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dc.rights.licenseopenen_US
dc.contributor.authorHOSHINO, Junichi
dc.contributor.authorTSUNODA, Ryoya
dc.contributor.authorNAGAI, Kei
dc.contributor.authorKAI, Hirayasu
dc.contributor.authorSAITO, Chie
dc.contributor.authorITO, Yukiko
dc.contributor.authorASAHI, Koichi
dc.contributor.authorKONDO, Masahide
dc.contributor.authorISEKI, Kunitoshi
dc.contributor.authorISEKI, Chiho
dc.contributor.authorOKADA, Hirokazu
dc.contributor.authorKASHIHARA, Naoki
dc.contributor.authorNARITA, Ichiei
dc.contributor.authorWADA, Takashi
hal.structure.identifierBioingénierie tissulaire [BIOTIS]
dc.contributor.authorCOMBE, Christian
dc.contributor.authorPISONI, Ronald L
dc.contributor.authorROBINSON, Bruce M
dc.contributor.authorYAMAGATA, Kunihiro
dc.date.accessioned2021-12-21T08:41:41Z
dc.date.available2021-12-21T08:41:41Z
dc.date.issued2021-08-01
dc.identifier.issn1437-7799en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/124233
dc.description.abstractEnDisease-specific trajectories of renal function in advanced chronic kidney disease (CKD) are not well defined. Here, we compared these trajectories in the estimated glomerular filtration rate (eGFR) by CKD stages. Patients with multiple eGFR measurements during the 5-year preregistration period of the REACH-J study were enrolled. Mean annual eGFR declines were calculated from linear mixed effect models with the adjustment variables of baseline CKD stage, age, sex and the current CKD stage and the level of proteinuria (CKDA1-3). Among 1,969 eligible patients with CKDG3b-5, the adjusted eGFR decline (ml/min/1.73 m/year) was significantly faster in diabetic kidney disease (DKD) patients and polycystic kidney disease (PKD) patients than in patients with other kidney diseases (DKD, - 2.96 ± 0.13; PKD, - 2.82 ± 0.17; and others, - 1.95 ± 0.05, p < 0.01). The declines were faster with higher CKD stages. In DKD patients, the eGFR decline was significantly faster in CKDG5 than CKDG4 (- 4.10 ± 0.18 vs - 2.76 ± 0.20, p < 0.01), while these declines in PKD patients were similar. The eGFR declines in PKD patients were significantly faster than DKD patients in CKDG4 (- 2.92 ± 0.23 vs - 2.76 ± 0.20, p < 0.01) and in CKDA2 (- 3.36 ± 0.35 vs - 1.40 ± 0.26, p < 0.01). Our study revealed the disease-specific annual eGFR declines by CKD stages and the level of proteinuria. Comparing to the other kidney diseases, the declines in PKD patients were getting faster from early stages of CKD. These results suggest the importance of CKD managements in PKD patients from the early stages.
dc.language.isoENen_US
dc.subject.enDiabetic kidney disease
dc.subject.enEGFR decline
dc.subject.enPolycystic kidney disease
dc.subject.enREACH-J
dc.title.enComparison of annual eGFR decline among primary kidney diseases in patients with CKD G3b-5: results from a REACH-J CKD cohort study.
dc.title.alternativeClin Exp Nephrolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s10157-021-02059-yen_US
dc.subject.halSciences du Vivant [q-bio]/Biotechnologiesen_US
dc.identifier.pubmed33881641en_US
bordeaux.journalClinical and Experimental Nephrologyen_US
bordeaux.page902-910en_US
bordeaux.volume25en_US
bordeaux.hal.laboratoriesBioingénierie Tissulaire (BioTis) - UMR_S 1026en_US
bordeaux.issue8en_US
bordeaux.institutionCNRSen_US
bordeaux.institutionINSERMen_US
bordeaux.institutionCHU de Bordeauxen_US
bordeaux.institutionInstitut Bergoniéen_US
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-03498558
hal.version1
hal.date.transferred2021-12-21T08:41:43Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Clinical%20and%20Experimental%20Nephrology&amp;rft.date=2021-08-01&amp;rft.volume=25&amp;rft.issue=8&amp;rft.spage=902-910&amp;rft.epage=902-910&amp;rft.eissn=1437-7799&amp;rft.issn=1437-7799&amp;rft.au=HOSHINO,%20Junichi&amp;TSUNODA,%20Ryoya&amp;NAGAI,%20Kei&amp;KAI,%20Hirayasu&amp;SAITO,%20Chie&amp;rft.genre=article


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