Abstract
Migraine is a recurrent ictal headache disorder accompanied by multisensory symptoms and pain-free interictal periods of variable length between attacks. During the last few decades, many research groups have used a variety of neurophysiological techniques to search for biomarkers of subtle CNS – factors that may predispose individuals to migraine attacks. Researchers have demonstrated significant changes in bioelectrical activity in the brains of migraineurs that change during the migraine cycle, although controversy remain regarding the reliability, effect size and utility of several findings. Notably, various abnormalities of spinal, brainstem and cortical responsivity to external innocuous or noxious stimuli have been described in several migraine groups by several research teams.
Progress over the next few years will largely depend on gaining a better understanding of the mechanisms underlying abnormal responsivity as measured by robust parameters. Also, the variations with the migraine cycle and its relationship with changes in thalamocortical rhythms and the activity of subcortico-(thalamo-)cortical pathways should be explored. Reliable biomarkers should be sought and identified by replication with thoroughly blinded studies, by collecting accurately clinical data and headache diaries before, during and after the test days and by prospectively monitoring the patients’ clinical fluctuations.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- BAEP:
-
Brainstem auditory evoked potential
- CAP:
-
Cyclic alternating pattern
- CM:
-
Chronic migraine
- CNV:
-
Contingent negative variation
- CR:
-
Corneal reflex
- CSP:
-
Cortical silent period
- EEG:
-
Electroencephalography
- EMG:
-
Electromyography
- ERP:
-
Event-related potential
- ES:
-
Exteroceptive suppression
- HR:
-
H-response-increased photic driving amplitude
- IDAP:
-
Intensity-dependent auditory evoked cortical potentials
- LEP:
-
Laser evoked potential
- MA:
-
Migraine with aura
- MEP:
-
Motor evoked potentials
- MO:
-
Migraine without aura
- MOH:
-
Medication overuse headache
- nBR:
-
Nociceptive blink reflex
- NSM:
-
Non-sleep-related migraine
- PAS:
-
Paired associative stimulation
- PD:
-
Photic driving
- PR:
-
Pattern reversal
- PSG:
-
Polysomnography
- PT:
-
Phosphene threshold
- qEEG:
-
Quantitative electroencephalography
- rTMS:
-
Repetitive transcranial magnetic stimulation
- SM:
-
Sleep-related migraine
- SSEP:
-
Somatosensory evoked potential
- sTMS:
-
Single-pulse transcranial magnetic stimulation
- TCR:
-
Trigemino-cervical reflex
- tDCS:
-
Transcranial direct-current stimulation
- TMS:
-
Transcranial magnetic stimulation
- TSR:
-
Trigemino-spinal reflex
- VEP:
-
Visual evoked potential
References
Sand T (1991) EEG in migraine: a review of the literature. Funct Neurol 6(1):7–22
Sand T (2003) Electroencephalography in migraine: a review with focus on quantitative electroencephalography and the migraine vs. epilepsy relationship. Cephalalgia 1:5–11
Parrino L, Pietrini V, Spaggiari M, Terzano M (1986) Acute confusional migraine attacks resolved by sleep: lack of significant abnormalities in post-ictal polysomnograms. Cephalalgia 6(2):95–100
Ganji S (1986) Basilar artery migraine: EEG and evoked potential patterns during acute stage. Headache 26(5):220–223
Pietrini V, Terzano M, D’Andrea G, Parrino L, Cananzi A, Ferro-Milone F (1987) Acute confusional migraine: clinical and electroencephalographic aspects. Cephalalgia 7(1):29–37
Haan J, Ferrari M, Brouwer O (1988) Acute confusional migraine. Case report and review of literature. Clin Neurol Neurosurg 90(3):275–278
Golla FL, Winter AL (1959) Analysis of cerebral responses to flicker in patients complaining of episodic headache. Electroencephalogr Clin Neurophysiol 11(3):539–549
