Update on giant cell arteritis (GCA)

Published on November 30, 2025   28 min

A selection of talks on Cardiovascular & Metabolic

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0:00
Hello and welcome to Update on Giant Cell Arteritis. My name is Alison Clifford, and I'm a rheumatologist and associate professor at the University of Alberta in Edmonton, Canada. In 2018, we produced a talk on giant cell arteritis or GCA, including an overview of the epidemiology, proposed pathogenesis, clinical features, and an approach to diagnosis and treatment. There've been a number of exciting advances in this disease. Today, we will review some of the major updates that have taken place.
0:29
First, with respect to disclosures, I've participated as a site investigator in clinical trials with Abbvie, and I've received honorarium in the past from UCB to my institution.
0:40
The objectives for today's talk are as follows. First, we will review the new classification criteria for GCA and discuss the implications of this work. Next, we'll discuss updates in advances in imaging for GCA. Then lastly, we'll consider new information available regarding the natural history and prognosis of GCA, and advances in treatment options.
1:03
In 2022, new classification criteria for identifying giant cell arteritis patients for research, were published and endorsed by the American College of Rheumatology and EULAR, together. This represents an important advance in GCA research to the previously available 1990 classification criteria, which frequently excluded GCA patients with predominantly large vessel disease. The 2022 criteria stipulate that for inclusion, patients must be 50 years or older at diagnosis, and a weighted score is provided to assess the presence of a variety of clinical, laboratory, imaging, or biopsy markers of disease, such as outlined here. As compared to the 1990 version, the 2022 version includes points for symptoms of polymyalgia rheumatica, assesses for the presence of elevated CRP, which is more commonly clinically available than ESR now, and importantly, emphasizes the role of imaging in addition to a biopsy for disease confirmation, including temporal artery ultrasound, imaging evidence of bilateral axillary artery involvement, or PET uptake consistent with aortitis. These updated criteria were validated in an independent dataset of over 400 patients, roughly half of whom had GCA and half of whom had other vasculitides or mimics. The new criteria were found to have an improved sensitivity of 87% over the 1990 criteria, with a similarly high specificity of 94.8%.

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