Non-invasive brain intervention techniques used in patients with disorders of consciousness

References

• Schnakers C, Monti MM. Disorders of consciousness after severe brain injury: therapeutic options. Curr Opin Neurol. 2017;30(6):573–579.
   PubMed Web of Science ®Google Scholar
• Giacino JT, Fins JJ, Laureys S, et al. Disorders of consciousness after acquired brain injury: the state of the science. Nat Rev Neurol. 2014;10(2):99–114.
   PubMed Web of Science ®Google Scholar
• Bernat JL. The natural history of chronic disorders of consciousness. Neurology. 2010;75(3):206–207.
   PubMed Web of Science ®Google Scholar
• Laureys S, Celesia GG, Cohadon F, et al. Unresponsive wakefulness syndrome: a new name for the vegetative state or apallic syndrome. BMC Med. 2010;8(1):68.
   PubMed Web of Science ®Google Scholar
• Naccache L. Minimally conscious state or cortically mediated state? Brain A J Neurol. 2018;141(4):949–960.
   Google Scholar
• Giacino JT, Malone R. The vegetative and minimally conscious states. Handb Clin Neurol. 2008;90:99–111.
   PubMedGoogle Scholar
• Giacino JT, Katz DI, Schiff ND, et al. Comprehensive systematic review update summary: disorders of consciousness. Arch Phys Med Rehabil. 2018;99(9): 1710–1719.
   PubMed Web of Science ®Google Scholar
• Giacino JT, Katz DI, Schiff ND, et al. Practice guideline update recommendations summary: disorders of consciousness. Arch Phys Med Rehabil. 2018;99(9):1699–1709
   PubMed Web of Science ®Google Scholar
• Giacino JT, Whyte J, Bagiella E, et al. Placebo-controlled trial of amantadine for severe traumatic brain injury. N Engl J Med. 2012;366(9):819–826.
   PubMed Web of Science ®Google Scholar
• Rezaei Haddad A, Lythe V, Green AL. Deep brain stimulation for recovery of consciousness in minimally conscious patients after traumatic brain injury: a systematic review. Neuromodulation. 2019;22(4):373–379.
   PubMed Web of Science ®Google Scholar
• Vanhoecke J, Hariz M. Deep brain stimulation for disorders of consciousness: Systematic review of cases and ethics. Brain Stimul. 2017;10(6):1013–1023.
   PubMed Web of Science ®Google Scholar
• Si J, Dang Y, Zhang Y, et al. Spinal cord stimulation frequency influences the hemodynamic response in patients with disorders of consciousness. Neurosci Bull. 2018;34(4):659–667.
   PubMed Web of Science ®Google Scholar
• Bai Y, Xia X, Li X, et al. Spinal cord stimulation modulates frontal delta and gamma in patients of minimally consciousness state. Neuroscience. 2017;346:247–254.
   PubMed Web of Science ®Google Scholar
• Yuan H, Silberstein SD. Vagus nerve and vagus nerve stimulation, a comprehensive review: part II. Headache. 2016;56(2):259–266.
   PubMed Web of Science ®Google Scholar
• Bourdillon P, Hermann B, Sitt JD, et al. Electromagnetic brain stimulation in patients with disorders of consciousness. Front Neurosci. 2019;13:223
   PubMed Web of Science ®Google Scholar
• Yavari F, Jamil A, Mosayebi Samani M, et al. Basic and functional effects of transcranial electrical stimulation (tES)-an introduction. Neurosci Biobehav Rev. 2018;85:81–92.
   PubMed Web of Science ®Google Scholar
• Jaberzadeh S, Bastani A, Zoghi M. Anodal transcranial pulsed current stimulation: a novel technique to enhance corticospinal excitability. Clin Neurophysiol. 2014;125(2):344–351.
   PubMed Web of Science ®Google Scholar
• Lapitska N, Gosseries O, Delvaux V, et al. Transcranial magnetic stimulation in disorders of consciousness. Rev Neurosci. 2009;20(3-4):235–250.
   PubMed Web of Science ®Google Scholar
• Rollnik JD, Altenmuller E. Music in disorders of consciousness. Front Neurosci. 2014;8:190
   PubMed Web of Science ®Google Scholar
• Magee WL. Music in the diagnosis, treatment and prognosis of people with prolonged disorders of consciousness. Neuropsychol Rehabil. 2018;28(8):1331–1339.
   PubMed Web of Science ®Google Scholar
• Zhang Y, Song W. Transcranial direct current stimulation in disorders of consciousness: a review. Int J Neurosci. 2018;128(3):255–261.
