Erschienen in:
01.01.2015 | Short Communication
Reduced retention of Pittsburgh compound B in white matter lesions
verfasst von:
Lidia Glodzik, Henry Rusinek, Jinyu Li, Cyrus Zhou, Wai Tsui, Lisa Mosconi, Yi Li, Ricardo Osorio, Schantel Williams, Catherine Randall, Nicole Spector, Pauline McHugh, John Murray, Elizabeth Pirraglia, Shankar Vallabhajolusa, Mony de Leon
Erschienen in:
European Journal of Nuclear Medicine and Molecular Imaging
|
Ausgabe 1/2015
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Abstract
Purpose
One of the interesting features of the amyloid tracer Pittsburgh compound B (PiB) is that it generates a signal in the white matter (WM) in both healthy subjects and cognitively impaired individuals. This characteristic gave rise to the possibility that PiB could be used to trace WM pathology. In a group of cognitively healthy elderly we examined PiB retention in normal-appearing WM (NAWM) and WM lesions (WML), one of the most common brain pathologies in aging.
Methods
We segmented WML and NAWM on fluid attenuation inversion recovery (FLAIR) images of 73 subjects (age 61.9 ± 10.0, 71 % women). PiB PET images were corrected for partial volume effects and coregistered to FLAIR images and WM masks. WML and NAWM PiB signals were then extracted.
Results
PiB retention in WML was lower than in NAWM (p < 0.001, 14.6 % reduction). This was true both for periventricular WML (p < 0.001, 17.8 % reduction) and deep WML (p = 0.001, 7.5 % reduction).
Conclusion
PiB binding in WM is influenced by the presence of WML, which lower the signal. Our findings add to the growing evidence that PiB can depict WM pathology and should prompt further investigations into PiB binding targets in WM.