Abstract
Purpose
Treatment of optic pathway gliomas is prompted by neuroradiological evidence of tumor growth, usually associated with progressive visual loss. Despite therapy, approximately 40% will show visual deterioration. Treatment outcome is largely based on the preservation of vision. However, current visual function assessment is often unreliable in children with optic pathway gliomas who have limited collaboration. Thus, there is a need for new clinical tools to evaluate visual functions in these children. The aim of the study was to assess the value of steady-state visual evoked potentials as a tool to assess function in the central and peripheral visual fields of children with optic pathway gliomas.
Method
Ten patients with optic pathway gliomas and 33 healthy controls (ages 3 to 18 years) were tested using steady-state visual evoked potentials. The dartboard stimulus consisted of one central circle alternating at 16 reversals/s and one peripheral hoop alternating at 14.4 reversals/s, separated by a hoop of gray space. It was presented monocularly at 30% and 96% contrasts.
Results
Results indicated that central signal-to-noise ratios were significantly lower in children with optic pathway gliomas compared to controls. However, no significant group difference was detected in the peripheral visual field.
Conclusion
Steady-state visual evoked potentials could eventually be implemented in the clinical assessment and follow-up of central visual field deficits in uncooperative or nonverbal children but seem to have limited usefulness for evaluation of peripheral visual field deficits. Additional studies are needed to identify testing parameters for full visual field assessment.
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References
Kelly JP, Weiss AH (2013) Detection of tumor progression in optic pathway glioma with and without neurofibromatosis type 1. Neuro-oncology 15(11):1560–1567
Ammendola A, Ciccone G, Ammendola E (2006) Utility of multimodal evoked potentials study in neurofibromatosis type 1 of childhood. Pediatr Neurol 34(4):276–280
Jahraus CD, Tarbell NJ (2006) Optic pathway gliomas. Pediatr Blood Cancer 46(5):586–596
World Health Organisation (2017) Cancer fact sheet
Fisher MJ et al (2013) Functional outcome measures for NF1-associated optic pathway glioma clinical trials. Neurology 81(21 supplement 1):S15–S24
Avery RA, Fisher MJ, Liu GT (2011) Optic pathway gliomas. J Neuroophthalmol 31(3):269–278
Robert-Boire V et al (2017) Clinical presentation and outcome of patients with optic pathway glioma. Pediatr Neurol 75:55–60
Aquilina K et al (2015) Optic pathway glioma in children: does visual deficit correlate with radiology in focal exophytic lesions? Child Nerv Syst 31(11):2041–2049
Listernick R et al (2007) Optic pathway gliomas in neurofibromatosis-1: controversies and recommendations. Ann Neurol 61(3):189–198
Van Mierlo C et al (2013) Role of visual evoked potentials in the assessment and management of optic pathway gliomas in children. Doc Ophthalmol 127(3):177–190
Binning MJ et al (2007) Optic pathway gliomas: a review. Neurosurg Focus 23(5):E2
Balcer LJ et al (2001) Visual loss in children with neurofibromatosis type 1 and optic pathway gliomas: relation to tumor location by magnetic resonance imaging. Am J Ophthalmol 131(4):442–445
de Freitas Dotto P et al (2018) Visual function assessed by visually evoked potentials in optic pathway low-grade gliomas with and without neurofibromatosis type 1. Doc Ophthalmol 136(3):177–189
Dhermain FG et al (2010) Advanced MRI and PET imaging for assessment of treatment response in patients with gliomas. Lancet Neurol 9(9):906–920
Avery RA et al (2015) Longitudinal change of circumpapillary retinal nerve fiber layer thickness in children with optic pathway gliomas. Am J Ophthalmol 160(5):944–952.e1
Kalin-Hajdu E et al (2014) Visual acuity of children treated with chemotherapy for optic pathway gliomas. Pediatr Blood Cancer 61(2):223–227
Hood DC et al (2004) Detecting early to mild glaucomatous damage: a comparison of the multifocal VEP and automated perimetry. Invest Ophthalmol Vis Sci 45(2):492–498
Fortune B et al (2007) Comparing multifocal VEP and standard automated perimetry in high-risk ocular hypertension and early glaucoma. Invest Ophthalmol Vis Sci 48(3):1173–1180
