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dc.contributor.authorDagestad, Magnhild Hammersland
dc.contributor.authorVetti, Nils
dc.contributor.authorKristoffersen, Per M
dc.contributor.authorZwart, John Anker Henrik
dc.contributor.authorStorheim, Kjersti
dc.contributor.authorBakland, Gunnstein
dc.contributor.authorBrox, Jens Ivar
dc.contributor.authorGrøvle, Lars
dc.contributor.authorMarchand, Gunn Hege
dc.contributor.authorAndersen, Erling
dc.contributor.authorAssmus, Jörg
dc.contributor.authorEspeland, Ansgar
dc.coverage.spatialNorwayen_US
dc.date.accessioned2022-10-03T09:36:09Z
dc.date.available2022-10-03T09:36:09Z
dc.date.created2022-08-17T16:03:09Z
dc.date.issued2022-07-22
dc.identifier.citationBMC Musculoskeletal Disorders. 2022, 23 .en_US
dc.identifier.issn1471-2474
dc.identifier.urihttps://hdl.handle.net/11250/3023274
dc.description.abstractBackground: Modic Changes (MCs) in the vertebral bone marrow were related to back pain in some studies but have uncertain clinical relevance. Difusion weighted MRI with apparent difusion coefcient (ADC)-measurements can add information on bone marrow lesions. However, few have studied ADC measurements in MCs. Further studies require reproducible and valid measurements. We expect valid ADC values to be higher in MC type 1 (oedema type) vs type 3 (sclerotic type) vs type 2 (fatty type). Accordingly, the purpose of this study was to evaluate ADC values in MCs for interobserver reproducibility and relation to MC type. Methods: We used ADC maps (b 50, 400, 800 s/mm2) from 1.5T lumbar spine MRI of 90 chronic low back pain patients with MCs in the AIM (Antibiotics In Modic changes)-study. Two radiologists independently measured ADC in fxed-sized regions of interests. Variables were MC-ADC (ADC in MC), MC-ADC% (0%=vertebral body, 100%=cere‑brospinal fuid) and MC-ADC-ratio (MC-ADC divided by vertebral body ADC). We calculated mean diference between observers ± limits of agreement (LoA) at separate endplates. The relation between ADC variables and MC type was assessed using linear mixed-effects models and by calculating the area under the receiver operating characteristic curve (AUC). Results: The 90 patients (mean age 44 years; 54 women) had 224 MCs Th12-S1 comprising type 1 (n=111), type 2 (n=91) and type 3 MC groups (n=22). All ADC variables had higher predicted mean for type 1 vs 3 vs 2 (p<0.001 to 0.02): MC-ADC (10−6 mm2/s) 1201/796/576, MC-ADC% 36/21/14, and MC-ADC-ratio 5.9/4.2/3.1. MC-ADC and MC ADC% had moderate to high ability to discriminate between the MC type groups (AUC 0.73–0.91). MC-ADC-ratio had low to moderate ability (AUC 0.67–0.85). At L4-S1, widest/narrowest LoA were for MC-ADC 20±407/12±254, MC-ADC% 1.6±18.8/1.4±10.4, and MC-ADC-ratio 0.3±4.3/0.2±3.9. Diference between observers >50% of their mean value was less frequent for MC-ADC (9% of MCs) vs MC-ADC% and MC-ADC-ratio (17–20%). Conclusions: The MC-ADC variable (highest mean ADC in the MC) had best interobserver reproducibility, discriminated between MC type groups, and may be used in further research. ADC values difered between MC types as expected from previously reported MC histology.en_US
dc.description.sponsorshipOpen access funding provided by University of Bergen. This study was funded by KLINBEFORSK (grant no. 2017–201), the Western Norway Regional Health Authority (grant nos. HV 911891 and HV 911938), and the South East Norway Regional Health Authority (grant no. 2015–090).en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.relation.ispartofseriesBMC Musculoskeletal Disorders;23, Article number: 695 (2022)
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectMR-imagingen_US
dc.subjectSpinesen_US
dc.subjectImaging sequencesen_US
dc.subjectAdultsen_US
dc.subjectSkeletal-axial spondyloarthritisen_US
dc.subjectObserver performancesen_US
dc.titleApparent diffusion coefficient values in Modic changes – interobserver reproducibility and relation to Modic typeen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s) 2022en_US
dc.source.articlenumber695en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttps://doi.org/10.1186/s12891-022-05610-4
dc.identifier.cristin2043937
dc.source.journalBMC Musculoskeletal Disordersen_US
dc.source.volume23en_US
dc.source.pagenumber12en_US
dc.relation.projectKLINBEFORSK: 2017–201en_US
dc.relation.projectHelse Vest: 911891en_US
dc.relation.projectHelse Vest: 911938en_US
dc.relation.projectHelse Sørøst: 2015–090en_US


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