Fogang Y, Gérard P, De P, Pepin J, Ndiaye M, Magis D et al (2014) Analysis and clinical correlates of 20 Hz photic driving on routine EEG in migraine. Acta Neurol Belg, DOI 10.1007/s13760-014-0309-8
Goto F, Oishi N, Tsutsumi T, Ito T, Arai M, Ogawa K (2013) Characteristic electroencephalographic findings by photic driving in patients with migraine-associated vertigo. Acta Otolaryngol 133(3):253–256
Puca FM, de Tommaso M, Tota P, Sciruicchio V (1996) Photic driving in migraine: correlations with clinical features. Cephalalgia 16(4):246–250
Bjørk M, Hagen K, Stovner L, Sand T (2011) Photic EEG-driving responses related to ictal phases and trigger sensitivity in migraine: a longitudinal, controlled study. Cephalalgia 31(4):444–455
Bjørk M, Stovner L, Hagen K, Sand T (2011) What initiates a migraine attack? Conclusions from four longitudinal studies of quantitative EEG and steady-state visual-evoked potentials in migraineurs. Acta Neurol Scand Suppl 191:56–63
de Tommaso M, Stramaglia S, Marinazzo D, Trotta G, Pellicoro M (2013) Functional and effective connectivity in EEG alpha and beta bands during intermittent flash stimulation in migraine with and without aura. Cephalalgia 33(11):938–947
Facchetti D, Marsile C, Faggi L, Donati E, Kokodoko A, Poloni M (1990) Cerebral mapping in subjects suffering from migraine with aura. Cephalalgia 10(6):279–284
Schoenen J, Jamart B, Delwaide P (1987) Topographic EEG mapping in common and classic migraine during and between attacks. In: Rose FC (ed) Advances in headache research. Smith Gordon, London, pp 25–33
Hughes J, Robbins L (1990) Brain mapping in migraine. Clin Electroencephalogr 21(1):14–24
Clemens B, Bánk J, Piros P, Bessenyei M, Veto S, Tóth M et al (2008) Three-dimensional localization of abnormal EEG activity in migraine: a low resolution electromagnetic tomography (LORETA) study of migraine patients in the pain-free interval. Brain Topogr 21(1):36–42
Bjørk MH, Stovner LJ, Nilsen BM, Stjern M, Hagen K, Sand T (2009) The occipital alpha rhythm related to the “migraine cycle” and headache burden: a blinded, controlled longitudinal study. Clin Neurophysiol 120(3):464–471
Sauer S, Schellenberg R, Hofmann H, Dimpfel W (1997) Functional imaging of headache – first steps in an objective quantitative classification of migraine. Eur J Med Res 2(9):367–376
Bjørk M, Sand T (2008) Quantitative EEG power and asymmetry increase 36 h before a migraine attack. Cephalalgia 28(9):960–968
Göder R, Fritzer G, Kapsokalyvas A, Kropp P, Niederberger U, Strenge H et al (2001) Polysomnographic findings in nights preceding a migraine attack. Cephalalgia 21(1):31–37
Della Marca G, Vollono C, Rubino M, Di Trapani G, Mariotti P, Tonali PA (2006) Dysfunction of arousal systems in sleep-related migraine without aura. Cephalalgia 26(7):857–864
Engstrøm M, Hagen K, Bjørk M, Gravdahl G, Sand T (2013) Sleep-related and non-sleep-related migraine: interictal sleep quality, arousals and pain thresholds. J Headache Pain 14:68
Engstrøm M, Hagen K, Bjørk M, Stovner L, Gravdahl G, Stjern M et al (2013) Sleep quality, arousal and pain thresholds in migraineurs: a blinded controlled polysomnographic study. J Headache Pain 14(1):12
Fritzer G, Strenge H, Göder R, Gerber WD, Aldenhoff J (2004) Changes in cortical dynamics in the preictal stage of a migraine attack. J Clin Neurophysiol 21(2):99–104
Coppola G, Pierelli F, Schoenen J (2007) Is the cerebral cortex hyperexcitable or hyperresponsive in migraine? Cephalalgia 27(12):1427–1439
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, 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
Ozkul Y, Bozlar S (2002) Effects of fluoxetine on habituation of pattern reversal visually evoked potentials in migraine prophylaxis. Headache 42(7):582–587
