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Abstract Number: 1901

Venous Thromboembolism Risk Is Consistently Increased in People with Rheumatoid Arthritis Across Different Ages, Sexes and Obesity Status: United Kingdom Population Based Study

James Galloway1, Victoria Basey2, Michael Mclean2, Simon de Lusignan3 and Maya H. Buch4, 1Centre for Rheumatic Diseases, King's College London, London, United Kingdom, 2Pfizer UK, Tadworth, United Kingdom, 3Royal College of General Practitioners Research and Surveillance Centre, Oxford, United Kingdom, 4Division of Musculoskeletal & Dermatological Sciences, University of Manchester, and NIHR Manchester Biomedical Research Centre, Manchester, United Kingdom

Meeting: ACR Convergence 2024

Keywords: Epidemiology, rheumatoid arthritis, risk factors

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Session Information

Date: Monday, November 18, 2024

Title: Epidemiology & Public Health Poster III

Session Type: Poster Session C

Session Time: 10:30AM-12:30PM

Background/Purpose: Risk of venous thromboembolism (VTE) is increased in people with rheumatoid arthritis (RA) when compared to the general population, but the variation of this risk among patients is not well understood. Acknowledging the heterogeneity in RA attributable VTE risk could support tailoring of treatment plans and screening protocols based on an individual’s specific risk profile. In a large population based study, we aimed to evaluate for variation in RA attributable VTE risk by age, sex and body mass index
(BMI).

Methods: Adults registered with a general practice from January 1999 to December 2018 were identified from the Royal College of
General Practitioners Research (RCGP) and Surveillance Centre (RSC) primary care database. RA patients and VTE outcome
(composite of pulmonary embolism and deep vein thrombosis) were determined using previously validated algorithms. RA unaffected
controls (UCs) were matched 4:1 with RA patients by current age, sex, calendar time, and years since practice registration
using nearest neighbour matching with replacement. Absolute VTE rates over 20 years were compared in RA patients versus
matched UCs, overall and by age category (18-49, 50-69, ≥70), sex, and BMI category (BMI < 25, 25-29.9, ≥30). Across the same
subgroups, relative VTE risk over the same period was estimated using Cox proportional hazards models adjusted for
sociodemographic and clinical features and established VTE risk factors (BMI, smoking status, alcohol use, reduced mobility evidence, thrombophilia, lower limb fracture and family history of VTE).

Results: 117,050 individuals were included of whom 23,410 were RA patients and 93,640 were UCs. Average follow up was 8.2 years
(standard deviation [SD]=6.6 years). RA patients (mean age 59.0, SD 15.5; 28.9% male [n=6776]; mean BMI 27.1, SD 5.6) were similar to matched UCs in clinical characteristics. Unadjusted VTE events rates were consistently higher in RA patients compared to UCs overall and across all subgroups (overall rates RA: 442.4 per 100,000 personyears [py], 95% confidence interval [CI]: 413.0, 473.2; UC: 262.2 per 100,000 py, 95%CI: 251.9, 273.9); subgroup rates). Similarly, overall relative VTE risk was 46% higher in people with RA compared to UCs (adjusted hazard ratio [aHR]= 1.46, 95%CI: 1.36, 1.56; p< 0.001), and was consistently higher across age, sex and BMI defined subgroups (aHR range: 1.34-2.13, all p< 0.001). Although relative risk was highest in RA patients < 50 years (aHR= 2.13, 95%CI: 1.62-2.79; p< 0.001), this patient subgroup had the lowest absolute risk of VTE (approximately 2.2 and 3.4fold lower than observed in those aged 50-69 and ≥70, respectively).

Conclusion: Clinicians should be aware that risk of VTE is consistently higher in people with RA compared to the general population, regardless of age, sex and BMI. Findings suggest close monitoring and assessment of VTE risk factors is required even in younger
individuals with RA.

This study was sponsored by Pfizer. Momentum Data UK provided project management, medical writing, and statistical support, funded by Pfizer.

This is an encore abstract previously presented/published for the British Society of Rheumatology Annual conference 2024 https://doi.org/10.1093/rheumatology/keae163.038


Disclosures: J. Galloway: AbbVie, 6, AstraZeneca, 5, Galapagos, 2, 6, Janssen, 2, 5, 6, Lilly, 2, 6, Pfizer, 2, 5, 6, UCB, 6; V. Basey: Pfizer, 3; M. Mclean: Pfizer, 3; S. de Lusignan: AstraZeneca, 5, Eli Lilly, 5, GlaxoSmithKlein(GSK), 5, Merck/MSD, 5, Moderna, 5, Sanofi, 5, Seqirus, 5, Takeda, 5; M. Buch: AbbVie, 2, 6, Arxx Therapeutics, 2, Boehringer Ingelheim, 6, CESAS Medical, 6, Galapagos, 2, 6, Gilead, 2, 5, 6, Medistream, 6, Pfizer, 2, 6.

To cite this abstract in AMA style:

Galloway J, Basey V, Mclean M, de Lusignan S, Buch M. Venous Thromboembolism Risk Is Consistently Increased in People with Rheumatoid Arthritis Across Different Ages, Sexes and Obesity Status: United Kingdom Population Based Study [abstract]. Arthritis Rheumatol. 2024; 76 (suppl 9). https://acrabstracts.org/abstract/venous-thromboembolism-risk-is-consistently-increased-in-people-with-rheumatoid-arthritis-across-different-ages-sexes-and-obesity-status-united-kingdom-population-based-study/. Accessed .
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