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: 896

Risk for Cardiovascular Disease in Giant Cell Arteritis and Polymyalgia Rheumatica

Florencia Beatriz Mollerach1, Emmanuel Bertiller1, Maria de los Angeles Gallardo2, Maximiliano José Martinez1, Marina Scolnik3, Javier Rosa1, Luis J. Catoggio4 and Enrique R. Soriano1, 1Rheumatology Unit, Internal Medicine Service, Hospital Italiano de Buenos Aires, Instituto Universitario Hospital Italiano de Buenos Aires, and Fundacion PM Catoggio, Buenos Aires, Argentina, 2Hospital Italiano de Buenos Aires, CABA, Argentina, 3Rheumatology Section, Rheumatology Unit, Internal Medicine Service, Hospital Italiano de Buenos Aires, Instituto Universitario Hospital Italiano de Buenos Aires, and Fundacion PM Catoggio, Buenos Aires, Argentina, 4Rheumatology Unit, Internal Medicine Service, Hospital Italiano de Buenos Aires, Instituto Universitario Hospital Italiano de Buenos Aires, and Fundacion PM Catoggio, Argentina., Buenos Aires, Argentina

Meeting: 2016 ACR/ARHP Annual Meeting

Date of first publication: September 28, 2016

Keywords: Cardiovascular disease, giant cell arteritis and polymyalgia rheumatica

  • Tweet
  • Email
  • Print
Session Information

Date: Sunday, November 13, 2016

Title: Vasculitis - Poster I: Large Vessel Vasculitis and Polymyalgia Rheumatica

Session Type: ACR Poster Session A

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

Background/Purpose:  chronic inflammatory diseases are at a substantially increased risk of cardiovascular events (CVE). Scarce data is available in patients with Giant cell arteritis (GCA) and Polymyalgia Rheumatica (PMR). Our objective was to analyze the incidence of CVE in these patients seen at a large University hospital.

Methods:  we retrospectively reviewed electronic medical records (EMR) of patients registered between years 2000-2015 with the diagnosis of GCA or PMR. Patients fulfilling ACR 1990 criteria for GCA or ACR PMR 2012 criteria or with a diagnose made by a rheumatologist were included. Patients with history of CVE before diagnosis were excluded. Data regarding smoking status, blood pressure, obesity, diabetes, dyslipidemia, disease characteristics and treatments were recorded. CVE such as stroke or transient ischemic attack, coronary and peripheral vascular disease were identified from the EMR, during follow up. For patients with more than one CVE only the first one was considered for global incidence. Aortic aneurism (AA) was considered separately. Incidence rate with 95% CI of CVE is reported. In PMR patients a Cox proportional hazards models was fitted to analyze variables associated with CVE including age, sex, smoking, hypertension, diabetes mellitus, obesity, total cholesterol level, time on steroids, and use of aspirin.

Results: 872 PMR and 105 GCA were included . Demographic characteristics are shown in table 1. Among the 872 PMR patients (3945 patient-years (pt-yrs) of follow up)76 CVE occurred: incidence rate (cases per 1000 pt-yrs) : 19.3 (95% CI: 15.4-24.1); Females (F): 18 (14-23) and males (M): 24 (15-37). 46 patients suffered AA: incidence rate: 11.3/per 1000 pt-yrs (95% CI: 8.5-15); M: 22.3 (14.2-35) and F: 8.3 (5.7-12.2). Among the 105 ACG patients, 15 CVE occurred (501 pt-yrs of follow up): incidence rate: 29.9/per 1000 pt-yrs (95% CI: 18 – 49.6); M: 31.3 (7.8-125.3) and F: 29.7 (17.2-51.2). Nine patients had AA: incidence rate per 1000 pt-yrs: 17.9 (95% CI: 9.3–34.4); M: 30.4 (7.6-121.6) and F: 16 (7.6-33.6). The incidence rate of different CVE by gender, are shown in table 2. In the multivariate Cox proportional hazards model, variables associated with CVE were: diabetes mellitus: HR 3.3 (95% CI: 1.8-6.1), age at diagnosis: HR: 1.05 (95% CI: 1.01-1.08) and time on steroids (months of use): HR: 1.01 (95% CI: 1-1.02).

