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We conducted a national in-depth analysis including pharmacovigilance reports and clinical study to assess the reporting rate (RR) and to determine the clinical profile of polymyalgia rheumatica (PMR) and giant cell arteritis (GCA) in COVID-19-vaccinated individuals. First, based on the French pharmacovigilance database, we estimated the RR of PMR and GCA cases in individuals aged over 50 who developed their initial symptoms within one month of receiving the BNT162b2 mRNA, mRNA-1273, ChAdOx1 nCoV-19, and Ad26.COV2.S vaccines. We then conducted a nationwide survey to gather clinical profiles, therapeutic management, and follow-up data from individuals registered in the pharmacovigilance study. A total of 70 854 684 COVID-19 vaccine doses were administered to 25 260 485 adults, among which, 179 cases of PMR (RR 7. 1 cases/1 000 000 persons) and 54 cases of GCA (RR 2. 1 cases/1 000 000 persons) have been reported. The nationwide survey allowed the characterization of 60 PMR and 35 GCA cases. Median time to the onset of first symptoms was 10 (range 2-30) and 7 (range 2-25) days for PMR and GCA, respectively. Phenotype, GCA-related ischemic complications and -large vessel vasculitis as well as therapeutic management and follow-up seemed similar according to the number of vaccine shots received and when compared to the literature data of unvaccinated population. Although rare, the short time between immunization and the onset of first symptoms of PMR and GCA suggests a temporal association. Physician should be aware of this potential vaccine-related phenomenon.
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http://dx.doi.org/10.1080/21645515.2024.2334084 | DOI Listing |
J Intern Med
September 2025
Université Paris-Saclay, UVSQ, Inserm CESP U1018, Gustave Roussy, Villejuif, France.
Objectives: To assess the association between infections, assessed by antibiotic reimbursement, and the occurrence of giant cell arteritis (GCA) and/or polymyalgia rheumatica (PMR).
Methods: We conducted a nested case-control study from the French cohort E3N-European Prospective Investigation into Cancer and Nutrition, which has followed 98,995 women since 1990. Cases, defined as patients who developed GCA and/or PMR during follow-up, were matched with 20 controls on age and vital status.
Front Immunol
August 2025
Department of Rheumatology, National Institute of Geriatrics, Rheumatology and Rehabilitation, Warsaw, Poland.
Giant cell arteritis (GCA) is an immune-mediated vasculitis predominantly affecting individuals aged 50 years and older, with clinical manifestations often overlapping with polymyalgia rheumatica (PMR). Despite advances in imaging and the advent of novel steroid-sparing agents, such as tocilizumab, challenges persist in accurately diagnosing and monitoring disease activity. Traditional inflammatory markers like C-reactive protein and erythrocyte sedimentation rate are frequently limited by their inability to fully capture disease dynamics, especially in patients receiving IL-6 inhibitors.
View Article and Find Full Text PDFSemin Arthritis Rheum
August 2025
Division of Rheumatology, Department of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address:
Objective: There is a need for better tools to monitor disease activity in giant cell arteritis (GCA). Prior studies demonstrated that vascular enhancement on cranial vessel wall magnetic resonance imaging (vw-MRI) decreases with treatment of GCA, but whether enhancement increases during relapse is not well known. This study examined changes on vw-MRI during relapse of cranial GCA.
View Article and Find Full Text PDFSemin Arthritis Rheum
August 2025
Objective: The increasing use of imaging techniques, particularly 18F-FDG PET-CT, together with autopsy findings, has significantly expanded our understanding of the clinical spectrum of giant cell arteritis (GCA). This study aimed to assess the frequency and spectrum of non-classical manifestations and other infrequent complications of the disease METHODS: This retrospective study analyzed a consecutive cohort of 174 patients with proven GCA diagnosed between 2005 and 2024.
Results: Among 174 GCA patients, 52 (29.
Ir J Med Sci
August 2025
Department of Ophthalmology, Royal Victoria Eye and Ear Hospital, Dublin, Ireland.
Background: Giant cell arteritis (GCA) is systemic vasculitis affecting medium and large-sized arteries that can result in vision-threatening complications. Temporal artery biopsy (TAB) has long been considered the gold standard method for diagnosing GCA; however, Doppler ultrasound offers a non-invasive alternative.
Objective: This study aims to evaluate the accuracy of Doppler ultrasound in comparison to TAB for diagnosing patients with suspected GCA and to determine its impact on treatment decisions.