Long-Term Effects of Self-Administered Transcranial Direct Current Stimulation in Episodic Migraine Prevention: Results of a Randomized Controlled Trial.
Hyperexcitability; migraine; migraine days; neuromodulation; neurostimulation; tDCS; Adolescent; Adult; Aged; Aged, 80 and over; Double-Blind Method; Electrodes; Humans; Middle Aged; Single-Blind Method; Young Adult; Migraine Disorders/therapy; Transcranial Direct Current Stimulation; Migraine Disorders; Neurology; Neurology (clinical); Anesthesiology and Pain Medicine; General Medicine
Abstract :
[en] ("[en] BACKGROUND: Migraine is a multifactorial neurovascular disorder, which affects about 12% of the general population. In episodic migraine, the visual cortex revealed abnormal processing, most likely due to decreased preactivation level. Transcranial direct current stimulation (tDCS) is able to modify cortical excitability and might result in an alleviation of migraine occurrence if used repetitively.
OBJECTIVE: To test the hypothesis that self-administered anodal tDCS over the visual cortex significantly decreases the number of monthly migraine days in episodic migraine.
MATERIALS AND METHODS: The study was single-blind, randomized, and sham-controlled. Inclusion criteria were age 18-80 years and an ICHD-3 diagnosis of episodic migraine. Exclusion criteria were pregnancy, presence of a neurodegenerative disorder, a contraindication against MRI examinations, and less than two migraine days during the 28-day baseline period. Patients in whom the baseline period suggested chronic migraine were excluded. After baseline, participants applied daily either verum (anodal-1 mA to 20 min) or sham tDCS (anodal-1 mA to 30 sec) at Oz (reference Cz electrode) for 28 days. Headache diaries were used to record the number of migraine days at baseline, during the stimulation period, and during four subsequent 28-day periods.
RESULTS: Twenty-eight patients were included; two were excluded after the baseline period because less than two migraine days occurred; three were excluded because their headache diaries suggested the diagnosis of chronic migraine. Twenty-three datasets were taken for further analysis. Compared to sham tDCS (n = 12), verum tDCS (n = 11) resulted in a lower number of migraine days (p = 0.010) across all follow-up periods. We found no significant change in total headache days (p = 0.165), anxiety (p = 0.884), or depression scores (p = 0.535). No serious adverse events occurred; minor side effects were similar in both groups.
CONCLUSIONS: This study provides Class II evidence that self-administered anodal tDCS over the visual cortex in episodic migraine results in a significantly lower number of monthly migraine days. However, it has neither an immediate nor a long-term effect.","[en] ","")
Disciplines :
Neurology
Author, co-author :
Pohl, Heiko ; Department of Neurology, University Hospital Zurich, Zurich, Switzerland
Moisa, Marius ; Zurich Center for Neuroeconomics (ZNE), Department of Economics, University of Zurich, Zurich, Switzerland
Jung, Hans-H; Department of Neurology, University Hospital Zurich, Zurich, Switzerland
Brenner, Kathrin; Department of Neuroradiology, University Hospital Zurich, Zurich, Switzerland
Aschmann, Jessica; Department of Neuroradiology, University Hospital Zurich, Zurich, Switzerland
Riederer, Franz ; Department of Neurology, University Hospital Zurich, Zurich, Switzerland ; Neurological Center Rosenhügel and Karl Landsteiner Institute for Epilepsy Research and Cognitive Neurology, Vienna, Austria
Ruff, Christian C ; Zurich Center for Neuroeconomics (ZNE), Department of Economics, University of Zurich, Zurich, Switzerland
Schoenen, Jean ; Centre Hospitalier Universitaire de Liège - CHU > > Service de neurologie (CHR)
Luechinger, Roger ; Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland
Widmer, Lukas; Department of Neurology, University Hospital Zurich, Zurich, Switzerland
Petersen, Jens A ; Neurozentrum Bern, Bern, Switzerland
Gantenbein, Andreas R; Department of Neurology, University Hospital Zurich, Zurich, Switzerland ; RehaClinic Bad Zurzach, Bad Zurzach, Switzerland
Sandor, Peter S; Department of Neurology, University Hospital Zurich, Zurich, Switzerland ; RehaClinic Bad Zurzach, Bad Zurzach, Switzerland
Michels, Lars ; Department of Neuroradiology, University Hospital Zurich, Zurich, Switzerland
Long-Term Effects of Self-Administered Transcranial Direct Current Stimulation in Episodic Migraine Prevention: Results of a Randomized Controlled Trial.
