• World Neurosurg · May 2021

    Optical Coherence Tomography Revealing Ganglion Cell Loss in idiopathic Normal Pressure Hydrocephalus.

    • Andreas Eleftheriou, Yumin Huang-Link, and Fredrik Lundin.
    • Department of Neurology, Division of Neurobiology, Linköping University, Linköping, Sweden; Department of Biomedical and Clinical Sciences, Division of Neurobiology, Linköping University, Linköping, Sweden. Electronic address: andelef2002@yahoo.gr.
    • World Neurosurg. 2021 May 1; 149: e1061-e1066.

    BackgroundAlthough there may theoretically be a disturbance in the eye or the visual pathways due to abnormal cerebrospinal fluid (CSF) dynamics in idiopathic normal pressure hydrocephalus (iNPH), it has not been studied systemically. Optical coherence tomography (OCT) is a noninvasive, reproducible procedure for quantitative and qualitative analysis of retinal morphology.MethodsOCT was used to study the eye fundus before and after a CSF tap test in patients with iNPH compared with healthy individuals (HIs). Twelve patients with iNPH (6 females and 6 males) with a median age of 76 years (64-84 years) and 21 HIs (11 females and 10 males) with a median age of 73 years (64-79 years) were included. The patients underwent neurological, cognitive, and physiotherapeutic evaluation. Brain magnetic resonance imaging, CSF tap test via lumbar puncture, and subsequently CSF analysis were performed. OCT was performed before and after CSF removal. HIs underwent OCT once.ResultsThe patients had significantly reduced retinal ganglion cell layer thickness 71 μm (56-81 μm) compared with the HIs, 79.5 μm (72-90 μm) (P = 0.001), but no significant changes were observed before or after the CSF tap test. All patients improved in motor function in a 10-m walk test after the CSF tap test. The median CSF pressure was 15 and 1 cm H2O, respectively, before and after lumbar puncture with removal of median 43.5 mL CSF.ConclusionsThis pilot study shows OCT findings that differ from HIs and implies a rational for becoming a valuable tool in the diagnosis of iNPH. Further studies are warranted to elucidate the pathology of the retina in iNPH.Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.

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