Harding G et al (2002) Field-specific visual-evoked potentials identifying field defects in vigabatrin-treated children. Neurology 58(8):1261–1265
Colenbrander A (2002) Visual standards aspects and ranges of vision loss with emphasis on population surveys. Report prepared for the International Council of Ophthalmology at the 29th International Congress of Ophthalmology, Sydney, Australia
Horton JC, Hoyt WF (1991) The representation of the visual field in human striate cortex. A revision of the classic Holmes map. Arch Ophthalmol 109(6):816–824
Norcia AM et al (2015) The steady-state visual evoked potential in vision research: a review. J Vis 15(6):4
Matsumoto CS et al (2013) Liquid crystal display screens as stimulators for visually evoked potentials: flash effect due to delay in luminance changes. Doc Ophthalmol 127(2):103–112
Bach M (1996) The Freiburg Visual Acuity test—automatic measurement of visual acuity. Optom Vis Sci 73(1):49–53
Jasper HH (1958) The ten twenty electrode system of the international federation. Electroencephalogr Clin Neurophysiol 10:371–375
Bach M, Meigen T (1999) Do’s and don’ts in Fourier analysis of steady-state potentials. Doc Ophthalmol 99(1):69–82
Meigen T, Bach M (1999) On the statistical significance of electrophysiological steady-state responses. Doc Ophthalmol 98(3):207–232
Holladay JT (2004) Visual acuity measurements. J Cataract Refract Surg 30(2):287–290
Abdullah S, Boon M, Maddess T (2012) Contrast-response functions of the multifocal steady-state VEP (MSV). Clin Neurophysiol 123(9):1865–1871
Wu J et al (2012) Retinotopic mapping of the peripheral visual field to human visual cortex by functional magnetic resonance imaging. Hum Brain Mapp 33(7):1727–1740
Kelly JP, Weiss AH (2006) Comparison of pattern visual-evoked potentials to perimetry in the detection of visual loss in children with optic pathway gliomas. J AAPOS 10(4):298–306
Wolsey DH et al (2006) Can screening for optic nerve gliomas in patients with neurofibromatosis type I be performed with visual-evoked potential testing? J AAPOS 10(4):307–311
Siatkowski RM (2006) VEP testing and visual pathway gliomas: not quite ready for prime time. J AAPOS 10(4):293–295
de Blank PM et al (2017) Optic pathway gliomas in neurofibromatosis type 1: an update: surveillance, treatment indications, and biomarkers of vision. J Neuroophthalmol 37:S23–S32
Falsini B et al (2008) Longitudinal assessment of childhood optic gliomas: relationship between flicker visual evoked potentials and magnetic resonance imaging findings. J Neurooncol 88(1):87–96
Trisciuzzi MTS et al (2004) A fast visual evoked potential method for functional assessment and follow-up of childhood optic gliomas. Clin Neurophysiol 115(1):217–226
Hébert-Lalonde N et al (2014) A frequency-tagging electrophysiological method to identify central and peripheral visual field deficits. Doc Ophthalmol 129(1):17–26
Hood DC et al (2006) The role of the multifocal visual evoked potential (mfVEP) latency in understanding optic nerve and retinal diseases. Trans Am Ophthalmol Soc 104:71
Kuenzle C et al (1994) Follow-up of optic pathway gliomas in children with neurofibromatosis type 1. Neuropediatrics 25(6):295–300
Acknowledgements
We would like to acknowledge the Brain Tumour Foundation of Canada and the Centre Hospitalier Universitaire de Sainte-Justine for their financial support. We would also like to thank our laboratory technician, Anthony Hosein Poitras Loewen for creation of the stimulus and technical support, as well as Hugues Leduc for his valuable help with the statistics. Lastly, we would like to thank the children and their families for their participation in this study.
Funding
The Brain Tumor Foundation of Canada provided financial support in the form of research funding but had no role in the design or conduct of this research.
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Rassi, S.Z., Ospina, L.H., Bochereau, A. et al. Central and peripheral steady-state visual evoked potentials in children with optic pathway gliomas. Doc Ophthalmol 139, 137–149 (2019). https://doi.org/10.1007/s10633-019-09703-9
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DOI: https://doi.org/10.1007/s10633-019-09703-9