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Depression Treatment Center:: Transcranial Magnetic Stimulation (TMS)
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rTMS in a rodent. From Oscar Arias-Carrión, 2008

Transcranial magnetic stimulation (TMS) is a noninvasive method to excite neurons in the brain: weak electric currents are induced in the tissue by rapidly changing magnetic fields (electromagnetic induction). This way, brain activity can be triggered with minimal discomfort, and the functionality of the circuitry and connectivity of the brain can be studied.

Repetitive transcranial magnetic stimulation is known as rTMS and can produce longer lasting changes. Numerous small-scale pilot studies have shown it could be a treatment tool for various neurological conditions (e.g. migraine, stroke, Parkinson's disease, dystonia, tinnitus) and psychiatric conditions (e.g. major depression, auditory hallucinations).

Contents

[edit] Background

The principle of inductive brain stimulation with eddy currents has been noted since the 19th century. The first successful TMS study was performed in 1985 by Anthony Barker et al.[1] in Sheffield, England. Its earliest application was in the demonstration of conduction of nerve impulses from the motor cortex to the spinal cord. This had been done with transcranial electrical stimulation a few years earlier, but use of this technique was limited by severe discomfort. By stimulating different points of the cerebral cortex and recording responses, e.g., from muscles, one may obtain maps of functional brain areas. By measuring functional imaging (e.g. MRI) or EEG, information may be obtained about the cortex (its reaction to TMS) and about area-to-area connections.

TMS publications.

Pioneers in the use of TMS in neuroscience research include Anthony Barker, Vahe Amassian, John Rothwell of the Institute of Neurology, Queen Square, London, Mark S. George, MD of the Medical University of South Carolina, David H. Avery, MD of the University of Washington at Seattle, Charles M. Epstein of Emory University, Drs. Mark Hallett, Leonardo G. Cohen, and Eric Wassermann of the National Institutes of Health, and Alvaro Pascual-Leone of Harvard Medical School. Currently, thousands of TMS stimulators are in use. More than 3000 scientific publications have been published describing scientific, diagnostic, and therapeutic trials.

[edit] Effects on the brain

The exact details of how TMS functions are still being explored. The effects of TMS can be divided into two types depending on the mode of stimulation:

  • Single or paired pulse TMS. The pulse(s) causes neurons in the neocortex under the site of stimulation to depolarise and discharge an action potential. If used in the primary motor cortex, it produces muscle activity referred to as a motor-evoked potential (MEP) which can be recorded on electromyography (EMG). If used on the occipital cortex, 'phosphenes' (flashes of light) might be detected by the subject. In most other areas of the cortex, the participant does not consciously experience any effect, but his or her behaviour may be slightly altered (e.g. slower reaction time on a cognitive task), or changes in brain activity may be detected using Positron Emission Tomography or fMRI. Effects resulting from single or paired pulses do not outlast the period of stimulation. A review of TMS can be found in the Handbook of Transcranial Magnetic Stimulation.[2]
  • Repetitive TMS (rTMS) produces effects which last longer than the period of stimulation. rTMS can increase or decrease the excitability of corticospinal or corticocortical pathways depending on the intensity of stimulation, coil orientation and frequency of stimulation. The mechanism of these effects is not clear although it is widely believed to reflect changes in synaptic efficacy akin to long-term potentiation (LTP) and long-term depression (LTD). A review of rTMS can be found in Fitzgerald et al., 2006[3].

As such, it is important to distinguish TMS from repetitive TMS (rTMS) as they are used in different ways for different purposes.

[edit] In research

One reason TMS is important in cognitive psychology/neuroscience is that it can help demonstrate causality. A noninvasive mapping technique such as fMRI allows researchers to see what regions of the brain are activated when a subject performs a certain task, but this is not proof that those regions are actually used for the task; it merely shows that a region is associated with a task. If activity in the associated region is suppressed (i.e. 'knocked out') with TMS stimulation and a subject then performs worse on a task, this is much stronger evidence that the region is used in performing the task.

For example: subjects asked to memorize and repeat a stream of numbers would be likely to show activation in the prefrontal cortex (PFC) via fMRI, indicating the association of this brain region in short-term memory. If the researcher then interfered with the PFC via TMS, the subjects' ability to remember numbers might decline, and the researcher would have evidence that the PFC is used for short-term memory, because reducing subjects' PFC capability led to reduced short-term memory.

