Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/45887
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dc.contributor.authorDeleersnijder, Dries-
dc.contributor.authorCleenders, Evert-
dc.contributor.authorCoemans, Maarten-
dc.contributor.authorDendooven, Amelie-
dc.contributor.authorKoshy, Priyanka-
dc.contributor.authorClaes, Kathleen-
dc.contributor.authorDe Vusser, Katrien-
dc.contributor.authorMeijers, Bjorn K.-
dc.contributor.authorSPRANGERS, Ben-
dc.contributor.authorVan Laecke, Steven-
dc.contributor.authorVan Craenenbroeck, Amaryllis H.-
dc.date.accessioned2025-04-22T09:54:15Z-
dc.date.available2025-04-22T09:54:15Z-
dc.date.issued2025-
dc.date.submitted2025-04-18T11:51:57Z-
dc.identifier.citationClinical Kidney Journal, 18 (4) (Art N° sfaf060)-
dc.identifier.urihttp://hdl.handle.net/1942/45887-
dc.description.abstractBackground Studies that compare kidney outcomes across patients with different forms of focal segmental glomerulosclerosis (FSGS) are lacking. Methods This retrospective study compared annual estimated glomerular filtration rate (eGFR) slope and kidney failure rate (eGFR <15 mL/min/1.73 m(2) or initiation of kidney replacement therapy) across patients with biopsy-proven primary, maladaptive, genetic and undetermined FSGS. Patients were included from two Belgian tertiary referral hospitals, from 2010 until 2022. Associations between covariates and kidney failure were estimated using Cox and Fine and Gray models. eGFR slopes were estimated using linear mixed-effects models. Results Eighty-two patients were subdivided into primary (28.1%), maladaptive (40.2%), genetic (14.6%) and undetermined FSGS (17.1%) groups. Kidney failure occurred in 22 patients (26.8%). Primary FSGS patients exhibited higher baseline eGFR and less chronic changes on biopsy. The annual eGFR slope was -2.5 mL/min in primary, -2.5 mL/min in maladaptive, -4.6 mL/min in genetic and -4.4 mL/min in undetermined FSGS. Female sex was associated with a lower kidney failure rate and higher eGFR slope. Higher proteinuria at biopsy was associated with a higher kidney failure rate, lower eGFR slope and a higher mortality rate. Global sclerosis on kidney biopsy was associated with lower baseline eGFR, while a higher percentage of segmental sclerosis rather associated with more rapid eGFR decline [-1.5 mL/min/year per 10% increase, 95% confidence interval (-2.2, -0.7)]. Conclusions Patients with primary FSGS were biopsied earlier in their disease course and exhibited surprisingly good kidney outcome. Overall, sex, baseline eGFR, proteinuria and the degree of focal and global glomerulosclerosis play a more important role in estimating the prognosis of patients with FSGS than merely the FSGS etiology.-
dc.description.sponsorshipFUNDING D.D. is supported by a PhD Fellowship grant fundamental research from the Research Foundation Flanders (F.W.O.) (grant number 11L5622N). M.C. is supported by the Research Foundation Flanders (F.W.O.) (grant 12D6423N). A.H.V.C. is supported by a postdoctoral grant from the University Hospitals Leuven (KOOR) and a Research Foundation Flanders (FWO) SBO project (S006722N). B.K.M. is a senior clinical investigator of F.W.O. (1 800 820 N) and received grant support from KU Leuven (3M190551 and C14/21/103). ACKNOWLEDGEMENTS This study was approved by the ethical committees of the academic hospitals of UZ Leuven and UZ Ghent (study reference S66295). All study participants were informed on the use of their data for this retrospective analysis.-
dc.language.isoen-
dc.publisherOXFORD UNIV PRESS-
dc.rightsThe Author(s) 2025. Published by Oxford University Press on behalf of the ERA. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.-
dc.subject.othereGFR slope-
dc.subject.otherepidemiology-
dc.subject.otherfocal segmental glomerulosclerosis-
dc.subject.otherFSGS-
dc.subject.otherprognosis-
dc.titlePrimary FSGS is not associated with worse kidney outcome compared with other FSGS subtypes-
dc.typeJournal Contribution-
dc.identifier.issue4-
dc.identifier.volume18-
local.format.pages12-
local.bibliographicCitation.jcatA1-
dc.description.notesVan Craenenbroeck, AH (corresponding author), Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Nephrol & Renal Transplantat Res Grp, Leuven, Belgium.; Van Craenenbroeck, AH (corresponding author), Univ Hosp Leuven, Div Nephrol, Leuven, Belgium.-
dc.description.notesamaryllis.vancraenenbroeck@kuleuven.be-
local.publisher.placeGREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.bibliographicCitation.artnrsfaf060-
dc.identifier.doi10.1093/ckj/sfaf060-
dc.identifier.pmid40207100-
dc.identifier.isi001461973800001-
local.provider.typewosris-
local.description.affiliation[Deleersnijder, Dries; Cleenders, Evert; Coemans, Maarten; Koshy, Priyanka; Claes, Kathleen; De Vusser, Katrien; Meijers, Bjorn K.; Van Craenenbroeck, Amaryllis H.] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Nephrol & Renal Transplantat Res Grp, Leuven, Belgium.-
local.description.affiliation[Dendooven, Amelie] Univ Hosp Ghent, Div Pathol, Ghent, Belgium.-
local.description.affiliation[Dendooven, Amelie] Univ Antwerp, Lab Expt Med & Pediat, Antwerp, Belgium.-
local.description.affiliation[Koshy, Priyanka] Univ Hosp Leuven, Dept Pathol, Leuven, Belgium.-
local.description.affiliation[Claes, Kathleen; De Vusser, Katrien; Meijers, Bjorn K.; Van Craenenbroeck, Amaryllis H.] Univ Hosp Leuven, Div Nephrol, Leuven, Belgium.-
local.description.affiliation[Sprangers, Ben] Ziekenhuis Oost Limburg, Dept Nephrol, Genk, Belgium.-
local.description.affiliation[Sprangers, Ben] UHasselt, Biomed Res Inst, Dept Immunol & Infect, Diepenbeek, Belgium.-
local.description.affiliation[Van Laecke, Steven] Ghent Univ Hosp, Dept Internal Med, Renal Div, Ghent, Belgium.-
local.uhasselt.internationalno-
item.fulltextWith Fulltext-
item.contributorDeleersnijder, Dries-
item.contributorCleenders, Evert-
item.contributorCoemans, Maarten-
item.contributorDendooven, Amelie-
item.contributorKoshy, Priyanka-
item.contributorClaes, Kathleen-
item.contributorDe Vusser, Katrien-
item.contributorMeijers, Bjorn K.-
item.contributorSPRANGERS, Ben-
item.contributorVan Laecke, Steven-
item.contributorVan Craenenbroeck, Amaryllis H.-
item.fullcitationDeleersnijder, Dries; Cleenders, Evert; Coemans, Maarten; Dendooven, Amelie; Koshy, Priyanka; Claes, Kathleen; De Vusser, Katrien; Meijers, Bjorn K.; SPRANGERS, Ben; Van Laecke, Steven & Van Craenenbroeck, Amaryllis H. (2025) Primary FSGS is not associated with worse kidney outcome compared with other FSGS subtypes. In: Clinical Kidney Journal, 18 (4) (Art N° sfaf060).-
item.accessRightsOpen Access-
crisitem.journal.issn2048-8505-
crisitem.journal.eissn2048-8513-
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