Parisi, V.; G.B. Bietti Foundation-IRCCS, Department of Neurophysiology of Vision and Neurophthalmology, Via Livenza 3, Rome, Italy
Di Renzo, A.; G.B. Bietti Foundation-IRCCS, Department of Neurophysiology of Vision and Neurophthalmology, Via Livenza 3, Rome, Italy
Martelli, F.; Istituto Superiore di Sanità, Dipartimento Tecnologie e Salute, Rome, Italy
Fadda, A.; Istituto Superiore di Sanità, Dipartimento Tecnologie e Salute, Rome, Italy
Schoenen, Jean ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Département des sciences biomédicales et précliniques
Pierelli, F.; Department of Medical and Surgical Sciences and Biotechnologies, “Sapienza” University of Rome Polo Pontino, Latina, Italy, IRCCS-Neuromed, Pozzilli, IS, Italy
Language :
English
Title :
Visual evoked potentials in subgroups of migraine with aura patients
Russell M, Olesen J (1996) A nosographic analysis of the migraine aura in a general population. Brain 119:355–361
Eriksen M, Thomsen L, Andersen I, Nazim F, Olesen J (2004) Clinical characteristics of 362 patients with familial migraine with aura. Cephalalgia 24:564–575
Rasmussen B, Olesen J (1992) Migraine with aura and migraine without aura: an epidemiological study. Cephalalgia 12:221–228
Lauritzen M (2001) Cortical spreading depression in migraine. Cephalalgia 21:757–760
Charles A, Baca S (2013) Cortical spreading depression and migraine. Nat Rev Neurol 9:637–644
Olesen J, Friberg L, Olsen T, Iversen H, Lassen N, Andersen A, et al (1990) Timing and topography of cerebral blood flow, aura, and headache during migraine attacks. Ann Neurol 28:791–798
Cao Y, Welch K, Aurora S, Vikingstad E (1999) Functional MRI-BOLD of visually triggered headache in patients with migraine. Arch Neurol 56:548–554
Hadjikhani N, Sanchez D, Wu O, Schwartz D, Bakker D, Fischl B, et al (2001) Mechanisms of migraine aura revealed by functional MRI in human visual cortex. Proc Natl Acad Sci U S A 98:4687–4692
Bowyer SM, Aurora KS, Moran JE, Tepley N, Welch KM (2001) Magnetoencephalographic fields from patients with spontaneous and induced migraine aura. Ann Neurol 50:582–587
Zhang X, Levy D, Noseda R, Kainz V, Jakubowski M, Burstein R, et al (2010) Activation of meningeal nociceptors by cortical spreading depression: implications for migraine with aura. J Neurosci 30:8807–8814
Zhang X, Levy D, Kainz V, Noseda R, Jakubowski M, Burstein R, et al (2011) Activation of central trigeminovascular neurons by cortical spreading depression. Ann Neurol 69:855–865
Omland P, Nilsen K, Uglem M, Gravdahl G, Linde M, Hagen K, et al (2013) Visual Evoked Potentials in Interictal Migraine: No Confirmation of Abnormal Habituation. Headache 53:1071–1086
Afra J, Cecchini AP, De Pasqua V, Albert A, Schoenen J (1998) Visual evoked potentials during long periods of pattern-reversal stimulation in migraine. Brain 121(Pt 2):233–241
Coppola G, Ambrosini A, Di Clemente L, Magis D, Fumal A, Gérard P, et al (2007) Interictal abnormalities of gamma band activity in visual evoked responses in migraine: an indication of thalamocortical dysrhythmia? Cephalalgia 27:1360–1367
Coppola G, Parisi V, Di Lorenzo C, Serrao M, Magis D, Schoenen J, et al (2013) Lateral inhibition in visual cortex of migraine patients between attacks. J Headache Pain 14:20
Coppola G, Di Lorenzo C, Schoenen J, Pierelli F (2013) Habituation and sensitization in primary headaches. J Headache Pain 14:65
Eriksen M, Thomsen L, Olesen J (2006) Implications of clinical subtypes of migraine with aura. Headache 46:286–297
Ambrosini A, de Noordhout A, Alagona G, Dalpozzo F, Schoenen J (1999) Impairment of neuromuscular transmission in a subgroup of migraine patients. Neurosci Lett 276:201–203
Ambrosini A, de Noordhout A, Schoenen J (2001) Neuromuscular transmission in migraine patients with prolonged aura. Acta Neurol Belg 101:166–170
