| Literature DB >> 35843134 |
Katharina Hohenfellner1, Christina Nießl2, Dieter Haffner3, Jun Oh4, Christine Okorn5, Katja Palm6, Karl-Peter Schlingmann7, Simone Wygoda8, William Allen Gahl9.
Abstract
Nephropathic cystinosis is a rare lysosomal storage disease whose basic defect, impaired transport of cystine out of lysosomes, results in intracellular cystine storage. Affected individuals exhibit renal Fanconi Syndrome in infancy, end-stage kidney disease at approximately 10 years of age, and many other systemic complications. Oral cysteamine therapy mitigates the detrimental effects on glomerular function and prevents most of the late complications of the disease but has not shown benefit with respect to the early tubular damage of cystinosis. This is because cystinosis is generally diagnosed in the second year of life, after the damage to kidney tubular function has already occurred. We longitudinally evaluated 6 infants diagnosed and treated with cysteamine from before 2 months of age. The 4 infants with good compliance with cysteamine and consistently low leucocyte cystine levels maintained normal eGFR values, exhibited only minor degrees of renal Fanconi Syndrome, and maintained normal serum levels of potassium, bicarbonate, phosphate, and calcium without electrolyte or mineral supplementation through 2, 4, 10 and 16 years of age. Thus, renal Fanconi syndrome can be attenuated by early administration of cysteamine and renew the call for molecular-based newborn screening for cystinosis.Entities:
Keywords: Cysteamine; Cystinosis; Fanconi syndrome; Glomerular function; Tubular function
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Year: 2022 PMID: 35843134 PMCID: PMC9413354 DOI: 10.1016/j.ymgme.2022.06.009
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.204