   PubMed Web of Science ®Google Scholar
• Ragazzoni A, Cincotta M, Giovannelli F, et al. Clinical neurophysiology of prolonged disorders of consciousness: From diagnostic stimulation to therapeutic neuromodulation. Clin Neurophysiol. 2017;128(9):1629–1646.
   PubMed Web of Science ®Google Scholar
• Thibaut A, Schiff N, Giacino J, et al. Therapeutic interventions in patients with prolonged disorders of consciousness. Lancet Neurol. 2019;18(6):600–614.
   PubMed Web of Science ®Google Scholar
• Kotchoubey B, Pavlov YG, Kleber B. Music in research and rehabilitation of disorders of consciousness: psychological and neurophysiological foundations. Front Psychol. 2015;6:1763
   PubMed Web of Science ®Google Scholar
• Xia X, Yang Y, Guo Y, et al. Current status of neuromodulatory therapies for disorders of consciousness. Neurosci Bull. 2018;34(4):615–625
   PubMed Web of Science ®Google Scholar
• Harris-Love ML, Cohen LG. Noninvasive cortical stimulation in neurorehabilitation: a review. Arch Phys Med Rehabil. 2006;87(12):84–93.
   Web of Science ®Google Scholar
• Tremblay S, Rogasch NC, Premoli I, et al. Clinical utility and prospective of TMS-EEG. Clin Neurophysiol. 2019;130(5):802–844.
   PubMed Web of Science ®Google Scholar
• Lapitskaya N, Gosseries O, De Pasqua V, et al. Abnormal corticospinal excitability in patients with disorders of consciousness. Brain Stimul. 2013;6(4):590–597.
   PubMed Web of Science ®Google Scholar
• Bagnato S, Boccagni C, Sant’Angelo A, et al. Patients in a vegetative state following traumatic brain injury display a reduced intracortical modulation. Clin Neurophysiol. 2012;123(10):1937–1941.
   PubMed Web of Science ®Google Scholar
• Ilmoniemi RJ, Kicic D. Methodology for combined TMS and EEG. Brain Topogr. 2010;22(4):233–248.
   PubMed Web of Science ®Google Scholar
• Gosseries O, Di H, Laureys S, et al. Measuring consciousness in severely damaged brains. Ann Rev Neurosci. 2014;37(1):457–478.
   PubMedGoogle Scholar
• Qin P, Di H, Liu Y, et al. Anterior cingulate activity and the self in disorders of consciousness. Hum Brain Mapp. 2010;31(12):1993–2002.
   PubMed Web of Science ®Google Scholar
• Massimini M, Ferrarelli F, Huber R, et al. Breakdown of cortical effective connectivity during sleep. Science, 2005;309(5744):2228–32.
   PubMed Web of Science ®Google Scholar
• Ferrarelli F, Massimini M, Sarasso S, et al. Breakdown in cortical effective connectivity during midazolam-induced loss of consciousness. Proc Natl Acad Sci U S A. 2010;107(6):2681–2686.
   PubMed Web of Science ®Google Scholar
• Rosanova M, Gosseries O, Casarotto S, et al. Recovery of cortical effective connectivity and recovery of consciousness in vegetative patients. Brain. 2012;135(4):1308–1320.
   PubMed Web of Science ®Google Scholar
• Ragazzoni A, Pirulli C, Veniero D, et al. Vegetative versus minimally conscious states: a study using TMS-EEG, sensory and event-related potentials. Plos One. 2013;8(2):e196–e196.
   Web of Science ®Google Scholar
• Gosseries O, Sarasso S, Casarotto S, et al. On the cerebral origin of EEG responses to TMS: insights from severe cortical lesions. Brain Stimul. 2015;8(1):142–149.
   PubMed Web of Science ®Google Scholar
• Casali AG, Gosseries O, Rosanova M, et al. A theoretically based index of consciousness independent of sensory processing and behavior. Sci Transl Med. 2013;5(198):198ra105–198ra105.
   PubMed Web of Science ®Google Scholar
• Casarotto S, Comanducci A, Rosanova M, et al. Stratification of unresponsive patients by an independently validated index of brain complexity. Ann Neurol. 2016;80(5):718–729.
   PubMed Web of Science ®Google Scholar
• Bodart O, Gosseries O, Wannez S, et al. Measures of metabolism and complexity in the brain of patients with disorders of consciousness. NeuroImage Clin. 2017;14:354–362.
   PubMed Web of Science ®Google Scholar
• Bai Y, Xia X, Kang J, et al. Evaluating the effect of repetitive transcranial magnetic stimulation on disorders of consciousness by using TMS-EEG. Front Neurosci. 2016;10(Pt 4):473.
