Exploiting Polynomial Chaos Expansion for Rapid Assessment of the Impact of Tissue Property Uncertainties in Low-Intensity Focused Ultrasound Stimulation.
Authors: Sumser K, Mestrom R, Tuysuz YE, Paulides MM
Neuromodulation with low-intensity focused ultrasound (LIFUS) holds significant promise for noninvasive treatment of neurological disorders, but its success relies heavily on accurately targeting specific brain regions. Computational model predictions can be used to optimize LIFUS, but uncertain acoustic tissue properties can affect prediction accuracy. The Monte Carlo method is often used to quantify the impact of uncertainties, but many iterations are generally needed for accurate estimates. We studied a surrogate model based on polynomial chaos expansion (PCE) to quantify the uncertainty in the LIFUS acoustic intensity field caused by tissue acoustic property uncertainties. The PCE approach was benchmarked against Monte Carlo method for LIFUS in three different head models. We also investigated the effect of the number of PCE samples on the accuracy of the surrogate model. Our results show that the PCE surrogate model requires only 20 simulation samples to estimate the mean and standard deviation of the acoustic intensity field with high accuracy compared to 100 samples needed for Monte Carlo method. The root mean squared percentage error (RMSPE) in the mean acoustic intensity field was less than 1.5%, with a maximum error of less than 0.5 W/cm<sup>2</sup> (< 1% of the focus peak intensity in water), while the RMSPE in the standard deviation was less than 9%, with a maximum error of less than 0.3 W/cm<sup>2</sup>. The accuracy of the PCE surrogate model, and the limited number of iterations it requires makes it a promising tool for quantifying the uncertainty in the acoustic intensity field in LIFUS applications.
Introduction
Purpose
Transcranial ultrasound stimulation
Study Objective
To evaluate and benchmark a polynomial chaos expansion (PCE) surrogate model for rapidly quantifying how tissue acoustic property uncertainties affect predicted low‑intensity focused ultrasound (LIFUS) acoustic intensity fields.
Animal model / Human subject
Human (Homo sapiens), strain: N/A (Population Head Model repository), age: 22–35 years, sex: not specified (MRI subjects)
Disease model
healthy
MRI or image guidance method
MRI Imaging
Targeted brain region(s)
Amygdala
Target coordinates
Not provided in the text
Cargo name and characteristics
Not Provided
Route of administration
Transcranial (external focused ultrasound applicator placed on the skin / transcutaneous)
Outcomes and Safety
Summary of Outcomes
the study developed a polynomial chaos expansion (PCE) surrogate model that accurately and efficiently quantifies uncertainties in low‑intensity focused ultrasound (LIFUS) acoustic intensity fields relevant to neuromodulation.
Duration of biological effect
1 h
Safety-related matter
The study notes that the PCE surrogate model can be extended to thermal safety assessment (including thermal property uncertainties) but does not report any observed safety incidents or adverse effects.
Brain Region
Ultrasound Parameters
Ultrasound instrument
NeuroFUS Cortical Focus Transducer (CTX)-250 (NeuroFUS, BrainBox Ltd, UK); CTX-250, 4-channel, 64 mm spherical radius, 64 mm aperture diameter; center frequency 250 kHz
FUS Frequency
250 kHz
FUS Intensity
50 W/cm2; 1 W/cm2 (analysis threshold, 2% of 50 W/cm2); 0.5 W/cm2 (reported maximum error)
FUS Pressure
Not reported
FUS Mode
pulsed
Pulse duration
55 s
Duration of a single FUS session
8 mins
Focal Characteristics
64 mm
Treatment frequency
multiple
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