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: 2377

The Impact of Chronologic versus Biologic Age on the Risk of Severe Infection, End-Stage Renal Disease, and Death in Older Adults with ANCA-Associated Vasculitis

Sebastian Sattui1, Xiaoqing Fu2, Claire Cook2, Shruthi Srivatsan2, Yuqing Zhang2 and Zachary Wallace3, 1University of Pittsburgh, Pittsburgh, PA, 2Massachusetts General Hospital, Boston, MA, 3Massachusetts General Hospital, Newton, MA

Meeting: ACR Convergence 2023

Keywords: Aging, ANCA associated vasculitis, Cohort Study, Infection

  • 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 14, 2023

Title: (2370–2386) Vasculitis – ANCA-Associated Poster III: Biomarkers & Renal Outcomes

Session Type: Poster Session C

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

Background/Purpose: Older adults with ANCA-associated vasculitis (AAV) have distinct clinical presentations and outcomes when compared to younger adults. Despite a high incidence of AAV in older adults, they are underrepresented in clinical trials. Studies have focused on age as a risk factor for poor outcomes. Frailty, a syndrome associated with increased morbidity and mortality, has not been adequately studied in older adults with AAV and provides a more holistic assessment.

The objective of this study was to compare the impact of age and frailty on early (≤ 2 years of diagnosis) end-stage renal disease (ESRD), severe infection, and death in adults with incident AAV who are ≥ 75 years old vs 65-74 years old.

Methods: Patients ≥ 65 years were included from the 2002-2019 Mass General Brigham AAV cohort, a consecutive inception cohort. EGPA patients were excluded. Covariates including demographics, disease characteristics, and the Charlson comorbidity index were assessed at baseline. Disease activity at diagnosis was assessed using the Birmingham Vasculitis Activity Score (BVAS/GPA). Baseline frailty was measured using the claims-based frailty index (CFI); pre-established cut-offs defined degrees of frailty (robust, pre-frail, mildly frail, and moderately/severely frail).1

Death and ESRD (composite outcome) were ascertained from linkage to national registries and/or medical records. Severe infections were identified utilizing inpatient data or as a code in death certificate. The cumulative incidence of the death/ESRD and severe infections at 2-years were estimated. Kaplan-Meier curves for the probability of composite outcome and severe infection by age and frailty were generated. Multivariable analysis was performed to compare the association of age and frailty with death/ESRD and severe infections within 2 years of treatment initiation.

Results: There were 298 patients included. Most were female (61%), white (86%), MPO-ANCA+ (80%), and had renal involvement (72%). Patients ≥ 75 years old (n=156) had a median age of 81 years, while median age was 69 years in the 65-74 years group (Table 1).

The cumulative incidence at 2 years of death/ESRD (23.1% [95% CI 16.5, 29.7]) vs 5.6% [95% CI 1.8, 9.4]) and severe infection (34.0% [95% CI 26.5, 41.4] vs 12% [95% CI 6.6, 17.3]) were higher in AAV patients ≥ 75 vs 65-74 years old. In the multivariable analysis, age ≥ 75 years was associated with an increased risk of composite outcome (hazard ratio (HR) 4.22, 95% CI 1.94-9.15); frailty was not (HR 2.02, 95% CI 0.46,8.81) (Table 2, Figure 1). In contrast, both frailty (HR 8.9, 95% CI 2.20,36.90) and age ≥ 75 years (HR 2.90, 95 CI% 1.73, 4.47) appeared to be independent risk factors for severe infections at 2-year follow-up; the association with frailty appeared greater.

Conclusion: AAV patients aged ≥ 75 vs 65-74 years had a higher incidence of death/ESRD and severe infections. Older age was associated with death/ESRD and severe infection risk. Frailty was a strong risk factor, independent of age, for severe infection. These findings highlight the need for innovative considerations beyond age when assessing outcome risks in older adults with AAV.

References
1. Kim DH, et al. J Gerontol A Biol Sci Med Sci

Supporting image 1

Table 1. Baseline Characteristics of patients with AAV by age group
AAV = ANCA-associated vasculitis, SD = standard deviation, PR3 = Proteinase 3, MPO = myeloperoxidase, eGFR = estimated glomerular filtration rate, BVAS/WG = Birmingham Vasculitis Activity Score, CCI = Charlson Comorbidity Index, CFI = Claims-based Frailty index, RTX = rituximab, CYC = cyclophosphamide

Supporting image 2

Table 2. Univariable and multivariable analyses for factors associated with outcomes in older adults with AAV at 2 years
ESRD = end-stage renal disease, CFI = Claims-based frailty index, BVAS = Birmingham Vasculitis Activity Score, CYC = cyclophosphamide
aAdjusted for sex, frailty, pulmonary involvement, renal involvement, and BVAS/GPA.
bAdjusted for age, sex, pulmonary involvement, renal involvement, and BVAS/GPA.

Supporting image 3

Figure 1. Kaplan-Meier curves for composite outcome (ESRD/death) and severe infections
Composite outcome (ESRD/death) by age category (A) and frailty status (B), and severe infections by age (C) and frailty status (D).


Disclosures: S. Sattui: AstraZeneca, 5, Bristol Myers Squibb Foundation, 5, Rheumatology Research Foundation, 5, Sanofi, 2, 5; X. Fu: None; C. Cook: None; S. Srivatsan: None; Y. Zhang: None; Z. Wallace: BioCryst, 2, Bristol-Myers Squibb(BMS), 5, Horizon, 1, 2, 5, MedPace, 2, Novartis, 1, PPD, 2, Sanofi, 1, 5, Shionogi, 1, Visterra, 1, 2, Zenas, 1, 2.

To cite this abstract in AMA style:

Sattui S, Fu X, Cook C, Srivatsan S, Zhang Y, Wallace Z. The Impact of Chronologic versus Biologic Age on the Risk of Severe Infection, End-Stage Renal Disease, and Death in Older Adults with ANCA-Associated Vasculitis [abstract]. Arthritis Rheumatol. 2023; 75 (suppl 9). https://acrabstracts.org/abstract/the-impact-of-chronologic-versus-biologic-age-on-the-risk-of-severe-infection-end-stage-renal-disease-and-death-in-older-adults-with-anca-associated-vasculitis/. 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 ACR Convergence 2023

ACR Meeting Abstracts - https://acrabstracts.org/abstract/the-impact-of-chronologic-versus-biologic-age-on-the-risk-of-severe-infection-end-stage-renal-disease-and-death-in-older-adults-with-anca-associated-vasculitis/

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