Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Brügelmann, M; Müller, S; Bohlen, AV; Hohenfellner, K; Büscher, A; Kemper, MJ; Fröde, K; Kanzelmeyer, N; Oh, J; Billing, H; Gellermann, J; Müller, D; Weber, LT; Acham-Roschitz, B; Arbeiter, K; Tönshoff, B; Hagenberg, M; Žebec, MS; Haffner, D; Zivicnjak, M.
Morphological changes and their associations with clinical parameters in children with nephropathic cystinosis and chronic kidney disease prior to kidney replacement therapy over 25 years.
Pediatr Nephrol. 2024; 39(10):3067-3077 Doi: 10.1007/s00467-024-06421-6 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Acham-Roschitz Birgit
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
BACKGROUND: Infantile nephropathic cystinosis (INC) is a rare lysosomal storage disorder, mostly and often firstly affecting the kidneys, together with impaired disharmonious growth and rickets, eventually resulting in progressive chronic kidney disease (CKD). With the introduction of cysteamine therapy, most pediatric patients reach adulthood with no need for kidney replacement therapy. Still, detailed changes in INC patients' clinical and morphological presentation over the past decades have not yet been thoroughly investigated. METHODS: Two groups with a respective total of 64 children with INC and 302 children with CKD, both treated conservatively and aged 2 to 18 years, were prospectively observed in the time span from 1998 to 2022 with 1186 combined annual clinical and morphological examinations clustered into two measurement periods (1998 to 2015 and ≥ 2016). RESULTS: In INC patients, thoracic proportion indices remained markedly increased, whereas body fat stores remained decreased over the past 25 years (+ 1 vs. below ± 0 z-score, respectively). Their CKD peers presented with overall improved growth, general harmonization of body proportions, and improved body fat stores, while INC patients only presented with an isolated significant increase in leg length over time (∆0.36 z-score). eGFR adjusted for age did not significantly change over the past 25 years in both groups. Alkaline phosphatase (ALP) showed a significant decrease in CKD patients over time, while remaining above normal levels in INC patients. CONCLUSIONS: Disproportionate thoracic shape and impaired body fat stores remain the most characteristic morphological traits in INC patients over the past 25 years, while causal mechanisms remain unclear.
Find related publications in this database (using NLM MeSH Indexing)
Humans - administration & dosage
Child - administration & dosage
Cystinosis - therapy, pathology, diagnosis, complications
Male - administration & dosage
Adolescent - administration & dosage
Female - administration & dosage
Child, Preschool - administration & dosage
Renal Insufficiency, Chronic - therapy, pathology
Renal Replacement Therapy - statistics & numerical data, methods
Prospective Studies - administration & dosage
Kidney - pathology
Disease Progression - administration & dosage
Cysteamine - therapeutic use, administration & dosage

Find related publications in this database (Keywords)
Infantile nephropathic cystinosis
Chronic kidney disease
Body fat mass
Thoracic proportions
Growth
Body mass index
© Med Uni Graz Impressum