Serveur d'exploration sur les relations entre la France et l'Australie

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The natural history of Modic changes in a community-based cohort.

Identifieur interne : 003735 ( Ncbi/Merge ); précédent : 003734; suivant : 003736

The natural history of Modic changes in a community-based cohort.

Auteurs : Andrew J. Teichtahl [Australie] ; Monica A. Finnin [Australie] ; Yuanyuan Wang [Australie] ; Anita E. Wluka [Australie] ; Donna M. Urquhart [Australie] ; Richard O'Sullivan [France] ; Graeme Jones [Australie] ; Flavia M. Cicuttini [Australie]

Source :

RBID : pubmed:27324605

Abstract

Vertebral endplate (Modic) lesions are gaining interest, with varied phenotypes recognised to have distinct clinical and histological correlates. Nevertheless, the natural history of these lesions is unclear. This study examined the natural history of Modic changes and their potential relationship to the intervertebral disc.

DOI: 10.1016/j.jbspin.2016.03.011
PubMed: 27324605

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pubmed:27324605

Le document en format XML

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<div type="abstract" xml:lang="en">Vertebral endplate (Modic) lesions are gaining interest, with varied phenotypes recognised to have distinct clinical and histological correlates. Nevertheless, the natural history of these lesions is unclear. This study examined the natural history of Modic changes and their potential relationship to the intervertebral disc.</div>
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<Month>06</Month>
<Day>21</Day>
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<Month>03</Month>
<Day>09</Day>
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<Volume>84</Volume>
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<Year>2017</Year>
<Month>Mar</Month>
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<Title>Joint, bone, spine : revue du rhumatisme</Title>
<ISOAbbreviation>Joint Bone Spine</ISOAbbreviation>
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<ArticleTitle>The natural history of Modic changes in a community-based cohort.</ArticleTitle>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Vertebral endplate (Modic) lesions are gaining interest, with varied phenotypes recognised to have distinct clinical and histological correlates. Nevertheless, the natural history of these lesions is unclear. This study examined the natural history of Modic changes and their potential relationship to the intervertebral disc.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Seventy-two community-based adults not selected for low back pain had lumbar spine magnetic resonance imaging (MRI) performed at baseline (2012) and approximately 2 years later to assess Modic lesions. Fifty-six participants completed the study. Intervertebral disc pathology was assessed by disc height and the Pfirrmann grading system at baseline.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">At baseline, 6 Modic type 1 lesions were present in 3 (4.2%) participants. At follow-up, 4 persisted, 2 changed to a Modic type 2 lesion, and there were 4 incident lesions. Only 1 participant (1.4%) had a baseline Modic type 3 lesion, which persisted at follow-up, with one further incident lesion. Modic type 2 lesions were most common (n=47, in 20 of 72 [27.8%] participants). Resolution of Modic type 2 lesions was uncommon (n=1, with 2 changing to a type 1 lesion). 18 incident lesions occurred in 7 (12.5%) participants, with most occurring both sides of the intervertebral disc. A reduction in the average baseline disc height was associated with an increased risk for type 2 incident lesions (OR 1.9, 95% CI 1.1 to 3.3, P=0.03). Similarly, severe baseline disc degeneration at L3/4, L4/5 and L5/S1 was associated with an increased risk for type 2 incident lesions (all P≤0.05).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">This longitudinal study has demonstrated that Modic type 2 are the most common of the Modic lesions in community-based adults and while resolution of these lesions is uncommon, incident disease develops on both sides of the intervertebral disc in the setting of severe disc degeneration. These results suggest that type 2 Modic changes are a sequel of disc degeneration.</AbstractText>
<CopyrightInformation>Copyright © 2016 Société française de rhumatologie. Published by Elsevier SAS. All rights reserved.</CopyrightInformation>
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<Affiliation>Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Alfred Hospital, 3004 Melbourne, Australia.</Affiliation>
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<name sortKey="Wang, Yuanyuan" sort="Wang, Yuanyuan" uniqKey="Wang Y" first="Yuanyuan" last="Wang">Yuanyuan Wang</name>
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Data generation: Tue Dec 5 10:43:12 2017. Site generation: Tue Mar 5 14:07:20 2024