Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/30095
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dc.contributor.authorÇalışkan, Yaşar-
dc.contributor.authorTorun, Ege Sinan-
dc.contributor.authorTiryaki, Tarık Onur-
dc.contributor.authorÖzlük, Yasemin-
dc.contributor.authorAkgül, Sebahat Usta-
dc.contributor.authorTemürhan, Sonay-
dc.contributor.authorÖztop, Nida-
dc.contributor.authorKılıçaslan, Işın-
dc.contributor.authorSever, Mehmet Şükrü-
dc.date.accessioned2022-12-26T12:48:13Z-
dc.date.available2022-12-26T12:48:13Z-
dc.date.issued2017-06-17-
dc.identifier.citationÇalışkan, Y. vd. (2017). ''Immunosuppressive treatment in C3 glomerulopathy: Is it really effective?''. American Journal of Nephrology, 46(2), 96-107.en_US
dc.identifier.issn0250-8095-
dc.identifier.urihttps://doi.org/10.1159/000479012-
dc.identifier.urihttps://www.karger.com/Article/FullText/479012-
dc.identifier.uri1421-9670-
dc.identifier.urihttp://hdl.handle.net/11452/30095-
dc.description.abstractBackground: C3 glomerulopathy (C3GP) is a recently identified and described disease that has a high risk of progressing into end-stage renal disease. We aimed to evaluate the effects of various immunosuppressive regimens on C3GP progression because there are conflicting data on the treatment modalities. Methods: In this retrospective study of 66 patients with C3GP, 27 patients received mycophenolate mofetil (MMF)-based treatment, 23 received non-MMF-based treatment (prednisolone or cyclophosphamide), and 16 received conservative care. The study groups were compared with each other with specific focus on primary outcomes defined as (1) kidney failure and (2) estimated glomerular filtration rate (eGFR) decline >= 50% from the baseline value. Results: Overall, 17 (25.8%) patients reached the primary outcome after a median period of 28 months. The number of patients who reached the primary outcome were similar among the study groups (MMF-based: 8/27 [29.6%], non-MMF-based: 4/23 [17.4%], and conservative care: 5/16 [31.3%], p = 0.520). In the Cox regression analysis, age (HR 0.912, p = 0.006), eGFR (HR 0.945, p = 0.001), and proteinuria levels (HR 1.418, p = 0.015) at the time of biopsy, percentage of crescentic (HR 1.035, p = 0.001) and sclerotic glomeruli (HR 1.041, p = 0.006), severity of interstitial fibrosis (HR 1.981, p = 0.048), as well as no remission of proteinuria (HR 2.418, p = 0.002) predicted the primary outcome. Conclusion: Although patients receiving immunosuppressive treatments had higher proteinuria and lower serum albumin at baseline, there were no differences between these patients and those receiving conservative care alone in proteinuria remission or in the decline of renal function. Younger age, higher proteinuria, lower eGFR, and the presence of crescentic and sclerotic glomeruli, severity of interstitial fibrosis, and no remission of proteinuria predicted the progression of kidney disease.en_US
dc.language.isoenen_US
dc.publisherKargeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectUrology & nephrologyen_US
dc.subjectC3 glomerulopathyen_US
dc.subjectComplement systemen_US
dc.subjectEnd-stage renal diseaseen_US
dc.subjectProteinuriaen_US
dc.subjectDense deposit diseaseen_US
dc.subjectHemolytic-uremic syndromeen_US
dc.subjectComplement abnormalitiesen_US
dc.subjectEculizumaben_US
dc.subjectGlomerulonephritisen_US
dc.subjectAdulten_US
dc.subject.meshAdulten_US
dc.subject.meshAge factorsen_US
dc.subject.meshAnti-Inflammatory agentsen_US
dc.subject.meshBiopsyen_US
dc.subject.meshComplement C3en_US
dc.subject.meshCreatinineen_US
dc.subject.meshDisease progressionen_US
dc.subject.meshFemaleen_US
dc.subject.meshFibrosisen_US
dc.subject.meshGlomerular filtration rateen_US
dc.subject.meshGlomerulonephritisen_US
dc.subject.meshHumansen_US
dc.subject.meshImmunosuppressive agentsen_US
