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Ratio of Urinary Proteins to Albumin Excretion Shifts Substantially during Progression of the Podocytopathy Alport Syndrome, and Spot Urine Is a Reliable Method to Detect These Pathologic Changes.
Boeckhaus, Jan; Mohr, Lea; Dihazi, Hassan; Tönshoff, Burkhard; Weber, Lutz T; Pape, Lars; Latta, Kay; Fehrenbach, Henry; Lange-Sperandio, Baerbel; Kettwig, Matthias; Staude, Hagen; König, Sabine; John-Kroegel, Ulrike; Gellermann, Jutta; Hoppe, Bernd; Galiano, Matthias; Haffner, Dieter; Rhode, Heidrun; Gross, Oliver.
Afiliação
  • Boeckhaus J; Clinic for Nephrology and Rheumatology, University Medical Center Goettingen, 37075 Goettingen, Germany.
  • Mohr L; Clinic for Nephrology and Rheumatology, University Medical Center Goettingen, 37075 Goettingen, Germany.
  • Dihazi H; Clinic for Nephrology and Rheumatology, University Medical Center Goettingen, 37075 Goettingen, Germany.
  • Tönshoff B; Department of Pediatrics I, University Children's Hospital Heidelberg, 69120 Heidelberg, Germany.
  • Weber LT; Pediatric Nephrology, Children's and Adolescents' Hospital, Faculty of Medicine and University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.
  • Pape L; Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, 30625 Hannover, Germany.
  • Latta K; Department of Pediatrics II, University Childrens' Hospital, University of Duisburg-Essen, 45147 Essen, Germany.
  • Fehrenbach H; Clementine Kinderhospital Frankfurt, 60316 Frankfurt, Germany.
  • Lange-Sperandio B; Pediatric Nephrology, Children's Hospital, 87700 Memmingen, Germany.
  • Kettwig M; Dr. v. Hauner Children's Hospital, Ludwig Maximilians University, 80337 Munich, Germany.
  • Staude H; Clinic of Pediatrics and Adolescent Medicine, University Medical Center Göttingen, 37075 Göttingen, Germany.
  • König S; Pediatric Nephrology, University Children's Hospital Rostock, 18057 Rostock, Germany.
  • John-Kroegel U; University Children's Hospital Münster, 48149 Münster, Germany.
  • Gellermann J; Division of Pediatric Nephrology, University Children's Hospital, 07743 Jena, Germany.
  • Hoppe B; Pediatric Nephrology, Charité Children's Hospital, 10117 Berlin, Germany.
  • Galiano M; Division of Pediatric Nephrology, Department of Pediatrics, University of Bonn, 53121 Bonn, Germany.
  • Haffner D; Department of Pediatrics and Adolescent Medicine, University Hospital, Friedrich-Alexander-University Erlangen, 91054 Erlangen, Germany.
  • Rhode H; Department of Pediatric Kidney, Liver and Metabolic Diseases, Hannover Medical School, 30625 Hannover, Germany.
  • Gross O; Department of Internal Medicine I, Cardiology, Angiology, Intensive Medical Care, University Hospital Jena, Am Klinikum 1, 07747 Jena, Germany.
Cells ; 12(9)2023 05 07.
Article em En | MEDLINE | ID: mdl-37174733
The urinary albumin- and protein-to-creatinine ratios (UACR and UPCR, respectively) are key endpoints in most clinical trials assessing risk of progression of chronic kidney disease (CKD). For the first time, the current study compares the UACR versus the UPCR head-to-head at early stages of CKD, taking use of the hereditary podocytopathy Alport syndrome (AS) as a model disease for any CKD. Urine samples originated from the prospective randomized, controlled EARLY PRO-TECT Alport trial (NCT01485978). Urine samples from 47 children with confirmed diagnoses of AS at very early stages of CKD were divided according to the current stage of AS: stage 0 (UACR < 30 mg/g), stage 1 (30-300 mg/g) or stage 2 (>300 mg/g). The range of estimated glomerular filtration rate was 75-187.6 mL/min. The mean age was 10.4 ± 4.5 years. In children at stage 0, proteinuria in spot urine, confirmed in 24 h urine, was almost ten times higher than albuminuria (106.4 ± 42.2 vs. 12.5 ± 9.7; p < 0.05); it was "only" about three times higher in stage 1 (328.5 ± 210.1 vs. 132.3 ± 80.5; p < 0.05) and almost equal in stage 2 (1481.9 ± 983.4 vs. 1109.7 ± 873.6; p = 0.36). In 17 children, UACRs and UPCRs were measured simultaneously in 24 h urine and spot urine in the same study visit. Interestingly, the UACR (and UPCR) in 24 h urine vs. in spot urine varied by less than 10% (266.8 ± 426.4 vs. 291.2 ± 530.2). In conclusion, our study provides the first evidence that in patients with normal glomerular filtration rate (GFR) and low amounts of albuminuria, especially in children with podocytopathies such as AS, measuring the UACR and UPCR in spot urine is a reliable and convenient alternative to 24 h urine collection. Our study advocates both the UACR and the UPCR as relevant diagnostic biomarkers in future clinical trials in children with glomerular diseases because the UPCR seems to be a very significant parameter at very early stages of podocytopathies. The German Federal Ministry of Education and Research funded this trial (01KG1104).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Nefrite Hereditária Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Humans Idioma: En Revista: Cells Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica / Nefrite Hereditária Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Humans Idioma: En Revista: Cells Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha