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Validation of T2* in-line analysis for tissue iron quantification at 1.5 T.

Alam, MH; He, T; Auger, D; Smith, GC; Drivas, P; Wage, R; Izgi, C; Symmonds, K; Greiser, A; Spottiswoode, BS; et al. Alam, MH; He, T; Auger, D; Smith, GC; Drivas, P; Wage, R; Izgi, C; Symmonds, K; Greiser, A; Spottiswoode, BS; Anderson, L; Firmin, D; Pennell, DJ (2016) Validation of T2* in-line analysis for tissue iron quantification at 1.5 T. Journal of Cardiovascular Magnetics Resonance, 18 (1). p. 23. ISSN 1532-429X https://doi.org/10.1186/s12968-016-0243-4
SGUL Authors: He, Taigang

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Abstract

BACKGROUND: There is a need for improved worldwide access to tissue iron quantification using T2* cardiovascular magnetic resonance (CMR). One route to facilitate this would be simple in-line T2* analysis widely available on MR scanners. We therefore compared our clinically validated and established T2* method at Royal Brompton Hospital (RBH T2*) against a novel work-in-progress (WIP) sequence with in-line T2* measurement from Siemens (WIP T2*). METHODS: Healthy volunteers (n = 22) and patients with iron overload (n = 78) were recruited (53 males, median age 34 years). A 1.5 T study (Magnetom Avanto, Siemens) was performed on all subjects. The same mid-ventricular short axis cardiac slice and transaxial slice through the liver were used to acquire both RBH T2* images and WIP T2* maps for each participant. Cardiac white blood (WB) and black blood (BB) sequences were acquired. Intraobserver, interobserver and interstudy reproducibility were measured on the same data from a subset of 20 participants. RESULTS: Liver T2* values ranged from 0.8 to 35.7 ms (median 5.1 ms) and cardiac T2* values from 6.0 to 52.3 ms (median 31 ms). The coefficient of variance (CoV) values for direct comparison of T2* values by RBH and WIP were 6.1-7.8 % across techniques. Accurate delineation of the septum was difficult on some WIP T2* maps due to artefacts. The inability to manually correct for noise by truncation of erroneous later echo times led to some overestimation of T2* using WIP T2* compared with the RBH T2*. Reproducibility CoV results for RBH T2* ranged from 1.5 to 5.7 % which were better than the reproducibility of WIP T2* values of 4.1-16.6 %. CONCLUSIONS: Iron estimation using the T2* CMR sequence in combination with Siemens' in-line data processing is generally satisfactory and may help facilitate global access to tissue iron assessment. The current automated T2* map technique is less good for tissue iron assessment with noisy data at low T2* values.

Item Type: Article
Additional Information: © 2016 Alam et al. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Keywords: CMR, Heart, In-line processing, Iron overload, Liver, T2*, CMR, T2*, In-line processing, Heart, Liver, Iron overload, CMR, Heart, In-line processing, Iron overload, Liver, T2*, Nuclear Medicine & Medical Imaging, 1102 Cardiovascular Medicine And Haematology
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cardiac (INCCCA)
Journal or Publication Title: Journal of Cardiovascular Magnetics Resonance
ISSN: 1532-429X
Language: ENG
Dates:
DateEvent
27 April 2016Published
20 April 2016Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
UNSPECIFIEDNational Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
PubMed ID: 27121114
Web of Science ID: WOS:000374865900001
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/108336
Publisher's version: https://doi.org/10.1186/s12968-016-0243-4

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