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Association of clinical events with everolimus exposure in kidney transplant patients receiving reduced cyclosporine

DC Field Value Language
dc.contributor.author김유선-
dc.date.accessioned2014-12-18T08:37:11Z-
dc.date.available2014-12-18T08:37:11Z-
dc.date.issued2013-
dc.identifier.issn0902-0063-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/86644-
dc.description.abstractBACKGROUND: The association between clinical events and everolimus exposure in patients receiving reduced-exposure calcineurin inhibitor therapy is poorly explored. METHODS: In a pre-planned, descriptive analysis of data from a randomized controlled trial, events were correlated with everolimus trough concentrations in 556 newly transplanted kidney transplant patients receiving everolimus with reduced-exposure cyclosporine (CsA) and steroids. Influence of everolimus exposure on clinical events was stratified according to predefined time-normalized concentrations. RESULTS: The incidence of treated biopsy-proven acute rejection and graft loss at month 12 was highest in patients with everolimus <3 ng/mL (36.4% and 28.6%, respectively, vs. 9.1-15.3% and 0.9-5.0% with higher concentration ranges). A higher mortality rate was observed in patients with an everolimus trough concentration ≥ 12 ng/mL (10.0% vs. 1.7-5.6% with lower concentration ranges). The lowest rates of renal dysfunction (defined as poor renal function [estimated GFR, serum creatinine] or proteinuria), wound healing events, peripheral edema, new-onset diabetes mellitus, hypercholesterolemia and hypertriglyceridemia were generally observed with everolimus trough concentration in the range 3-8 ng/mL and CsA <100 ng/mL. Proteinuria occurred most frequently in patients with very low or very high everolimus trough concentrations. CONCLUSIONS: These results support an exposure-response relationship between clinical events and everolimus trough concentrations in kidney transplant patients receiving reduced-exposure CsA.-
dc.description.statementOfResponsibilityopen-
dc.relation.isPartOfCLINICAL TRANSPLANTATION-
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.MESHCyclosporine/administration & dosage*-
dc.subject.MESHCyclosporine/adverse effects-
dc.subject.MESHCyclosporine/pharmacokinetics-
dc.subject.MESHCyclosporine/therapeutic use-
dc.subject.MESHDose-Response Relationship, Drug-
dc.subject.MESHDrug Administration Schedule-
dc.subject.MESHDrug Monitoring-
dc.subject.MESHDrug Therapy, Combination-
dc.subject.MESHEverolimus-
dc.subject.MESHFemale-
dc.subject.MESHFollow-Up Studies-
dc.subject.MESHGraft Rejection/epidemiology-
dc.subject.MESHGraft Rejection/prevention & control*-
dc.subject.MESHGraft Survival-
dc.subject.MESHHumans-
dc.subject.MESHImmunosuppressive Agents/administration & dosage-
dc.subject.MESHImmunosuppressive Agents/adverse effects-
dc.subject.MESHImmunosuppressive Agents/pharmacokinetics-
dc.subject.MESHImmunosuppressive Agents/therapeutic use*-
dc.subject.MESHKidney Transplantation*-
dc.subject.MESHLinear Models-
dc.subject.MESHLogistic Models-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPostoperative Complications/chemically induced-
dc.subject.MESHPostoperative Complications/epidemiology-
dc.subject.MESHPostoperative Complications/prevention & control*-
dc.subject.MESHSirolimus/adverse effects-
dc.subject.MESHSirolimus/analogs & derivatives*-
dc.subject.MESHSirolimus/pharmacokinetics-
dc.subject.MESHSirolimus/therapeutic use-
dc.subject.MESHSurvival Analysis-
dc.subject.MESHTreatment Outcome-
dc.titleAssociation of clinical events with everolimus exposure in kidney transplant patients receiving reduced cyclosporine-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Surgery (외과학)-
dc.contributor.googleauthorFuad S. Shihab-
dc.contributor.googleauthorDiane Cibrik-
dc.contributor.googleauthorLaurence Chan-
dc.contributor.googleauthorYu Seun Kim-
dc.contributor.googleauthorMario Carmellini-
dc.contributor.googleauthorRowan Walker-
dc.contributor.googleauthorGazi Zibari-
dc.contributor.googleauthorJames Pattison-
dc.contributor.googleauthorCatherine Cornu-Artis-
dc.contributor.googleauthorZailong Wang-
dc.contributor.googleauthorHelio Tedesco-Silva Jr-
dc.identifier.doi10.1111/ctr.12045.-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00785-
dc.relation.journalcodeJ00615-
dc.identifier.eissn1399-0012-
dc.identifier.pmid23230975-
dc.identifier.urlhttp://onlinelibrary.wiley.com/doi/10.1111/ctr.12045/abstract-
dc.subject.keywordCalcineurin inhibitor toxicity-
dc.subject.keywordCyclosporine-
dc.subject.keywordEverolimus-
dc.subject.keywordRenal function-
dc.subject.keywordRenal transplantation-
dc.contributor.alternativeNameKim, Yu Seun-
dc.contributor.affiliatedAuthorKim, Yu Seun-
dc.rights.accessRightsnot free-
dc.citation.volume27-
dc.citation.number2-
dc.citation.startPage217-
dc.citation.endPage226-
dc.identifier.bibliographicCitationCLINICAL TRANSPLANTATION, Vol.27(2) : 217-226, 2013-
dc.identifier.rimsid29116-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers

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