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Assessment of structural lesions in sacroiliac joints enhances diagnostic utility of MRI in early spondyloarthritis


Weber, U; Lambert, R G W; Pedersen, S J; Hodler, J; Ostergaard, M; Maksymowych, W P (2010). Assessment of structural lesions in sacroiliac joints enhances diagnostic utility of MRI in early spondyloarthritis. Arthritis Care and Research, 62(12):1763-1771.

Abstract

OBJECTIVE:: We aimed to compare the diagnostic utility of T1-weighted (T1w) and STIR MRI sequences in early spondyloarthritis (SpA) using a standardized approach to the evaluation of sacroiliac joints (SIJ) and to test whether systematic calibration of readers directed at recognition of abnormalities on T1w MRI would enhance diagnostic utility. METHODS:: Six readers independently assessed T1w and STIR MRI scans of the SIJ from 187 subjects: 75 AS and 27 preradiographic IBP patients; 26 mechanical back pain and 59 healthy volunteer controls aged </=45 years. The exercise was repeated 6 months later on a random selection of 30 AS patients and 34 controls after calibration directed at lesions visible on T1w MRI. Specific MRI lesions were recorded according to standardized definitions. In addition to deciding on the presence/absence of SpA readers were asked which MRI sequence and which type of lesion was the primary basis for their diagnostic conclusion. RESULTS:: Structural lesions were detected in 98% of AS and in 64% of IBP patients. A diagnosis of SpA was based on T1w or combined T1w/STIR sequences in 82% of AS and 41% of IBP patients. Calibration enhanced diagnostic utility of MRI in the majority of readers, especially those considered less experienced; mean (of 6 readers) pre-calibration likelihood ratio (LR) (+/-) was 14.5/0.08 and post-calibration was 22.2/0.02. CONCLUSION:: Recognition of structural lesions on T1w MRI contributes significantly to its diagnostic utility in early SpA. Rheumatologist training directed at detection of lesions visible on T1w MRI enhances diagnostic utility.

Abstract

OBJECTIVE:: We aimed to compare the diagnostic utility of T1-weighted (T1w) and STIR MRI sequences in early spondyloarthritis (SpA) using a standardized approach to the evaluation of sacroiliac joints (SIJ) and to test whether systematic calibration of readers directed at recognition of abnormalities on T1w MRI would enhance diagnostic utility. METHODS:: Six readers independently assessed T1w and STIR MRI scans of the SIJ from 187 subjects: 75 AS and 27 preradiographic IBP patients; 26 mechanical back pain and 59 healthy volunteer controls aged </=45 years. The exercise was repeated 6 months later on a random selection of 30 AS patients and 34 controls after calibration directed at lesions visible on T1w MRI. Specific MRI lesions were recorded according to standardized definitions. In addition to deciding on the presence/absence of SpA readers were asked which MRI sequence and which type of lesion was the primary basis for their diagnostic conclusion. RESULTS:: Structural lesions were detected in 98% of AS and in 64% of IBP patients. A diagnosis of SpA was based on T1w or combined T1w/STIR sequences in 82% of AS and 41% of IBP patients. Calibration enhanced diagnostic utility of MRI in the majority of readers, especially those considered less experienced; mean (of 6 readers) pre-calibration likelihood ratio (LR) (+/-) was 14.5/0.08 and post-calibration was 22.2/0.02. CONCLUSION:: Recognition of structural lesions on T1w MRI contributes significantly to its diagnostic utility in early SpA. Rheumatologist training directed at detection of lesions visible on T1w MRI enhances diagnostic utility.

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Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > University Hospital Zurich > Clinic for Diagnostic and Interventional Radiology
04 Faculty of Medicine > Balgrist University Hospital, Swiss Spinal Cord Injury Center
Dewey Decimal Classification:610 Medicine & health
Scopus Subject Areas:Health Sciences > Rheumatology
Language:English
Date:December 2010
Deposited On:01 Oct 2010 14:37
Last Modified:28 Jun 2022 10:24
Publisher:Wiley-Blackwell
ISSN:2151-464X
OA Status:Hybrid
Publisher DOI:https://doi.org/10.1002/acr.20312
PubMed ID:20665745
  • Content: Accepted Version