# Relationship between ultrasound damage score of peripheral entheses and spinal bone formation in long-standing radiographic axial spondyloarthritis

**Authors:** Anna Deminger, Mats Geijer, Magnus Hallström, Lennart T H Jacobsson, Helena Forsblad-d’Elia

PMC · DOI: 10.1136/rmdopen-2025-006388 · RMD Open · 2026-03-04

## TL;DR

This study explores how damage at peripheral entheses, measured by ultrasound, relates to spinal bone formation in patients with long-standing axial spondyloarthritis.

## Contribution

The study identifies sex and age-related differences in the association between peripheral entheses damage and spinal bone formation in axial spondyloarthritis.

## Key findings

- Structural lesions at peripheral entheses are common in long-standing axial spondyloarthritis and increase with age.
- The association between ultrasound damage scores and spinal bone formation is stronger in males and diminishes with older age.
- Adjusting for symptom duration shows a significant association between ultrasound damage scores and spinal bone formation in males.

## Abstract

To assess structural changes at peripheral entheses and the association with spinal bone formation in patients with long-standing radiographic axial spondyloarthritis (r-axSpA) overall and stratified by sex.

Peripheral entheses were examined cross-sectionally using ultrasound (US) in patients fulfilling the modified New York criteria for ankylosing spondylitis (AS) and assessed for Outcome Measures in Rheumatology consensus-based structural lesions (enthesophytes, calcifications and erosions) summed to a damage US score (0–42). Spinal radiographs were graded with the modified Stoke AS Spinal Score (mSASSS). Associations between US damage score and mSASSS were assessed with negative binomial regression analyses overall, by sex and by age quartiles.

US was performed in 173 patients, 54% males, with a mean (SD) age of 55 (13) years and symptom duration of 29 (13) years. The prevalence of any structural US lesion was 92%. The US damage score was higher in males than females (mean (SD) 4.7 (3.0) versus 3.3 (2.4), p<0.001) and increased significantly with age, as did mSASSS. Univariate associations between US damage score and mSASSS were found overall and in males, but diminished with older age. The association remained significant for males when the multivariable model was adjusted for symptom duration (rate ratio (95% CI) for log-transformed mSASSS+1: 1.32 (1.04 to 1.67)). Overall, mSASSS was not associated with the US damage score when the multivariable model was adjusted for age or symptom duration.

Structural lesions at the peripheral entheses are common in long-standing r-axSpA and accumulate with age, which may obscure the possible association with spinal bone formation.

## Linked entities

- **Diseases:** ankylosing spondylitis (MONDO:0005306)

## Full-text entities

- **Genes:** HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** psoriasis (MESH:D011565), ankylosis of the spine (MESH:D000844), Osteoarthritis (MESH:D010003), PsA (MESH:D015535), Chronic Inflammatory Diseases (MESH:D002908), lesions (MESH:D009059), IBD (MESH:D015212), ectopic bone formation (MESH:D000072717), AS (MESH:D013167), dementia (MESH:D003704), calcification (MESH:D002114), AxSpA (MESH:D000089183), Stoke (MESH:D000219), fibromyalgia (MESH:D005356), osteoporosis (MESH:D010024), bursitis (MESH:D002062), sacroiliitis (MESH:D058566), Erosion (MESH:D014077), Enthesitis (MESH:D001171), DISH (MESH:D004057), metabolic syndrome (MESH:D024821), arthritis (MESH:D001168), inflammation (MESH:D007249), IBP (MESH:D001416), impairment of physical function (MESH:D059445)
- **Chemicals:** TNFi (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12970138/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12970138/full.md

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Source: https://tomesphere.com/paper/PMC12970138