Evidence map›Paper›PMID 40001661›Full record

ArticleBioengineering (Basel, Switzerland)2025

Characterization of Normal and Degenerative Discovertebral Complexes Using Qualitative and Quantitative Magnetic Resonance Imaging at 4.7T: Longitudinal Evaluation of Immature and Mature Rats.

Benjamin Dallaudière, Emeline J Ribot, Aurélien J Trotier, Laurence Dallet, Olivier Thibaudeau, Sylvain Miraux, Olivier Hauger

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Benjamin DallaudièreCentre de Résonance Magnétique des Systèmes Biologiques, UMR 5536, CNRS. Université de Bordeaux, 146 rue Léo Saignat, 33076 Bordeaux, France.
Emeline J RibotCentre de Résonance Magnétique des Systèmes Biologiques, UMR 5536, CNRS. Université de Bordeaux, 146 rue Léo Saignat, 33076 Bordeaux, France.ORCID 0000-0002-3063-1263
Aurélien J TrotierCentre de Résonance Magnétique des Systèmes Biologiques, UMR 5536, CNRS. Université de Bordeaux, 146 rue Léo Saignat, 33076 Bordeaux, France.ORCID 0000-0001-8860-1406
Laurence DalletCentre de Résonance Magnétique des Systèmes Biologiques, UMR 5536, CNRS. Université de Bordeaux, 146 rue Léo Saignat, 33076 Bordeaux, France.
Olivier ThibaudeauInserm UMS 34 Claude Bernard, Université de Paris Cité / UFR de Médecine Site Bichat, 16, rue Henri Huchard-BP 416, 75870 Paris Cedex 1, France.
Sylvain MirauxCentre de Résonance Magnétique des Systèmes Biologiques, UMR 5536, CNRS. Université de Bordeaux, 146 rue Léo Saignat, 33076 Bordeaux, France.
Olivier HaugerCentre de Résonance Magnétique des Systèmes Biologiques, UMR 5536, CNRS. Université de Bordeaux, 146 rue Léo Saignat, 33076 Bordeaux, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe assessed the feasibility of qualitative, semiquantitative, and multiparametric quantitative magnetic resonance imaging (MRI) using a three-dimensional (3D) ultrashort echo time (3D-UTE) sequence together with 2D-T2 and 3D-T1 mapping sequences to evaluate normal and pathological discovertebral complexes (DVCs). We assessed the disc (nucleus pulposus [NP] and annulus fibrosus [AF]), vertebral endplate (cartilage endplate [CEP] and growth plate [GP]), and subchondral bone (SB) using a rat model of degenerative disc disease (DDD). We also assessed whether this complete MRI cartography can improve the monitoring of DDD.

methodsDDD was induced by percutaneous disc trituration and collagenase injection of the tail. Then, the animals were imaged at 4.7T. The adjacent disc served as the control. The MRI protocol was performed at baseline and each week (W) postoperatively for 2 weeks. Visual analysis and signal intensity measurements from the 3D-UTE images, as well as T2 and T1 measurements, were carried out in all DVC portions. Histological analysis with hematoxylin-eosin and Masson trichrome staining was performed following euthanization of the rats at 2 weeks and the results were compared to the MRI findings.

resultsComplete qualitative identification of the normal zonal anatomy of the DVC, including the AF, CEP, and GP, was achieved using the 3D-UTE sequence. Quantitative measurements of the signal-to-noise ratio in the AF and NP enabled healthy DVCs to be distinguished from surgery-induced DDD, based on an increase in these values post-surgery. The 2D-T2 mapping results showed a significant increase in the T2 values of the AF and a decrease in the values of the NP between the baseline and W1 and W2 postoperatively (

conclusionsUse of the 3D-UTE sequence enabled a complete, robust, and reproducible visualization of DVC anatomy in both immature and mature rats under both normal and pathological conditions. The findings were supported quantitatively by the T2 and T1 mapping sequences and histologically. This sequence is therefore of prime interest in spinal imaging and should be regularly be performed.

Indexed as

anatomydiscendplatemappingMRIT1T2UTE

Identifiers

PMID40001661
PMCPMC11851778

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.