This ‘knock-out’ technique (also known as virtual lesioning) can be done in two ways:

  • Online TMS: where subjects perform the task and at a specific time in the task (usually after less than 200ms), a TMS pulse is given to a particular part of the brain. If this affects task performance it may be deduced that this part of the brain was involved with the task at that particular time point.
  • Offline repetitive TMS: where performance at a task is measured initially and then repetitive TMS is given over a few minutes, and the performance is measured again. This technique has the advantage of not requiring a time line of how the brain processes the task. A variant of this technique is the ‘enhancement’ technique, where repetitive TMS is delivered to enhance performance. But the latter is even harder to achieve than the ‘knock-out’ technique.[citation needed]

In a 2008 article in the UK's “The Psychologist” Dr. Chris Chambers, Senior Research Fellow at the (School of Psychology, University of Cardiff and the Institute of Cognitive Neuroscience, University College London) focused on recent advances in the cognitive neuroscience of attention using TMS [4].

Transcranial magnetic is used in research to dissect the physiological mechanisms underlying motor deficits, spontaneous motor recovery, and the beneficial effects of therapeutic interventions. In this field, a lot of parameters related with both cortcicospinal and corticocortical excitability are studied in order to evaluate the diagnosis and prognosis of stroke patients.

[edit] Risks

Single pulse TMS is regarded as safe although seizures following single pulse TMS stimulation have have been reported in some patients with stroke or other disorders involving the central nervous system.[5][6] Seizures from single or paired pulse TMS are rare, especially in patients without pre-existing conditions that affect the central nervous system such as epilepsy. rTMS has been reported to cause seizures in normal individuals at certain combinations of stimulation frequency and intensity. Guidelines have since been instituted regarding the maximum safe frequency and intensity combinations of rTMS [5]
Common adverse effects of TMS are:

  • Discomfort or pain from the stimulation of the scalp and associated nerves and muscles on the overlying skin[6] Discomfort is rarely a problem for single pulse TMS but some people may find rTMS quite uncomfortable [5]
  • Rapid deformation of the TMS coil produces a loud clicking sound which scales with stimulator intensity. The sound has been characterized as deceptively mild sounding and has the potential to affect hearing, given sufficient exposure (particularly relevant for rTMS). Hearing protection may be offered to prevent this. [5]
  • rTMS in the presence of EEG electrodes can result in electrode heating and, in severe cases, skin burns[7]

[edit] Clinical uses

The uses of TMS and rTMS can be divided into diagnostic and therapeutic uses.

[edit] Diagnosis

TMS is used currently clinically to measure activity and function of specific brain circuits in humans. The most robust and widely-accepted use is in measuring the connection between the primary motor cortex and a muscle (i.e. MEP amplitude, MEP latency, central motor conduction time). This is most useful in stroke, spinal cord injury, multiple sclerosis and motor neuron disease. There are numerous other measures which have been shown to be abnormal in various diseases but few are validated or reproduced and more importantly, no one knows the significance of these measures. The most famous is short-interval intracortical inhibition (SICI) which measures the internal circuitry (intracortical circuits) of the motor cortex described by Kujirai et al. in 1993.[8]

Plasticity of the human brain can also be measured now with repetitive TMS (and variants of the technique, e.g. theta-burst stimulation, paired associative stimulation) and it has been suggested that this abnormality of plasticity is the primary abnormality in a number of conditions.

[edit] Therapy

A large number of studies with TMS and rTMS have been conducted for a variety of neurological and psychiatric conditions but few have been confirmed and most show very modest effects, if any. Multiple controlled studies support the use of this method in treatment-resistant depression; it has been approved for this indication in Europe, Canada, Australia, and the US.[9][10][11] Some conditions which have been reported to be responsive to TMS-based therapy are:

[edit] FDA approval

A TMS device was cleared by the Food and Drug Administration (FDA) in the United States for use in adult patients with major depression who have failed to benefit from prior antidepressant medications. [17]

For information on this device, see Neuronetics

Most TMS use is currently done off label or under research protocols approved by hospital ethics boards and, in the US, often under Investigational Device Exemption from the U.S. Food and Drug Administration (FDA). The requirement for FDA approval for research use of TMS is determined by the degree of risk as assessed by the investigators, the FDA, and the local ethics authority.