Sándor P, Dydak U, Schoenen J, Kollias S, Hess K, Boesiger P, et al (2005) MR-spectroscopic imaging during visual stimulation in subgroups of migraine with aura. Cephalalgia 25:507–518
Sickmann H, Walls A, Schousboe A, Bouman S, Waagepetersen H (2009) Functional significance of brain glycogen in sustaining glutamatergic neurotransmission. J Neurochem 1:80–86
Bozzo L, Puyal J, Chatton J (2013) Lactate modulates the activity of primary cortical neurons through a receptor-mediated pathway. PLoS One 8:10
Matsui T, Soya S, Kawanaka K, Soya H (2015) Brain Glycogen Decreases During Intense Exercise Without Hypoglycemia: The Possible Involvement of Serotonin. Neurochem Res 40:1333–1340
Gilbert E, Tang J, Ludvig N, Bergold P (2006) Elevated lactate suppresses neuronal firing in vivo and inhibits glucose metabolism in hippocampal slice cultures. Brain Res 1117:213–223
Shimizu H, Watanabe E, Hiyama T, Nagakura A, Fujikawa A, Okado H et al (2007) Glial Nax channels control lactate signaling to neurons for brain [Na+] sensing. Neuron 54:59–72
Sappey-Marinier D, Calabrese G, Fein G, Hugg J, Biggins C, Weiner M, et al (1992) Effect of photic stimulation on human visual cortex lactate and phosphates using 1H and 31P magnetic resonance spectroscopy. J Cereb Blood Flow Metab 12:584–592
Barbiroli B, Montagna P, Cortelli P, Funicello R, Iotti S, Monari L, et al (1992) Abnormal brain and muscle energy metabolism shown by 31P magnetic resonance spectroscopy in patients affected by migraine with aura. Neurology 42:1209–1214
Watanabe H, Kuwabara T, Ohkubo M, Tsuji S, Yuasa T (1996) Elevation of cerebral lactate detected by localized 1H-magnetic resonance spectroscopy in migraine during the interictal period. Neurology 47:1093–1095
Judit A, Sándor PS, Schoenen J (2000) Habituation of visual and intensity dependence of auditory evoked cortical potentials tends to normalize just before and during the migraine attack. Cephalalgia 20:714–719
Coutin-Churchman P, Padrón de Freytez A (2003) Vector analysis of visual evoked potentials in migraineurs with visual aura. Clin Neurophysiol 114:2132–2137
Shibata K, Osawa M, Iwata M (1997) Pattern reversal visual evoked potentials in classic and common migraine. J Neurol Sci 145:177–181
Shibata K, Osawa M, Iwata M (1998) Pattern reversal visual evoked potentials in migraine with aura and migraine aura without headache. Cephalalgia 18:319–323
Oelkers R, Grosser K, Lang E, Geisslinger G, Kobal G, Brune K, et al (1999) Visual evoked potentials in migraine patients: alterations depend on pattern spatial frequency. Brain 122(Pt 6):1147–1155
Zaletel M, Strucl M, Bajrović F, Pogacnik T (2005) Coupling between visual evoked cerebral blood flow velocity responses and visual evoked potentials in migraneurs. Cephalalgia 25:567–574
Shibata K, Yamane K, Iwata M, Ohkawa S (2005) Evaluating the effects of spatial frequency on migraines by using pattern-reversal visual evoked potentials. Clin Neurophysiol 116:2220–2227
Sand T, Zhitniy N, White LR, Stovner LJ (2008) Visual evoked potential latency, amplitude and habituation in migraine: a longitudinal study. Clin Neurophysiol 119:1020–1027
Sand T, White L, Hagen K, Stovner L (2009) Visual evoked potential and spatial frequency in migraine: a longitudinal study. Acta Neurol Scand Suppl 189:33–37
Shibata K, Yamane K, Otuka K, Iwata M (2008) Abnormal visual processing in migraine with aura: a study of steady-state visual evoked potentials. J Neurol Sci 271:119–126
Nguyen B, McKendrick A, Vingrys A (2012) Simultaneous retinal and cortical visually evoked electrophysiological responses in between migraine attacks. Cephalalgia 32:896–907
Khalil NM, Legg NJ, Anderson DJ (2000) Long term decline of P100 amplitude in migraine with aura. J Neurol Neurosurg Psychiatry 69:507–511
