Simultaneous assessment of cerebral hemodynamics and contrast agent uptake in lesions with disrupted blood– brain–barrier

The purpose of this study was to develop a method that eliminates the influence of the T1 relaxation time upon the signal-time course in perfusion-weighted imaging of cerebral lesions with blood–brain–barrier (BBB) disruption. On a 1.5 T whole body clinical magnetic resonance (MR) imager, we impleme...

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Veröffentlicht in:Magnetic resonance imaging 1999-01, Vol.17 (1), p.21-27
Hauptverfasser: Heiland, Sabine, Benner, Thomas, Debus, Jürgen, Rempp, Katrin, Reith, Wolfgang, Sartor, Klaus
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Sprache:eng
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Zusammenfassung:The purpose of this study was to develop a method that eliminates the influence of the T1 relaxation time upon the signal-time course in perfusion-weighted imaging of cerebral lesions with blood–brain–barrier (BBB) disruption. On a 1.5 T whole body clinical magnetic resonance (MR) imager, we implemented a dual-echo RF-spoiled FLASH sequence (TE = 6/23.6 ms). We developed a postprocessing routine that allowed to calculate a signal-time course representing only the change in T2∗ and another one representing only the change in T1. Using this method, we examined 7 patients with various brain lesions showing evidence of BBB disruption. In the signal-time-curves obtained from the early echo we found a distinct signal drop due to the T2∗ effect. These effects could be eliminated by the correction algorithm yielding a 67% higher signal increase. Correction of the signal-time curve of the late echo yielded a more pronounced maximum signal drop and a decrease in postcontrast signal intensity. We found that without this correction the relative regional cerebral blood volume and the first moment of the concentration-time curve were underestimated by 72% and 22%, respectively. The dual echo-sequence combined with the postprocessing algorithm separates T1 and T2∗ effects and thus allows to assess cerebral hemodynamics and contrast agent kinetics simultaneously. This method may be a useful tool for characterizing, staging, and therapy monitoring of brain tumors.
ISSN:0730-725X
1873-5894
DOI:10.1016/S0730-725X(98)00149-0