Please use this identifier to cite or link to this item: https://accedacris.ulpgc.es/handle/10553/139950
DC FieldValueLanguage
dc.contributor.authorFernandez, Juan M.en_US
dc.contributor.authorRodríguez Pérez, José Carlosen_US
dc.contributor.authorLorenzo-Medina, M. Mercedesen_US
dc.contributor.authorRodriguez-Esparragon, Fanciscoen_US
dc.contributor.authorQuevedo-Reina, Juan C.en_US
dc.contributor.authorHernandez-Socorro, Carmen R.en_US
dc.date.accessioned2025-06-11T14:31:15Z-
dc.date.available2025-06-11T14:31:15Z-
dc.date.issued2025en_US
dc.identifier.otherScopus-
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/139950-
dc.description.abstractEquations for estimation glomerular filtration rate (eGFR) have been associated with poor clinical performance and their clinical accuracy and reliability have been called into question. AIM To assess the longitudinal changes in measured glomerular filtration rate (mGFR) in patients with autosomal dominant polycystic kidney disease (ADPKD). METHODS Analysis of an ambispective data base conducted on consecutive patients diagnosed with ADPKD. The mGFR was assessed by iohexol clearance; while eGFR was calculated by three different formulas: (1) The chronic kidney disease epidemiology collaboration (CKD-EPI); (2) Modification of diet in renal disease (MDRD); and (3) The 24-hour urine creatinine clearance (CrCl). The primary end-points were the mean change in mGFR between the baseline and final visit, as well as the comparison of the mean change in mGFR with the change estimated by the different formulas. RESULTS Thirty-seven patients were included in the study. As compared to baseline, month-6 mGFR was significantly decrease by-4.4 mL/minute ± 10.3 mL/minute (P = 0.0132). However, the CKD-EPI, MDRD, and CrCl formulas underestimated this change by 48.3%, 89.0%, and 45.8% respectively, though none of these differences reached statistical significance (P = 0.3647; P = 0.0505; and P = 0.736, respectively). The discrepancies between measured and estimated glomerular filtration rate values, as evaluated by CKD-EPI (r = 0.29, P = 0.086); MDRD (r = 0.19, P = 0.272); and CrCl (r = 0.09, P = 0.683), were not correlated with baseline mGFR values. CONCLUSION This study indicated that eGFR inaccurately reflects the decline in mGFR and cannot reliably track changes over time. This poses significant challenges for clinical decision-making, particularly in treatment strategies.en_US
dc.languageengen_US
dc.relation.ispartofWorld Journal of Nephrologyen_US
dc.sourceWorld Journal of Nephrology [EISSN 2220-6124], v. 14 (1), (Marzo 2025)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320102 Genética clínicaen_US
dc.subject320506 Nefrologíaen_US
dc.subject.otherAutosomal Dominant Polycystic Kidney Diseaseen_US
dc.subject.otherChronic Kidney Disease Epidemiology Collaborationen_US
dc.subject.otherEnd-Stage Kidney Diseaseen_US
dc.subject.otherGlomerular Filtration Rateen_US
dc.subject.otherIohexolen_US
dc.subject.otherModification Of Diet In Renal Diseaseen_US
dc.titleLongitudinal assessment of measured and estimated glomerular filtration-rate in autosomal dominant polycystic kidney disease: Real practice experienceen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.5527/wjn.v14.i1.99044en_US
dc.identifier.scopus85216482573-
dc.contributor.orcid0000-0003-3907-6005-
dc.contributor.orcid0000-0003-0023-1063-
dc.contributor.orcid0000-0003-4854-2303-
dc.contributor.orcid0000-0003-1663-3673-
dc.contributor.orcid0000-0001-5595-0298-
dc.contributor.orcid0000-0002-9753-2550-
dc.contributor.authorscopusid55455064000-
dc.contributor.authorscopusid7005446255-
dc.contributor.authorscopusid22980400500-
dc.contributor.authorscopusid6603262370-
dc.contributor.authorscopusid57218592801-
dc.contributor.authorscopusid6505758785-
dc.identifier.eissn2220-6124-
dc.identifier.issue1-
dc.relation.volume14en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.date.coverdateMarzo 2025en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,344
dc.description.sjrqQ3
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptGIR IUIBS: Patología y Tecnología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0003-0023-1063-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameRodríguez Pérez,José Carlos-
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