Abstract

BackgroundNative T1 mapping is a cardiovascular magnetic resonance (CMR) technique that associates with markers of fibrosis and strain in hemodialysis patients. The reproducibility of T1 mapping in hemodialysis patients, prone to changes in fluid status, is unknown. Accurate quantification of myocardial fibrosis in this population has prognostic potential.MethodsUsing 3 Tesla CMR, we report the results of 1) the inter-study, inter-observer and intra-observer reproducibility of native T1 mapping in 10 hemodialysis patients; 2) inter-study reproducibility of left ventricular (LV) structure and function in 10 hemodialysis patients; 3) the agreement of native T1 map and native T1 phantom analyses between two centres in 20 hemodialysis patients; 4) the effect of changes in markers of fluid status on native T1 values in 10 hemodialysis patients.ResultsInter-study, inter-observer and intra-observer variability of native T1 mapping were excellent with co-efficients of variation (CoV) of 0.7, 0.3 and 0.4% respectively. Inter-study CoV for LV structure and function were: LV mass = 1%; ejection fraction = 1.1%; LV end-diastolic volume = 5.2%; LV end-systolic volume = 5.6%. Inter-centre variability of analysis techniques were excellent with CoV for basal and mid-native T1 slices between 0.8–1.2%. Phantom analyses showed comparable native T1 times between centres, despite different scanners and acquisition sequences (centre 1: 1192.7 ± 7.5 ms, centre 2: 1205.5 ± 5 ms). For the 10 patients who underwent inter-study testing, change in body weight (Δweight) between scans correlated with change in LV end-diastolic volume (ΔLVEDV) (r = 0.682;P = 0.03) representing altered fluid status between scans. There were no correlations between change in native T1 between scans (ΔT1) and ΔLVEDV or Δweight (P > 0.6). Linear regression confirmed ΔT1 was unaffected by ΔLVEDV or Δweight (P > 0.59).ConclusionsMyocardial native T1 is reproducible in HD patients and unaffected by changes in fluid status at the levels we observed. Native T1 mapping is a potential imaging biomarker for myocardial fibrosis in patients with end-stage renal disease.

Highlights

  • Native T1 mapping is a cardiovascular magnetic resonance (CMR) technique that associates with markers of fibrosis and strain in hemodialysis patients

  • Myocardial native T1 times have been shown to be significantly higher in HD patients compared to control subjects [17, 18] and to associate with circulating markers of cardiac disease [17] and measures of myocardial systolic strain [18], but the reproducibility of native T1 mapping has not been assessed in HD patients who are prone to shifts in extracellular volume

  • Native T1 times are prolonged with increasing water content of tissue and the presence of intermittent myocardial edema from alterations in fluid status may in theory affect native T1 time confounding results and reducing native T1 time reproducibility

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Summary

Introduction

Native T1 mapping is a cardiovascular magnetic resonance (CMR) technique that associates with markers of fibrosis and strain in hemodialysis patients. Native T1 mapping is a novel, non-contrast CMR technique that correlates well with biopsy measured myocardial fibrosis in aortic stenosis [11, 12] and can differentiate patients with hypertrophic cardiomyopathy from hypertensive cardiac disease [13]. Myocardial native T1 times have been shown to be significantly higher in HD patients compared to control subjects [17, 18] and to associate with circulating markers of cardiac disease [17] and measures of myocardial systolic strain [18], but the reproducibility of native T1 mapping has not been assessed in HD patients who are prone to shifts in extracellular volume. Concerns remain about the use of this technique to assess myocardial fibrosis in patients with ESRD on HD, who are subject to significant changes in fluid status and who may potentially have intermittent myocardial oedema [19]

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