Fumal A, Coppola G, Bohotin V, Gérardy PY, Seidel L, Donneau AF et al (2006) Induction of long-lasting changes of visual cortex excitability by five daily sessions of repetitive transcranial magnetic stimulation (rTMS) in healthy volunteers and migraine patients. Cephalalgia 26(2):143–149
Coppola G, Di Lorenzo C, Schoenen J, Pierelli F (2013) Habituation and sensitization in primary headaches. J Headache Pain 14(1):65
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
Sand T, Vingen JV (2000) Visual, long-latency auditory and brainstem auditory evoked potentials in migraine: relation to pattern size, stimulus intensity, sound and light discomfort thresholds and pre-attack state. Cephalalgia 20(9):804–820
Sand T, Zhitniy N, White LR, Stovner LJ (2008) Visual evoked potential latency, amplitude and habituation in migraine: a longitudinal study. Clin Neurophysiol 119(5):1020–1027
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(7):1071–1086
Chen W, Wang S, Fuh J, Lin C, Ko Y, Lin Y (2011) Persistent ictal-like visual cortical excitability in chronic migraine. Pain 152(2):254–258
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(6):1223–1230
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, 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(12):1360–1367
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(6):497–503
Coppola G, Crémers J, Gérard P, Pierelli F, Schoenen J (2011) Effects of light deprivation on visual evoked potentials in migraine without aura. BMC Neurol 11:91
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(8):714–719
Chen W, Wang S, Fuh J, Lin C, Ko Y, Lin Y (2009) Peri-ictal normalization of visual cortex excitability in migraine: an MEG study. Cephalalgia 29(11):1202–1211
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
Sand T, Zhitniy N, White LR, Stovner LJ (2008) Brainstem auditory-evoked potential habituation and intensity-dependence related to serotonin metabolism in migraine: a longitudinal study. Clin Neurophysiol 119(5):1190–1200
Schlake HP, Grotemeyer KH, Hofferberth B, Husstedt IW, Wiesner S (1990) Brainstem auditory evoked potentials in migraine–evidence of increased side differences during the pain-free interval. Headache 30(3):129–132
Wang W, Timsit-Berthier M, Schoenen J (1996) Intensity dependence of auditory evoked potentials is pronounced in migraine: an indication of cortical potentiation and low serotonergic neurotransmission? Neurology 46(5):1404–1409
Ambrosini A, Rossi P, De Pasqua V, Pierelli F, Schoenen J (2003) Lack of habituation causes high intensity dependence of auditory evoked cortical potentials in migraine. Brain 126(Pt 9):2009–2015
Ambrosini A, De Pasqua V, Afra J, Sandor PS, Schoenen J (2001) Reduced gating of middle-latency auditory evoked potentials (P50) in migraine patients: another indication of abnormal sensory processing? Neurosci Lett 306(1–2):132–134
Siniatchkin M, Kropp P, Gerber WD (2003) What kind of habituation is impaired in migraine patients? Cephalalgia 23(7):511–518
Chayasirisobhon S (1995) Somatosensory evoked potentials in acute migraine with sensory aura. Clin Electroencephalogr 26(1):65–69
de Tommaso M, Sciruicchio V, Tota P, Megna M, Guido M, Genco S et al (1997) Somatosensory evoked potentials in migraine. Funct Neurol 12(2):77–82
Ozkul Y, Uckardes A (2002) Median nerve somatosensory evoked potentials in migraine. Eur J Neurol 9(3):227–232
Coppola G, Currà A, Di Lorenzo C, Parisi V, Gorini M, Sava SL et al (2010) Abnormal cortical responses to somatosensory stimulation in medication-overuse headache. BMC Neurol 10:126
Coppola G, De Pasqua V, Pierelli F, Schoenen J (2012) Effects of repetitive transcranial magnetic stimulation on somatosensory evoked potentials and high frequency oscillations in migraine. Cephalalgia 32(9):700–709