ERC - European Research Council SNF - Schweizerische Nationalfonds zur Förderung der wissenschaftlichen Forschung
Funding text :
Source(s) of financial support: Heiko Pohl was funded by the Werner Dessauer Stiftung. Christian C. Ruff received support from the SNSF (grant no. 100019L_173248) and from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation program (grant agreement No 725355, BRAINCODES).
Goadsby PJ, Holland PR, Martins-Oliveira M, Hoffmann J, Schankin C, Akerman S. Pathophysiology of migraine: a disorder of sensory processing. Physiol Rev 2017;97:553–622.
Evans RW, Seifert T, Kailasam J, Mathew NT. The use of questions to determine the presence of photophobia and phonophobia during migraine. Headache 2008;48:395–397.
Headache Classification Committee of the International Headache Society (IHS). The international classification of headache disorders, 3rd edition. Cephalalgia 2018;38:1–211.
Vanagaite J, Pareja JA, Storen O, White LR, Sand T, Stovner LJ. Light-induced discomfort and pain in migraine. Cephalalgia 1997;17:733–741.
Vingen JV, Pareja JA, Storen O, White LR, Stovner LJ. Phonophobia in migraine. Cephalalgia 1998;18:243–249.
Ozkul Y, Uckardes A. Median nerve somatosensory evoked potentials in migraine. Eur J Neurol 2002;9:227–232.
Schoenen J, Wang W, Albert A, Delwaide PJ. Potentiation instead of habituation characterizes visual evoked potentials in migraine patients between attacks. Eur J Neurol 1995;2:115–122.
Ambrosini A, Rossi P, De Pasqua V, Pierelli F, Schoenen J. Lack of habituation causes high intensity dependence of auditory evoked cortical potentials in migraine. Brain 2003;126:2009–2015.
Valeriani M, de Tommaso M, Restuccia D et al. Reduced habituation to experimental pain in migraine patients: a CO2 laser evoked potential study. Pain 2003;105:57–64.
Bohotin V, Fumal A, Vandenheede M, Bohotin C, Schoenen J. Excitability of visual V1-V2 and motor cortices to single transcranial magnetic stimuli in migraine: a reappraisal using a figure-of-eight coil. Cephalalgia 2003;23:264–270.
Mulleners WM, Chronicle EP, Palmer JE, Koehler PJ, Vredeveld JW. Visual cortex excitability in migraine with and without aura. Headache 2001;41:565–572.
Chen WT, Wang SJ, Fuh JL, Lin CP, Ko YC, Lin YY. Persistent ictal-like visual cortical excitability in chronic migraine. Pain 2011;152:254–258.
Coppola G, Schoenen J. Cortical excitability in chronic migraine. Curr Pain Headache Rep 2012;16:93–100.
Coppola G, Pierelli F, Schoenen J. Is the cerebral cortex hyperexcitable or hyperresponsive in migraine? Cephalalgia 2007;27:1427–1439.
Bindman LJ, Lippold OC, Redfearn JW. The action of brief polarizing currents on the cerebral cortex of the rat (1) during current flow and (2) in the production of long-lasting after-effects. J Physiol 1964;172:369–382.
Antal A, Nitsche MA, Paulus W. Transcranial direct current stimulation and the visual cortex. Brain Res Bull 2006;68:459–463.
Accornero N, Li Voti P, La Riccia M, Gregori B. Visual evoked potentials modulation during direct current cortical polarization. Exp Brain Res 2007;178:261–266.
Antal A, Kincses TZ, Nitsche MA, Bartfai O, Paulus W. Excitability changes induced in the human primary visual cortex by transcranial direct current stimulation: direct electrophysiological evidence. Invest Ophthalmol Vis Sci 2004;45:702–707.
