AB0219 ASSOCIATION OF DISEASE ACTIVITY AND THE PRESENCE OF BILATERAL CAROTID PLAQUE IN RHEUMATOID ARTHRITIS PATIENTS
Annals of the rheumatic diseases(2022)
摘要
BackgroundCardiovascular (CV) disease is the major cause of death of RA patients. There is a direct association of systemic inflammation and an accelerated process of atherosclerosis, which is related to higher CV morbimortality (1). Additionally, RA patients with bilateral carotid plaque (CP) had a two-fold risk of developing a CV event compared to patients with unilateral CP (2).ObjectivesTo compare disease activity and other disease characteristics of RA patients with bilateral and unilateral CP.MethodsThis was a cross-sectional study nested of a RA patients’ cohort. We recruited RA patients who fulfilled the 2010 ACR/EULAR classification criteria. Patients with a previous CV event, another connective tissue disease, or pregnancy were excluded. Disease activity was assessed with DAS28-CRP. A carotid ultrasound was performed to all RA patients, and the presence of CP was considered as a carotid intima media thickness ≥ 1.2 mm or a focal narrowing ≥ 0.5 mm. All RA patients with bilateral CP were included in this study and matched by age (± 5 years), gender, and traditional CV risk factors to RA patients with unilateral CP by a rheumatologist blinded to clinical information. Comparisons were done with Chi-square test for qualitative variables and Student’s T test or Mann-Whitney’s U test for quantitative variables. A p-value < 0.05 was considered statistically significant.ResultsMean age of RA patients with bilateral CP was 61.98 ± 6.82 years as compared to 59.70 ± 6.74 years in patients with unilateral CP (p = NS). Demographic characteristics are shown in Figure 1. When comparing disease characteristics, we found a difference in C-reactive protein (CRP) levels, higher in patients with bilateral CP (1.06 mg/dl vs 0.64 mg/dl, p = 0.012), in disease activity assessed with DAS28-CRP as a continuous variable, higher in patients with bilateral CP (3.83 vs 3.05, p = 0.023), and as moderate-high disease activity classification, more prevalent in patients with bilateral CP (70.0% vs 43.3%, p = 0.037) (Table 1). A binary logistic regression, including traditional CV risk factors and disease activity, showed that classification of disease activity in the moderate-high activity category is an independent risk factor for the presence of bilateral CP, OR 3.18, 95% CI 1.033-9.812, p = 0.044.Table 1.Comparison of disease characteristics.VariablesRA patients with bilateral CP (n=30)RA patients with unilateral CP (n=30)p-valueDisease duration, years, median (IQR)7.86 (2.97-19.18)9.02 (6.45-13.66)NSCRP, mg/dl, median (IQR)1.06 (0.67-1.93)0.64 (0.43-1.06)0.012DAS28-CRP, mean ± SD3.83 ± 1.273.05 ± 1.320.023Moderate-high activity, n (%)21 (70.0)13 (43.3)0.037Anti-CCP, median (IQR)15.30 (3.16-196.15)115.73 (1.60-196.05)NSFR IgG, median (IQR)5.84 (2.00-17.13)5.25 (2.00-20.41)NSFR IgM, median (IQR)156.86 (27.91-200.00)197.22 (65.71-200.00)NSFR IgA, median (IQR)85.87 (13.60-200.00)46.83 (5.33-129.93)NSMTX, n (%)22 (75.9)21 (70.0)NSGC, n (%)16 (55.2)11 (36.7)NSbDMARD, n (%)3 (10.3)6 (20.0)NSNS, no significant; RA, rheumatoid arthritis; CRP, C-reactive protein; anti-CCP, anti-cyclic citrullinated peptide antibodies; RF, rheumatoid factor; MTX, methotrexate; GC, glucocorticoids; bDMARD, biologic disease modifying antirheumatic drugs.ConclusionWe found that RA patients with bilateral CP had higher levels of CRP levels, higher DAS28-CRP, and a higher prevalence of being classified in the moderate-high disease activity category, which was independently associated to the presence of bilateral CP. Emphasis should be placed on tight disease control to prevent the development of a major CV events in RA patients.References[1]Skeoch S, Bruce IN. Atherosclerosis in rheumatoid arthritis: is it all about inflammation? Nat Rev Rheumatol. 2015;11(7):390-400.[2]Evans MR, Escalante A, Battafarano DF, et al. Carotid atherosclerosis predicts incident acute coronary syndromes in rheumatoid arthritis. Arthritis Rheum. 2011;63(5):1211-20.Disclosure of InterestsNone declared
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