Sakuma K, Takeshima T, Ishizaki K, Nakashima K (2004) Somatosensory evoked high-frequency oscillations in migraine patients. Clin Neurophysiol 115(8):1857–1862
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(Pt 1):98–103
Coppola G, Iacovelli E, Bracaglia M, Serrao M, Di Lorenzo C, Pierelli F (2013) Electrophysiological correlates of episodic migraine chronification: evidence for thalamic involvement. J Headache Pain 14(1):76
Restuccia D, Vollono C, Virdis D, del Piero I, Martucci L, Zanini S (2014) Patterns of habituation and clinical fluctuations in migraine. Cephalalgia 34(3):201–210
Darabaneanu S, Kropp P, Niederberger U, Strenge H, Gerber W (2008) Effects of pregnancy on slow cortical potentials in migraine patients and healthy controls. Cephalalgia 28(10):1053–1060
Kropp P, Siniatchkin M, Gerber WD (2000) Contingent negative variation as indicator of duration of migraine disease. Funct Neurol 15(Suppl 3):78–81
Kropp P, Brecht I, Niederberger U, Kowalski J, Schröder D, Thome J et al (2012) Time-dependent post-imperative negative variation indicates adaptation and problem solving in migraine patients. J Neural Transm 119(10):1213–1221
Schoenen J, Maertens A, Timsit-Berthier M, Timsit M (1985) Contingent negative variation (CNV) as a diagnostic and physiopathologic tool in headache patients. In: Rose F (ed) Migraine. Clinical and research advances. Karger, Basel, pp 17–25
Kropp P, Gerber WD (1993) Contingent negative variation–findings and perspectives in migraine. Cephalalgia 13(1):33–36
Siniatchkin M, Gerber WD, Kropp P, Voznesenskaya T, Vein AM (2000) Are the periodic changes of neurophysiological parameters during the pain-free interval in migraine related to abnormal orienting activity? Cephalalgia 20(1):20–29
Siniatchkin M, Kropp P, Gerber WD (2001) Contingent negative variation in subjects at risk for migraine without aura. Pain 94(2):159–167
Siniatchkin M, Andrasik F, Kropp P, Niederberger U, Strenge H, Averkina N et al (2007) Central mechanisms of controlled-release metoprolol in migraine: a double-blind, placebo-controlled study. Cephalalgia 27(9):1024–1032
Siniatchkin M, Kropp P, Gerber WD, Stephani U (2000) Migraine in childhood–are periodically occurring migraine attacks related to dynamic changes of cortical information processing? Neurosci Lett 279(1):1–4
Schoenen J, Maertens de Noordhout A, Timsit-Berthier M, Timsit M (1986) Contingent negative variation and efficacy of beta-blocking agents in migraine. Cephalalgia 6(4):229–233
Tommaso M, Guido M, Sardaro M, Serpino C, Vecchio E, De S et al (2008) Effects of topiramate and levetiracetam vs placebo on habituation of contingent negative variation in migraine patients. Neurosci Lett 442(2):81–85
Overath C, Darabaneanu S, Evers M, Gerber W, Graf M, Keller A et al (2014) Does an aerobic endurance programme have an influence on information processing in migraineurs? J Headache Pain 15(1):11
Morlet D, Demarquay G, Brudon F, Fischer C, Caclin A (2014) Attention orienting dysfunction with preserved automatic auditory change detection in migraine. Clin Neurophysiol 125(3):500–511
de Tommaso M, Difruscolo O, Sardaro M, Libro G, Pecoraro C, Serpino C et al (2007) Effects of remote cutaneous pain on trigeminal laser-evoked potentials in migraine patients. J Headache Pain 8(3):167–174
de Tommaso M, Baumgartner U, Sardaro M, Difruscolo O, Serpino C, Treede RD (2008) Effects of distraction versus spatial discrimination on laser-evoked potentials in migraine. Headache 48(3):408–416
de Tommaso M, Valeriani M, Sardaro M, Serpino C, Fruscolo OD, Vecchio E et al (2009) Pain perception and laser evoked potentials during menstrual cycle in migraine. J Headache Pain 10(6):423–429
de Tommaso M, Calabrese R, Vecchio E, De Vito Francesco V, Lancioni G, Livrea P (2009) Effects of affective pictures on pain sensitivity and cortical responses induced by laser stimuli in healthy subjects and migraine patients. Int J Psychophysiol 74(2):139–148