   PubMedGoogle Scholar
• Wu M, Wu Y, Yu Y, et al. Effects of theta burst stimulation of the left dorsolateral prefrontal cortex in disorders of consciousness. Brain Stimul. 2018;11(6):1382–1384.
   PubMed Web of Science ®Google Scholar
• Manganotti P, Formaggio E, Storti SF, et al. Effect of high-frequency repetitive transcranial magnetic stimulation on brain excitability in severely brain-injured patients in minimally conscious or vegetative state. Brain Stimul. 2013;6(6):913–921.
   PubMed Web of Science ®Google Scholar
• Xie Y, Zhang T, Chen AC. Repetitive Transcranial Magnetic Stimulation for the Recovery of Stroke Patients With Disturbance of Consciousness. Brain Stimul. 2015;8(3):674–675.
   PubMed Web of Science ®Google Scholar
• Liu X, Meng F, Gao J, et al. Behavioral and resting state functional connectivity effects of high frequency rTMS on disorders of consciousness: a sham-controlled study. Front Neurol. 2018;9:982.
   PubMed Web of Science ®Google Scholar
• Antonino Naro M, Russo M, Leo A, et al. A single session of repetitive transcranial magnetic stimulation over the dorsolateral prefrontal cortex in patients with unresponsive wakefulness syndrome: preliminary results. Neurorehabil Neural Repair. 2015;29(7):603–613
   PubMed Web of Science ®Google Scholar
• Xia X, Liu Y, Bai Y, et al. Long-lasting repetitive transcranial magnetic stimulation modulates electroencephalography oscillation in patients with disorders of consciousness. Neuroreport. 2017;28(15):1022–1029.
   PubMed Web of Science ®Google Scholar
• Cincotta M, Giovannelli F, Chiaramonti R, et al. No effects of 20 Hz-rTMS of the primary motor cortex in vegetative state: A randomised, sham-controlled study. Cortex. 2015;71:368–376.
   PubMed Web of Science ®Google Scholar
• Louise-Bender Pape T, Rosenow J, Lewis G, et al. Repetitive transcranial magnetic stimulation-associated neurobehavioral gains during coma recovery. Brain Stimul. 2009;2(1):22–35.
   PubMed Web of Science ®Google Scholar
• Naro A, Bramanti A, Leo A, et al. Metaplasticity: A promising tool to disentangle chronic disorders of consciousness differential diagnosis. Int J Neur Syst. 2018;28(06):1750059.
   PubMedGoogle Scholar
• Chen R, Classen J, Gerloff C, et al. Depression of motor cortex excitability by low-frequency transcranial magnetic stimulation. Neurology. 1997;48(5):1398–1403.
   PubMed Web of Science ®Google Scholar
• Conti CL, Nakamura-Palacios EM. Bilateral transcranial direct current stimulation over dorsolateral prefrontal cortex changes the drug-cued reactivity in the anterior cingulate cortex of crack-cocaine addicts. Brain Stimul. 2014;7(1):130–132.
   PubMed Web of Science ®Google Scholar
• Hummel FC, Voller B, Celnik P, et al. Effects of brain polarization on reaction times and pinch force in chronic stroke. BMC Neurosci. 2006;7(1):73.
   PubMedGoogle Scholar
• Dimitri D, De Filippis D, Galetto V, et al. Evaluation of the effectiveness of transcranial direct current stimulation (tDCS) and psychosensory stimulation through DOCS scale in a minimally conscious subject. Neurocase. 2017;23(2):96–104.
   PubMed Web of Science ®Google Scholar
• Fregni F, Boggio PS, Santos MC, et al. Noninvasive cortical stimulation with transcranial direct current stimulation in Parkinson’s disease. Mov Disord. 2006;21(10):1693–1702.
   PubMed Web of Science ®Google Scholar
• Fregni F, Freedman S, Pascual-Leone A. Recent advances in the treatment of chronic pain with non-invasive brain stimulation techniques. Lancet Neurol. 2007;6(2):188–191.
   PubMed Web of Science ®Google Scholar
• Nitsche MA, Boggio PS, Fregni F, et al. Treatment of depression with transcranial direct current stimulation (tDCS): a review. Exp Neurol. 2009;219(1):14–19.
   PubMed Web of Science ®Google Scholar
• Angelakis E, Liouta E, Andreadis N, et al. Transcranial direct current stimulation effects in disorders of consciousness. Arch Phys Med Rehabil. 2014;95(2):283–289.
