Hurler syndrome glycosaminoglycans decrease in cerebrospinal fluid without brain-targeted therapy.
Troy C LundElizabeth BraunlinLynda E PolgreenAshish O GuptaPaul J OrchardJulie B EisengartPublished in: Annals of neurology (2023)
Novel therapies for Hurler syndrome aim to cross the blood-brain barrier (BBB) to target neurodegeneration by degrading glycosaminoglycans (GAG). BBB penetration has been assumed with decreased cerebrospinal fluid (CSF) GAG, yet little is known about CSF GAG without brain-targeting therapies. We compared pre-transplant CSF GAG in patients who were treatment naïve (n=19) versus receiving standard non-BBB penetrating enzyme replacement therapy (ERT, n=12). In the ERT versus treatment naïve groups, CSF GAG was significantly lower across all content assayed, raising questions about using CSF GAG decrements to show BBB penetration. Future studies should compare GAG reduction in standard versus novel therapies. This article is protected by copyright. All rights reserved.