Schoenen J, Wang W, Albert A, Delwaide P (1995) Potentiation instead of habituation characterizes visual evoked potentials in migraine patients between attacks. Eur J Neurol 2:115–122
Afra J, Ambrosini A, Genicot R, Albert A, Schoenen J (2000) Influence of colors on habituation of visual evoked potentials in patients with migraine with aura and in healthy volunteers. Headache 40:36–40
Afra J, Proietti Cecchini A, Sándor PS, Schoenen J (2000) Comparison of visual and auditory evoked cortical potentials in migraine patients between attacks. Clin Neurophysiol 111:1124–1129
Ozkul Y, Bozlar S (2002) Effects of fluoxetine on habituation of pattern reversal visually evoked potentials in migraine prophylaxis. Headache 42:582–587
Coppola G, Currà A, Sava SL, Alibardi A, Parisi V, Pierelli F et al (2010) Changes in visual-evoked potential habituation induced by hyperventilation in migraine. J Headache Pain 11:497–503
Coppola G, Pierelli F, Schoenen J (2007) Is the cerebral cortex hyperexcitable or hyperresponsive in migraine? Cephalalgia 27:1427–1439
Coppola G, Iacovelli E, Bracaglia M, Serrao M, Di Lorenzo C, Pierelli F et al (2013) Electrophysiological correlates of episodic migraine chronification: evidence for thalamic involvement. J Headache Pain 14:76
Chen W, Wang S, Fuh J, Lin C, Ko Y, Lin Y et al (2011) Persistent ictal-like visual cortical excitability in chronic migraine. Pain 152:254–258
Floery D, Vosko M, Fellner F, Fellner C, Ginthoer C, Gruber F, et al (2012) Acute-onset migrainous aura mimicking acute stroke: MR perfusion imaging features. AJNR Am J Neuroradiol 33:1546–1552
Iizuka T, Tominaga N, Kaneko J, Sato M, Akutsu T, Hamada J et al (2015) Biphasic neurovascular changes in prolonged migraine aura in familial hemiplegic migraine type 2. J Neurol Neurosurg Psychiatry 86:344–353
Piilgaard H, Lauritzen M (2009) Persistent increase in oxygen consumption and impaired neurovascular coupling after spreading depression in rat neocortex. J Cereb Blood Flow Metab 29:1517–1527
Hamel E (1985) (1985) Perivascular nerves and the regulation of cerebrovascular tone. J Appl Physiol 100:1059–1064
Gordon G, Choi H, Rungta R, Ellis-Davies G, MacVicar B (2008) Brain metabolism dictates the polarity of astrocyte control over arterioles. Nature 456:745–749
Descamps B, Vandemaele P, Reyngoudt H, Deblaere K, Leybaert L, Paemeleire K, et al (2011) Absence of haemodynamic refractory effects in patients with migraine without aura: an interictal fMRI study. Cephalalgia 31:1220–1231
Griebe M, Flux F, Wolf M, Hennerici M, Szabo K (2014) Multimodal assessment of optokinetic visual stimulation response in migraine with aura. Headache 54:131–141
Hamel E (2007) Serotonin and migraine: biology and clinical implications. Cephalalgia 27:1293–1300
Schoenen J (1996) Deficient habituation of evoked cortical potentials in migraine: a link between brain biology, behavior and trigeminovascular activation? Biomed Pharmacother 50:71–78
Schulz U, Blamire A, Corkill R, Davies P, Styles P, Rothwell P, et al (2007) Association between cortical metabolite levels and clinical manifestations of migrainous aura: an MR-spectroscopy study. Brain 130:3102–3110
Di Lorenzo C, Pierelli F, Coppola G, Grieco GS, Rengo C, Ciccolella M, et al (2009) Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs. Neurology 72:1588–1594
Eikermann-Haerter K, Dileköz E, Kudo C, Savitz SI, Waeber C, Baum MJ, et al (2009) Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1. J Clin Invest 119:99–109
Leo L, Gherardini L, Barone V, De F, Pietrobon D, Pizzorusso T, et al (2011) Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2. PLoS Genet 7:10
Nyholt D, Anttila V, Winsvold B, Kurth T, Stefansson H, Kallela M, et al (2015) Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies. Cephalalgia 35:489–499
