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AB1330 (2024)
PREVALENCE OF CAROTID ATHEROSCLEROSIS IN PATIENTS WITH GIANT CELL ARTERITIS
Keywords: Ultrasound, Cardiovascular diseases, Atherosclerosis, Imaging
J. Fernandes Serodio1,2, C. Saca1, F. Batista1,2, F. Seguro Paula1,2, S. Oliveira1, J. Delgado Alves1,2
1Hospital Prof. Doutor Fernando Fonseca, Unit for Systemic Immune-Mediated Diseases (UDIMS), Amadora, Portugal
2Nova Medical School, Immune Response and Vascular Disease Group, Lisbon, Portugal

Background: Giant Cell Arteritis (GCA) is the most frequent vasculitis in patients older than 50 years-old. Increasing use of imaging tools for the diagnosis of GCA led to recognition of extracranial Large-Vessel (LV-GCA) involvement in a significant proportion of patients. Around two-thirds of patients with GCA are reported to have extracranial LV-GCA [1,2]. GCA phenotypes may vary according to age at diagnosis, with cranial manifestations being more prominent in older patients and LV-GCA more frequent in patients younger than 65 years-old [3]. Atherosclerosis is highly prevalent among patients with an advanced age. However, little is known about the coexistence of these two vascular diseases.


Objectives: The aim of this work is to describe the prevalence of atherosclerosis in patients with GCA.


Methods: Thirty-eight patients with GCA followed at our vasculitis clinic were included. GCA was diagnosed according to local imaging protocol with subsequent Vascular Ultrasound (VUS) followed by FDG-Positron Emission Tomography (PET-FDG). VUS protocol includes the systematic assessment of the following artery territories: common carotid, proximal internal and external carotid, vertebral, subclavian, axillary and temporal. VUS was also used to assess for the presence of carotid atherosclerotic plaques. Patients with GCA were compared with a 38 Polymialgia Rheumatica (PMR) patients and 80 controls, matched for age and sex. GCA was also subclassified as Cranial (C-GCA, only cranial vessels involved), or Large-Vessel (LV-GCA when any degree of extracranial Large Arteries were involved).


Results: Patients with GCA included were diagnosed at age of 71 (65-79) years, 21/38 were male. GCA was newly diagnosed in 31 and relapsing in 7 patients at the time of VUS. Regarding disease phenotype, 27 (71%) of patients had LV-GCA and 11 (29%) had C-GCA. The occurrence of other cardiovascular risk factors was not different among groups, although there was a trend towards lower prevalence of diabetes mellitus among patients with GCA (Table 1). The prevalence of carotid atherosclerotic plaque in GCA patients was of 17/38 (45%), which was not different from PMR (53%, p=0,491) and from controls (59%, p=0,153). The presence of carotid plaques in C-GCA patients was of 9/11 (82%), whereas in LV-GCA was of 8/27 (30%, p=0,005). As shown in Table 2, C-GCA was more frequent in older age >75 years-old 6/11 (55%) and LV-GCA in younger ≤ 75 years-old 19/24 (79%), although without statistical significance (p=0,142).


Conclusion: In our study cohort, the prevalence of carotid atherosclerotic plaques was considerable in GCA and only slightly inferior to PMR and controls. There was an association between the GCA phenotype and the presence of carotid plaques, but not with the age at diagnosis. These results should be validated in larger cohorts.


REFERENCES: [1] Prieto-González S, et al. Ann Rheum Dis. 2012; 71(7):1170-6.

[2] Förster S, et al. Vasa 2011; 40(3):219-27.

[3] Monti S, et al. Ann Rheum Dis. 2023; 82(8):1098-1106.

Comparison of GCA with PMR and controls---

GCA PMR p-value Controls p-value
n 38 38 80
Female 17 (45%) 15 (40%) 0,642 43 (54%) 0,432
Age 73 (67-79) 75 (69-81) 0,183 71 (65-79) 0,689
Age >75 years-old 14 (37%) 18 (47%) 0,353 33 (41%) 0,648
Hypertension 28 (74%) 28 (74%) 0,999 55 (69%) 0,583
Diabetes mellitus 6 (16%) 13 (34%) 0,111 26 (33%) 0,056
Hyperlipidemia 27 (71%) 15 (40%) 0,006 47 (59%) 0,197
Smoking 10 (26%) 6 (15%) 0,188 19 (24%) 0,624
Previous MI 1 (3%) 5 (13%) 0,200 9 (11%) 0,164
Previous stroke 2 (5%) 5 (13%) 0,215 7 (9%) 0,399
Peripheral artery disease 0 0 - 3 0,308
Carotid IMT 0,80 (0,70-1,00) 0,70 (0,70-0,90) 0,251 0,80 (0,70-0,90) 0,230
Carotid plaque 17 (45%) 20 (53%) 0,491 47 (59%) 0,153

Comparison between LV-GCA and C-GCA-

LV-GCA C-GCA p-value
n 27 11
Female 14 (52%) 3 (27%) 0,153
Age 70 (62-78) 79 (69-83) 0,154
Age >75 years-old 8 (30%) 6 (55%) 0,149
Hypertension 20 (74%) 8 (73%) 0,615
Diabetes mellitus 3 (11%) 3 (27%) 0,221
Hyperlipidemia 17 (63%) 10 (90%) 0,088
Smoking 8 (29%) 2 (18%) 0,837
Carotid plaque 8 (30% ) 9 (82% ) 0,005

Acknowledgements: NIL.


Disclosure of Interests: João Fernandes Serodio Novartis, Carolina Saca: None declared, Frederico Batista: None declared, Filipe Seguro Paula: None declared, Susana Oliveira: None declared, Jose Delgado Alves Novartis, Lilly, AbbVie.


DOI: 10.1136/annrheumdis-2024-eular.6321
Keywords: Ultrasound, Cardiovascular diseases, Atherosclerosis, Imaging
Citation: , volume 83, supplement 1, year 2024, page 2015
Session: Vasculitis, large vessels including polymyalgia rheumatica (Publication Only)