[edit] Technical information

TMS focal field .png

TMS is simply the application of the principle of induction to get electrical current across the insulating tissues of the scalp and skull without discomfort. A coil of wire, encased in plastic, is held to the head. When the coil is energized by the rapid discharge of a large capacitor, a rapidly changing current flows in its windings. This produces a magnetic field oriented orthogonally to the plane of the coil. The magnetic field passes unimpeded through the skin and skull, inducing an oppositely directed current in the brain that flows tangentially with respect to skull. The current induced in the structure of the brain activates nearby nerve cells in much the same way as currents applied directly to the cortical surface. The path of this current is complex to model because the brain is a non-uniform conductor with an irregular shape. These magnetic fields do not directly affect the whole brain; they only reach about 2-3 centimeters into the brain directly beneath the treatment coil.[18] With stereotactic MRI-based control, the precision of targeting TMS can be approximated to a few millimeters (Hannula et al., Human Brain Mapping 2005).

Typical data: [19]

  • magnetic field: often about 2 teslas on the coil surface and 0.5 T in the cortex
  • current rise time: zero to peak, often around 70-100 microseconds
  • wave form: monophasic or biphasic
  • repetition rate for rTMS: below 1 Hz (slow TMS), above 1 Hz (rapid-rate TMS)

[edit] Coil types

TMS - Butterfly Coils

The design of transcranial magnetic stimulation coils used in either treatment or diagnostic/experimental studies may differ in a variety of ways. These differences should be considered in the interpretation of any study result, and the type of coil used should be specified in the study methods for any published reports.

The most important considerations include:

  • the type of material used to construct the core of the coil
  • the geometry of the coil configuration
  • the biophysical characteristics of the pulse produced by the coil.

With regard to coil composition, the core material may be either a magnetically inert substrate (ie, the so-called ‘air-core’coil design), or possess a solid, ferromagnetically active material (ie, the so-called ‘solid-core’ design). Solid core coil design result in a more efficient transfer of electrical energy into a magnetic field, with a substantially reduced amount of energy dissipated as heat, and so can be operated under more aggressive duty cycles often mandated in therapeutic protocols, without treatment interruption due to heat accumulation, or the use of an accessory method of cooling the coil during operation. Varying the geometric shape of the coil itself may also result in variations in the focality, shape, and depth of cortical penetration of the magnetic field. Differences in the coil substance as well as the electronic operation of the power supply to the coil may also result in variations in the biophysical characteristics of the resulting magnetic pulse (eg, width or duration of the magnetic field pulse). All of these features should be considered when comparing results obtained from different studies, with respect to both safety and efficacy. [20][21]

A number of different types of coils exist, each of which produce different magnetic field patterns. Some examples:

  • round coil: the original type of TMS coil
  • figure-eight coil (i.e. butterfly coil): results in a more focal pattern of activation
  • double-cone coil: conforms to shape of head, useful for deeper stimulation
  • Deep TMS (or H-coil): currently being used in a clinical trial for the treatment of patients suffering from clinical depression.[22]
  • four-leaf coil: for focal stimulation of peripheral nerves[23]

