Publication:
Sirolimus Attenuates the Rate of Progression of Early Chronic Allograft Nephropathy

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.date.issuedBE2549
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.format.mimetypeapplication/pdf
dc.identifier.citationTransplantation Proceedings. Vol 38, No.10 (2006), p.3470-3472
dc.identifier.doi10.1016/j.transproceed.2006.10.097
dc.identifier.issn411345
dc.identifier.other2-s2.0-33845452280
dc.identifier.urihttps://hdl.handle.net/20.500.14740/5258
dc.rights.holderScopus
dc.subject.otherAzathioprine
dc.subject.otherCyclosporin A
dc.subject.otherDipeptidyl carboxypeptidase inhibitor
dc.subject.otherHydroxymethylglutaryl coenzyme A reductase inhibitor
dc.subject.otherMycophenolic acid 2 morpholinoethyl ester
dc.subject.otherPrednisolone
dc.subject.otherRapamycin
dc.subject.otherAdult
dc.subject.otherArticle
dc.subject.otherAttenuation
dc.subject.otherBlood pressure
dc.subject.otherChronic allograft nephropathy
dc.subject.otherClinical article
dc.subject.otherClinical trial
dc.subject.otherControlled clinical trial
dc.subject.otherControlled study
dc.subject.otherDemography
dc.subject.otherDisease course
dc.subject.otherDrug blood level
dc.subject.otherFollow up
dc.subject.otherGlomerulus filtration rate
dc.subject.otherHigh performance liquid chromatography
dc.subject.otherHuman
dc.subject.otherKidney biopsy
dc.subject.otherLinear regression analysis
dc.subject.otherPrescription
dc.subject.otherPriority journal
dc.subject.otherRank sum test
dc.subject.otherRating scale
dc.subject.otherStatistical analysis
dc.subject.otherStatistical significance
dc.subject.otherAdult
dc.subject.otherAzathioprine
dc.subject.otherBiopsy
dc.subject.otherBlood Pressure
dc.subject.otherChronic Disease
dc.subject.otherCreatinine
dc.subject.otherCyclosporine
dc.subject.otherDisease Progression
dc.subject.otherDrug Therapy, Combination
dc.subject.otherGlomerular Filtration Rate
dc.subject.otherHumans
dc.subject.otherImmunosuppressive Agents
dc.subject.otherKidney Function Tests
dc.subject.otherKidney Transplantation
dc.subject.otherMiddle Aged
dc.subject.otherMycophenolic Acid
dc.subject.otherPostoperative Complications
dc.subject.otherSirolimus
dc.subject.otherTransplantation, Homologous
dc.subject.otherTreatment Outcome
dc.titleSirolimus Attenuates the Rate of Progression of Early Chronic Allograft Nephropathy
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-33845452280&doi=10.1016%2fj.transproceed.2006.10.097&partnerID=40&md5=68a6fc500623d77e93a18a64d8fae067

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