Nitsche MA, Paulus W. Excitability changes induced in the human motor cortex by weak transcranial direct current stimulation. J Physiol 2000;527:633–639.
Tfelt-Hansen P, Olesen J. Taking the negative view of current migraine treatments: the unmet needs. CNS Drugs 2012;26:375–382.
Vigano A, D'Elia TS, Sava SL et al. Transcranial direct current stimulation (tDCS) of the visual cortex: a proof-of-concept study based on interictal electrophysiological abnormalities in migraine. J Headache Pain 2013;14:23.
Rocha S, Melo L, Boudoux C, Foerster A, Araujo D, Monte-Silva K. Transcranial direct current stimulation in the prophylactic treatment of migraine based on interictal visual cortex excitability abnormalities: a pilot randomized controlled trial. J Neurol Sci 2015;349:33–39.
Antal A, Kriener N, Lang N, Boros K, Paulus W. Cathodal transcranial direct current stimulation of the visual cortex in the prophylactic treatment of migraine. Cephalalgia 2011;31:820–828.
Ahdab R, Mansour AG, Khazen G et al. Cathodal transcranial direct current stimulation of the occipital cortex in episodic migraine: a randomized sham-controlled crossover study. J Clin Med 2019;9.
Dasilva AF, Mendonca ME, Zaghi S et al. tDCS-induced analgesia and electrical fields in pain-related neural networks in chronic migraine. Headache 2012;52:1283–1295.
Andrade SM, de Brito Aranha REL, de Oliveira EA et al. Transcranial direct current stimulation over the primary motor vs prefrontal cortex in refractory chronic migraine: A pilot randomized controlled trial. J Neurol Sci 2017;378:225–232.
Auvichayapat P, Janyacharoen T, Tiamkao S, Krisanaprakornkit T, Thinkhamrop B, Auvichayapat N. Transcranial direct current stimulation on prophylactic treatment in migraine patients, an open-label pilot study. Srinagarind Med J 2012;27:49–57.
Baschi R, Sava S, La Salvia V et al. EHMTI-0317. Transcranial direct current stimulation in chronic migraine: a pilot trial combining cathodal visual and anodal dlpfc stimulation. J Headache Pain 2014;15:G4.
Cortese F, Pierelli F, Bove I et al. Anodal transcranial direct current stimulation over the left temporal pole restores normal visual evoked potential habituation in interictal migraineurs. J Headache Pain 2017;18:70.
Wiethoff S, Hamada M, Rothwell JC. Variability in response to transcranial direct current stimulation of the motor cortex. Brain Stimul 2014;7:468–475.
Lopez-Alonso V, Cheeran B, Rio-Rodriguez D, Fernandez-Del-Olmo M. Inter-individual variability in response to non-invasive brain stimulation paradigms. Brain Stimul 2014;7:372–380.
Minen MT, Begasse De Dhaem O, Kroon Van Diest A et al. Migraine and its psychiatric comorbidities. J Neurol Neurosurg Psychiatr 2016;87:741–749.
Woods AJ, Bryant V, Sacchetti D, Gervits F, Hamilton R. Effects of electrode drift in transcranial direct current stimulation. Brain Stimul 2015;8:515–519.
Bikson M, Datta A, Rahman A, Scaturro J. Electrode montages for tDCS and weak transcranial electrical stimulation: role of "return" electrode's position and size. Clin Neurophysiol 2010;121:1976–1978.
Kim JH, Kim DW, Chang WH, Kim YH, Kim K, Im CH. Inconsistent outcomes of transcranial direct current stimulation may originate from anatomical differences among individuals: electric field simulation using individual MRI data. Neurosci Lett 2014;564:6–10.
Auvichayapat P, Janyacharoen T, Rotenberg A et al. Migraine prophylaxis by anodal transcranial direct current stimulation, a randomized, placebo-controlled trial. J Med Assoc Thailand 2012;95:1003–1012.
