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Serum fibroblast growth factor-21 concentration is associated with residual renal function and insulin resistance in end-stage renal disease patients receiving long-term peritoneal dialysis

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dc.contributor.author강신욱-
dc.contributor.author한대석-
dc.contributor.author한승혁-
dc.date.accessioned2015-04-23T17:42:38Z-
dc.date.available2015-04-23T17:42:38Z-
dc.date.issued2010-
dc.identifier.issn0026-0495-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/102981-
dc.description.abstractFibroblast growth factor-21 (FGF-21) is a new metabolic regulator, which is related to antiobesity and insulin sensitivity in vivo. However, the clinical implication of FGF-21 is poorly understood. To investigate whether FGF-21 may play a role as a metabolic regulator in patients with end-stage renal disease, we measured serum concentrations of FGF-21, inflammatory markers, and metabolic parameters in healthy people (n = 63) and nondiabetic patients receiving peritoneal dialysis (PD, n = 72). The patients were treated with angiotensin receptor blocker for 6 months, and the changes in FGF-21 concentration and metabolic parameters were assessed. Compared with controls, serum FGF-21 concentration was 8 times higher in patients undergoing PD (754.2 ± 463.5 vs 86.9 ± 60.2 pg/mL, P < .001). In controls, only lipid parameters correlated positively with FGF-21 concentration. In contrast, inflammatory markers (interleukin-6, fibrinogen, high-sensitivity C-reactive protein) and homeostasis model assessment of insulin resistance (HOMA-IR) correlated positively and residual renal function correlated inversely with serum FGF-21 concentration in PD patients. In a multivariate analysis adjusting these factors, residual renal function, HOMA-IR, and fibrinogen concentration were independent determinants of serum FGF-21 concentration. After 6-month angiotensin receptor blocker treatment, serum FGF-21 concentration declined significantly by 13% and HOMA-IR and inflammatory markers improved in PD patients. These findings suggest that FGF-21 may play a role in insulin resistance in patients with end-stage renal disease-
dc.description.statementOfResponsibilityopen-
dc.format.extent1656~1662-
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.MESHAngiotensin Receptor Antagonists/administration & dosage-
dc.subject.MESHAngiotensin Receptor Antagonists/pharmacology-
dc.subject.MESHAngiotensin Receptor Antagonists/therapeutic use-
dc.subject.MESHBiomarkers-
dc.subject.MESHCase-Control Studies-
dc.subject.MESHFemale-
dc.subject.MESHFibrinogen/analysis-
dc.subject.MESHFibroblast Growth Factors/blood*-
dc.subject.MESHFibroblast Growth Factors/drug effects-
dc.subject.MESHFibroblast Growth Factors/metabolism-
dc.subject.MESHHumans-
dc.subject.MESHInflammation-
dc.subject.MESHInsulin Resistance*-
dc.subject.MESHKidney/physiopathology*-
dc.subject.MESHKidney Failure, Chronic/blood*-
dc.subject.MESHKidney Failure, Chronic/therapy-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPeritoneal Dialysis*-
dc.titleSerum fibroblast growth factor-21 concentration is associated with residual renal function and insulin resistance in end-stage renal disease patients receiving long-term peritoneal dialysis-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학)-
dc.contributor.googleauthorSeung Hyeok Han-
dc.contributor.googleauthorSung Hee Choi-
dc.contributor.googleauthorBong Jun Cho-
dc.contributor.googleauthorYenna Lee-
dc.contributor.googleauthorSoo Lim-
dc.contributor.googleauthorYoung Joo Park-
dc.contributor.googleauthorMin Kyung Moon-
dc.contributor.googleauthorHong Kyu Lee-
dc.contributor.googleauthorShin-Wook Kang-
dc.contributor.googleauthorDae Suk Han-
dc.contributor.googleauthorYoung-Bum Kim-
dc.contributor.googleauthorHak C. Jang-
dc.contributor.googleauthorKyong Soo Park-
dc.identifier.doi10.1016/j.metabol.2010.03.018-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00053-
dc.contributor.localIdA04272-
dc.contributor.localIdA04304-
dc.relation.journalcodeJ02223-
dc.identifier.eissn1532-8600-
dc.identifier.pmid20423749-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S0026049510001083-
dc.contributor.alternativeNameKang, Shin Wook-
dc.contributor.alternativeNameHan, Dae Suk-
dc.contributor.alternativeNameHan, Seung Hyeok-
dc.contributor.affiliatedAuthorKang, Shin Wook-
dc.contributor.affiliatedAuthorHan, Dae Suk-
dc.contributor.affiliatedAuthorHan, Seung Hyeok-
dc.citation.volume59-
dc.citation.number11-
dc.citation.startPage1656-
dc.citation.endPage1662-
dc.identifier.bibliographicCitationMETABOLISM-CLINICAL AND EXPERIMENTAL, Vol.59(11) : 1656-1662, 2010-
dc.identifier.rimsid35138-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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