Neuromodulation

deep brain stimulation

Deep Brain Stimulation

Deep brain stimulation (DBS) is a neurosurgical treatment that modulates abnormal neural circuit activity by inserting electrodes into specific areas of the brain and applying high-frequency electrical stimulation.

AT A GLANCE

At a glance

DBS is the standard surgical treatment for Parkinson's disease, essential tremor, and dystonia that do not respond sufficiently to drug treatment. Electrodes are inserted into the subthalamic nucleus (STN) or globus pallidus internus (GPi) to provide continuous electrical stimulation. In Parkinson's disease, motor symptoms can be improved by about 50-70% and drug dosage can be reduced by 30-50% [1]. It is a reversible procedure and has the advantage of allowing stimulation conditions to be changed or the device to be removed.

Definition and Overview

Deep brain stimulation (DBS) is a neurosurgical procedure that controls abnormal neural circuit activity by stereotactically inserting microelectrodes into specific target nuclei of the brain and applying continuous high-frequency electrical stimulation from an implantable pulse generator (IPG) implanted under the skin of the chest.

Since it was first introduced in the treatment of tremor by Benabid et al. in 1987, its effectiveness against Parkinson's disease, essential tremor, and dystonia has been proven in large-scale randomized controlled trials. It has been performed on more than 200,000 patients worldwide, and its indications are still expanding.

Principle and mechanism

Mechanism of Action

The exact mechanism of DBS is not fully understood, but it is understood that high-frequency (130-180 Hz) electrical stimulation modulates abnormal neural activity patterns in the target area. In the past, it was explained as a 'functional lesion' effect, but now a complex mechanism is proposed, including suppression of pathological oscillation, changes in neurotransmitter release, and promotion of neuroplasticity.

stimulus goal

  • Subthalamic nucleus (STN): The most common target in Parkinson's disease. It is effective in improving motor symptoms and reducing drug dosage.
  • Globus pallidus internus (GPi): Used to control dyskinesia and treat dystonia in Parkinson's disease.
  • Ventral intermediate nucleus (VIM): A standard target in the treatment of essential tremor.

Indications

Parkinson's disease

The most representative indication is moderate to advanced Parkinson's disease in which motor fluctuations and dyskinesia occur after drug treatment. In the EARLYSTIM study, DBS showed superior results than drug treatment alone, even in patients with early motor complications.

Essential tremor

VIM-DBS is effective in severe essential tremor that does not respond to drugs (propranolol, primidone), and tremor is significantly reduced in approximately 80-90% of patients.

dystonia

It has been reported that GPi-DBS improves symptoms by approximately 50-70% in generalized or segmental dystonia. It is most effective in primary dystonia caused by DYT1 gene mutation.

expanded indications

Studies are ongoing in obsessive-compulsive disorder (OCD), treatment-resistant depression, Tourette syndrome, and epilepsy, and some have received limited approval.

surgical procedure

Preoperative evaluation

A multidisciplinary team (neurology, neurosurgery, neuropsychology, and psychiatry) comprehensively evaluates the suitability for surgery. The location of the target nucleus is confirmed with a brain MRI, and cognitive function is evaluated with a neuropsychological test.

electrode insertion

Electrodes are accurately inserted into the target nucleus using a stereotactic frame or robotic assistance system. The target location is confirmed electrophysiologically using microelectrode recording. In the case of Parkinson's disease, the traditional method was to perform awake surgery to check real-time symptom changes, but recently, image-guided procedures under general anesthesia are also increasing.

stimulator implant

IPG is implanted subcutaneously under the chest and clavicle, and connected to electrodes in the brain with an extension line that passes under the scalp.

programming

Programming to optimize stimulation conditions (voltage, frequency, pulse width, stimulation contact point) begins 2 to 4 weeks after surgery. It may take several months to find optimal conditions.

treatment effect

Parkinson's disease

In a large randomized controlled trial, STN-DBS improved motor symptoms by approximately 50-70% in the off-medication state. Dyskinesia under drug administration is also reduced by about 60-70%, and the daily dose of levodopa can be reduced by about 30-50%. Even in long-term follow-up of more than 5 years, the effect on tremor and stiffness is maintained, but the effect on walking and speech disorders tends to decrease over time.

dystonia

After GPi-DBS, the Burke-Fahn-Marsden dystonia score improves by about 50-70%, and the difference from Parkinson's disease is that the effect appears gradually over several months.

Side effects and complications

surgery related

Intracranial hemorrhage (1-2%), infection (3-5%), electrode migration, and skin erosion are reported.

stimulus related

Depending on the stimulation conditions, dysarthria, muscle contraction, sensory abnormalities, and balance disorders may occur, but most of them can be controlled by changing the stimulation conditions. Mood changes and impulse control disorders are reported in some patients, so regular follow-up is necessary.

Technological advancements such as directional leads, adaptive stimulation (adaptive DBS, aDBS), and MRI-compatible devices are progressing rapidly. Adaptive DBS analyzes brain signals in real time and applies stimulation only when necessary, and is expected to extend battery life and reduce side effects.

QUESTIONS

Frequently asked questions

Q01For which patients is deep brain stimulation suitable?

The most representative patients are Parkinson's disease patients who do not respond sufficiently to drug treatment or have severe drug side effects (dyskinesia). It is also performed in essential tremor and drug-refractory dystonia. In general, it is effective in patients with levodopa-responsive Parkinson's disease and patients with preserved cognitive function [1].

Q02Is DBS surgery dangerous?

Although all brain surgery carries risks, the rate of serious complications from DBS is relatively low. Intracranial hemorrhage is reported in approximately 1-2%, infection is reported in approximately 3-5%, and electrode migration is reported [4]. When performed at an experienced center, safety is high, and the reversibility of the procedure is a major advantage.

Q03If I have DBS, can I not take medication?

This does not mean completely stopping the medication. DBS enhances drug effects and reduces drug dosage. According to studies, the levodopa dose can be reduced by about 30-50% after STN-DBS, and motor symptoms are improved by about 50-70% [1].

Q04How long does the battery in my DBS device last?

Non-rechargeable batteries can be used for about 3 to 5 years, and rechargeable batteries can be used for about 15 to 25 years. When the battery life expires, it can be replaced with a relatively simple procedure that only replaces the stimulation generator (IPG) in the chest area, while the electrodes in the brain remain the same [5].

Q05Can I have an MRI scan after DBS?

Most of the latest DBS systems are MRI-compatible (MR-conditional) products. However, because there are restrictions on imaging conditions (magnetic field strength, coil type, SAR restrictions, etc.), MRI must be performed after consulting with the DBS medical staff. For older devices, MRI may be limited.

This article provides general medical information and does not replace an individual diagnosis or treatment plan. Please seek a medical assessment if symptoms persist.

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