Nonuniform sliding-window reconstruction for accelerated dual contrast agent quantification with MR fingerprinting.

Objective: MR fingerprinting (MRF) can enable preclinical studies of cell tracking by quantifying multiple contrast agents simultaneously, but faster scan times are required for in vivo applications. Sliding window (SW)-MRF is one option for accelerating MRF, but standard implementations are not sufficient to preserve the accuracy of T₂*, which is critical for tracking iron-labelled cells in vivo. Purpose: To develop a SW approach to MRF which preserves the T₂* accuracy required for accelerated concentration mapping of iron-labelled cells on single-channel preclinical systems. Methods: A nonuniform SW was applied to the MRF sequence and dictionary. Segments of the sequence most sensitive to T₂* were subject to a shorter window length, preserving the T₂* sensitivity. Phantoms containing iron-labelled CD8+ T cells and gadolinium were used to compare 24× undersampled uniform and nonuniform SW-MRF parameter maps. Dual concentration maps were generated for both uniform and nonuniform MRF and compared. Results: Lin's concordance correlation coefficient, compared to gold standard parameter values, was much greater for nonuniform SW-MRF than for uniform SW-MRF. A Wilcoxon signed-rank test showed no significant difference between nonuniform SW-MRF and gold standards. Nonuniform SW-MRF outperformed the uniform SW-MRF concentration maps for all parameters, providing a balance between T₂* sensitivity of short window lengths, and SNR of longer window lengths. Conclusions: Nonuniform SW-MRF improves the accuracy of matching compared to uniform SW-MRF, allowing higher accelerated concentration mapping for preclinical systems. [ABSTRACT FROM AUTHOR]