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Large vessel vasculitis is a risk factor for relapse only in giant cell arteritis patients without polymyalgia rheumatica.
Moreel, Lien; Betrains, Albrecht; Boeckxstaens, Lennert; Molenberghs, Geert; Van Laere, Koen; De Langhe, Ellen; Vanderschueren, Steven; Blockmans, Daniel.
Afiliación
  • Moreel L; Department of General Internal Medicine, UZ Leuven, Leuven, Belgium.
  • Betrains A; Department of Microbiology, Immunology, and Transplantation, KU Leuven, Leuven, Belgium.
  • Boeckxstaens L; Department of General Internal Medicine, UZ Leuven, Leuven, Belgium.
  • Molenberghs G; Department of Microbiology, Immunology, and Transplantation, KU Leuven, Leuven, Belgium.
  • Van Laere K; Department of Nuclear Medicine, UZ Leuven, Leuven, Belgium.
  • De Langhe E; Department of Imaging and Pathology, Nuclear Medicine and Molecular Imaging, Leuven, KU, Belgium.
  • Vanderschueren S; Interuniversity Institute for Biostatistics and Statistical Bioinformatics (I-BioStat), KU Leuven and Hasselt University, Leuven, Belgium.
  • Blockmans D; Department of Nuclear Medicine, UZ Leuven, Leuven, Belgium.
Article en En | MEDLINE | ID: mdl-39173669
ABSTRACT

OBJECTIVES:

To evaluate differences in presentation and outcome of giant cell arteritis (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 and followed for ≥12 months at the University Hospitals Leuven (Belgium), were included retrospectively. PET scans were visually scored (0-3) in 7 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 glucocorticoids (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 glucocorticoids (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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Bélgica

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Rheumatology (Oxford) Asunto de la revista: REUMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Bélgica
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