Abstract
As a vascular-inflammatory disease, migraine affects the brain and some other organs, such as the eye. The aim of this study was to measure and compare the peripapillary retinal nerve fiber layer (RNFL) thickness, macular ganglion cell layer thickness and optic nerve head parameters to detect structural damage in children with migraine using swept-source optical coherence tomography. Twenty-four children with migraine in the painless period and 26 controls were included in the study. The vast majority of the groups consisted of females (75% for patients and 77% for controls). Certain RNFL quadrants and optic disc parameters revealed significant differences between the patients and controls. In the right and left eyes of children with migraine, nasal quadrant RNFL was significantly thicker than that in healthy subjects (88.82 ± 11.03 vs 77.80 ± 13.77, P = 0.004 for right eyes and 87.71 ± 11.79 vs 77.80 ± 13.77, P = 0.01 for left eyes). Temporal quadrant RNFL in the left eyes was thinner (78.67 ± 9.57 vs 84.44 ± 9.68, P = 0.04). Disc area in the left eyes of the patients was greater (2.29 ± 0.46 vs 1.94 ± 0.28, P = 0.003). There were significant expansions in cup volumes in favor of the patients for right and left eyes (0.15 ± .0.19 vs 0.05 ± 0.05, P = 0.03 and 0.17 ± 0.14 vs 0.05 ± 0.05, P = 0.001, respectively). The only significant difference between the left and right eyes of the migraineurs was the RNFL thickness in the superior quadrant. Ganglion cell layer thickness did not differ between the right eyes, left eyes and controls. In conclusion, children with migraine showed significant variations in specific RNFL and optic disc parameters compared to control subjects.
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References
Özge A, Termine C, Antonaci F et al (2011) Overview of diagnosis and management of pediatric headache. Part I: diagnosis. J Headache Pain 12:13–23
Al-Twajiri WA, Shevell MI (2002) Pediatric migraine equivalents occurrence and clinical features in practice. Pediatr Neurol 26:365–368
Abu-Arefeh I, Russell G (1994) Prevalence of headache and migraine in school children. BMJ 309:765–769
Lynberg AC, Rasmussen BK, Jorgensen T, Jensen R (2005) Incidence of primary headache: a Danish epidemiological follow-up study. Am J Epidemiol 161:1066–1073
Mavromichalis I, Anagnostopoulos D, Metaxas N, Papanastassiou E (1999) Prevalence of migraine in school children and some clinical comparisons between migraine with and without aura. Headache 39:728–736
Battistella PA, Fiumana E, Binelli M et al (2006) Primary headaches in preschool age children: clinical study and follow-up in 163 patients. Cephalalgia 26:162–171
Wober-Bingöl C, Wober C, Karwautz A et al (2004) Clinical features of migraine: a cross-sectional study in patients aged three to sixty-nine. Cephalalgia 24:12–17
Antonaci F, Voiticovschi-Iosob C, Di Stefano AL et al (2014) The evolution of headache from childhood to adulthood: a review of the literature. J Headache Pain. https://doi.org/10.1186/1129-2377-15-15
Lewis DW (2009) Pediatric migraine. Neurol Clin 27:481–501
Eidlitz-Marcus T, Gorali O, Haimi-Cohen Y, Zeharia A (2008) Symptoms of migraine in the pediatric population by age group. Cephalalgia 28:1259–1263
Petrusic I, Pavlovski V, Vucinic D, Jancic J (2014) Features of migraine aura in teenagers. J Headache Pain https://doi.org/10.1186/1129-2377-15-87
Karsan N, Prabhakar P, Goadsby PJ (2016) Characterising the premonitory stage of migraine in children: a clinic-based study of 100 patients in a specialist headache service. J Headache Pain. https://doi.org/10.1186/s10194-016-0689-7
Mamouri O, Cuvellier JC, Duhamel A et al (2017) Postdrome symptoms in pediatric migraine: A questionnaire retrospective study by phone in 100 patients. Cephalalgia. https://doi.org/10.1177/0333102417721132
Genizi J, Gordon S, Kerem NC et al (2013) Primary headaches, attention deficit disorder and learning disabilities in children and adolescents. J Headache Pain 14:4–60
D’Andrea G, Nertempi P, Ferro Milone F et al (1989) Personality and memory in childhood migraine. Cephalalgia 9:25–28
Waldie KE, Hausmann M, Milne BJ, Poulton R (2002) Migraine and cognitive function: a life-course study. Neurology 59:904–908
Parisi P, Verrotti A, Paolino MC et al (2010) Headache and cognitive profile in children: a cross-sectional controlled study. J Headache Pain 11:45–51
Haverkamp F, Hornscheid A, Muller-Sinik K (2002) Cognitive development in children with migraine and their unaffected siblings. Headache 42:776–779
Fercher AF (2010) Optical coherence tomography-development, principles, applications. Z Med Phys 20:251–276
Huang D, Swanson EA, Lin CP et al (1991) Optical coherence tomography. Science 254:178–181
Headache Classification Committee of the International Headache Society (IHS) (2013) The international classification of headache disorders: 3rd edition (beta version). Cephalalgia 33:629–808
Goadsby PJ, Charbit AP, Andreou S et al (2009) Neurobiology of migraine. Neuroscience 161:327–341
Ayata C (2010) Cortical spreading depression triggers migraine attack pro. Headache 50:725–730
Silberstein SD (2004) Migraine pathophysiology and its clinical implications. Cephalalgia 24:2–7
