Improved contrast for myeloma focal lesions with T2-weighted Dixon images compared to T1-weighted images.


Journal

Diagnostic and interventional imaging
ISSN: 2211-5684
Titre abrégé: Diagn Interv Imaging
Pays: France
ID NLM: 101568499

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 12 01 2019
revised: 25 04 2019
accepted: 04 05 2019
pubmed: 28 5 2019
medline: 25 3 2020
entrez: 28 5 2019
Statut: ppublish

Résumé

The purpose of this study was twofold. First, to compare the contrast between spinal multiple myeloma (MM) focal lesions and surrounding bone marrow obtained on T2-weighted Dixon fat-only MR images to that obtained on T1-weighted spin-echo images. Second, to search for correlation between bone marrow fat fraction assessed by T2-weighted Dixon sequence and International Myeloma Working Group myeloma defining events. A total of 39 patients with 112 focal MM lesions were included. There were 25 men and 14 women with a mean age of 68.8±9.8 [SD] years (range: 49-88 years). Contrast between focal MM lesions and surrounding bone marrow was calculated on T1-weighted spin-echo and T2-weighted Dixon (including water-only and fat-only) images. Contrast between focal MM lesions and bone marrow was compared using ANOVA and post-hoc Tukey tests. Correlation between bone marrow fat fraction and myeloma defining events was assessed using Spearman's correlation test. MM lesion contrast was greater on T2-weighted Dixon (F (2;93)=35.10) than on T1-weighted images (P<0.0001). Greatest MM lesion contrast was achieved with T2-weighted Dixon fat-only (0.63±0.21 [SD]; range: 0.06-0.91) compared to T2-weighted Dixon water-only (0.45±0.20 [SD]; range: 0.07-0.8) (P=0.0003) and T1-weighted (0.23±0.19 [SD]; range: 0.04-0.87) (P<0.0001) images. There were no significant correlations between myeloma defining events and fat fraction. T2-weighted Dixon fat-only images provide greater contrast between MM lesions and adjacent bone marrow than T1-weighted images. The usefulness of a T1-weighted sequence associated to a T2-weighted Dixon sequence has to be determined.

Identifiants

pubmed: 31130374
pii: S2211-5684(19)30110-X
doi: 10.1016/j.diii.2019.05.001
pii:
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

513-519

Informations de copyright

Copyright © 2019 Société française de radiologie. Published by Elsevier Masson SAS. All rights reserved.

Auteurs

A Danner (A)

Department of Musculoskeletal Imaging. CHU de Besancon, 25000 Besancon, France.

E Brumpt (E)

Department of Musculoskeletal Imaging. CHU de Besancon, 25000 Besancon, France; Laboratoire d'Anatomie, Université de Bourgogne-Franche-comté, 25000 Besancon, France.

M Alilet (M)

Department of Musculoskeletal Imaging. CHU de Besancon, 25000 Besancon, France.

G Tio (G)

Clinical investigation center. INSERM CIT808. CHU de Besancon, 25000 Besancon, France.

P Omoumi (P)

Department of Diagnostic and Interventional Radiology. Lausanne University Hospital, 1011 Lausanne, Swizerland.

S Aubry (S)

Department of Musculoskeletal Imaging. CHU de Besancon, 25000 Besancon, France; Nanomedecine Laboratory inserm EA 4662, Université de Bourgogne-Franchecomté, 25000 Besancon, France. Electronic address: radio.aubry@free.fr.

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Classifications MeSH