Siniatchkin M, Moeller F, Shepherd A, Siebner H, Stephani U (2007) Altered cortical visual processing in individuals with a spreading photoparoxysmal EEG response. Eur J Neurosci 26:529–536
Moeller F, Siebner H, Wolff S, Muhle H, Granert O, Jansen O et al (2009) Mapping brain activity on the verge of a photically induced generalized tonic-clonic seizure. Epilepsia 50:1632–1637
Moeller F, Muthuraman M, Stephani U, Deuschl G, Raethjen J, Siniatchkin M (2013) Representation and propagation of epileptic activity in absences and generalized photoparoxysmal responses. Hum Brain Mapp 34:1896–1909
Hanganu A, Groppa S, Deuschl G, Siebner H, Moeller F, Siniatchkin M et al (2015) Cortical Thickness Changes Associated with Photoparoxysmal Response. Brain Topogr 28:702–709
Tepe N, Filiz A, Dilekoz E, Akcali D, Sara Y, Charles A, et al (2015) The thalamic reticular nucleus is activated by cortical spreading depression in freely moving rats: prevention by acute valproate administration. Eur J Neurosci 41:120–128
Coppola G, Vandenheede M, Di Clemente L, Ambrosini A, Fumal A, De Pasqua V et al (2005) Somatosensory evoked high-frequency oscillations reflecting thalamo-cortical activity are decreased in migraine patients between attacks. Brain 128:98–103
DaSilva AFM, Granziera C, Tuch DS, Snyder J, Vincent M, Hadjikhani N (2007) Interictal alterations of the trigeminal somatosensory pathway and periaqueductal gray matter in migraine. Neuroreport 18:301–305
Rocca MA, Pagani E, Colombo B, Tortorella P, Falini A, Comi G, et al (2008) Selective diffusion changes of the visual pathways in patients with migraine: a 3-T tractography study. Cephalalgia 28:1061–1068
Datta R, Aguirre G, Hu S, Detre G, Cucchiara B (2013) Interictal cortical hyperresponsiveness in migraine is directly related to the presence of aura. Cephalalgia 33:365–374
Shepherd A, Wyatt G, Tibber M (2011) Visual metacontrast masking in migraine. Cephalalgia 31:346–356
Bednář M, Kubová Z, Kremláček J (2014) Lack of visual evoked potentials amplitude decrement during prolonged reversal and motion stimulation in migraineurs. Clin Neurophysiol 125:1223–1230
Omland P, Uglem M, Engstrøm M, Linde M, Hagen K, Sand T, et al. (2014) Modulation of visual evoked potentials by high-frequency repetitive transcranial magnetic stimulation in migraineurs. Clin Neurophysiol. doi:10.1016/j.clinph.2014.12.035
Omland P, Uglem M, Hagen K, Linde M, Tronvik E, Sand T (2015) Visual evoked potentials in migraine: Is the “neurophysiological hallmark” concept still valid? Clin Neurophysiol. doi:10.1016/j.clinph.2014.12.035.
Brighina F, Cosentino G, Fierro B (2015) Habituation or lack of habituation: What is really lacking in migraine? Clin Neurophysiol. doi:10.1016/j.clinph.2015.05.028.
Harter MR, White CT (1968) Effects of contour sharpness and check-size on visually evoked cortical potentials. Vision Res 8:701–711
Thompson RF, Spencer WA (1966) Habituation: a model phenomenon for the study of neuronal substrates of behavior. Psychol Rev 73:16–43
Rankin CH, Abrams T, Barry RJ, Bhatnagar S, Clayton DF, Colombo J, et al (2009) Habituation revisited: an updated and revised description of the behavioral characteristics of habituation. Neurobiol Learn Mem 92:135–138
Skuse N, Burke D (1992) Sequence-dependent deterioration in the visual evoked potential in the absence of drowsiness. Electroencephalogr Clin Neurophysiol 84:20–25
Hoshiyama M, Kakigi R (2001) Effects of attention on pattern-reversal visual evoked potentials: foveal field stimulation versus peripheral field stimulation. Brain Topogr 13:293–298
Heinrich T, Bach M (2002) Contrast adaptation in retinal and cortical evoked potentials: no adaptation to low spatial frequencies. Vis Neurosci 19:645–650
Heinrich S, Bach M (2001) Adaptation dynamics in pattern-reversal visual evoked potentials. Doc Ophthalmol 102:141–156