TY - GEN
T1 - A new similarity metric for groupwise registration of variable flip angle sequences for improved T10 estimation in DCE-MRI
AU - Hallack, Andre
AU - Chappell, Michael A.
AU - Gooding, Mark J.
AU - Schnabel, Julia A.
PY - 2014
Y1 - 2014
N2 - Relaxation time (T10) estimation using variable flip angle sequences is a key step for pharmacokinetic (PK) analysis of tumours in DCE-MRI exams. In this study, the effects of motion within flip angle sequences on the T10 and subsequent Ktrans and kep estimation were examined. It was found that errors in T10 estimation caused by motion had a significant impact on subsequent PK analysis. A new similarity metric, based on the T10 regression error, for groupwise motion correction of variable flip angle sequences is proposed and compared against Groupwise Normalized Mutual Information (GNMI). In rigid registration experiments on simulated data, the new metric outperformed GNMI, showing an improvement alignment of over 14% in terms of average target registration error, which is also reflected by a lower T10 estimation error. Finally, registration was applied to 46 clinical sequences to identify the average amount of motion found in this type of acquisition; this showed an estimated displacement of 0.98mm, which could lead to over 25% Ktrans estimation error if motion were not corrected.
AB - Relaxation time (T10) estimation using variable flip angle sequences is a key step for pharmacokinetic (PK) analysis of tumours in DCE-MRI exams. In this study, the effects of motion within flip angle sequences on the T10 and subsequent Ktrans and kep estimation were examined. It was found that errors in T10 estimation caused by motion had a significant impact on subsequent PK analysis. A new similarity metric, based on the T10 regression error, for groupwise motion correction of variable flip angle sequences is proposed and compared against Groupwise Normalized Mutual Information (GNMI). In rigid registration experiments on simulated data, the new metric outperformed GNMI, showing an improvement alignment of over 14% in terms of average target registration error, which is also reflected by a lower T10 estimation error. Finally, registration was applied to 46 clinical sequences to identify the average amount of motion found in this type of acquisition; this showed an estimated displacement of 0.98mm, which could lead to over 25% Ktrans estimation error if motion were not corrected.
UR - https://www.scopus.com/pages/publications/84903709057
U2 - 10.1007/978-3-319-08554-8_16
DO - 10.1007/978-3-319-08554-8_16
M3 - Conference contribution
AN - SCOPUS:84903709057
SN - 9783319085531
T3 - Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)
SP - 154
EP - 163
BT - Biomedical Image Registration - 6th International Workshop, WBIR 2014, Proceedings
PB - Springer Verlag
T2 - 6th International Workshop on Biomedical Image Registration, WBIR 2014
Y2 - 7 July 2014 through 8 July 2014
ER -