   PubMed Web of Science ®Google Scholar
• Yeh KL, Fong PY, Huang YZ. Intensity sensitive modulation effect of theta burst form of median nerve stimulation on the monosynaptic spinal reflex. Neural Plast. 2015;2015:1–8.
   Web of Science ®Google Scholar
• Cavaliere C, Aiello M, Di Perri C, et al. Functional connectivity substrates for tDCS response in minimally conscious state patients. Front Cell Neurosci. 2016;10:257
   PubMed Web of Science ®Google Scholar
• Thibaut A, Di Perri C, Chatelle C, et al. Clinical response to tDCS depends on residual brain metabolism and grey matter integrity in patients with minimally conscious state. Brain Stimul. 2015;8(6):1116–1123.
   PubMed Web of Science ®Google Scholar
• Huang W, Wannez S, Fregni F, et al. Repeated stimulation of the posterior parietal cortex in patients in minimally conscious state: a sham-controlled randomized clinical trial. Brain Stimul. 2017;10(3):718–720.
   PubMed Web of Science ®Google Scholar
• Thibaut A, Bruno M-A, Ledoux D, et al. tDCS in patients with disorders of consciousness: sham-controlled randomized double-blind study. Neurology. 2014;82(13):1112–1118.
   PubMed Web of Science ®Google Scholar
• Wu M, Yu Y, Luo L, et al. Efficiency of repetitive transcranial direct current stimulation of the dorsolateral prefrontal cortex in disorders of consciousness: a randomized sham-controlled study. Neural Plast. 2019;2019:1–11.
   Web of Science ®Google Scholar
• Alonzo A, Brassil J, Taylor JL, et al. Daily transcranial direct current stimulation (tDCS) leads to greater increases in cortical excitability than second daily transcranial direct current stimulation. Brain Stimul. 2012;5(3):208–213.
   PubMed Web of Science ®Google Scholar
• Thibaut A, Wannez S, Donneau A-F, et al. Controlled clinical trial of repeated prefrontal tDCS in patients with chronic minimally conscious state. Brain Inj. 2017;31(4):466–474.
   PubMed Web of Science ®Google Scholar
• Bai Y, Xia X, Kang J, et al. TDCS modulates cortical excitability in patients with disorders of consciousness. Neuroimage Clin. 2017;15:702–709.
   PubMed Web of Science ®Google Scholar
• Wach C, Krause V, Moliadze V, et al. Effects of 10 Hz and 20 Hz transcranial alternating current stimulation (tACS) on motor functions and motor cortical excitability. Behav Brain Res. 2013;241:1–6.
   PubMed Web of Science ®Google Scholar
• Naro A, Bramanti P, Leo A, et al. Transcranial alternating current stimulation in patients with chronic disorder of consciousness: a possible way to cut the diagnostic Gordian knot? Brain Topogr. 2016;29(4):623–644.
   PubMed Web of Science ®Google Scholar
• Bergmann TO, Groppa S, Seeger M, et al. Acute changes in motor cortical excitability during slow oscillatory and constant anodal transcranial direct current stimulation. J Neurophysiol. 2009;102(4):2303–2311.
   PubMed Web of Science ®Google Scholar
• Groppa S, Bergmann TO, Siems C, et al. Slow-oscillatory transcranial direct current stimulation can induce bidirectional shifts in motor cortical excitability in awake humans. Neuroscience. 2010;166(4):1219–1225.
   PubMed Web of Science ®Google Scholar
• Naro A, Russo M, Leo A, et al. Cortical connectivity modulation induced by cerebellar oscillatory transcranial direct current stimulation in patients with chronic disorders of consciousness: A marker of covert cognition?. Clin Neurophysiol. 2016;127(3):1845–1854.
   PubMed Web of Science ®Google Scholar
• Cai T, Xia X, Zhang H, et al. High-definition transcranial direct current stimulation modulates neural activities in patients with prolonged disorders of consciousness. Brain Stimul. 2019;12(6):1619–1621.
   PubMed Web of Science ®Google Scholar
• Tillmann B. Implicit investigations of tonal knowledge in nonmusician listeners. Ann N Y Acad Sci. 2005;1060(1):100–110.
   PubMedGoogle Scholar
• Thaut MH. Neurologic Music Therapy in Cognitive Rehabilitation. Music Percept. 2010;27(4):281–285.
   Web of Science ®Google Scholar
• Zatorre RJ. Predispositions and plasticity in music and speech learning: neural correlates and implications. Science. 2013;342(6158):585–589.
   PubMed Web of Science ®Google Scholar
• Koelsch S. Towards a neural basis of music-evoked emotions. Trends Cogn Sci. 2010;14(3):131–137.
