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

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 confi...

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Veröffentlicht in:Magnetic resonance in medicine 2004-05, Vol.51 (5), p.913-923
Hauptverfasser: McDannold, Nathan, Vykhodtseva, Natalia, Jolesz, Ferenc A., Hynynen, Kullervo
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Sprache:eng
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Zusammenfassung: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 T2‐weighted imaging and T1‐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 T1‐weighted imaging shortly after the ultrasound exposures, sometimes accompanied by changes in T2‐weighted imaging. Two days later, changes in T2‐weighted imaging were observed, sometimes accompanied by changes in T1‐weighted imaging. In histology, tissue damage was seen at every location where MRI changes were observed, ranging from small (diameter
ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.20060