Feasibility of dynamic T2*-based oxygen-enhanced lung MRI at 3T
Mina Kim, Josephine H. Naish, Sarah H. Needleman, Marta Tibiletti, Yohn Taylor, James P. B. O’Connor, Geoff J. M. Parker
Abstract
Purpose
To demonstrate proof-of-concept of a T2*-sensitized oxygen-enhanced MRI (OE-MRI) method at 3T by assessing signal characteristics, repeatability, and reproducibility of dynamic lung OE-MRI metrics in healthy volunteers.
Methods
We performed sequence-specific simulations for protocol optimisation and acquired free-breathing OE-MRI data from 16 healthy subjects using a dual-echo RF-spoiled gradient echo approach at 3T across two institutions. Non-linear registration and tissue density correction were applied. Derived metrics included percent signal enhancement (PSE), ∆R2* and wash-in time normalized for breathing rate (τ-nBR). Inter-scanner reproducibility and intra-scanner repeatability were evaluated using intra-class correlation coefficient (ICC), repeatability coefficient, reproducibility coefficient, and Bland–Altman analysis.
Results
Simulations and experimental data show negative contrast upon oxygen inhalation, due to substantial dominance of ∆R2* at TE > 0.2 ms. Density correction improved signal fluctuations. Density-corrected mean PSE values, aligned with simulations, display TE-dependence, and an anterior-to-posterior PSE reduction trend at TE1. ∆R2* maps exhibit spatial heterogeneity in oxygen delivery, featuring anterior-to-posterior R2* increase. Mean T2* values across 32 scans were 0.68 and 0.62 ms for pre- and post-O2 inhalation, respectively. Excellent or good agreement emerged from all intra-, inter-scanner and inter-rater variability tests for PSE and ∆R2*. However, ICC values for τ-nBR demonstrated limited agreement between repeated measures.
Conclusion
Our results demonstrate the feasibility of a T2*-weighted method utilizing a dual-echo RF-spoiled gradient echo approach, simultaneously capturing PSE, ∆R2* changes, and oxygen wash-in during free-breathing. The excellent or good repeatability and reproducibility on intra- and inter-scanner PSE and ∆R2* suggest potential utility in multi-center clinical applications.