Deutsche Migräne- und Kopfschmerzgesellschaft e.V. Kopfschmerzkalender [Available from: http://www.dmkg.de/files/dmkg.de/PDF-Dokumente/Kopfschmerzkalender_DEUTSCH_5.11.2019.pdf.
Tassorelli C, Diener HC, Dodick DW et al. Guidelines of the international headache society for controlled trials of preventive treatment of chronic migraine in adults. Cephalalgia 2018;38:815–832.
Nitsche MA, Doemkes S, Karakose T et al. Shaping the effects of transcranial direct current stimulation of the human motor cortex. J Neurophysiol 2007;97:3109–3117.
Opitz A, Legon W, Rowlands A, Bickel WK, Paulus W, Tyler WJ. Physiological observations validate finite element models for estimating subject-specific electric field distributions induced by transcranial magnetic stimulation of the human motor cortex. Neuroimage 2013;81:253–264.
Makarov S, Horner M, Noetscher G (Eds.). Brain and human body modeling: computational human modeling at EMBC 2018. Cham, Switzerland: Springer International Publishing, 2019.
Lipton RB. Establishing the clinical utility of the Migraine Disability Assessment (MIDAS) Questionnaire. Eur J Neurol 1998;5:S253.
Shajahan PM, Glabus MF, Gooding PA, Shah PJ, Ebmeier KP. Reduced cortical excitability in depression. Impaired post-exercise motor facilitation with transcranial magnetic stimulation. Brit J Psychiatr 1999;174:449–454.
Croarkin PE, Nakonezny PA, Lewis CP et al. Developmental aspects of cortical excitability and inhibition in depressed and healthy youth: an exploratory study. Front Hum Neurosci 2014;8:669.
Concerto C, Lanza G, Cantone M et al. Different patterns of cortical excitability in major depression and vascular depression: a transcranial magnetic stimulation study. BMC Psychiatr 2013;13:300.
Salustri C, Tecchio F, Zappasodi F et al. Cortical excitability and rest activity properties in patients with depression. J Psychiatr Neurosci 2007;32:259–266.
Westfall PH, Krishen A. Optimally weighted, fixed sequence and gatekeeper multiple testing procedures. J Stat Plann Infer 2001;99:25–40.
Gronseth GS, Cox J, Getchius TSD. Amendments to the 2011 American Academy of Neurology Clinical Practice Guideline Process Manual 2015. https://webcache.googleusercontent.com/search?q=cache:_72YcmnVGr0J:https://www.aan.com/siteassets/home-page/policy-and-guidelines/guidelines/about-guidelines/15processmanualamendment_v607.pdf+&cd=1&hl=en&ct=clnk&gl=us#5.
Alonzo A, Brassil J, Taylor JL, Martin D, Loo CK. Daily transcranial direct current stimulation (tDCS) leads to greater increases in cortical excitability than second daily transcranial direct current stimulation. Brain Stimul 2012;5:208–213.
Di Clemente L, Puledda F, Biasiotta A et al. Topiramate modulates habituation in migraine: evidences from nociceptive responses elicited by laser evoked potentials. J Headache Pain 2013;14:25.
Hoppe A, Weidenhammer W, Wagenpfeil S, Melchart D, Linde K. Correlations of headache diary parameters, quality of life and disability scales. Headache 2009;49:868–878.
Turi Z, Bjorkedal E, Gunkel L, Antal A, Paulus W, Mittner M. Evidence for cognitive placebo and Nocebo effects in healthy individuals. Sci Rep 2018;8:17443.
Gallagher RM, Kunkel R. Migraine medication attributes important for patient compliance: concerns about side effects may delay treatment. Headache 2003;43:36–43.
Danno D, Iigaya M, Imai N, Igarashi H, Takeshima T. The safety and preventive effects of a supraorbital transcutaneous stimulator in Japanese migraine patients. Sci Rep 2019;9:9900.
Vikelis M, Dermitzakis EV, Spingos KC, Vasiliadis GG, Vlachos GS, Kararizou E. Clinical experience with transcutaneous supraorbital nerve stimulation in patients with refractory migraine or with migraine and intolerance to topiramate: a prospective exploratory clinical study. BMC Neurol 2017;17:97.