de Tommaso M, Brighina F, Fierro B, Francesco V, Santostasi R, Sciruicchio V et al (2010) Effects of high-frequency repetitive transcranial magnetic stimulation of primary motor cortex on laser-evoked potentials in migraine. J Headache Pain 11(6):505–512
de Tommaso M, Federici A, Franco G, Ricci K, Lorenzo M, Delussi M et al (2012) Suggestion and pain in migraine: a study by laser evoked potentials. CNS Neurol Disord Drug Targets 11(2):110–126
de Tommaso M, Guido M, Libro G, Losito L, Sciruicchio V, Monetti C et al (2002) Abnormal brain processing of cutaneous pain in migraine patients during the attack. Neurosci Lett 333(1):29–32
de Tommaso M, Guido M, Libro G, Losito L, Difruscolo O, Puca F et al (2004) Topographic and dipolar analysis of laser-evoked potentials during migraine attack. Headache 44(10):947–960
de Tommaso M, Libro G, Guido M, Losito L, Lamberti P, Livrea P (2005) Habituation of single CO2 laser-evoked responses during interictal phase of migraine. J Headache Pain 6(4):195–198
de Tommaso M, Lo Sito L, Di Fruscolo O, Sardaro M, Pia Prudenzano M, Lamberti P et al (2005) Lack of habituation of nociceptive evoked responses and pain sensitivity during migraine attack. Clin Neurophysiol 116(6):1254–1264
Afra J, Mascia A, Gérard P, Maertens de Noordhout A, Schoenen J (1998) Interictal cortical excitability in migraine: a study using transcranial magnetic stimulation of motor and visual cortices. Ann Neurol 44(2):209–215
Conforto A, Moraes M, Amaro E, Young W, Lois L, Gonçalves A et al (2012) Increased variability of motor cortical excitability to transcranial magnetic stimulation in migraine: a new clue to an old enigma. J Headache Pain 13(1):29–37
Siniatchkin M, Kröner-Herwig B, Kocabiyik E, Rothenberger A (2007) Intracortical inhibition and facilitation in migraine–a transcranial magnetic stimulation study. Headache 47(3):364–370
Gunaydin S, Soysal A, Atay T, Arpaci B (2006) Motor and occipital cortex excitability in migraine patients. Can J Neurol Sci 33(1):63–67
Curra A, Pierelli F, Coppola G, Barbanti P, Buzzi MG, Galeotti F et al (2007) Shortened cortical silent period in facial muscles of patients with migraine. Pain 132(1–2):124–131
Currà A, Coppola G, Gorini M, Porretta E, Bracaglia M, Di Lorenzo C et al (2011) Drug-induced changes in cortical inhibition in medication overuse headache. Cephalalgia 31(12):1282–1290
Brighina F, Palermo A, Panetta M, Daniele O, Aloisio A, Cosentino G et al (2009) Reduced cerebellar inhibition in migraine with aura: a TMS study. Cerebellum 8(3):260–266
Aurora SK, Ahmad BK, Welch KM, Bhardhwaj P, Ramadan NM (1998) Transcranial magnetic stimulation confirms hyperexcitability of occipital cortex in migraine. Neurology 50(4):1111–1114
Bohotin V, Fumal A, Vandenheede M, Bohotin C, Schoenen J (2003) Excitability of visual V1-V2 and motor cortices to single transcranial magnetic stimuli in migraine: a reappraisal using a figure-of-eight coil. Cephalalgia 23(4):264–270
Chadaide Z, Arlt S, Antal A, Nitsche M, Lang N, Paulus W (2007) Transcranial direct current stimulation reveals inhibitory deficiency in migraine. Cephalalgia 27(7):833–839
Omland P, Uglem M, Engstrøm M, Linde M, Hagen K, Sand T (2014) Modulation of visual evoked potentials by high-frequency repetitive transcranial magnetic stimulation in migraineurs. Clin Neurophysiol 125(10):2090–9
Brigo F, Storti M, Tezzon F, Manganotti P, Nardone R (2013) Primary visual cortex excitability in migraine: a systematic review with meta-analysis. Neurol Sci 34(6):819–830
Brighina F, Giglia G, Scalia S, Francolini M, Palermo A, Fierro B (2005) Facilitatory effects of 1 Hz rTMS in motor cortex of patients affected by migraine with aura. Exp Brain Res 161(1):34–38
