Three-dimensional ultrashort echo time (3D UTE) magnetic resonance imaging (MRI) of the normal and degenerative disco-vertebral complex at 4.7 T: a feasibility study with longitudinal evaluation.


Journal

European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society
ISSN: 1432-0932
Titre abrégé: Eur Spine J
Pays: Germany
ID NLM: 9301980

Informations de publication

Date de publication:
05 2021
Historique:
received: 09 10 2020
accepted: 26 01 2021
revised: 19 01 2021
pubmed: 21 2 2021
medline: 6 7 2021
entrez: 20 2 2021
Statut: ppublish

Résumé

To assess feasibility of a three-dimensional ultrashort echo time (3D-UTE)-sequence to evaluate normal and pathological disco-vertebral complex (DVC), with assessment of its different portions in a rat model of degenerative disk disease (DDD) with histological correlation. To assess whether this sequence, in comparison with long echo time T2-weighted sequence, is able to monitor DDD with differentiation of early from chronic DVC changes in pathological mechanical conditions. Five rats were induced with DDD model by percutaneous disk trituration of the tail with an 18-G needle under US-guidance and imaged at 4.7 T. MRI protocol included fat-saturated-T2 (RARE) and 3D-UTE-sequences performed at baseline (day 0. n = 5 animals /10 DVC) and each week (W) from W1 to W10 postoperatively. Visual analysis and signal intensity measurements of SNR and CNR of all DVC portions were performed on RARE and UTE images. Following killing (baseline, n = 1/2 DVC; W2, n = 2/4 DVC; W10, n = 2/4 DVC), histological analysis was performed and compared with MRI. In normal DVC, unlike conventional RARE-sequences, 3D-UTE allowed complete identification of DVC zonal anatomy including on visual analysis and CNR measurements. In pathological conditions, SNR and CNR measurements of the annulus fibrosus and nucleus pulposus on 3D-UTE distinguished early discitis at W1 from chronic discopathy (P < 0.001 for SNR and P < 0.001 for CNR). Neither the normal complete anatomy of the DVC nor its pathological patterns could be assessed on conventional sequences. Unlike conventional sequences, 3D-UTE enables visualization of the complete normal DVC anatomy and enables monitoring of DDD differentiating between early DVC changes from chronic ones. Diagnostic: individual cross-sectional studies with the consistently applied reference standard and blinding.

Identifiants

pubmed: 33609189
doi: 10.1007/s00586-021-06755-x
pii: 10.1007/s00586-021-06755-x
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1144-1154

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Auteurs

Benjamin Dallaudière (B)

Department of Radiology, University Hospital of Bordeaux, Bordeaux, France. Benjamin.dallaudiere@gmail.com.
Centre de Résonance Magnétique des Systèmes Biologiques, CNRS/University of Bordeaux, Bordeaux, France. Benjamin.dallaudiere@gmail.com.

Emeline J Ribot (EJ)

Centre de Résonance Magnétique des Systèmes Biologiques, CNRS/University of Bordeaux, Bordeaux, France.

Aurélien J Trotier (AJ)

Centre de Résonance Magnétique des Systèmes Biologiques, CNRS/University of Bordeaux, Bordeaux, France.

Stéphane Loubrie (S)

Centre de Résonance Magnétique des Systèmes Biologiques, CNRS/University of Bordeaux, Bordeaux, France.

Laurence Dallet (L)

Centre de Résonance Magnétique des Systèmes Biologiques, CNRS/University of Bordeaux, Bordeaux, France.

Olivier Thibaudeau (O)

Plateau de Morphologie, Inserm, Université Paris Diderot-Paris 7, UMR 1152, Paris, France.

Sylvain Miraux (S)

Centre de Résonance Magnétique des Systèmes Biologiques, CNRS/University of Bordeaux, Bordeaux, France.

Olivier Hauger (O)

Department of Radiology, University Hospital of Bordeaux, Bordeaux, France.
Centre de Résonance Magnétique des Systèmes Biologiques, CNRS/University of Bordeaux, Bordeaux, France.

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