[edit] See also

[edit] References

  1. ^ Barker AT, Jalinous R, Freeston IL. (May 1985). "Non-invasive magnetic stimulation of human motor cortex". The Lancet 1 (8437): 1106–1107. doi:10.1016/S0140-6736(85)92413-4. PMID 2860322. 
  2. ^ Alvaro Pascual-Leone, Nick Davey, John Rothwell, Eric M. Wassermann, Besant K. Puri (January 2002). Handbook of Transcranial Magnetic Stimulation. Hodder Arnold. ISBN 0340720093. 
  3. ^ Paul B. Fitzgerald, Sarah Fountain, Zafiris J. Daskalakis (December 2006). "A comprehensive review of the effects of rTMS on motor cortical excitability and inhibition". Clinical Neurophysiology 117 (12): 2584–96. doi:10.1016/j.clinph.2006.06.712. PMID 16890483. 
  4. ^ Chambers, C., (2008), A stimulating take on attention, The Psychologist, Vol 21, Part 6, June 2008, 502–505
  5. ^ a b c d Wassermann, Eric. M (1998). "Risk and safety of repetitive transcranial magnetic stimulation: report and suggested guidelines from the International Workshop on the Safety of Repetitive Transcranial Magnetic Stimulation, June 5–7, 1996". Electroencephalography and clinical Neurophysiology 108: 1–16. http://www.icts.uci.edu/neuroimaging/Wassermann_rTMS_Safety1998.pdf. 
  6. ^ a b "Transcranial Magnetic Stimulation (TMS)". National Alliance on Mental Illness. http://www.nami.org/Content/ContentGroups/Helpline1/Transcranial_Magnetic_Stimulation_(rTMS).htm. Retrieved 15 December 2008. 
  7. ^ Roth BJ, Pascual-Leone A, Cohen LG, Hallett M (1992). "The heating of metal electrodes during rapid-rate magnetic stimulation: A possible safety hazard.". Electroenceph. clin. Neurophysiol. 85: 116–123. 
  8. ^ Kujirai T, Caramia MD, Rothwell JC, et al. (November 1993). "Corticocortical inhibition in human motor cortex". J. Physiol. (Lond.) 471: 501–19. PMID 8120818. PMC 1143973. http://www.jphysiol.org/cgi/pmidlookup?view=long&pmid=8120818. 
  9. ^ Marangell LB, Martinez M, Jurdi RA, Zboyan H (September 2007). "Neurostimulation therapies in depression: A review of new modalities". Acta Psychiatrica Scandinavica 116 (3): 174–81. doi:10.1111/j.1600-0447.2007.01033.x. PMID 17655558. 
  10. ^ Schutter DJ (April 2008). "Antidepressant efficacy of high-frequency transcranial magnetic stimulation over the left dorsolateral prefrontal cortex in double-blind sham-controlled designs: A meta-analysis". Psychological Medicine: 1–11. doi:10.1017/S0033291708003462. PMID 18447962. 
  11. ^ DeNoon, Daniel J. (October 8, 2008). "FDA OKs TMS Depression Device: Brain-Stimulating Device Cleared for Depression Treatment After 1 Drug Failure". WebMD. WebMD. http://www.webmd.com/depression/news/20081008/fda-oks-tms-depression-device. Retrieved 10 November 2008. 
  12. ^ Benjamin Thompson, Behzad Mansouri, Lisa Koski, and Robert F. Hess (2008). "Brain Plasticity in the Adult: Modulation of Function in Amblyopia with rTMS". Current Biology 18: 1067–1071. doi:10.1016/j.cub.2008.06.052. http://www.current-biology.com/content/article/abstract?uid=PIIS0960982208008087. 
  13. ^ National Public Radio. "Magnetic Pulses To Brain Help 'Lazy Eye'". http://www.npr.org/templates/story/story.php?storyId=92965339. 
  14. ^ Press Releases
  15. ^ Naeser Aphasia Research
  16. ^ Kleinjung T, Vielsmeier V, Landgrebe M, Hajak G, Langguth B (2008). "Transcranial magnetic stimulation: a new diagnostic and therapeutic tool for tinnitus patients". Int Tinnitus J 14 (2): 112–8. PMID 19205161. 
  17. ^ "FDA clears Neuronetics’ depression therapy". 2008-10-08. http://www.philly.com/inquirer/breaking/business_breaking/20081008_FDA_clears_Neuronetics_depression_therapy.html. 
  18. ^ "TMS Center of New York"
  19. ^ "TMS terminology", BioMag Laboratory at Helsinki University Central Hospital
  20. ^ Riehl M (2008). "TMS Stimulator Design". in Wassermann EM, Epstein CM, Ziemann U, Walsh V, Paus T, Lisanby SH. Oxford Handbook of Transcranial Stimulation. Oxford: Oxford University Press. pp. 13–23. ISBN 0198568924. 
  21. ^ Epstein CM (2008). "TMS Stimulation Coils". in Wassermann EM, Epstein CM, Ziemann U, Walsh V, Paus T, Lisanby SH. Oxford Handbook of Transcranial Stimulation. Oxford: Oxford University Press. pp. 25–32. ISBN 0198568924. 
  22. ^ "Israeli scientists probe deeper to lift depression", Reuters.com
  23. ^ Roth BJ, Maccabee PJ, Eberle L, Amassian VE, Hallett M, Cadwell J, Anselmi GD, Tatarian GT (1994). "In-vitro evaluation of a four-leaf coil design for magnetic stimulation of peripheral nerve.". Electroenceph. clin. Neurophysiol. 93: 68–74. 

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