Pitt Shield

MRI investigation of the threshold for thermally induced blood-brain barrier disruption and brain tissue damage in the rabbit brain.

Authors: McDannold N, Vykhodtseva N, Jolesz FA, Hynynen K

The ability of MRI-derived thermometry to predict thermally induced tissue changes in the brain was tested, and the thermal thresholds for blood-brain barrier (BBB) disruption and brain tissue damage were estimated. In addition, the ability of standard MRI to detect threshold-level effects was confirmed. These safety thresholds are being investigated to provide guidelines for clinical thermal ablation studies in the brain. MRI-monitored focused ultrasound heating was delivered to 63 locations in 26 rabbits. Tissue changes were detected in T(2)-weighted imaging and T(1)-weighted imaging (with and without contrast) and with light microscopy. The probability for tissue damage as a function of the accumulated thermal dose, the peak temperature achieved, the applied acoustic energy, and the peak acoustic power was estimated with probit regression. The discriminative abilities of these parameters were compared using the areas under the receiver operator characteristic (ROC) curves. In MRI, BBB disruption was observed in contrast-enhanced T(1)-weighted imaging shortly after the ultrasound exposures, sometimes accompanied by changes in T(2)-weighted imaging. Two days later, changes in T(2)-weighted imaging were observed, sometimes accompanied by changes in T(1)-weighted imaging. In histology, tissue damage was seen at every location where MRI changes were observed, ranging from small (diameter <1.0 mm) areas of tissue necrosis to severe vascular damage and associated hemorrhagic infarct. In one location, small (diameter: 0.8 mm) damage was not detected in MRI. The thermal dose and peak temperature thresholds were between 12.3-40.1 equivalent min at 43 degrees C and 48.0-50.8 degrees C, respectively, and values of 17.5 equivalent min at 43 degrees C and 48.4 degrees C were estimated to result in tissue damage with 50% probability. Thermal dose and peak temperature were significantly better predictors than the applied acoustic energy and peak acoustic power (P < 0.01). BBB disruption was always accompanied by tissue damage. The temperature information was better than the applied acoustic power or energy for predicting the damage than the ultrasound parameters. MRI was sensitive in detecting threshold-level damage.

Introduction

Purpose Thermal ablation
Study Objective To determine, using MRI, the temperature threshold at which thermal exposure causes blood-brain barrier disruption and brain tissue damage in the rabbit brain.
Animal model / Human subject rabbit, New Zealand White, 3–4 kg, not reported
Disease model healthy
Targeted brain region(s) Thalamus

Outcomes and Safety

Summary of Outcomes MR-thermometry determined the thermal dose thresholds in rabbits, showing that BBB disruption occurs at lower heating levels ($CEM_{43} < 17$ min) before irreversible tissue damage ($CEM_{43} > 17$ min).
Duration of biological effect not reported
Safety-related matter The study identified a safe "therapeutic window" for BBBO; exceeding 17 mins of $CEM_{43}$ resulted in permanent thermal necrosis and microhemorrhage detectable on T2-weighted MRI.

Brain Region

Ultrasound Parameters

Ultrasound instrument single-element focused ultrasound transducer with MR-thermometry
FUS Frequency 1.5 MHz
FUS Intensity not reported
FUS Pressure not reported
FUS Mode not reported
Pulse duration not reported
Duration of a single FUS session 30 s

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