Large vessel vasculitis is a risk factor for relapse only in giant cell arteritis patients without polymyalgia rheumatica

Author:

Moreel Lien12ORCID,Betrains Albrecht12ORCID,Boeckxstaens Lennert34,Molenberghs Geert5,Van Laere Koen34,De Langhe Ellen678ORCID,Vanderschueren Steven128,Blockmans Daniel128ORCID

Affiliation:

1. Department of General Internal Medicine, UZ Leuven , Leuven, Belgium

2. Department of Microbiology, Immunology, and Transplantation, KU Leuven , Leuven, Belgium

3. Department of Nuclear Medicine, UZ Leuven , Leuven, Belgium

4. Department of Imaging and Pathology, Nuclear Medicine and Molecular Imaging, KU Leuven , Leuven, Belgium

5. Interuniversity Institute for Biostatistics and Statistical Bioinformatics (I-BioStat), KU Leuven and Hasselt University , Leuven, Belgium

6. Department of Rheumatology, UZ Leuven , Leuven, Belgium

7. Department of Development and Regeneration, KU Leuven , Leuven, Belgium

8. European Reference Network for Immunodeficiency, Autoinflammatory, Autoimmune and Pediatric Rheumatic Disease (ERN-RITA) , Utrecht, The Netherlands

Abstract

Abstract Objectives To evaluate differences in presentation and outcome of GCA patients with and without large vessel vasculitis (LVV) and according to the extent and severity of LVV. Methods Consecutive patients diagnosed with GCA between 2003 and 2020 who have had FDG PET imaging at diagnosis ≤3 days after initiation of glucocorticoids (GC) and followed for ≥12 months at the University Hospitals Leuven (Belgium) were included retrospectively. PET scans were visually scored (0–3) in seven vascular areas and a total vascular score (TVS) was calculated. LVV was defined as FDG uptake ≥2 in any large vessel. Results We included 238 GCA patients, of which 169 (71%) had LVV. LVV patients were younger (69 vs 74 years, P < 0.001) and more frequently female (72% vs 49%, P = 0.001). In patients without PMR symptoms, the presence of LVV was associated with relapse (aOR 3.05 [95% CI 1.32–7.43], P = 0.011) and with a lower probability of stopping GC (aHR 0.59 [95% CI 0.37–0.94], P = 0.025). However, in those with PMR symptoms, there was no difference in relapse risk (aOR 1.20 [95% CI 0.53–2.66], P = 0.657) and in the probability of stopping GC (aHR 1.25 [95% CI 0.75–2.09], P = 0.394) between patients with and without LVV. A higher TVS was associated with an increased risk of relapse (aOR 1.09 [95% CI 1.04–1.15], P = 0.001) in patients without PMR symptoms, but not in those with PMR symptoms (aOR 1.01 [95% CI 0.96–1.07], P = 0.693). Conclusion LVV is a risk factor for relapse in GCA patients without PMR symptoms with a higher relapse risk in those with higher TVS.

Publisher

Oxford University Press (OUP)

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