TY - JOUR
T1 - Glucocorticoid discontinuation and clinical phenotypes in patients with giant cell arteritis
T2 - A retrospective cohort study from a fast track clinic
AU - Gorlen, Tanja Fromberg
AU - Møller Døhn, Uffe
AU - Heymonet, Marie Celeste
AU - Brittain, Jane Maestri
AU - Østergaard, Mikkel
AU - Ripa, Rasmus Sejersten
AU - Hansen, Peter Riis
AU - Jacobsen, Søren
AU - Terslev, Lene
N1 - Publisher Copyright:
© The Author(s) 2026. This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
PY - 2026/1/1
Y1 - 2026/1/1
N2 - Background: Previous studies have shown that many patients with giant cell arteritis (GCA) remain on glucocorticoid (GC) therapy for several years, though mostly based on older data. Identifying predictors of successful GC tapering is increasingly relevant. Objectives: to 1) determine the probability of discontinuing GC treatment, 2) characterise clinical phenotypes within the GCA spectrum, and 3) their predictive value for successful GC discontinuation. Design: A retrospective cohort study of all patients diagnosed with GCA in our fast track Clinic (FTC) between September 2018 and December 2021. Methods: Clinical, biochemical and imaging data were obtained from patient records from the time of the FTC visit until 31.12.2023. The cumulative incidence of GC discontinuation was estimated using a competing risks model. Symptom- and laboratory-based phenotypes were identified through hierarchical cluster analysis. Results: During the study period, 172 patients were diagnosed with GCA. At baseline, 26% had a prior diagnosis of GCA or polymyalgia rheumatica (PMR). The cumulative incidence of GC discontinuation was 10% at one year, 43% at two years, 58% at three years, and 69% at four and five years after the FTC visit, respectively. Patients with prior GCA/PMR had a lower probability of discontinuing GC treatment than those with new-onset disease. Four symptom-based and three laboratory-based phenotypic clusters were identified, but none of these variables predicted successful GC discontinuation. Multivariable Fine-Gray regression confirmed that previous GCA/PMR was an independent predictor of reduced probability of GC discontinuation. Conclusions: In this real-world cohort, many patients required GC therapy for more than two years. The identified phenotypes did not predict treatment discontinuation. A previous diagnosis of GCA/PMR was associated with a persistent disease course.
AB - Background: Previous studies have shown that many patients with giant cell arteritis (GCA) remain on glucocorticoid (GC) therapy for several years, though mostly based on older data. Identifying predictors of successful GC tapering is increasingly relevant. Objectives: to 1) determine the probability of discontinuing GC treatment, 2) characterise clinical phenotypes within the GCA spectrum, and 3) their predictive value for successful GC discontinuation. Design: A retrospective cohort study of all patients diagnosed with GCA in our fast track Clinic (FTC) between September 2018 and December 2021. Methods: Clinical, biochemical and imaging data were obtained from patient records from the time of the FTC visit until 31.12.2023. The cumulative incidence of GC discontinuation was estimated using a competing risks model. Symptom- and laboratory-based phenotypes were identified through hierarchical cluster analysis. Results: During the study period, 172 patients were diagnosed with GCA. At baseline, 26% had a prior diagnosis of GCA or polymyalgia rheumatica (PMR). The cumulative incidence of GC discontinuation was 10% at one year, 43% at two years, 58% at three years, and 69% at four and five years after the FTC visit, respectively. Patients with prior GCA/PMR had a lower probability of discontinuing GC treatment than those with new-onset disease. Four symptom-based and three laboratory-based phenotypic clusters were identified, but none of these variables predicted successful GC discontinuation. Multivariable Fine-Gray regression confirmed that previous GCA/PMR was an independent predictor of reduced probability of GC discontinuation. Conclusions: In this real-world cohort, many patients required GC therapy for more than two years. The identified phenotypes did not predict treatment discontinuation. A previous diagnosis of GCA/PMR was associated with a persistent disease course.
KW - fast track clinic
KW - giant cell arteritis
KW - glucocorticoid therapy
UR - https://www.scopus.com/pages/publications/105047934956
U2 - 10.1177/1759720X261477872
DO - 10.1177/1759720X261477872
M3 - Journal article
AN - SCOPUS:105047934956
SN - 1759-720X
VL - 18
JO - Therapeutic Advances in Musculoskeletal Disease
JF - Therapeutic Advances in Musculoskeletal Disease
M1 - 1759720X261477872
ER -