=0.186) and low level of high-density lipoprotein-cholesterol (HDL-C <40 mg/dl, r=0.214) were significantly related to carotid IMT. Over the 24 months, carotid IMT increased from 0.670 ± 0.089 mm to 0.696 ± 0.095 mm. There was a positive correlation between sFlt-1 tertiles and IMT change (P=0.05 by ANOVA). Upon multivariate analysis, log-transformed sFlt-1 level (β=0.137, P=0.003) and low HDL-C (β=0.048, P=0.04) were identified as predictors of IMT progression, independent of other confounding variables. CONCLUSIONS: High sFlt-1 level is predictive of carotid IMT progression in hypertensive patients. Low HDL-C level was also associated with IMT change. These observations support a high sFlt-1 level being indicative of progression of atherosclerosis-
dc.description.statementOfResponsibilityopen-
dc.format.extent2211~2215-
dc.relation.isPartOfCIRCULATION JOURNAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAged-
dc.subject.MESHCarotid Artery Diseases/pathology*-
dc.subject.MESHCholesterol, HDL/blood-
dc.subject.MESHDisease Progression-
dc.subject.MESHFollow-Up Studies-
dc.subject.MESHHumans-
dc.subject.MESHHypertension-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPredictive Value of Tests*-
dc.subject.MESHTunica Intima/pathology*-
dc.subject.MESHVascular Endothelial Growth Factor A/blood-
dc.subject.MESHVascular Endothelial Growth Factor Receptor-1/blood*-
dc.titleSoluble fms-like tyrosine kinase-1 and the progression of carotid intima-media thickness – 24-month follow-up study –.-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorSanghoon Shin-
dc.contributor.googleauthorSang-Hak Lee-
dc.contributor.googleauthorSungha Park-
dc.contributor.googleauthorSeok-Min Kang-
dc.contributor.googleauthorNamsik Chung-
dc.contributor.googleauthorWon-Heum Shim-
dc.contributor.googleauthorSeung-Yun Cho-
dc.contributor.googleauthorIchiro Manabe-
dc.contributor.googleauthorYangsoo Jang-
dc.identifier.doi10.1253/circj.CJ-10-0432-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA02202-
dc.contributor.localIdA03448-
dc.contributor.localIdA03585-
dc.contributor.localIdA03844-
dc.contributor.localIdA00037-
dc.contributor.localIdA01512-
dc.contributor.localIdA02107-
dc.contributor.localIdA02833-
dc.relation.journalcodeJ00534-
dc.identifier.eissn1347-4820-
dc.identifier.pmid20689217-
dc.subject.keywordAtherosclerosis-
dc.subject.keywordCarotid arteries-
dc.subject.keywordHypertension-
dc.subject.keywordVascular endothelial growth factor-
dc.subject.keywordVascular endothelial growth factor receptor 1-
dc.contributor.alternativeNameShim, Won Heum-
dc.contributor.alternativeNameLee, Sang Hak-
dc.contributor.alternativeNameJang, Yang Soo-
dc.contributor.alternativeNameChung, Nam Sik-
dc.contributor.alternativeNameCho, Seung Yun-
dc.contributor.alternativeNameKang, Seok Min-
dc.contributor.alternativeNamePark, Sung Ha-
dc.contributor.alternativeNameShin, Sang Hoon-
dc.contributor.affiliatedAuthorShim, Won Heum-
dc.contributor.affiliatedAuthorJang, Yang Soo-
dc.contributor.affiliatedAuthorChung, Nam Sik-
dc.contributor.affiliatedAuthorCho, Seung Yun-
dc.contributor.affiliatedAuthorKang, Seok Min-
dc.contributor.affiliatedAuthorPark, Sung Ha-
dc.contributor.affiliatedAuthorShin, Sang Hoon-
dc.contributor.affiliatedAuthorLee, Snag Hak-
dc.citation.volume74-
dc.citation.number10-
dc.citation.startPage2211-
dc.citation.endPage2215-
dc.identifier.bibliographicCitationCIRCULATION JOURNAL, Vol.74(10) : 2211-2215, 2010-
dc.identifier.rimsid40143-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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