T₁ mapping performance and measurement repeatability: results from the multi-national T₁ mapping standardization...

The T₁ Mapping and Extracellular volume (ECV) Standardization (T1MES) program explored T₁ mapping quality assurance using a purpose-developed phantom with Food and Drug Administration (FDA) and Conformité Européenne (CE) regulatory clearance. We report T₁ measurement repeatability across centers describing sequence, magnet, and vendor performance.

Phantoms batch-manufactured in August 2015 underwent 2 years of structural imaging, B₀ and B₁, and "reference" slow T₁ testing. Temperature dependency was evaluated by the United States National Institute of Standards and Technology and by the German Physikalisch-Technische Bundesanstalt. Center-specific T₁ mapping repeatability (maximum one scan per week to minimum one per quarter year) was assessed over mean 358 (maximum 1161) days on 34 1.5 T and 22 3 T magnets using multiple T₁ mapping sequences. Image and temperature data were analyzed semi-automatically. Repeatability of serial T₁ was evaluated in terms of coefficient of variation (CoV), and linear mixed models were constructed to study the interplay of some of the known sources of T₁ variation.

Over 2 years, phantom gel integrity remained intact (no rips/tears), B₀ and B₁ homogenous, and "reference" T₁ stable compared to baseline (% change at 1.5 T, 1.95 ± 1.39%; 3 T, 2.22 ± 1.44%). Per degrees Celsius, 1.5 T, T₁ (MOLLI 5s(3s)3s) increased by 11.4 ms in long native blood tubes and decreased by 1.2 ms in short post-contrast myocardium tubes. Agreement of estimated T₁ times with "reference" T₁ was similar across Siemens and Philips CMR systems at both field strengths (adjusted R² ranges for both field strengths, 0.99-1.00). Over 1 year, many 1.5 T and 3 T sequences/magnets were repeatable with mean CoVs < 1 and 2% respectively. Repeatability was narrower for 1.5 T over 3 T. Within T1MES repeatability for native T₁ was narrow for several sequences, for example, at 1.5 T, Siemens MOLLI 5s(3s)3s prototype number 448B (mean CoV = 0.27%) and Philips modified Look-Locker inversion recovery (MOLLI) 3s(3s)5s (CoV 0.54%), and at 3 T, Philips MOLLI 3b(3s)5b (CoV 0.33%) and Siemens shortened MOLLI (ShMOLLI) prototype 780C (CoV 0.69%). After adjusting for temperature and field strength, it was found that the T₁ mapping sequence and scanner software version (both P < 0.001 at 1.5 T and 3 T), and to a lesser extent the scanner model (P = 0.011, 1.5 T only), had the greatest influence on T₁ across multiple centers.

The T1MES CE/FDA approved phantom is a robust quality assurance device. In a multi-center setting, T₁ mapping had performance differences between field strengths, sequences, scanner software versions, and manufacturers. However, several specific combinations of field strength, sequence, and scanner are highly repeatable, and thus, have potential to provide standardized assessment of T₁ times for clinical use, although temperature correction is required for native T₁ tubes at least.