Subscribe to RSS
DOI: 10.1055/s-0040-1722687
Lumbar Puncture Opening Pressure in Patients with Spinal Muscular Atrophy
Abstract
The announcement of a hydrocephalus as a possible side effect in patients with spinal muscular atrophy (SMA) receiving the drug nusinersen, promoted major concern and warrants further evaluation. In this retrospective monocentric study, we analyzed clinical data, lumbar puncture opening pressure (LOP) measurement, and ophthalmologic and neuroimaging results in 34 patients with SMA types 1 to 3 undergoing treatment with nusinersen. None of the patients reported symptoms indicative of increased intracranial pressure. In our cohort, the LOP was >20 cm H2O in 25 patients (70.5%), and within this group ≥28 cm H2O in 12 patients (35.3%), in two patients, it was increased prior to treatment initiation. Signs of increased intracranial pressure in ophthalmological assessments or brain imaging were only seen in one patient. We did not identify a correlation between increased LOP and SMA type, scoliosis, or age of the patients; however, it was slightly higher in patients receiving sedation. Our results raise the question whether the LOP is generally increased in SMA as part of the underlying disease, if so, what the etiology is, and whether the increased LOP needs to be treated.
Keywords
spinal muscular atrophy - intracranial pressure - nusinersen - hydrocephalus - MRI - lumbar puncture opening pressureContributor's Statement Page
L.L.B. collected data, drafted the initial manuscript, performed the analysis, and reviewed and revised the manuscript. A.T., C.W., and V.M. collected data, interpreted data, and reviewed and revised the manuscript. A.M.K. conceptualized and designed the study, coordinated and supervised data collection, and critically reviewed the manuscript for important intellectual content. All authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.
Publication History
Received: 31 March 2020
Accepted: 15 October 2020
Article published online:
12 February 2021
© 2021. Thieme. All rights reserved.
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References
- 1 Mercuri E, Darras BT, Chiriboga CA. et al; CHERISH Study Group. Nusinersen versus sham control in later-onset spinal muscular atrophy. N Engl J Med 2018; 378 (07) 625-635
- 2 Chiriboga CA, Swoboda KJ, Darras BT. et al. Results from a phase 1 study of nusinersen (ISIS-SMN(Rx)) in children with spinal muscular atrophy. Neurology 2016; 86 (10) 890-897
- 3 Michelson D, Ciafaloni E, Ashwal S. et al. Evidence in focus: Nusinersen use in spinal muscular atrophy: report of the guideline development, dissemination, and implementation subcommittee of the American Academy of Neurology. Neurology 2018; 91 (20) 923-933
- 4 Grotto S, Cuisset JM, Marret S. et al. Type 0 spinal muscular atrophy: further delineation of prenatal and postnatal features in 16 patients. J Neuromuscul Dis 2016; 3 (04) 487-495
- 5 Lefebvre S, Burlet P, Liu Q. et al. Correlation between severity and SMN protein level in spinal muscular atrophy. Nat Genet 1997; 16 (03) 265-269
- 6 Taylor JE, Thomas NH, Lewis CM. et al. Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy. Eur J Hum Genet 1998; 6 (05) 467-474
- 7 Pechmann A, Langer T, Wider S, Kirschner J. Single-center experience with intrathecal administration of Nusinersen in children with spinal muscular atrophy type 1. Eur J Paediatr Neurol 2018; 22 (01) 122-127
- 8 Avery RA. Reference range of cerebrospinal fluid opening pressure in children: historical overview and current data. Neuropediatrics 2014; 45 (04) 206-211
- 9 Wurster CD, Winter B, Wollinsky K. et al. Intrathecal administration of nusinersen in adolescent and adult SMA type 2 and 3 patients. J Neurol 2019; 266 (01) 183-194
- 10 Lunskens S, Lammertijn L, Deeren D, Bergmans B, Maertens J, Vandenberghe R. Intracranial hypertension following intrathecal administration of liposomal cytarabine. J Neurol 2011; 258 (01) 162-163
- 11 Groen EJN, Perenthaler E, Courtney NL. et al. Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy. Hum Mol Genet 2018; 27 (16) 2851-2862
- 12 Wishart TM, Huang JP, Murray LM. et al. SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy. Hum Mol Genet 2010; 19 (21) 4216-4228
- 13 Querin G, El Mendili MM, Lenglet T. et al. The spinal and cerebral profile of adult spinal-muscular atrophy: a multimodal imaging study. Neuroimage Clin 2019; 21: 101618
- 14 Tozawa T, Kasai T, Tatebe H. et al. Intrathecal nusinersen treatment after ventriculo-peritoneal shunt placement: a case report focusing on the neurofilament light chain in cerebrospinal fluid. Brain Dev 2020; 42 (03) 311-314
- 15 Kilgore KP, Bhatti MT, Cutsforth-Gregory JK, Hodge DO, Chen JJ. Variability of consecutive lumbar puncture opening pressures. J Neuroophthalmol 2019