AI Article Synopsis

  • The study examines the effect of HLA-B27 status on MRI findings in the sacroiliac joint among patients with chronic low back pain who do not have inflammatory conditions.
  • It analyzes data from 139 non-axSpA patients, scoring for various lesions and comparing results based on HLA-B27 positivity and sex.
  • The findings indicate that HLA-B27 status does not significantly affect the presence or severity of lesions in either men or women with low back pain of non-inflammatory origin.

Article Abstract

Objective: The assessment of inflammatory and structural lesions in the sacroiliac joint (SIJ) is crucial in axial spondyloarthritis (axSpA). HLA-B27 status plays an important role in axSpA diagnosis and has been linked to MRI lesion burden in the general population. We aimed to investigate the sex-specific influence of HLA-B27 status on inflammatory and structural MRI findings in patients with low back pain of non-inflammatory origin.

Methods: This post hoc analysis included 139 non-axSpA patients (90 women) with chronic low back pain. Two readers scored MRIs of the SIJ for the presence of sclerosis, erosion, fat metaplasia, bone marrow oedema (BMO) and ankylosis. Frequencies and extent of lesions were compared regarding the HLA-B27 status using χ tests and t-tests. Regression models to assess the sex-dependent influence of HLA-B27 on lesion burden were computed.

Results: HLA-B27 was positive in 33 women (36.7%) and 23 men (46.9%). The overall occurrence of all SIJ lesions did not differ in HLA-B27 negative and positive individuals. There were no significant differences in the extent of lesions considering the HLA-B27 positivity, for erosion (mean sum score (MSS) of 0.91 vs 0.48; p=0.144), sclerosis (MSS 1.65 vs 1.88; p=0.576), fat metaplasia (MSS 0.56 vs 0.27; p=0.425), BMO (MSS 0.75 vs 0.59; p=0.460) and ankylosis (MSS 0.06 vs 0.04; p=0.659).

Conclusion: HLA-B27 status has no significant influence on the occurrence and extent of SIJ lesions in patients with low back pain of non-inflammatory origin in either men or women.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533781PMC
http://dx.doi.org/10.1136/rmdopen-2023-003357DOI Listing

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