Related Experiment Video
Updated: Aug 27, 2026

In Vivo Quantitative Assessment of Myocardial Structure, Function, Perfusion and Viability Using Cardiac Micro-computed Tomography
Published on: February 16, 2016
Simultaneous 3-D Adiabatic T1ρ, T2*, and Quantitative Susceptibility Mapping for Characterization of Myocardial
Iida Räty1, Olli Nykänen2,3, Sanna Kettunen1
1A.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.
Abstract:
To develop a T1ρ-weighted quantitative susceptibility mapping (QSM) technique for simultaneous imaging of T1ρ and T2* relaxation and magnetic susceptibility in ex vivo mouse hearts after myocardial infarction (MI). MI was induced in C75Bl/6JOlaHsd mice, and their hearts (nMI = 7, nCTRL = 6) were imaged ex vivo by combining adiabatic T1ρ preparation with a 3-D multi-echo gradient recalled echo (GRE) sequence for simultaneous T1ρ-weighted QSM. As a reference, 2-D adiabatic T1ρ mapping and QSM without preparation were used. T2* and susceptibility maps were calculated for both T1ρ-QSM and QSM measurements. Additionally, T1ρ maps were calculated from T1ρ-T2*-QSM. Region of interest analysis was performed using American Heart Association (AHA) segments. Correlation and Bland-Altman bias between 2-D/3-D T1ρ and T1ρ-T2*-QSM/QSM segments were assessed, respectively. Statistical significance between the segments was tested using Mann-Whitney U test. Histological validation was conducted using Picro Sirius red (SR), hematoxylin and eosin (HE), and Perls' Prussian Blue (PPB) stainings. T1ρ relaxation times were elevated significantly in basal AHA segments 1, 2, and 6, compared to the corresponding control segments. T2* relaxation times decreased significantly in basal and apical segments 4, 6, 13, and 14. QSM revealed visible heterogeneity within the same segments, and greater variance in basal, mid, and apical segments 6, 7, 11, 12, and 13 compared to controls. Histology confirmed the formation of myocardial fibrosis and hemosiderin-laden macrophages within the corresponding MRI segments with minimal residual blood in MI hearts. Quantitative analysis showed a moderate agreement between 2-D and 3-D T1ρ mapping (Spearman's r = 0.71). Bland-Altman analysis between T1ρ-T2*-QSM and reference QSM showed minimal bias (-7.6 · 10-4) and Pearson's correlation coefficient rp = 0.69. For T2* (T1ρ-T2*-QSM) and QSM, the Bland-Altman analysis bias was -0.84 and rp = 0.77. The developed T1ρ-weighted QSM technique enabled simultaneous acquisition of T1ρ, T2*, and susceptibility maps in ex vivo mouse hearts. All imaging contrasts showed good correlation with reference methods, and MI regions were visible using either T1ρ, T2*, or susceptibility mapping. The identified MI areas were in line with histological findings, supporting the accuracy of the proposed imaging approach.