Martinez A, Proupim N, Sanchez M (2008) Retinal nerve fiber layer thickness measuremets using optical coherence tomography in migraine patients. Br J Ophthalmol 92:1069–1075
Gipponi S, Scaroni N, Venturelli E et al (2013) Reduction in retinal nerve fiber layer thickness in migraine patients. Neurol Sci 34:841–845
Yülek E, Dirik EB, Eren Y et al (2015) Macula and retinal nerve fiber layer in migraine patients: analysis by spectral domain optic coherence tomography. Semin Ophthalmol 30:124–128
Reggio E, Chisari CG, Ferrigno G et al (2017) Migraine causes retinal and choroidal structural changes: evaluation with ocular coherence tomography. J Neurol 26:494–502
Monterio MI, Fernandes DB, Apostolos-Pereira SL, Callegaro D (2012) Quantification of retinal neural loss in patients with neuromyelitis optica and multiple sclerosis with or without optic neuritis using Fourier-domain optical coherence tomography. Invest Ophthalmol Vis Sci 53:3959–3966
Kırbaş S, Türkyılmaz K, Anlar O et al (2013) Retinal nerve fiber layer thickness in Alzheimer disease. J Neuroophthalmol 33:58–61
Yener A, Korucu O (2018) Quantitative analysis of retinal nerve fiber layer, ganglion cell layer and optic disc parameters in patients with migraine and patients with tension type headache by swept source optical coherence tomography. Acta Neurol Belg. https://doi.org/10.1007/s13760-018-1041-6
Tan FU, Akarsu C, Güllü R (2005) Retinal nerve fiber layer thickness is unaffected in migraine patients. Acta Neurol Scand 112:19–23
Ekinci M, Ceylan E, Çağatay HH et al (2014) Retinal nerve fiber layer, ganglion cell layer and choroid thinning in migraine with aura. BMC Ophthalmol. https://doi.org/10.1186/1471-2415-14-75
Ascaso FJ, Marco S, Mateo J et al (2017) Optical coherence tomography in patients with chronic migraine: Literature review and update. Front Neurol. https://doi.org/10.3389/fneur.2017.00684
Yang Z, Tatham AJ, Zangwill LM et al (2015) Diagnostic ability of retinal nerve fiber layer imaging by swept source optical coherence tomography in glaucoma. Am J Ophthalmol 159:193–201
Sung KR, Wollstein G, Kim NR et al (2012) Macular assessment using optical coherence tomography for glaucoma diagnosis. Br J Ophthalmol 96:1452–1455
McKendrick AM, Vingrys AJ, Badcock DR, Heywood JT (2000) Visual field losses in subjects with migraine headache. Invest Ophthalmol Vis Sci 41:1239–1247
Drance S, Anderson DR, Schulzer M (2001) Collaborative Normal-Tension Glaucoma Study Group. Risk factors for progression of visual field abnormalities in normal-tension glaucoma. Am J Ophthalmol 131:699–708
Phelps CD, Corbett JJ (1985) Migraine and low tension glaucoma. A case control study. Invest Ophthalmol Vis Sci 26:1105–1108
Flammer J, Pache M, Resink T (2001) Vasospasm, its role in the pathogenesis of diseases with articular reference to the eye. Prog Retin Eye Res 20:319–349
Koban Y, Özlece HK, Bilgin G et al (2016) Intraocular pressure and ocular biometric parameters changes in migraine. BMC Ophthalmol. https://doi.org/10.1186/s12886-016-0258-5
Kara SA, Erdemoğlu AK, Karadeniz MY, Altınok D (2003) Color doppler sonography of orbital and vertebral arteries in migraineurs without aura. J Clin Ultrasound 31:308–314
Schwedt TI, Chiang CC, Chong CD, Dodick DW (2015) Functional MRI of migraine. Lancet Neurol 14:81–91
Killer HE, Forrer A, Flammer J (2003) Retinal vasospasm during an attack of migraine. Retina 23:253–254
Güneş A, Demirci S, Tok L et al (2016) Is retinal nerve fiber layer thickness change related to headache lateralization in migraine? Korean J Ophthalmol 30:134–139
Feng YF, Guo H, Huang JH et al (2016) Retinal nerve fiber layer thickness changes in migraine: a meta-analysis of case-control studies. Curr Eye Res 41:814–822
Stewart WF, Lipton RB, Dowson AJ, Sawyer J (2001) Development and testing of the migraine disability assessment (MIDAS) questionnaire to assess headache related disability. Neurology 56:520–528
Zengin MO, Elmas Z, Çınar E, Küçükerdönmez C (2015) Choroidal thickness changes in patients with migraine. Acta Neurol Belg 115:33–37
Karaca EE, Koçer EB, Özdek Ş et al (2016) Choroidal thickness measurements in migraine patients during attack-free period. Neurol Sci 37:81–88
Dadacı Z, Doğanay F, Öncel Acır N (2014) Enhanced depth imaging optical coherence tomography of the choroid in migraine patients: implications for the association of migraine and glaucoma. Br J Ophthalmol 98:972–975
Karalezli A, Şimşek C, Çelik G, Eroğlu FC (2014) Evaluation of choroidal thickness using spectral- domain optical coherence tomography in migraine patients during acute migraine attacks: a comparative study. Eye (Lond) 28:1477–1481
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This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors. The authors thank Vedat Selamoğlu for providing help in the construction of the figures in the text.
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Yener, A.Ü., Yılmaz, D. Topographic changes measured by the swept source optical coherence tomography in retinal nerve fiber layer, optic nerve head and macula in children with migraine. Acta Neurol Belg 120, 661–668 (2020). https://doi.org/10.1007/s13760-019-01123-5
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DOI: https://doi.org/10.1007/s13760-019-01123-5