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Evaluation of serum and urinary angiogenic factors in patients with endometriosis

DC Field Value Language
dc.contributor.author김재훈-
dc.contributor.author김혜연-
dc.contributor.author남안나-
dc.contributor.author박기현-
dc.contributor.author이병석-
dc.contributor.author조동제-
dc.contributor.author조시현-
dc.date.accessioned2014-12-21T16:22:12Z-
dc.date.available2014-12-21T16:22:12Z-
dc.date.issued2007-
dc.identifier.issn1046-7408-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/95563-
dc.description.abstractPROBLEM: The aim of this study was to evaluate serum and urinary levels of vascular endothelial growth factors, tumor necrosis factor-alpha (TNF-alpha), and soluble fms-like tyrosine kinase (sFlt-1) in patients with endometriosis. METHOD OF STUDY: During surgery for pelvic pain, pelvic mass or infertility, serum and urine were collected. Of 70 patients, 46 had histology-proven endometriosis and 24 patients without endometriosis participated as controls. RESULTS: Serum TNF-alpha levels and urinary sFlt-1 levels corrected for creatinine excretion were significantly increased in the endometriosis group (P=0.001 and P=0.011 respectively). Serum sFlt-1 levels and urinary sFlt-1 levels corrected for creatinine were significantly higher in patients with minimal-to-mild disease (P=0.014 and P=0.015 respectively), where serum TNF-alpha levels were increased in moderate-to-severe endometriosis (P<0.001). CONCLUSION: The pathogenesis of minimal-to-mild endometriosis and moderate-to-severe endometriosis seems to be different. Increased sFlt-1 levels in serum and urine of minimal-to-mild disease indicate that sFlt-1 may have an important role in inhibiting angiogenic process of the disease.-
dc.description.statementOfResponsibilityopen-
dc.format.extent497~504-
dc.relation.isPartOfAMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleEvaluation of serum and urinary angiogenic factors in patients with endometriosis-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Obstetrics & Gynecology (산부인과학)-
dc.contributor.googleauthorSi Hyun Cho-
dc.contributor.googleauthorYoon Jin Oh-
dc.contributor.googleauthorByung Seok Lee-
dc.contributor.googleauthorDong Je Cho-
dc.contributor.googleauthorKi Hyun Park-
dc.contributor.googleauthorJae Hoon Kim-
dc.contributor.googleauthorJoo Hyun Park-
dc.contributor.googleauthorHye Yeon Kim-
dc.contributor.googleauthorAnna Nam-
dc.identifier.doi10.1111/j.1600-0897.2007.00535.x-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00876-
dc.contributor.localIdA01174-
dc.contributor.localIdA01257-
dc.contributor.localIdA01450-
dc.contributor.localIdA02795-
dc.contributor.localIdA03814-
dc.contributor.localIdA03846-
dc.relation.journalcodeJ00111-
dc.identifier.eissn1600-0897-
dc.identifier.urlhttp://onlinelibrary.wiley.com/doi/10.1111/j.1600-0897.2007.00535.x/abstract-
dc.contributor.alternativeNameKim, Jae Hoon-
dc.contributor.alternativeNameKim, Hye Yeon-
dc.contributor.alternativeNameNam, An Na-
dc.contributor.alternativeNamePark, Ki Hyun-
dc.contributor.alternativeNameLee, Byung Seok-
dc.contributor.alternativeNameCho, Dong Je-
dc.contributor.alternativeNameCho, Si Hyun-
dc.contributor.affiliatedAuthorKim, Jae Hoon-
dc.contributor.affiliatedAuthorKim, Hye Yeon-
dc.contributor.affiliatedAuthorNam, An Na-
dc.contributor.affiliatedAuthorPark, Ki Hyun-
dc.contributor.affiliatedAuthorLee, Byung Seok-
dc.contributor.affiliatedAuthorCho, Dong Je-
dc.contributor.affiliatedAuthorCho, Si Hyun-
dc.rights.accessRightsnot free-
dc.citation.volume58-
dc.citation.number6-
dc.citation.startPage497-
dc.citation.endPage504-
dc.identifier.bibliographicCitationAMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, Vol.58(6) : 497-504, 2007-
dc.identifier.rimsid43335-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers

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