Conclusion: There was a high incidence of CVE and AA, in both patients with PMR and ACG. Diabetes, older age at diagnosis and prolonged use of steroids were significantly associated with more CVE. Table 1. Patient characteristics

Variable PMR (n=872) ACG (n=105)
Females, n (%) 678 (78) 88 (84)
Mean age at diagnosis (SD) 75.2 (7.9) 76.5 (5.9)
Mean time follow up (years), (SD) 4.8 (3.7) 12.1 (6.1)
Mean erythrocyte sedimentation rate (SD) 56.8 (25.4) 70.6 (25)
Polymyalgia symptoms, n (%) 872 (100) 59 (56)
Hypertension at baseline, n (%) 599 (68) 73 (69.5)
Diabetes at baseline, n (%) 64 (7.3) 10 (9.5)
Obesity at baseline (BMI (weight(kg)/Height(m)2)>30, n (%) 137 (16) 11 (10.5)
Smoking, n (%)
Never 676 (77.5) 83 (79)
Former 144 (16.5) 12 (11.4)
Current 52 (5.9) 10 (9.5)
Median time on steroids (months) (IQR) 18 (12-29) 27.5 (18-42)

Table 2. Incidence rate of CV events by gender

PMR (n=872) ACG (n=105)
CV Event Incidence rate/1000 patients-year (95 % CI) Incidence rate/1000 patients-year (95 % CI)
CV Deaths
Global 7.9 (5.6 -11) 13.3 (6.3 – 27.9)
Males 9.1 (4 – 18) 14.4 (2 – 102.3)
Females 7.6 (5.2 – 11) 13.1 (5.9 – 20.2)
Myocardial infarction
Global 7.6 (5.3 – 11) 9.5 (3.9 – 22.8)
Males 12.6 (7.0 – 22.8) 14.6 (2.1 – 103.6)
Females 6.2 (4.0 –9.6) 8.7 (3.3 – 23.3)
Cerebrovascular accident
Global 4.2 (2.8 – 6.3) 9.7 (4.1 – 23.4)
Males 2.8 (0.92 – 8.8) 14.7 (2.1 – 104.3)
Females 4.5 (2.9 – 7.0) 8.9 (3.4 – 23.9)
Peripheral vascular disease
Global 4.4 (2.8 – 6.9) 9.8 (4.1 – 23.6)
Males 5.8 (2.4 – 13.9) 0
Females 4.0 (2.3 – 6.9) 11.3 (4.7 – 27)

Disclosure: F. B. Mollerach, None; E. Bertiller, None; M. D. L. A. Gallardo, None; M. J. Martinez, None; M. Scolnik, None; J. Rosa, None; L. J. Catoggio, None; E. R. Soriano, Abbvie, 2,Pfizer Inc, 3,UCB, 2,Janssen Pharmaceutica Product, L.P., 2,Roche Pharmaceuticals, 2,Bristol-Myers Squibb, 2,Abbvie, 5,Pfizer Inc, 5,UCB, 5,Janssen Pharmaceutica Product, L.P., 5,Roche Pharmaceuticals, 5,Novartis Pharmaceutical Corporation, 5,Bristol-Myers Squibb, 5.

To cite this abstract in AMA style:

Mollerach FB, Bertiller E, Gallardo MDLA, Martinez MJ, Scolnik M, Rosa J, Catoggio LJ, Soriano ER. Risk for Cardiovascular Disease in Giant Cell Arteritis and Polymyalgia Rheumatica [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/risk-for-cardiovascular-disease-in-giant-cell-arteritis-and-polymyalgia-rheumatica/. Accessed .
  • Tweet
  • Email
  • Print

« Back to 2016 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/risk-for-cardiovascular-disease-in-giant-cell-arteritis-and-polymyalgia-rheumatica/

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