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dc.contributor.authorBråten, Lars Christian Haugli
dc.contributor.authorSchistad, Ellina Iordanova
dc.contributor.authorEspeland, Ansgar
dc.contributor.authorKristoffersen, Per M
dc.contributor.authorHaugen, Anne Julsrud
dc.contributor.authorMarchand, Gunn Hege
dc.contributor.authorVetti, Nils
dc.contributor.authorPripp, Are Hugo
dc.contributor.authorKadar, Thomas
dc.contributor.authorSkouen, Jan Sture
dc.contributor.authorGrotle, Margreth
dc.contributor.authorGrøvle, Lars
dc.contributor.authorZwart, John-Anker
dc.contributor.authorBrox, Jens Ivar
dc.contributor.authorStorheim, Kjersti
dc.coverage.spatialNorwayen_US
dc.date.accessioned2021-05-10T07:41:01Z
dc.date.available2021-05-10T07:41:01Z
dc.date.created2021-01-12T13:13:19Z
dc.date.issued2020-06-10
dc.identifier.citationBMC Musculoskeletal Disorders. 2020, 21 .en_US
dc.identifier.issn1471-2474
dc.identifier.urihttps://hdl.handle.net/11250/2754493
dc.description.abstractBackground: Modic Changes (MCs, magnetic resonance imaging (MRI) signal changes in the vertebral bone marrow extending from the vertebral endplate) may represent a subgroup of nonspecific chronic low back pain that could benefit from a specific management. The primary aim was to compare clinical characteristics between patients with type 1 versus type 2 MCs. The secondary aim was to explore associations between clinical characteristics and MC related short tau inversion recovery (STIR) signals. Methods: This cross-sectional study used baseline data prospectively collected between 2015 and 2017 on the 180 patients included in the AIM-study (Antibiotics In Modic changes), a randomized controlled trial in a Norwegian hospital out-patient setting of patients with chronic low back pain, a lumbar disc herniation within the last 2 years, low back pain intensity score ≥ 5 (on a 0–10 scale) and current type 1 or type 2 MCs at the previously herniated lumbar disc level. We used prespecified clinical characteristics including self-report measures, physiologic measures and functional measures from clinical history and examination. The diagnostic accuracy of various clinical characteristics to discriminate between patients with type 1 MCs (with or without additional type 2 MCs) and patents with type 2 MCs only (not type 1) were assessed by calculating the area under the receiver-operating curve. We assessed the correlations of clinical characteristics with details of MC related STIR signal increase. Results: No clinical characteristic differed between patients with type 1 (n = 118) versus type 2 (but not type 1) (n = 62) MCs. The clinical characteristics showed no/minor differences or no/weak correlations with MC related STIR signal increase. Patients with a positive Springing test (at any lumbar level) had slightly less volume of STIR signal increase than those with a negative test (mean difference 1.3 on a 0–48 scale, 95% CI 0.3 to 2.3). Conclusion: Clinical characteristics were similar for patients with type 1 MCs and patients with type 2 MCs, and showed no clinically relevant correlations with MC related STIR signal increase.en_US
dc.description.sponsorshipThe trial was funded by governmental organisations; Helse Sør-Øst (grant no: 2015090) and Helse Vest (grant no: 911938 and 911891).en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.relation.ispartofseriesBMC Musculoskeletal Disorders;21, Article number: 368 (2020)
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectModic changesen_US
dc.subjectLow back painen_US
dc.subjectClinical characteristicsen_US
dc.subjectDiagnostic accuracyen_US
dc.subjectShort tau inversion recoveriesen_US
dc.subjectBone marrow edemaen_US
dc.subjectMagnetic resonance imagesen_US
dc.titleAssociation of Modic change types and their short tau inversion recovery signals with clinical characteristics : a cross sectional study of chronic low back pain patients in the AIM-studyen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s).en_US
dc.source.articlenumber368en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttps://doi.org/10.1186/s12891-020-03381-4
dc.identifier.cristin1869821
dc.source.journalBMC Musculoskeletal Disordersen_US
dc.source.volume21en_US
dc.source.pagenumber10en_US


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