Native T value in the remote myocardium is independently associated with left ventricular dysfunction in patients with prior myocardial infarction.

Purpose: To compare remote myocardium native T in patients with chronic myocardial infarction (MI) and controls without MI and to elucidate the relationship of infarct size and native T in the remote myocardium for the prediction of left ventricular (LV) systolic dysfunction after MI.

Materials And Methods: A total of 41 chronic MI (18 anterior MI) patients and 15 age-matched volunteers with normal LV systolic function and no history of MI underwent cardiac magnetic resonance imaging (MRI) at 1.5T.

Comparison of spoiled gradient echo and steady-state free-precession imaging for native myocardial T1 mapping using the slice-interleaved T1 mapping (STONE) sequence.

Cardiac T1 mapping allows non-invasive imaging of interstitial diffuse fibrosis. Myocardial T1 is commonly calculated by voxel-wise fitting of the images acquired using balanced steady-state free precession (SSFP) after an inversion pulse. However, SSFP imaging is sensitive to B1 and B0 imperfection, which may result in additional artifacts.

Myocardial Native T1 Time in Patients With Hypertrophic Cardiomyopathy.

In hypertrophic cardiomyopathy (HC), there are significant variations in left ventricular (LV) wall thickness and fibrosis, which necessitates a volumetric coverage. Slice-interleaved T1 (STONE) mapping sequence allows for the assessment of native T1 time with complete coverage of LV myocardium. The aims of this study were to evaluate spatial heterogeneity of native T1 time in patients with HC.

Reproducibility of myocardial T and T relaxation time measurement using slice-interleaved T and T mapping sequences.

Purpose: To assess measurement reproducibility and image quality of myocardial T and T maps using free-breathing slice-interleaved T and T mapping sequences at 1.5 Tesla (T).

Materials And Methods: Eleven healthy subjects (33 ± 16 years; 6 males) underwent a slice-interleaved T and T mapping test/retest cardiac MR study at 1.

Native Myocardial T1 as a Biomarker of Cardiac Structure in Non-Ischemic Cardiomyopathy.

Diffuse myocardial fibrosis is involved in the pathology of nonischemic cardiomyopathy (NIC). Recently, the application of native (noncontrast) myocardial T1 measurement has been proposed as a method for characterizing diffuse interstitial fibrosis. To determine the association of native T1 with myocardial structure and function, we prospectively studied 39 patients with NIC (defined as left ventricular ejection fraction (LVEF) ≤ 50% without cardiac magnetic resonance (CMR) evidence of previous infarction) and 27 subjects with normal LVEF without known overt cardiovascular disease.