ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 2170

Cardiovascular Risk in Patients with Psoriasis, Psoriatic and Rheumatoid Arthritis: A Prospective Study Using Secured Anonymised Information Technology Databank in Wales, United Kingdom

Ernest H. Choy1, Roxanne Cooksey2, Sinead Brophy2, Jonathan Kennedy2, Fabiola Fernandez-Gutierrez3, Ruth Davies4, Timothy Pickles5 and Vincent Piguet6, 1CREATE Center, Division of Infection and Immunity,, Cardiff University, Cardiff, United Kingdom, 2College of Medicine, Swansea University, Swansea, United Kingdom, 3Cancer Research UK Manchester Institute, Manchester, United Kingdom, 4CREATE Centre, Division of Infection and Immunity, Cardiff University, Cardiff, United Kingdom, 5CREATE Center, Division of Infection and Immunity, Cardiff University, Cardiff, United Kingdom, 6Division of Infection and Immunity, Cardiff University, Cardiff, United Kingdom

Meeting: 2016 ACR/ARHP Annual Meeting

Date of first publication: September 28, 2016

Keywords: Cardiovascular disease, psoriasis, psoriatic arthritis and rheumatoid arthritis (RA)

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Tuesday, November 15, 2016

Title: Epidemiology and Public Health - Poster III

Session Type: ACR Poster Session C

Session Time: 9:00AM-11:00AM

Background/Purpose: Compared with cardiovascular (CV) risk in rheumatoid arthritis (RA), precise CV risk in psoriatic arthritis (PsA) and psoriasis is less established, particularly the relative contribution of traditional CV risk factors versus systemic inflammation. The objective of this study is to compare the incidence of Major Adverse Cardiac Events (MACE) among patients with RA, PsA and psoriasis with population controls adjusting for traditional CV risk factors, systemic inflammation, and Disease Modifying Anti-Rheumatic Drug s(DMARDs).

Methods: Using linked, routinely collected health data from 1999 to 2013 in Wales UK, available from the Secure Anonymised Information Linkage (SAIL) databank, which includes general practitioner, and hospital datasets, the incidence of a MACE was investigated in individuals with RA (n=8,650), PsA (n=2,128), psoriasis (n=24,630) and population controls (n= 1,187,706), while controlling for traditional CV risk factors, systemic inflammation (measured by erythrocyte sedimentation rate (ESR)), and DMARDs.

Results: Demographic details and incidence of MACE are listed in Table 1. After controlling for traditional risk factors, CV risk was significantly increased for individuals with RA (HR: 1.2, 95% CI: 1.0-1.3, p=0.038) and psoriasis (HR: 1.1, 95% CI: 1.0-1.3, p=0.025) but not for PsA (HR: 1.0, 95% CI: 0.7-1.5, p=0.887). ESR was significantly higher in patients with RA compared with patients with psoriasis, PsA and controls. ESR was associated with increased in CV risk in RA but not psoriasis or PsA. No interaction between DMARDs and MACE occurrence was observed. Table 1: Baseline Characteristics AND INCIDENCE OF MACE ControlRAPsAPsoriasis(n=1187706)(n=8650)(n=2128)(n=24630)Age at diagnosis (SD)50 (17.2)59.6 (14.6)50.3 (13.1)51.4 (16.2)Male49%32%47%49%Baseline BMI (SD)25.5 (5.1)26.8 (5.5)27.8 (5.9)26.5 (5.4)Hyperlipidemia7.30%13.90%12.60%11.40%Diabetes 7.80%14.10%13.10%11.90%Hypertension21.60%39.70%33.30%29.90%Smoker21.20%24.60%21.90%27.90%MACE Incidence rate per 1000PY (95% CI)4.5 (4.5 to 4.6)9.6 (8.8 to 10.5)2.9 (2.2 to 3.9)5.3 (5.0 to 5.7)

Conclusion: In addition to traditional CV risk factors, there is an increased incidence of CV disease for RA and psoriasis, but not for PsA. This demonstrates the varying mediators of CV risk across the conditions and highlights the need for different CV risk reduction strategies for specific diseases.


Disclosure: E. H. Choy, Pfizer Inc, 2,Pfizer Inc, 5,Pfizer Inc, 8,UCB, 2,Roche Pharmaceuticals, 2,Roche Pharmaceuticals, 5,Roche Pharmaceuticals, 8,Regeneron, 5,Regeneron, 8,Sanofi-Aventis Pharmaceutical, 5,Sanofi-Aventis Pharmaceutical, 8,Amgen, 5,UCB, 8,Celgene, 5,Bristol-Myers Squibb, 5,Bristol-Myers Squibb, 8,Janssen Pharmaceutica Product, L.P., 5; R. Cooksey, None; S. Brophy, None; J. Kennedy, None; F. Fernandez-Gutierrez, None; R. Davies, None; T. Pickles, None; V. Piguet, None.

To cite this abstract in AMA style:

Choy EH, Cooksey R, Brophy S, Kennedy J, Fernandez-Gutierrez F, Davies R, Pickles T, Piguet V. Cardiovascular Risk in Patients with Psoriasis, Psoriatic and Rheumatoid Arthritis: A Prospective Study Using Secured Anonymised Information Technology Databank in Wales, United Kingdom [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/cardiovascular-risk-in-patients-with-psoriasis-psoriatic-and-rheumatoid-arthritis-a-prospective-study-using-secured-anonymised-information-technology-databank-in-wales-united-kingdom/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2016 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/cardiovascular-risk-in-patients-with-psoriasis-psoriatic-and-rheumatoid-arthritis-a-prospective-study-using-secured-anonymised-information-technology-databank-in-wales-united-kingdom/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology