Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children
dc.authorid | Baskin, Esra/0000-0003-4361-8508 | |
dc.authorid | Canpolat, Nur/0000-0002-3420-9756 | |
dc.authorid | Canpolat, Nur/0000-0002-3420-9756 | |
dc.authorid | Balat, Ayse/0000-0002-8904-1348 | |
dc.authorid | Vidal, Enrico/0000-0003-3963-0803 | |
dc.authorid | Liebau, Max Christoph/0000-0003-0494-9080 | |
dc.authorid | Zurowska, Aleksandra/0000-0002-3354-5344 | |
dc.authorwosid | Baskin, Esra/B-5785-2018 | |
dc.authorwosid | Candan, Cengiz/ABC-6193-2021 | |
dc.authorwosid | Canpolat, Nur/AHE-2082-2022 | |
dc.authorwosid | Canpolat, Nur/V-6807-2017 | |
dc.authorwosid | Balat, Ayse/JOZ-8426-2023 | |
dc.authorwosid | Vidal, Enrico/AAL-9105-2021 | |
dc.authorwosid | Liebau, Max Christoph/K-3470-2019 | |
dc.contributor.author | Azukaitis, Karolis | |
dc.contributor.author | Ju, Wenjun | |
dc.contributor.author | Kirchner, Marietta | |
dc.contributor.author | Nair, Viji | |
dc.contributor.author | Smith, Michelle | |
dc.contributor.author | Fang, Zhiyin | |
dc.contributor.author | Thurn-Valsassina, Daniela | |
dc.date.accessioned | 2024-08-04T20:45:53Z | |
dc.date.available | 2024-08-04T20:45:53Z | |
dc.date.issued | 2019 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Urinary epidermal growth factor (uEGF) has recently been identified as a promising biomarker of chronic kidney disease (CKD) progression in adults with glomerular disease. Low levels of uEGF predict CKD progression and appear to reflect the extent of tubulointerstitial damage. We investigated the relevance of uEGF in pediatric CKD. We performed a post hoc analysis of the Cardiovascular Comorbidity in Children with CKD (4C) study, which prospectively follows children aged 6-17 years with baseline estimated glomerular filtration rate (eGFR) of 10-60 ml/min/1.73 m(2). uEGF levels were measured in archived urine collected within 6 months of enrollment. Congenital abnormalities of the kidney and urinary tract were the most common cause of CKD, with glomerular diseases accounting for <10% of cases. Median eGFR at baseline was 28 ml/min/1.73 m(2), and 288 of 623 participants (46.3%) reached the composite endpoint of CKD progression (50% eGFR loss, eGFR < 10 ml/min/1.73 m(2), or initiation of renal replacement therapy). In a Cox proportional hazards model, higher uEGF/Cr was associated with a decreased risk of CKD progression (HR 0.76; 95% CI 0.69-0.84) independent of age, sex, baseline eGFR, primary kidney disease, proteinuria, and systolic blood pressure. The addition of uEGF/Cr to a model containing these variables resulted in a significant improvement in C-statistics, indicating better prediction of the 1-, 2- and 3-year risk of CKD progression. External validation in a prospective cohort of 222 children with CKD demonstrated comparable results. Thus, uEGF may be a useful biomarker to predict CKD progression in children with CKD. | en_US |
dc.description.sponsorship | ERA-EDTA Research Programme; KfH Foundation for Preventive Medicine; German Federal Ministry of Education and Research [01EO0802]; European Community's Seventh Framework Programme (FP7/2007-2013) [2012-305608] | en_US |
dc.description.sponsorship | Support for the 4C Study was received from the ERA-EDTA Research Programme, the KfH Foundation for Preventive Medicine, and the German Federal Ministry of Education and Research (reference number: 01EO0802). FS and MK received support for this study from the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement No. 2012-305608 (EURenOmics). FS, EW, FL, EV, and AM are members of the European Reference Network for Rare Kidney Diseases (ERKNet). | en_US |
dc.identifier.doi | 10.1016/j.kint.2019.01.035 | |
dc.identifier.endpage | 221 | en_US |
dc.identifier.issn | 0085-2538 | |
dc.identifier.issn | 1523-1755 | |
dc.identifier.issue | 1 | en_US |
dc.identifier.pmid | 31005273 | en_US |
dc.identifier.scopus | 2-s2.0-85064440108 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 214 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.kint.2019.01.035 | |
dc.identifier.uri | https://hdl.handle.net/11616/98762 | |
dc.identifier.volume | 96 | en_US |
dc.identifier.wos | WOS:000472024100029 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science Inc | en_US |
dc.relation.ispartof | Kidney International | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | chronic kidney disease | en_US |
dc.subject | CKD progression | en_US |
dc.subject | epidermal growth factor | en_US |
dc.subject | pediatric CKD | en_US |
dc.title | Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children | en_US |
dc.type | Article | en_US |