Abstract

BackgroundT2 mapping indicates to be a sensitive method for detection of tissue oedema hidden beyond the detection limits of T2-weighted Cardiovascular Magnetic Resonance (CMR). However, due to variability of baseline T2 values in volunteers, reference values need to be defined. Therefore, the aim of the study was to investigate the effects of age and sex on quantitative T2 mapping with a turbo gradient-spin-echo (GRASE) sequence at 1.5 T. For that reason, we studied sensitivity issues as well as technical and biological effects on GRASE-derived myocardial T2 maps. Furthermore, intra- and interobserver variability were calculated using data from a large volunteer group.MethodsGRASE-derived multiecho images were analysed using dedicated software. After sequence optimization, validation and sensitivity measurements were performed in muscle phantoms ex vivo and in vivo. The optimized parameters were used to analyse CMR images of 74 volunteers of mixed sex and a wide range of age with typical prevalence of hypertension and diabetes. Myocardial T2 values were analysed globally and according to the 17 segment model. Strain-encoded (SENC) imaging was additionally performed to investigate possible effects of myocardial strain on global or segmental T2 values.ResultsEx vivo studies in muscle phantoms showed, that GRASE-derived T2 values were comparable to those acquired by a standard multiecho spinecho sequence but faster by a factor of 6. Besides that, T2 values reflected tissue water content. The in vivo measurements in volunteers revealed intra- and interobserver correlations with R2=0.91 and R2=0.94 as well as a coefficients of variation of 2.4% and 2.2%, respectively. While global T2 time significantly decreased towards the heart basis, female volunteers had significant higher T2 time irrespective of myocardial region. We found no correlation of segmental T2 values with maximal systolic, diastolic strain or heart rate. Interestingly, volunteers´ age was significantly correlated to T2 time while that was not the case for other coincident cardiovascular risk factors.ConclusionGRASE-derived T2 maps are highly reproducible. However, female sex and aging with typical prevalence of hypertension and diabetes were accompanied by increased myocardial T2 values. Thus, sex and age must be considered as influence factors when using GRASE in a diagnostic manner.Electronic supplementary materialThe online version of this article (doi:10.1186/s12968-015-0118-0) contains supplementary material, which is available to authorized users.

Highlights

  • T2 mapping indicates to be a sensitive method for detection of tissue oedema hidden beyond the detection limits of T2-weighted Cardiovascular Magnetic Resonance (CMR)

  • On the other hand, using the appropriate sequence, T1 and T2 relaxation times can directly be derived from the images, Bönner et al Journal of Cardiovascular Magnetic Resonance (2015) 17:9 and the relaxation values can be investigated with greater objectivity than a threshold-based grading of myocardial signal intensity [5]

  • Adjustment of GRASE for in vivo measurements of the human heart In order to evaluate the effect of EPI on T2 values, we performed experiments in muscle-phantoms ex vivo and found that GRASE derived T2 values were in good agreement with T2 values of a standard multi echo spin echo (MESE) in repeated experiments (Additional file 1: Figure S1) by saving measurement time of factor 6

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Summary

Introduction

T2 mapping indicates to be a sensitive method for detection of tissue oedema hidden beyond the detection limits of T2-weighted Cardiovascular Magnetic Resonance (CMR). One of the major advantages of Cardiovascular Magnetic Resonance (CMR) in comparison to other non-invasive imaging modalities represents its superior soft tissue contrast. This contrast is determined by myocardial T1 and T2 relaxation properties which can be used for. The biological heterogeneity of myocardial texture in hearts of volunteers and patients as a result of age and sex might have a significant impact on myocardial T2 reference values [16,17]. Myocardial T2 values should be obtained in a large group of non-diseased controls for reference purposes in each T2 mapping sequence

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