BIOLOGIC USE REGULATES THE IMPACT OF INFLAMMATION ON ISCHEMIC CARDIOVASCULAR RISK IN RHEUMATOID ARTHRITIS

G. Karpouzas, S. Ormseth, P. Van Riel, E. Myasoedova, M. A. González-Gay, A. Corrales, S. Rantapää Dahlqvist, P. Sfikakis, P. Dessein, L. Tsang, C. Hitchon, V. Pascual, I. J. Colunga-Pedraza, D. Á. Galarza-Delgado, J. R. Azpiri-López, S. Rollefstad, A. G. Semb, D. P. Misra, E. M. Hauge, G. KitasHarbor-UCLA Medical Center, Rheumatology, Torrance, United States of America The Lundquist Institute, Rheumatology, Torrance, United States of America Radboud University Medical Center, Rheumatology, Nijmegen, Netherlands Mayo Clinic Rochester MN, Rheumatology, Rochester, United States of America Marqués de Valdecilla University Hospital, Rheumatology, Santander, Spain Umeå universitet, Rheumatology, Umea, Sweden Laikon Hospital, Rheumatology, Athina, Greece University Of Witwatersrand, Rheumatology, Johannesburg, South Africa University of Manitoba, Rheumatology, Winnipeg, Canada Salvador Zubirán National Institute of Health Sciences and Nutrition, Rheumatology, Ciudad de México, Mexico Hospital Universitario Dr. José Eleuterio González, Rheumatology, Monterrey, Mexico Diakonhjemmet Hospital, Cardiology, Oslo, Norway Sanjay Gandhi Postgraduate Institute of Medical Sciences, Rheumatology, Lucknow, India Aarhus University Hospital, Rheumatology, Aarhus, Denmark Aarhus University, Rheumatology, Aarhus, Denmark The Dudley Group NHS Foundation Trust, Rheumatology, Brierley Hill, United Kingdom  Background Chronic inflammation contributes to enhanced cardiovascular risk in patients with rheumatoid arthritis (RA). Biologic disease modifying antirheumatic drugs (bDMARDs) have been shown to effectively control inflammation in many conventional synthetic DMARD non-responders and improve cardiovascular outcomes. Objectives We here explored whether baseline bDMARD use may influence the impact of disease activity and systemic inflammation on long-term cardiovascular risk in patients with RA. Methods We studied 4370 patients with RA who were free of cardiovascular disease upon registration to An International Cardiovascular Consortium for people with RA (ATACC-RA) and followed prospectively. Prespecified outcomes included (a) major adverse cardiovascular events (MACE) defined as non-fatal myocardial infarction, non-fatal stroke, or cardiovascular death and (b) any ischemic cardiovascular events (CVE) comprising MACE, coronary revascularization, stable angina pectoris, transient ischemic attack and peripheral arterial disease with or without revascularization. Missing covariate data were imputed using multiple imputation with 10 repetitions. Multivariable Cox models stratified by center evaluated the impact of disease activity [based on 28 joint counts and C-reactive protein (DAS28-CRP)], systemic inflammation (CRP), bDMARD use and their respective interactions on CVE risk after adjusting for age, gender, hypertension, diabetes, family history of CAD, smoking and total cholesterol to high-density lipoprotein ratio. Two corroborating sensitivity analyses were performed; the first included patients enrolled in the cohort on or after January 1, 2000, when bDMARD use became more prevalent among enrollees. The second used inverse probability of treatment weights (IPTW) to balance differences in bDMARD treated and untreated patients. Results Throughout 26534 patient years of follow-up, 239 first MACE and 362 total ischemic CVE were recorded. Among bDMARD nonusers, incidence of MACE and any ischemic CVE was [9.3 (95% CI 8.2-10.6) and 14.2 (12.8-15.8) events/1000PY respectively. Corresponding rates for bDMARD users were [5.4 (95% CI 2.9-10.1) and 8.2 (5.0-13.6) events/1000PY respectively. In the entire cohort, DAS-28 CRP and CRP(ln) associated with greater risk of MACE [(adjusted hazards ratio [HR] 1.19 (95%CI 1.06-1.34), p=0.004 and HR 1.15 (1.02-1.28), p=0.017 respectively], while for all ischemic CVE the association was significant for DAS-28 CRP [adjusted HR 1.1 (95%CI 1.07 to 1.30)], but not CRP(ln) [HR 1.06 (0.97 to 1.16)]. In bDMARD nonusers at baseline, higher DAS28-CRP and CRP(ln) associated with greater risk of MACE [adjusted HR 1.21 (95%CI 1.07-1.37), p=0.002 and HR 1.16 (1.04-1.30), p=0.009 respectively]. However, this was not the case in bDMARD users [p-for-interaction= 0.017 and 0.011 correspondingly, Figure 1]. In contrast, no significant interaction between DAS28-CRP or CRP and bDMARD use on any ischemic CVE risk was observed (p-for-interaction= 0.167 and 0.237 respectively). Both sensitivity analyses yielded similar results. Conclusion Higher disease activity and systemic inflammation at baseline associated with greater risk of MACE in bDMARD nonusers but not in patients receiving bDMARDs. This may suggest the presence of additional bDMARD-specific benefits directly on atherosclerotic plaque —such as plaque stabilization— above and beyond their effects on systemic inflammation. Reference [1]Karpouzas GA, Ormseth SR, Hernandez E, Budoff MJ. Biologics may prevent cardiovascular events in rheumatoid arthritis by inhibiting coronary plaque formation and stabilizing high-risk lesions. Arthritis Rheumatol. 2020 Sep;72(9):1467-1475. doi: 10.1002/art.41293. Image/graph:Figure 1. bDMARD use regulates the effect of inflammation on ischemic cardiovascular risk in patients with RA. Acknowledgements: NIL. Disclosure of Interests George Karpouzas Speakers bureau: Sanofi/Genzyme/Regeneron, BMS, Consultant of: Sanofi/Genzyme/Regeneron, Janssen, Scipher, Grant/research support from: Pfizer, Sarah Ormseth: None declared, Piet van Riel: None declared, Elena Myasoedova: None declared, Miguel A González-Gay: None declared, Alfonso Corrales: None declared, Solbritt Rantapää Dahlqvist: None declared, Petros Sfikakis: None declared, Patrick Dessein: None declared, Linda Tsang: None declared, Carol Hitchon: None declared, Virginia Pascual: None declared, Iris Jazmin Colunga-Pedraza: None declared, Dionicio Ángel Galarza-Delgado: None declared, José Ramón Azpiri-López: None declared, Silvia Rollefstad: None declared, Anne Grete Semb: None declared, Durga Prasanna Misra: None declared, Ellen-Margrethe Hauge: None declared, George Kitas: None declared. Keywords: Cardiovascular disease, Rheumatoid arthritis DOI: 10.1136/annrheumdis-2023-eular.2784Citation: , volume 82, supplement 1, year 2023, page 225Session: RA is more than just joints (Poster Tours)