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Effects of tracer arrival time on flow estimates in MR perfusion-weighted imaging
Ona Wu1, Leif Østergaard, Walter J Koroshetz
1Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology/Harvard Medical School, Boston, 02129, USA. ona@nmr.mgh.harvard.edu
Abstract:
A common technique for calculating cerebral blood flow (CBF) and mean transit time (MTT) is to track a bolus of contrast agent using perfusion-weighted MRI (PWI) and to deconvolve the change in concentration with an arterial input function (AIF) using singular value decomposition (SVD). This method has been shown to often overestimate the volume of tissue that infarcts and in cases of severe vasculopathy to produce CBF maps that are inconsistent with clinical presentation. This study examines the effects of tracer arrival time differences between tissue and a user-selected global AIF on flow estimates. CBF and MTT were calculated in both numerically simulated and clinically acquired PWI data where the AIF and tissue signals were shifted backward and forward in time with respect to one another. Results show that when the AIF leads the tissue, CBF is underestimated independent of extent of delay, but dependent on MTT. When the AIF lags the tissue, flow may be over- or underestimated depending on MTT and extent of timing differences. These conditions may occur in practice due to the application of a user-selected AIF that is not the "true AIF" and therefore caution must be taken in interpreting CBF and MTT estimates.
Insights
Timing differences between the arterial input function (AIF) and tissue signals in perfusion-weighted MRI (PWI) can significantly alter cerebral blood flow (CBF) and mean transit time (MTT) calculations. Careful interpretation of PWI-derived flow metrics is crucial due to potential inaccuracies.
Area of Science:
- Medical Imaging
- Neuroscience
- Biophysics
Background:
- Perfusion-weighted MRI (PWI) with deconvolution using singular value decomposition (SVD) is a standard method for calculating cerebral blood flow (CBF) and mean transit time (MTT).
- Existing PWI methods can overestimate infarct volume and produce flow maps inconsistent with clinical findings, particularly in severe vasculopathy.
- The accuracy of CBF and MTT estimates is sensitive to the arterial input function (AIF) used in the deconvolution process.
Purpose of the Study:
- To investigate the impact of temporal discrepancies between the AIF and tissue signals on CBF and MTT calculations.
- To evaluate how variations in tracer arrival times affect quantitative perfusion parameters derived from PWI data.
- To identify potential sources of error in PWI-based flow estimation related to AIF selection.
Main Methods:
- Calculated CBF and MTT using simulated and real PWI data.
- Introduced controlled time shifts between the user-selected global AIF and tissue concentration signals.
- Analyzed the effects of AIF leading and lagging the tissue signal on flow estimates.
Main Results:
- When the AIF precedes the tissue signal, CBF is consistently underestimated, with dependence on MTT.
- When the AIF lags the tissue signal, CBF can be over- or underestimated, influenced by MTT and the magnitude of the time delay.
- These timing differences, arising from non-ideal AIF selection, directly impact the reliability of calculated CBF and MTT.
Conclusions:
- Temporal alignment between the AIF and tissue signals is critical for accurate PWI-derived CBF and MTT quantification.
- User-selected global AIFs may not perfectly represent the true AIF, leading to significant estimation errors.
- Caution is advised when interpreting CBF and MTT values, especially in the presence of potential timing mismatches in PWI data.
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