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Published on: February 8, 2019
Subclinical giant cell arteritis increases the risk of relapse in polymyalgia rheumatica
Eugenio De Miguel1, Rositsa Karalilova2, Pierluigi Macchioni3
1Rheumatology, La Paz University Hospital, Madrid, Spain eugenio.demiguel@gmail.com.
Objective:
The aim of the present study was to determine the clinical significance of subclinical giant cell arteritis (GCA) in polymyalgia rheumatica (PMR) and ascertain its optimal treatment approach.
Methods:
Patients with PMR who fulfilled the 2012 European Alliance of Associations for Rheumatology/American College of Rheumatology Provisional Classification Criteria for PMR, did not have GCA symptoms and were routinely followed up for 2 years and were stratified into two groups, according to their ultrasound results: isolated PMR and PMR with subclinical GCA. The outcomes (relapses, glucocorticoid use and disease-modifying antirheumatic drug treatments) between groups were compared.
Results:
We included 150 patients with PMR (50 with subclinical GCA) with a median (IQR) follow-up of 22 (20-24) months. Overall, 47 patients (31.3 %) had a relapse, 31 (62%) in the subclinical GCA group and 16 (16%) in the isolated PMR group (p<0.001). Among patients with subclinical GCA, no differences were found in the mean (SD) prednisone starting dosage between relapsed and non-relapsed patients (32.4±15.6 vs 35.5±12.1 mg, respectively, p=0.722). Patients with subclinical GCA who relapsed had a faster prednisone dose tapering in the first 3 months compared with the non-relapsed patients, with a mean dose at the third month of 10.0±5.2 versus 15.2±7.9 mg daily (p<0.001). No differences were found between relapsing and non-relapsed patients with subclinical GCA regarding age, sex, C reactive protein and erythrocyte sedimentation rate.
Conclusions:
Patients with PMR and subclinical GCA had a significantly higher number of relapses during a 2-year follow-up than patients with isolated PMR. Lower starting doses and rapid glucocorticoid tapering in the first 3 months emerged as risk factors for relapse.
Insights
Polymyalgia rheumatica (PMR) patients with subclinical giant cell arteritis (GCA) experience more relapses. Lower initial glucocorticoid doses and rapid tapering increase relapse risk in PMR with subclinical GCA.
Area of Science:
- Rheumatology
- Internal Medicine
- Clinical Immunology
Background:
- Polymyalgia rheumatica (PMR) is a common inflammatory condition.
- Giant cell arteritis (GCA) can be present subclinically in PMR patients.
- Identifying subclinical GCA in PMR is crucial for optimal management.
Purpose of the Study:
- To evaluate the clinical significance of subclinical GCA in PMR patients.
- To determine the optimal treatment strategy for PMR with subclinical GCA.
- To compare outcomes between isolated PMR and PMR with subclinical GCA.
Main Methods:
- 150 PMR patients were classified into isolated PMR or PMR with subclinical GCA groups based on ultrasound.
- Patients were followed for 2 years, monitoring relapses and treatment.
- Outcomes including glucocorticoid use and DMARDs were compared between groups.
Main Results:
- Patients with subclinical GCA had a significantly higher relapse rate (62%) compared to isolated PMR (16%).
- Lower initial prednisone doses and rapid tapering within 3 months were associated with relapses in subclinical GCA.
- No differences in age, sex, CRP, or ESR were found between relapsing and non-relapsing subclinical GCA patients.
Conclusions:
- Subclinical GCA in PMR patients leads to a significantly higher risk of relapses.
- Lower starting glucocorticoid doses and accelerated tapering in the first 3 months are risk factors for relapse.
- These findings highlight the importance of tailored glucocorticoid management in PMR with subclinical GCA.
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