Session Information
Session Type: ACR Poster Session B
Session Time: 9:00AM-11:00AM
Background/Purpose: Chylomicrons, with apolipoprotein (apo) B48 as a structural protein, induce leukocyte and complement activation and contribute to atherosclerosis. ApoB48 is higher in conditions associated with a higher degree of systemic inflammation and apoB48 helps to identify patients at increased cardiovascular risk. There are no data available on apoB48 levels in rheumatoid arthritis (RA) in relation to atherosclerosis. Since classical risk factors do not predict the cardiovascular risk well in RA, search for novel markers of risk is relevant. The objective of this study was to investigate the levels of apoB48 in RA patients compared to patients with coronary artery disease (CAD) and its association with metabolic and other lipid parameters, carotid intima media thickness (cIMT) and the estimated cardiovascular risk.
Methods: RA patients, without the presence of clinical cardiovascular disease or diabetes mellitus and participating in the FRANCIS study, were included. Also subjects with CAD (CAD+) and without RA were included. Blood samples were collected after an overnight fast and a complete lipid profile, including total plasma apoB and apoB48 (ELISA) were measured. cIMT was measured using ultrasound.
Results: 328 Patients with RA and 56 CAD+ patients were included. RA patients were younger (53±11 vs. 68±11 yrs; P<0.001), more often female (68% vs. 34%; P<0.001) and had lower remnant cholesterol (remnant-C) concentrations (0.52±0.26 vs. 0.75±34 mmol/l; P<0.001) and triglycerides (1.25±0.88 vs. 1.83±1.12 mmol/l; P<0.001) compared to CAD+ patients. Median apoB48 was significantly higher in RA patients compared to CAD+ patients (8.6 [IQR 5.2-12.5] vs. 7.1 [IQR 4.9-10.4] mg/L; P=0.026). In RA apoB48 correlated positively with triglycerides (r=0.616; P<0.001), remnant-C (r=0.479; P<0.001), LDL-cholesterol (r=0.123; P=0.03) and the cardiovascular risk score according to the SCORE model (r=0,141; P=0.011). No significant correlation between apoB48 and cIMT (r=0.103; P=0.07), BMI (r=0.014; P=0.81), systolic blood pressure (r=0.095; P=0.09), glucose (r=0.106; p=0.06)and RA DAS28 (-0.32; P=0.58) was found.
Conclusion: In RA apoB48 is associated with an increased cardiovascular risk score and may contribute to the increased atherogenesis of RA. Since apoB48 in RA was higher compared to CAD+ patients, despite lower triglycerides and remnant-C, chylomicron remnant clearance may be impaired in RA.
To cite this abstract in AMA style:
van Breukelen-van der Stoep D, van Zeben D, de Vries M, Klop B, van der Meulen N, van de Geijn GJ, Janssen H, Valdivielso P, Rioja J, Ramirez-Bollero J, Hazes M, Birnie E, Castro Cabezas M. Plasma Apolipoprotein B48 Levels in Patients with Rheumatoid Arthritis: Evaluating Novel Cardiovascular Risk Factors [abstract]. Arthritis Rheumatol. 2015; 67 (suppl 10). https://acrabstracts.org/abstract/plasma-apolipoprotein-b48-levels-in-patients-with-rheumatoid-arthritis-evaluating-novel-cardiovascular-risk-factors/. Accessed .« Back to 2015 ACR/ARHP Annual Meeting
ACR Meeting Abstracts - https://acrabstracts.org/abstract/plasma-apolipoprotein-b48-levels-in-patients-with-rheumatoid-arthritis-evaluating-novel-cardiovascular-risk-factors/