Sustained reduction of Essential Tremor with low-power non-thermal transcranial focused ultrasound stimulations in humans.

Accelerometry Essential Tremor MR-guidance Skull Aberration Correction Transcranial Ultrasound Stimulation

Journal

Brain stimulation
ISSN: 1876-4754
Titre abrégé: Brain Stimul
Pays: United States
ID NLM: 101465726

Informations de publication

Date de publication:
09 May 2024
Historique:
received: 12 12 2023
revised: 03 05 2024
accepted: 03 05 2024
medline: 12 5 2024
pubmed: 12 5 2024
entrez: 11 5 2024
Statut: aheadofprint

Résumé

Transcranial ultrasound stimulation (TUS) is a non-invasive brain stimulation technique; when skull aberrations are compensated for, this technique allows, with millimetric accuracy, circumvention of the invasive surgical procedure associated with deep brain stimulation (DBS) and the limited spatial specificity of transcranial magnetic stimulation. /hypothesis: We hypothesize that MR-guided low-power TUS can induce a sustained decrease of tremor power in patients suffering from medically refractive essential tremors. The dominant hand only was targeted, and two anatomical sites were sonicated in this exploratory study: the ventral intermediate nucleus of the thalamus (VIM) and the dentato-rubro-thalamic tract (DRT). Patients (N=9) were equipped with MR-compatible accelerometers attached to their hands to monitor their tremor in real-time during TUS. VIM neurostimulations followed by a low-duty cycle (5%) DRT stimulation induced a substantial decrease in the tremor power in four patients, with a minimum of 89.9% reduction when compared with the baseline power a few minutes after the DRT stimulation. The only patient stimulated in the VIM only and with a low duty cycle (5%) also experienced a sustained reduction of the tremor (up to 93.4%). Four patients (N=4) did not respond. The temperature at target was 37.2 ± 1.4°C compared to 36.8 ± 1.4°C for a 3cm away control point. MR-guided low power TUS can induce a substantial and sustained decrease of tremor power. Follow-up studies need to be conducted to reproduce the effect and better to understand the variability of the response amongst patients. MR thermometry during neurostimulations showed no significant thermal rise, supporting a mechanical effect.

Sections du résumé

BACKGROUND BACKGROUND
Transcranial ultrasound stimulation (TUS) is a non-invasive brain stimulation technique; when skull aberrations are compensated for, this technique allows, with millimetric accuracy, circumvention of the invasive surgical procedure associated with deep brain stimulation (DBS) and the limited spatial specificity of transcranial magnetic stimulation.
OBJECTIVE OBJECTIVE
/hypothesis: We hypothesize that MR-guided low-power TUS can induce a sustained decrease of tremor power in patients suffering from medically refractive essential tremors.
METHODS METHODS
The dominant hand only was targeted, and two anatomical sites were sonicated in this exploratory study: the ventral intermediate nucleus of the thalamus (VIM) and the dentato-rubro-thalamic tract (DRT). Patients (N=9) were equipped with MR-compatible accelerometers attached to their hands to monitor their tremor in real-time during TUS.
RESULTS RESULTS
VIM neurostimulations followed by a low-duty cycle (5%) DRT stimulation induced a substantial decrease in the tremor power in four patients, with a minimum of 89.9% reduction when compared with the baseline power a few minutes after the DRT stimulation. The only patient stimulated in the VIM only and with a low duty cycle (5%) also experienced a sustained reduction of the tremor (up to 93.4%). Four patients (N=4) did not respond. The temperature at target was 37.2 ± 1.4°C compared to 36.8 ± 1.4°C for a 3cm away control point.
CONCLUSIONS CONCLUSIONS
MR-guided low power TUS can induce a substantial and sustained decrease of tremor power. Follow-up studies need to be conducted to reproduce the effect and better to understand the variability of the response amongst patients. MR thermometry during neurostimulations showed no significant thermal rise, supporting a mechanical effect.

Identifiants

pubmed: 38734066
pii: S1935-861X(24)00085-8
doi: 10.1016/j.brs.2024.05.003
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest ☐ The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. ☒The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: IR and YS are employees of Insightec. JFA received a research grant from Insightec for preclinical work on transcranial ultrasound.

Auteurs

Thomas Bancel (T)

Physics for Medicine Paris, Inserm U1273, ESPCI Paris, CNRS UMR8361, PSL University, Paris, France.

Benoît Béranger (B)

Institut du Cerveau, ICM, Centre de NeuroImagerie de Recherche, CENIR, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France.

Maxime Daniel (M)

Physics for Medicine Paris, Inserm U1273, ESPCI Paris, CNRS UMR8361, PSL University, Paris, France.

Mélanie Didier (M)

Institut du Cerveau, ICM, Centre de NeuroImagerie de Recherche, CENIR, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France.

Mathieu Santin (M)

Institut du Cerveau, ICM, Centre de NeuroImagerie de Recherche, CENIR, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France.

Itay Rachmilevitch (I)

Insightec, Tirat Carmel, Israel.

Yeruham Shapira (Y)

Insightec, Tirat Carmel, Israel.

Mickael Tanter (M)

Physics for Medicine Paris, Inserm U1273, ESPCI Paris, CNRS UMR8361, PSL University, Paris, France.

Eric Bardinet (E)

Institut du Cerveau, ICM, Centre de NeuroImagerie de Recherche, CENIR, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France.

Sara Fernandez Vidal (S)

Institut du Cerveau, ICM, Centre de NeuroImagerie de Recherche, CENIR, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France.

David Attali (D)

Physics for Medicine Paris, Inserm U1273, ESPCI Paris, CNRS UMR8361, PSL University, Paris, France.

Cécile Galléa (C)

Institut du Cerveau, ICM, Centre de NeuroImagerie de Recherche, CENIR, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France.

Alexandre Dizeux (A)

Physics for Medicine Paris, Inserm U1273, ESPCI Paris, CNRS UMR8361, PSL University, Paris, France.

Marie Vidailhet (M)

Institut du Cerveau, ICM, Centre de NeuroImagerie de Recherche, CENIR, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France; Neurology Department, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, Paris, France.

Stéphane Lehéricy (S)

Institut du Cerveau, ICM, Centre de NeuroImagerie de Recherche, CENIR, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France; Neuroradiology Department, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, Paris, France.

David Grabli (D)

Neurology Department, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, Paris, France.

Nadya Pyatigorskaya (N)

Institut du Cerveau, ICM, Centre de NeuroImagerie de Recherche, CENIR, Inserm U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France; Neuroradiology Department, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, Paris, France.

Carine Karachi (C)

Neurosurgery Department, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, Paris, France.

Elodie Hainque (E)

Neurology Department, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, Paris, France.

Jean-François Aubry (JF)

Physics for Medicine Paris, Inserm U1273, ESPCI Paris, CNRS UMR8361, PSL University, Paris, France. Electronic address: jean-francois.aubry@espci.fr.

Classifications MeSH