Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14989
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSumethkul V.
dc.contributor.authorChangsirikulchai S.
dc.contributor.authorLothuvachai T.
dc.contributor.authorChalermsanyakorn P.
dc.date.accessioned2021-04-05T04:32:17Z-
dc.date.available2021-04-05T04:32:17Z-
dc.date.issued2006
dc.identifier.issn411345
dc.identifier.other2-s2.0-33845452280
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14989-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-33845452280&doi=10.1016%2fj.transproceed.2006.10.097&partnerID=40&md5=68a6fc500623d77e93a18a64d8fae067
dc.description.abstractOptimal treatment for patients with chronic allograft nephropathy (CAN) is not known. Early intervention is preferred. We examined the benefit of adding sirolimus (SRL; C0 5-12 ng/mL: HPLC) on the rate of progression of early CAN. We identified patients with biopsy-confirmed Banff grade 1 CAN. After biopsy, patients were switched to SRL + CsA + prednisolone (SRL), MMF + CsA + prednisolone (MMF), or CsA + AZA + prednisolone (AZA). GFR was estimated by Cockcroft-Gault and MDRD formulae. The rate of GFR decline (delta GFR) was determined by calculating the slope of the regression line of estimated GFR (MDRD and Cockcroft-Gault method) at different times. Statistical analysis was performed by the Wilcoxon test. The 41 patients with CAN grade 1 were assigned to SRL: MMF: AZA = 12: 20: 9. Before biopsy; the graft age for SRL: MMF: AZA were 56 ± 27: 70 ± 48: 51 ± 36 months; and the GFR (MDRD method), 38 ± 8: 42 ± 15: 36 ± 14 mL/min; GFR (C-G method) 45 ± 13, 42 ± 12, 41 ± 15 mL/min; trough CsA levels 152 ± 36: 145 ± 46: 177 ± 61 ng/dL; delta GFR (MDRD method) -0.18 ± 0.20: -0.15 ± 0.59: -0.20 ± 1.08; delta GFR (C-G method) -0.13 ± 0.37: -0.19 ± 0.24: -0.65 ± 0.99. Follow-up time for SRL: MMF: AZA was 19 ± 4: 35 ± 32: 59 ± 54 months. At last follow-up; GFR (MDRD method) for SRL: MMF: AZA were 39 ± 13: 35 ± 21: 40 ± 24 mL/min; GFR (C-G method) 46 ± 17, 37 ± 18, 46 ± 25 mL/min; BP 128 ± 11/79 ± 7: 131 ± 22/80 ± 14: 132 ± 20/82 ± 11 mm Hg; and CsA level 52 ± 25: 122 ± 41: 155 ± 49. After biopsy, statin was prescribed in nine SRL, 10 MMF, and three AZA. ACEI was prescribed in two SRL, three MMF, and two AZA. Compared with the prebiopsy values, the delta GFR (MDRD method) changed to -0.04 ± 0.31 (SRL; P = .04), -0.17 ± 0.40 (MMF; P = .60), and -0.97 ± 1.52 (AZA: P = .16). Delta GFR (C-G method) was also significantly improved in the SRL group (-0.02 ± 0.47; P = .05) but not in the MMF (-0.13 ± 0.51; P = .53) or AZA (-0.54 ± 1.78; P = .44). We concluded that patients with early CAN who are switched to SRL and low-dose CsA have a significant attenuation of the rate of GFR declination when compared with patients who receive MMF or AZA addition. © 2006 Elsevier Inc. All rights reserved.
dc.subjectazathioprine
dc.subjectcyclosporin A
dc.subjectdipeptidyl carboxypeptidase inhibitor
dc.subjecthydroxymethylglutaryl coenzyme A reductase inhibitor
dc.subjectmycophenolic acid 2 morpholinoethyl ester
dc.subjectprednisolone
dc.subjectrapamycin
dc.subjectadult
dc.subjectarticle
dc.subjectattenuation
dc.subjectblood pressure
dc.subjectchronic allograft nephropathy
dc.subjectclinical article
dc.subjectclinical trial
dc.subjectcontrolled clinical trial
dc.subjectcontrolled study
dc.subjectdemography
dc.subjectdisease course
dc.subjectdrug blood level
dc.subjectfollow up
dc.subjectglomerulus filtration rate
dc.subjecthigh performance liquid chromatography
dc.subjecthuman
dc.subjectkidney biopsy
dc.subjectlinear regression analysis
dc.subjectprescription
dc.subjectpriority journal
dc.subjectrank sum test
dc.subjectrating scale
dc.subjectstatistical analysis
dc.subjectstatistical significance
dc.subjectAdult
dc.subjectAzathioprine
dc.subjectBiopsy
dc.subjectBlood Pressure
dc.subjectChronic Disease
dc.subjectCreatinine
dc.subjectCyclosporine
dc.subjectDisease Progression
dc.subjectDrug Therapy, Combination
dc.subjectGlomerular Filtration Rate
dc.subjectHumans
dc.subjectImmunosuppressive Agents
dc.subjectKidney Function Tests
dc.subjectKidney Transplantation
dc.subjectMiddle Aged
dc.subjectMycophenolic Acid
dc.subjectPostoperative Complications
dc.subjectSirolimus
dc.subjectTransplantation, Homologous
dc.subjectTreatment Outcome
dc.titleSirolimus Attenuates the Rate of Progression of Early Chronic Allograft Nephropathy
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationTransplantation Proceedings. Vol 38, No.10 (2006), p.3470-3472
dc.identifier.doi10.1016/j.transproceed.2006.10.097
Appears in Collections:Scopus 1983-2021

Files in This Item:
There are no files associated with this item.


Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.