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Abstract Number: 2435

Prevalence Of Inflammatory Lesions MRI-Spine In Patients With Chronic Back Pain Of ≤2 Years Duration Included In The SPACE-Cohort

Manouk de Hooge1, Rosaline van den Berg2, Monique Reijnierse3, Victoria Navarro-Compán2, Floris van Gaalen2, Karen Fagerli4, Maureen C. Turina5, Maikel van Oosterhout6, Roberta Ramonda7, Tom Huizinga2 and Désirée van der Heijde8, 1Leiden University Medical Center, Leiden, Netherlands, 2Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 3Radiology, Leiden University Medical Center, Leiden, Netherlands, 4Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 5Department of Clinical Immunology and Rheumatology, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 6Rheumatology, GHZ Hospital, Gouda, Netherlands, 7Rheumatology Unit, University of Padova, Padova, Italy, 8Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: MRI and spondylarthritis

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Session Information

Title: Spondylarthropathies and Psoriatic Arthritis: Clinical Aspects and Treatment III

Session Type: Abstract Submissions (ACR)

Background/Purpose: Inflammatory lesions of the spine are not included in the ASAS definition of a positive MRI for fulfilment of the ASAS axial spondyloarthritis (axSpA) criteria1. However, inflammatory lesions in the spine on MRI (MRI-spine) may occur in the absence of affected sacroiliac joints (SIJ). Therefore the aim of this study is to determine the prevalence of inflammatory lesions on MRI-spine and to investigate if axSpA patients with inflammatory lesions in the spine only exist.

Methods: The SPondyloArthritis Caught Early (SPACE)-cohort includes patients with chronic back pain (≥3 months, ≤2 years, onset <45 years) recruited from 5 participating centres in Europe. All patients underwent MRI of the SIJ (MRI-SI) and MRI-spine scored by 3 well-calibrated readers independently. MRI-SI were scored according to the ASAS definition1 (the presence of ≥1 lesion on ≥2 consecutive slices or the presence of >1 lesion on a single slice). Inflammatory lesions on MRI-spine suggestive of spondylitis were scored when visible on ≥2 consecutive slices and according to the ASAS/OMERACT consensus definition2 (the presence of ≥3 lesions on ≥2 consecutive slices). Lesions were considered present if 2/3 readers agreed.

Results: All patients with MRI-spine (n=306) were included to determine the prevalence of BME lesions in patients grouped according to the ASAS axSpA criteria (radiographic, non-radiographic (imaging & clinical arm), possible SpA (presence of ≥1  SpA features with a Likelihood Ratio (LR+) of ≥6 or ≥2 SpA features with a LR+ <6) and no-SpA (see table). In 292 patients MRI-SI and MRI-spine data were both available. There were 51 patients with a positive MRI-spine, of which 30 patients (58.8%) had a negative MRI-SI. Nine of these 30 patients fulfilled the ASAS axSpA criteria via the clinical-arm. Of the remaining 21 patients, 3 patients had no SpA features at all, 7 patients had 1 SpA feature, 8 patients had 2 SpA features, 1 patient had 3 SpA features and 2 patients had 4 SpA features. Only the sole patient with 4 SpA features had a probability (calculated from the LR+) ≥80%. When using the ASAS consensus definition of a positive MRI-spine in post-test probability calculations, another 6 patients would reach a probability ≥80% of having axSpA.

Conclusion: A cut-off of ≥3 BME lesions discriminates well between patients with and without axSpA. A positive MRI-spine can be present in patients without inflammation on MRI-SI. MRI-spine might have (limited) additional value to MRI-SI in a group of patients with a certain level of suspicion of axSpA.

Reference: 1Rudwaleit ARD 2009;68:1520-7 2Hermann ARD 2012;71:1278-88

MRI-Spine

 

AxSpA (ASAS axSpA)

n=126

Possible axSpA

(≥1  SpA features with LR+ ≥6 or 2 with LR+ <6)

n=116

No-SpA

n=64

Imaging-arm

n=72

Clinical-arm, n=54

 

mNY+

n=26

mNY-

n=46

BME lesion >1

12 (46.2%)

23 (50%)

17 (31.5%)

29 (25%)

17 (26.6%)

BME lesion >2

10 (38.5%)

16 (34.8%)

11 (20.4%)

21 (18.1%)

9 (14.1%)

BME lesion >3

8 (30.8%)

11 (23.9%)

3 (5.6%)

12 (10.3%)

4 (6.3%)

BME lesion >4

7 (26.9%)

7 (15.2%)

2 (3.7%)

5 (4.3%)

3 (4.7%)

BME lesion >5

6 (23.1%)

4 (8.7%)

1 (1.9%)

3 (2.6%)

2 (3.1%)

BME lesion >6

4 (15.4%)

3 (6.5%)

1 (1.9%)

2 (1.7%)

1 (1.6%)

BME lesion >7

4 (15.4%)

2 (4.3%)

1 (1.9%)

2 (1.7%)

0


Disclosure:

M. de Hooge,
None;

R. van den Berg,
None;

M. Reijnierse,
None;

V. Navarro-Compán,
None;

F. van Gaalen,
None;

K. Fagerli,
None;

M. C. Turina,
None;

M. van Oosterhout,
None;

R. Ramonda,
None;

T. Huizinga,
None;

D. van der Heijde,
None.

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