Conte A, Barbanti P, Frasca V, Iacovelli E, Gabriele M, Giacomelli E et al (2010) Differences in short-term primary motor cortex synaptic potentiation as assessed by repetitive transcranial magnetic stimulation in migraine patients with and without aura. Pain 148(1):43–48
Brighina F, Cosentino G, Vigneri S, Talamanca S, Palermo A, Giglia G et al (2011) Abnormal facilitatory mechanisms in motor cortex of migraine with aura. Eur J Pain 15(9):928–935
Cosentino G, Fierro B, Vigneri S, Talamanca S, Paladino P, Baschi R et al (2014) Cyclical changes of cortical excitability and metaplasticity in migraine: evidence from a repetitive transcranial magnetic stimulation study. Pain 155(6):1070–1078
Pierelli F, Iacovelli E, Bracaglia M, Serrao M, Coppola G (2013) Abnormal sensorimotor plasticity in migraine without aura patients. Pain 154(9):1738–1742
Siniatchkin M, Sendacki M, Moeller F, Wolff S, Jansen O, Siebner H et al (2012) Abnormal changes of synaptic excitability in migraine with aura. Cereb Cortex 22(10):2207–2216
Viganò A, D’Elia T, Sava S, Auvé M, De P, Colosimo A et al (2013) Transcranial Direct Current Stimulation (tDCS) of the visual cortex: a proof-of-concept study based on interictal electrophysiological abnormalities in migraine. J Headache Pain 14(1):23
Aktekin B, Yaltkaya K, Ozkaynak S, Oguz Y (2001) Recovery cycle of the blink reflex and exteroceptive suppression of temporalis muscle activity in migraine and tension-type headache. Headache 41(2):142–149
Sand T, Zwart J (1994) The blink reflex in chronic tension-type headache, migraine, and cervicogenic headache. Cephalalgia 14(6):447–450
Sand T, Møll-Nilsen B, Zwart J (2006) Blink reflex R2 amplitudes in cervicogenic headache, chronic tension-type headache and migraine. Cephalalgia 26(10):1186–1191
Bánk J, Bense E, Király C (1992) The blink reflex in migraine. Cephalalgia 12(5):289–292
Avramidis T, Podikoglou D, Anastasopoulos I, Koutroumanidis M, Papadimitriou A (1998) Blink reflex in migraine and tension-type headache. Headache 38(9):691–696
de Tommaso M, Murasecco D, Libro G, Guido M, Sciruicchio V, Specchio L et al (2002) Modulation of trigeminal reflex excitability in migraine: effects of attention and habituation on the blink reflex. Int J Psychophysiol 44(3):239–249
Shibata K, Yamane K, Iwata M (2006) Change of excitability in brainstem and cortical visual processing in migraine exhibiting allodynia. Headache 46(10):1535–1544
Katsarava Z, Giffin N, Diener HC, Kaube H (2003) Abnormal habituation of ‘nociceptive’ blink reflex in migraine–evidence for increased excitability of trigeminal nociception. Cephalalgia 23(8):814–819
Di Clemente L, Coppola G, Magis D, Fumal A, De Pasqua V, Di Piero V et al (2007) Interictal habituation deficit of the nociceptive blink reflex: an endophenotypic marker for presymptomatic migraine? Brain 130(Pt 3):765–770
Kaube H, Katsarava Z, Przywara S, Drepper J, Ellrich J, Diener HC (2002) Acute migraine headache: possible sensitization of neurons in the spinal trigeminal nucleus? Neurology 58(8):1234–1238
Katsarava Z, Limmroth V, Baykal O, Akguen D, Diener H, Kaube H (2004) Differences of anti-nociceptive mechanisms of migraine drugs on the trigeminal pain processing during and outside acute migraine attacks. Cephalalgia 24(8):657–662
Coppola G, Di Clemente L, Fumal A, Magis D, De Pasqua V, Pierelli F et al (2007) Inhibition of the nociceptive R2 blink reflex after supraorbital or index finger stimulation is normal in migraine without aura between attacks. Cephalalgia 27(7):803–808
Sandrini G, Proietti C, Milanov I, Tassorelli C, Buzzi M, Nappi G (2002) Electrophysiological evidence for trigeminal neuron sensitization in patients with migraine. Neurosci Lett 317(3):135–138
