UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

Neurologic involvement in cystinosis: Focus on brain lesions and new evidence of four-repeat (4R-) Tau immunoreactivity

Nicoletti, T; Bink, A; Helmchen, B; Briel, N; Frontzek, K; Vlad, B; Gaspert, A; ... Hortobágyi, T; + view all (2024) Neurologic involvement in cystinosis: Focus on brain lesions and new evidence of four-repeat (4R-) Tau immunoreactivity. Journal of the Neurological Sciences , 456 , Article 122841. 10.1016/j.jns.2023.122841.

[thumbnail of Frontzek_Manuscript_Cystinosis_Rev_CLEAN.pdf] Text
Frontzek_Manuscript_Cystinosis_Rev_CLEAN.pdf - Accepted Version
Access restricted to UCL open access staff until 15 December 2024.

Download (425kB)

Abstract

Nephropathic cystinosis is a rare autosomal recessive storage disorder caused by CTNS gene mutations, leading to autophagy-lysosomal pathway impairment and cystine crystals accumulation. Neurologic involvement is highly variable and includes both neurodevelopmental and neurodegenerative disturbances, as well as focal neurologic deficits. By presenting longitudinal data of a 28-year-old patient with a large infratentorial lesion, we summarized the pathology, clinical and imaging features of neurological involvement in cystinosis patients. Brain damage in form of cystinosis-related cerebral lesions occurs in advanced disease phases and is characterized by the accumulation of cystine crystals, subsequent inflammation with vasculitis-like features, necrosis, and calcification. Epilepsy is a frequent comorbidity in affected individuals. Steroids might play a role in the symptomatic treatment of “stroke-like” episodes due to edematous-inflammatory lesions, but probably do not change the overall prognosis. Lifelong compliance to depleting therapy with cysteamine still represents the main therapeutic option. However, consequences of CTNS gene defects are not restricted to cystine accumulation. New evidence of four-repeat (4R-) Tau immunoreactivity suggests concurrent progressive neurodegeneration in cystinosis patients, highlighting the need of innovative therapeutic strategies, and shedding light on the crosstalk between proteinopathies and autophagy-lysosomal system defects. Eventually, emerging easily accessible biomarkers such as serum neurofilament light chains (NfL) might detect subclinical neurologic involvement in cystinosis patients.

Type: Article
Title: Neurologic involvement in cystinosis: Focus on brain lesions and new evidence of four-repeat (4R-) Tau immunoreactivity
Location: Netherlands
DOI: 10.1016/j.jns.2023.122841
Publisher version: http://dx.doi.org/10.1016/j.jns.2023.122841
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: 4R-tauopathy, CTNS, Calcification, Cristallopathy, Crystals, Cysteamine, Necroptosis, TFEB, Humans, Adult, Cystinosis, Cystine, Amino Acid Transport Systems, Neutral, Cysteamine, Inflammation, Brain
URI: https://discovery.ucl.ac.uk/id/eprint/10185983
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item