Association of anti-neutrophil cytoplasmic antibody-associated vasculitis and cardiovascular events: a population-based cohort study

Author:

Massicotte-Azarniouch David1ORCID,Petrcich William2,Walsh Michael345,Canney Mark6,Hundemer Gregory L6ORCID,Milman Nataliya7,Hladunewich Michelle A8,Fairhead Todd6,Sood Manish M26

Affiliation:

1. Department of Medicine, University of Ottawa, Ontario, Canada

2. Institute for Clinical Evaluative Sciences, Ottawa, Ontario, Canada

3. Departments of Medicine and Health Research Methods, Evidence & Impact, McMaster University, Hamilton, Canada

4. Population Health Research Institute, Hamilton Health Sciences/McMaster University, Hamilton, Canada

5. St Joseph's Healthcare Hamilton, Hamilton, Canada

6. Division of Nephrology, The Ottawa Hospital Research Institute, Department of Medicine, University of Ottawa, Ontario, Canada

7. Division of Rheumatology, Department of Medicine, University of Ottawa, Ontario, Canada

8. Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Ontario, Canada

Abstract

ABSTRACT Background Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is implicated in elevating the risk for cardiovascular (CV) disease; whether the elevated risk applies to all types of CV diseases or specific types is unclear. This study examined the association of AAV and adverse CV outcomes compared with the non-AAV population. Methods We conducted a population-based, retrospective cohort study of adults (mean age 61 years, 51% female) with a new diagnosis of AAV in Ontario, Canada from 2007 to 2017. