TY - JOUR
T1 - Repeatability and reproducibility of joint T1-T2 transient-state relaxometry across multiple vendors and implementations at 3T in phantom and human brain
AU - Lancione, Marta
AU - Cencini, Matteo
AU - Aquino, Domenico
AU - Baldoli, Cristina
AU - Elia, Maurizio
AU - Ghielmetti, Francesco
AU - Montanaro, Domenico
AU - Neri, Ilaria
AU - Nigri, Anna
AU - Pasquariello, Rosa
AU - Pettinato, Salvatore
AU - Romano, Salvatore
AU - Sbrizzi, Alessandro
AU - Scifo, Paola
AU - van der Heide, Oscar
AU - Versteeg, Edwin
AU - Biagi, Laura
AU - Tosetti, Michela
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025/10/15
Y1 - 2025/10/15
N2 - Transient-state relaxometry (TSR) enables rapid estimation of T1 and T2 relaxation times. To support its broader adoption in multi-center studies, it is essential to assess the consistency of its implementation across different MRI vendors. This work aimed to assess accuracy, repeatability, and inter-vendor reproducibility of jointly measured T1 and T2 maps based on TSR at 3T. To achieve this goal, a phantom and five volunteers were scanned in a traveling-brain study at four 3T MRI systems from three manufacturers. In the phantom study, Bland-Altman analysis and coefficients of variation (CV) were used to assess accuracy, and repeatability and reproducibility, respectively. Subsequently, in-vivo inter-site variability was evaluated via ANOVA and by computing voxelwise CVs and biases associated with sites were measured via a general linear model (GLM). Excellent accuracy, repeatability, and reproducibility were obtained for the phantom. In-vivo, we found excellent repeatability (CV < 4.5%) and generally good inter-site and inter-vendor reproducibility, though significant variability was found across different TSR implementations. The GLM analysis revealed site-related biases of approximately 100 ms for T1 and 2 ms for T2 in solid brain tissues. These differences may be attributable to different magnetization transfer effects and residual B1+ inhomogeneities due to imperfect calibration. Our findings demonstrate that the bias introduced by the use of different TSR implementations needs to be considered carefully in order to perform in-vivo multi-center studies.
AB - Transient-state relaxometry (TSR) enables rapid estimation of T1 and T2 relaxation times. To support its broader adoption in multi-center studies, it is essential to assess the consistency of its implementation across different MRI vendors. This work aimed to assess accuracy, repeatability, and inter-vendor reproducibility of jointly measured T1 and T2 maps based on TSR at 3T. To achieve this goal, a phantom and five volunteers were scanned in a traveling-brain study at four 3T MRI systems from three manufacturers. In the phantom study, Bland-Altman analysis and coefficients of variation (CV) were used to assess accuracy, and repeatability and reproducibility, respectively. Subsequently, in-vivo inter-site variability was evaluated via ANOVA and by computing voxelwise CVs and biases associated with sites were measured via a general linear model (GLM). Excellent accuracy, repeatability, and reproducibility were obtained for the phantom. In-vivo, we found excellent repeatability (CV < 4.5%) and generally good inter-site and inter-vendor reproducibility, though significant variability was found across different TSR implementations. The GLM analysis revealed site-related biases of approximately 100 ms for T1 and 2 ms for T2 in solid brain tissues. These differences may be attributable to different magnetization transfer effects and residual B1+ inhomogeneities due to imperfect calibration. Our findings demonstrate that the bias introduced by the use of different TSR implementations needs to be considered carefully in order to perform in-vivo multi-center studies.
KW - Brain
KW - Magnetic resonance fingerprinting
KW - Multi-vendor
KW - Quantitative MRI
KW - Reproducibility
KW - T1 and T2 mapping
KW - Transient state relaxometry
UR - https://www.scopus.com/pages/publications/105016611962
U2 - 10.1016/j.neuroimage.2025.121471
DO - 10.1016/j.neuroimage.2025.121471
M3 - Article
C2 - 40967293
AN - SCOPUS:105016611962
SN - 1053-8119
VL - 320
JO - NeuroImage
JF - NeuroImage
M1 - 121471
ER -