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Evidence for a different anatomic basis for joint disease localization in polymyalgia rheumatica in comparison with
Helena Marzo-Ortega1, Laura A Rhodes, Ai Lyn Tan
1University of Leeds, and Chapel Allerton Hospital, Leeds, UK.
Objective:
The anatomic basis for joint disease localization in polymyalgia rheumatica (PMR) is poorly understood. This study used contrast-enhanced and fat suppression magnetic resonance imaging (MRI) to evaluate the relationship between synovial and extracapsular inflammation in PMR and early rheumatoid arthritis (RA).
Methods:
Ten patients with new-onset PMR and 10 patients with early RA underwent dynamic contrast-enhanced MRI and conventional MRI of affected metacarpophalangeal (MCP) joints. Synovitis and tenosynovitis were calculated based on the number of enhancing voxels, initial rate of enhancement, and maximal enhancement of gadolinium diethylenetriaminepentaacetic acid (Gd-DTPA). Periarticular bone erosion and bone edema were scored according to the OMERACT (Outcome Measures in Rheumatology Clinical Trials) scoring system in both groups. The degree of extracapsular Gd-DTPA enhancement was assessed in both conditions using semiquantitative scoring.
Results:
No significant differences were seen in the volume of synovitis (P = 0.294), degree of flexor tenosynovitis (P = 0.532), periarticular erosions (P = 0.579), or degree of bone edema (P = 0.143) between RA and PMR joints. However, despite comparable degrees of synovitis, the proportion of MCP joints showing extracapsular enhancement was higher in the PMR group (100%) than in the RA group (50%) (P = 0.030). One PMR patient, but none of the RA patients, had bone edema at the capsular insertion.
Conclusion:
Despite degrees of synovitis and tenosynovitis comparable with those in RA, PMR-related hand disease is associated with prominent extracapsular changes, suggesting that inflammation in these tissues is more prominent than joint synovitis, which is common in both conditions. This suggests that the anatomic basis for joint disease localization differs between RA and PMR.
Insights
Polymyalgia rheumatica (PMR) hand disease shows significant extracapsular inflammation, unlike rheumatoid arthritis (RA). This suggests different anatomical origins for joint disease in PMR and RA, despite similar synovitis levels.
Area of Science:
- Rheumatology
- Medical Imaging
- Immunology
Background:
- The anatomical basis of joint disease in polymyalgia rheumatica (PMR) is not well understood.
- Evaluating synovial and extracapsular inflammation is crucial for differentiating PMR from other inflammatory arthropathies like rheumatoid arthritis (RA).
Purpose of the Study:
- To compare synovial and extracapsular inflammation in metacarpophalangeal (MCP) joints of patients with new-onset PMR and early RA.
- To investigate the anatomical basis of joint disease localization in PMR using advanced MRI techniques.
Main Methods:
- Dynamic contrast-enhanced MRI and conventional MRI were performed on MCP joints of 10 PMR and 10 early RA patients.
- Synovitis, tenosynovitis, bone erosion, and bone edema were quantified using established scoring systems and MRI parameters.
- Extracapsular inflammation was assessed using semiquantitative scoring of gadolinium diethylenetriaminepentaacetic acid (Gd-DTPA) enhancement.
Main Results:
- No significant differences in synovitis, tenosynovitis, or bone erosion were observed between PMR and RA groups.
- A significantly higher proportion of PMR joints (100%) showed extracapsular enhancement compared to RA joints (50%).
- Bone edema at the capsular insertion was present in one PMR patient but absent in RA patients.
Conclusions:
- PMR-related hand disease is characterized by prominent extracapsular inflammation, even with comparable synovitis to RA.
- Inflammation in extracapsular tissues appears more significant in PMR than joint synovitis.
- The findings suggest distinct anatomical patterns of joint disease localization in PMR compared to RA.
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