Busch V, Kaube S, Schulte-Mattler W, Kaube H, May A (2007) Sumatriptan and corneal reflexes in headache-free migraine patients: a randomized and placebo-controlled crossover study. Cephalalgia 27(2):165–172
Nardone R, Ausserer H, Bratti A, Covi M, Lochner P, Marth R et al (2008) Trigemino-cervical reflex abnormalities in patients with migraine and cluster headache. Headache 48(4):578–585
Serrao M, Perrotta A, Bartolo M, Fiermonte G, Pauri F, Rossi P et al (2005) Enhanced trigemino-cervical-spinal reflex recovery cycle in pain-free migraineurs. Headache 45(8):1061–1068
Perrotta A, Serrao M, Sandrini G, Burstein R, Sances G, Rossi P et al (2010) Sensitisation of spinal cord pain processing in medication overuse headache involves supraspinal pain control. Cephalalgia 30(3):272–284
Weissman-Fogel I, Sprecher E, Granovsky Y, Yarnitsky D (2003) Repeated noxious stimulation of the skin enhances cutaneous pain perception of migraine patients in-between attacks: clinical evidence for continuous sub-threshold increase in membrane excitability of central trigeminovascular neurons. Pain 104(3):693–700
Perrotta A, Serrao M, Tassorelli C, Arce-Leal N, Guaschino E, Sances G et al (2011) Oral nitric-oxide donor glyceryl-trinitrate induces sensitization in spinal cord pain processing in migraineurs: a double-blind, placebo-controlled, cross-over study. Eur J Pain 15(5):482–490
Ayzenberg I, Obermann M, Nyhuis P, Gastpar M, Limmroth V, Diener HC et al (2006) Central sensitization of the trigeminal and somatic nociceptive systems in medication overuse headache mainly involves cerebral supraspinal structures. Cephalalgia 26(9):1106–1114
de Tommaso M, Valeriani M, Guido M, Libro G, Specchio LM, Tonali P et al (2003) Abnormal brain processing of cutaneous pain in patients with chronic migraine. Pain 101(1–2):25–32
de Tommaso M, Losito L, Difruscolo O, Libro G, Guido M, Livrea P (2005) Changes in cortical processing of pain in chronic migraine. Headache 45(9):1208–1218
Lorenzo C, Coppola G, Currà A, Grieco G, Santorelli F, Lepre C et al (2012) Cortical response to somatosensory stimulation in medication overuse headache patients is influenced by angiotensin converting enzyme (ACE) I/D genetic polymorphism. Cephalalgia 32(16):1189–1197
Siniatchkin M, Gerber WD, Kropp P, Vein A (1998) Contingent negative variation in patients with chronic daily headache. Cephalalgia 18(8):565–569; discussion 531
Ferraro D, Vollono C, Miliucci R, Virdis D, De A, Pazzaglia C et al (2012) Habituation to pain in “medication overuse headache”: a CO2 laser-evoked potential study. Headache 52(5):792–807
Aurora S, Barrodale P, Tipton R, Khodavirdi A (2007) Brainstem dysfunction in chronic migraine as evidenced by neurophysiological and positron emission tomography studies. Headache 47(7):996–1003
De Marinis M, Pujia A, Colaizzo E, Accornero N (2007) The blink reflex in “chronic migraine”. Clin Neurophysiol 118(2):457–463
Sandrini G, Friberg L, Coppola G, Jänig W, Jensen R, Kruit M et al (2011) Neurophysiological tests and neuroimaging procedures in non-acute headache (2nd edition). Eur J Neurol 18(3):373–381
Sacks O, Siegel R (2012) Migraine aura and hallucinatory constants. In: Sacks O (ed) Migraine. Picador, London, pp 273–297
Author information
Authors and Affiliations
Corresponding authors
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2015 Springer International Publishing Switzerland
About this chapter
Cite this chapter
Coppola, G., Pierelli, F., Omland, P.M., Sand, T. (2015). Neurophysiology of Migraine. In: Ashina, M., Geppetti, P. (eds) Pathophysiology of Headaches. Headache. Springer, Cham. https://doi.org/10.1007/978-3-319-15621-7_8
Download citation
DOI: https://doi.org/10.1007/978-3-319-15621-7_8
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-15620-0
Online ISBN: 978-3-319-15621-7
eBook Packages: MedicineMedicine (R0)