Purpose: To evaluate the effectiveness of a mathematical model for histogram analysis of DCE-MRI in distinguishing responders from non-responders during RA drug treatment. Method: Twenty-three consecutive RA patients with clinically active inflammation prospectively underwent DCEMRI at baseline and after treatment. Manual segmentation of the enhanced synovium was performed on the last phase of DCE-MRI. The voxel-based contrast enhancement was calculated in each phase to obtain 75th percentile values. Kinetic curves made from the 75th percentile values were fitted to mathematical model as follows, delta S(t) = A(1-e- alpha t)e-beta t, where A is the upper limit of signal intensity (%), alpha (sec-1) is the rate of signal increase, and beta (sec-1) is the rate of signal decrease during washout. AUC30 was calculated by integration of 30 s. SER was calculated as the signal intensity at the initial time point (t = 60) relative to the delayed time point (t = 300). The volumes of enhanced synovium (sum of the number of voxels) were also calculated. Results: After treatment, alpha, A alpha, AUC30 and SER were significantly lower in the responder group than in the nonresponder group (p = 0.033, 0.024, 0.015, and 0.007). The p value of SER was lowest. A alpha, AUC30, and the volume of enhanced synovium had significantly larger changes from baseline to after treatment in the responder group than in the non-responder group (p = 0.045, 0.017, and 0.008). The volume of enhanced synovium had the lowest p value. Conclusions: SER after treatment and change in the volume of enhanced synovium might be effective for distinguishing responders from non-responders.
机构:
Univ Ulsan, Coll Med, Asan Med Ctr, Ctr Bioimaging New Drug Dev,Asan Inst Life Sci, Seoul, South Korea
Univ Ulsan, Coll Med, Asan Med Ctr, Dept Clin Pharmacol & Therapeut, Seoul, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Radiol,Res Inst Radiol, Seoul, South Korea
Lim, Hyeong-Seok
Woo, Dong-Cheol
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Radiol,Res Inst Radiol, Seoul, South Korea
Univ Ulsan, Coll Med, Asan Med Ctr, Ctr Bioimaging New Drug Dev,Asan Inst Life Sci, Seoul, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Radiol,Res Inst Radiol, Seoul, South Korea
Woo, Dong-Cheol
Kim, Kyung Won
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Radiol,Res Inst Radiol, Seoul, South Korea
Univ Ulsan, Coll Med, Asan Med Ctr, Ctr Bioimaging New Drug Dev,Asan Inst Life Sci, Seoul, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Radiol,Res Inst Radiol, Seoul, South Korea
Kim, Kyung Won
Kim, Jeong Kon
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Radiol,Res Inst Radiol, Seoul, South Korea
Univ Ulsan, Coll Med, Asan Med Ctr, Ctr Bioimaging New Drug Dev,Asan Inst Life Sci, Seoul, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Radiol,Res Inst Radiol, Seoul, South Korea