Abstract

BackgroundHigh resolution 3D T1 mapping is important for assessment of diffuse myocardial fibrosis in left atrium or other thin-walled structures. In this work, we investigated a fast single-TI 3D high resolution T1 mapping method that directly transforms a 3D late gadolinium enhancement (LGE) volume to a 3D T1 map.MethodsThe proposed method, T1-refBlochi, is based on Bloch equation modeling of the LGE signal, a single-point calibration, and assumptions that proton density and T2* are relatively uniform in the heart. Several sources of error of this method were analyzed mathematically and with simulations. Imaging was performed in phantoms, eight swine and five patients, comparing T1-refBlochi to a standard spin-echo T1 mapping, 3D multi-TI T1 mapping, and 2D ShMOLLI, respectively.ResultsThe method has a good accuracy and adequate precision, even considering various sources of error. In phantoms, over a range of protocols, heart-rates and T1 s, the bias ±1SD was -3 ms ± 9 ms. The porcine studies showed excellent agreement between T1-refBlochi and the multi-TI method (bias ±1SD = −6 ± 22 ms). The proton density and T2* weightings yielded ratios for scar/blood of 0.94 ± 0.01 and for myocardium/blood of 1.03 ± 0.02 in the eight swine, confirming that sufficient uniformity of proton density and T2* weightings exists among heterogeneous tissues of the heart. In the patients, the mean T1 bias ±1SD in myocardium and blood between T1-refBlochi and ShMOLLI was -9 ms ± 21 ms.ConclusionT1-refBlochi provides a fast single-TI high resolution 3D T1 map of the heart with good accuracy and adequate precision.

Highlights

  • High resolution 3D T1 mapping is important for assessment of diffuse myocardial fibrosis in left atrium or other thin-walled structures

  • T1 mapping has been recognized in recent years as an important potential biomarker for tissue characterization in cardiovascular magnetic resonance (CMR)

  • Several clinical studies have shown that post-contrast T1 values, the focus of this paper, are significantly shorter in the left ventricular (LV) myocardium for several cardiac diseases, beyond myocardial infarction [1, 2], including dilated cardiomyopathy

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Summary

Introduction

High resolution 3D T1 mapping is important for assessment of diffuse myocardial fibrosis in left atrium or other thin-walled structures. T1 mapping has been recognized in recent years as an important potential biomarker for tissue characterization in cardiovascular magnetic resonance (CMR). Postcontrast T1 enables calculation of extracellular volume (ECV) fraction, which is a robust and sensitive biomarker to diffuse myocardial fibrosis, undetectable by late gadolinium enhancement [7]. Navigator-Gated Look-Locker IMaging (ANGIE) and an interleaved T1/T2 method [11, 13], provide higher in-plane spatial resolution and use navigator-gating. All these techniques focus on 2D T1 mapping

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