dc.subject.meshKidney failure, chronicen_US
dc.subject.meshKidney glomerulusen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshProteinuriaen_US
dc.subject.meshRetrospective studiesen_US
dc.subject.meshRisk factorsen_US
dc.subject.meshTreatment outcomeen_US
dc.subject.meshYoung adulten_US
dc.titleImmunosuppressive treatment in C3 glomerulopathy: Is it really effective?en_US
dc.typeArticleen_US
dc.identifier.wos000408371900002tr_TR
dc.identifier.scopus2-s2.0-85023751797tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı/Nefroloji Anabilim Dalı.tr_TR
dc.identifier.startpage96tr_TR
dc.identifier.endpage107tr_TR
dc.identifier.volume46tr_TR
dc.identifier.issue2tr_TR
dc.relation.journalAmerican Journal of Nephrologyen_US
dc.contributor.buuauthorOruç, Ayşegül-
dc.contributor.researcheridAAH-4002-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed28700996tr_TR
dc.subject.wosUrology & nephrologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid55133912100tr_TR
dc.subject.scopusImmunoglobulin A Nephropathy; Proteinuria; Kidney Diseasesen_US
dc.subject.emtreeAlbuminen_US
dc.subject.emtreeComplement component C1qen_US
dc.subject.emtreeComplement component C3en_US
dc.subject.emtreeCyclophosphamideen_US
dc.subject.emtreeImmunoglobulin Aen_US
dc.subject.emtreeImmunoglobulin Gen_US
dc.subject.emtreeImmunoglobulin Men_US
dc.subject.emtreeMycophenolate mofetilen_US
dc.subject.emtreePrednisoloneen_US
dc.subject.emtreeAntiinflammatory agenten_US
dc.subject.emtreeC3 protein, humanen_US
dc.subject.emtreeComplement component C3en_US
dc.subject.emtreeCreatinineen_US
dc.subject.emtreeImmunosuppressive agenten_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAnemiaen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBladder diseaseen_US
dc.subject.emtreeBlood cell counten_US
dc.subject.emtreeClinical outcomeen_US
dc.subject.emtreeConservative treatmenten_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeCreatinine blood levelen_US
dc.subject.emtreeDiarrheaen_US
dc.subject.emtreeDrug dose reductionen_US
dc.subject.emtreeDrug megadoseen_US
dc.subject.emtreeDrug withdrawalen_US
dc.subject.emtreeEstimated glomerular filtration rateen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFibrosing alveolitisen_US
dc.subject.emtreeGenderen_US
dc.subject.emtreeGlomerulopathyen_US
dc.subject.emtreeHematuriaen_US
dc.subject.emtreeHistopathologyen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHypocomplementemiaen_US
dc.subject.emtreeImmunofluorescenceen_US
dc.subject.emtreeImmunofluorescence testen_US
dc.subject.emtreeImmunosuppressive treatmenten_US
dc.subject.emtreeKidney biopsyen_US
dc.subject.emtreeKidney failureen_US
dc.subject.emtreeLeukopeniaen_US
dc.subject.emtreeLow drug doseen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMembranoproliferative glomerulonephritisen_US
dc.subject.emtreeNauseaen_US
dc.subject.emtreeNephrotic syndromeen_US
dc.subject.emtreePneumoniaen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeProteinuriaen_US
dc.subject.emtreeRemissionen_US
dc.subject.emtreeRetrospective studyen_US
dc.subject.emtreeSanger sequencinen_US
dc.subject.emtreeThrombocytopeniaen_US
dc.subject.emtreeAgeen_US
dc.subject.emtreeBiopsyen_US
dc.subject.emtreeBlooden_US
dc.subject.emtreeChronic kidney failureen_US
dc.subject.emtreeComparative studyen_US
dc.subject.emtreeDisease exacerbationen_US
dc.subject.emtreeFibrosisen_US
dc.subject.emtreeGlomerulonephritisen_US
dc.subject.emtreeGlomerulusen_US
dc.subject.emtreeGlomerulus filtration rateen_US
dc.subject.emtreeMetabolismen_US
dc.subject.emtreeMiddle ageden_US
dc.subject.emtreePathologyen_US
dc.subject.emtreeProteinuriaen_US
dc.subject.emtreeRisk factoren_US
dc.subject.emtreeTreatment outcomeen_US
dc.subject.emtreeUrineen_US
dc.subject.emtreeYoung adulten_US
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