   PubMed Web of Science ®Google Scholar
• Schellenberg EG. Exposure to music: the truth about the consequences. 2006.
   Google Scholar
• Kotz SA, Gunter TC, Wonneberger S. The basal ganglia are receptive to rhythmic compensation during auditory syntactic processing: ERP patient data. Brain Lang. 2005;95(1):70–71.
   Web of Science ®Google Scholar
• Kotz SA, Gunter TC. Can rhythmic auditory cuing remediate language-related deficits in Parkinson’s disease? Ann NY Acad Sci. 2015;1337(1):62–68.
   PubMedGoogle Scholar
• Przybylski L. Rhythmic auditory stimulation influences syntactic processing in children with developmental language disorders. Neuropsychology. 2013; 27(1):121–131.
   Google Scholar
• Magee WL. Music therapy with patients in low awareness states: approaches to assessment and treatment in multidisciplinary care. Neuropsychol Rehabil. 2005;15(3-4):522–536.
   PubMed Web of Science ®Google Scholar
• Magee WL. Development of a music therapy assessment tool for patients in low awareness states. NeuroRehabilitation. 2007;22(4):319–324.
   Google Scholar
• Riganello F, Cortese MD, Arcuri F, et al. How can music influence the autonomic nervous system response in patients with severe disorder of consciousness? Front Neurosci. 2015;9:461
   PubMed Web of Science ®Google Scholar
• Okumura Y, Asano Y, Takenaka S, et al. Brain activation by music in patients in a vegetative or minimally conscious state following diffuse brain injury. Brain Inj. 2014;28(7):944–950.
   PubMed Web of Science ®Google Scholar
• Heine L, Castro M, Martial C, et al. Exploration of functional connectivity during preferred music stimulation in patients with disorders of consciousness. Front Psychol. 2015;6:1704
   PubMed Web of Science ®Google Scholar
• Li J, Shen J, Liu S, et al. Responses of patients with disorders of consciousness to habit stimulation: a quantitative EEG study. Neurosci Bull. 2018;34(4):691–699.
   PubMed Web of Science ®Google Scholar
• Hashmi JT, Huang Y-Y, Osmani BZ, et al. Role of low-level laser therapy in neurorehabilitation. PM R. 2010;2(12 Suppl 2):S292–S305.
   PubMedGoogle Scholar
• Lohse-Busch H, Reime U, Falland R. Symptomatic treatment of unresponsive wakefulness syndrome with transcranially focused extracorporeal shock waves. NeuroRehabilitation. 2014;35(2):235–244.
   PubMed Web of Science ®Google Scholar
• Werner C, Byhahn M, Hesse S. Non-invasive brain stimulation to promote alertness and awareness in chronic patients with disorders of consciousness: Low-level, near-infrared laser stimulation vs. focused shock wave therapy. Restor Neurol Neurosci. 2016;34(4):561–569.
   PubMed Web of Science ®Google Scholar
• Bystritsky A, Korb AS, Douglas PK, et al. A review of low-intensity focused ultrasound pulsation. Brain Stimul. 2011;4(3):125–136.
   PubMed Web of Science ®Google Scholar
• Monti MM, Schnakers C, Korb AS, et al. Non-invasive ultrasonic thalamic stimulation in disorders of consciousness after severe brain injury: a first-in-man report. Brain Stimul. 2016;9(6):940–941.
   PubMed Web of Science ®Google Scholar
• He W, Wang X, Shi H, et al. Auricular acupuncture and vagal regulation. Evid Based Complement Alternat Med. 2012;2012:1–6.
   Web of Science ®Google Scholar
• Yu Y-T, Yang Y, Wang L-B, et al. Transcutaneous auricular vagus nerve stimulation in disorders of consciousness monitored by fMRI: The first case report. Brain Stimul. 2017;10(2):328–330.
   PubMed Web of Science ®Google Scholar
• Thies M, Zrenner C, Ziemann U, et al. Sensorimotor mu-power is positively related to corticospinal excitability. Brain Stimul. 2018;11(5):1119–1122.
   PubMed Web of Science ®Google Scholar
• Zrenner C, et al. Real-time EEG-defined excitability states determine efficacy of TMS-induced plasticity in human motor cortex. Brain Stimul. 2017;11(2):S1935861X17309725.
   Web of Science ®Google Scholar
• Grossman N, Bono D, Dedic N, et al. Noninvasive deep brain stimulation via temporally interfering electric fields. Cell. 2017;169(6):1029–1041.e16.
   PubMed Web of Science ®Google Scholar