Video: Every Case Tells a Story| Webinar: ACR/CHEST ILD Guidelines in Practice

An official publication of the ACR and the ARP serving rheumatologists and rheumatology professionals

  • Conditions
    • Axial Spondyloarthritis
    • Gout and Crystalline Arthritis
    • Myositis
    • Osteoarthritis and Bone Disorders
    • Pain Syndromes
    • Pediatric Conditions
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Sjögren’s Disease
    • Systemic Lupus Erythematosus
    • Systemic Sclerosis
    • Vasculitis
    • Other Rheumatic Conditions
  • FocusRheum
    • ANCA-Associated Vasculitis
    • Axial Spondyloarthritis
    • Gout
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Systemic Lupus Erythematosus
  • Guidance
    • Clinical Criteria/Guidelines
    • Ethics
    • Legal Updates
    • Legislation & Advocacy
    • Meeting Reports
      • ACR Convergence
      • Other ACR meetings
      • EULAR/Other
    • Research Rheum
  • Drug Updates
    • Analgesics
    • Biologics/DMARDs
  • Practice Support
    • Billing/Coding
    • EMRs
    • Facility
    • Insurance
    • QA/QI
    • Technology
    • Workforce
  • Opinion
    • Patient Perspective
    • Profiles
    • Rheuminations
      • Video
    • Speak Out Rheum
  • Career
    • ACR ExamRheum
    • Awards
    • Career Development
  • ACR
    • ACR Home
    • ACR Convergence
    • ACR Guidelines
    • Journals
      • ACR Open Rheumatology
      • Arthritis & Rheumatology
      • Arthritis Care & Research
    • From the College
    • Events/CME
    • President’s Perspective
  • Search

ANCA Mortality: Are Patients Doing Better?

Lara C. Pullen, PhD  |  December 13, 2019

The collection of small-vessel vasculitides known as anti-neutrophil cytoplasmic antibody-associated vasculitides (AAV) can affect nearly every organ system. The different categories of vasculitis, including granulomatosis with polyangiitis (GPA), a life-threatening form of small-vessel vasculitis, were described in the 2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Since the 1980s, rheumatologists have treated AAV patients with a combination of daily cyclophosphamide and alternate-day prednisone therapy. For many patients, this approach has successfully induced and maintained long-term remission. Recent trends in treatment have emphasized less cumulative cyclophosphamide exposure and greater use of azathioprine and other steroid-sparing agents.1

Although AAV patients appear to be responding to newer treatment approaches, they still have an increased risk of mortality relative to the general population. Example: In 2016, investigators reported a 2.7-fold increase in mortality among patients with AAV relative to the general population.2

ad goes here:advert-1
ADVERTISEMENT
SCROLL TO CONTINUE

That same year, another population-based study found that although the survival of GPA patients had improved considerably over the past two decades, it still had a hazard ratio of mortality of 2.5, which was somewhat lower than previous reports.3 However, the study was limited, relying on physician diagnoses of GPA unconfirmed by pre-specified criteria. Nevertheless, the study was one of the largest of a population-based cohort to evaluate mortality in patients diagnosed with GPA. GPA had previously been associated with increased mortality due to the disease itself, as well as complications due to treatment.This study affirmed the benefits of recent trends in GPA and AAV management.

Recently, Alexander W. Steinberg, MD, an internal medicine specialist at St. Joseph Hospital, Denver, and Michael E. Wechsler, MD, MMSc, a pulmonologist at National Jewish Health, Denver, sought to describe age-adjusted AAV mortality trends in the U.S. across demographic groups and geographic regions. For this analysis, they examined the multiple-cause-of-death records from the Centers of Disease Control & Prevention’s Wide-Ranging Online Data for Epidemiologic Research Database from 1999 to 2017. The results were published Oct. 8 in the Annals of Internal Medicine.4

ad goes here:advert-2
ADVERTISEMENT
SCROLL TO CONTINUE

The investigators found that from 1999–2017 11,316 AAV-related deaths occurred in the U.S. They calculated an age-adjusted mortality rate of 1.86 per 1 million people.

“Our results provide novel insights into mortality in persons with AAV in the U.S. between 1999 and 2017,” write the authors. “During this period, the age-adjusted AAV mortality declined by nearly 2% per year. The decrease in overall mortality and mortality among persons aged 65 to 74 years may reflect increased longevity due to improved treatment of AAV and common comorbid conditions.”

Page: 1 2 | Single Page
Share: 

Filed under:ConditionsVasculitis Tagged with:ANCAanti-neutrophil cytoplasmic antibodies (ANCA)mortality

Related Articles
    Figure 2: Renal Biopsy

    The Classification & Diagnosis of Granulomatosis with Polyangiitis

    August 16, 2018

    Based on the classification system developed by the Chapel Hill Consensus Conference, anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis is defined as a necrotizing vasculitis involving small vessels that is associated with myeloperoxidase (MPO) ANCA or proteinase 3 (PR3) ANCA and displays minimal immune deposits. The mechanism behind the pathogenesis of ANCA-associated vasculitis is not fully…

    Mortality from Anti-neutrophil Cytoplasmic Autoantibody-Associated Vasculitis Falling Slightly

    October 9, 2019

    NEW YORK (Reuters Health)—Mortality rates in patients with antineutrophil cytoplasmic autoantibody-associated vasculitis (AAV) decreased from 1999 to 2017, according to records from the Centers for Disease Control and Prevention (CDC). “The mortality attributed to several rare diseases [e.g., hypersensitivity pneumonitis] has increased in recent years,” Alexander W. Steinberg, MD, from Saint Joseph Hospital, Denver, tells…

    The Granulomatosis of Wegener’s

    May 16, 2011

    Delving deeper into the nonvasculitis aspects of the disease

    Case Report: GPA Presenting as Neuropathy

    December 16, 2021

    Granulomatosis with polyangiitis (GPA), is a type of anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV) that affects small- to medium-sized vessels.1 It can occur equally in both men and women, with a reported mean age at onset of 55 years.2 The classical presentation of GPA includes upper respiratory tract (i.e., chronic sinusitis, serous otitis and…

  • About Us
  • Meet the Editors
  • Issue Archives
  • Contribute
  • Advertise
  • Contact Us
  • Copyright © 2025 by John Wiley & Sons, Inc. All rights reserved, including rights for text and data mining and training of artificial technologies or similar technologies. ISSN 1931-3268 (print). ISSN 1931-3209 (online).
  • DEI Statement
  • Privacy Policy
  • Terms of Use
  • Cookie Preferences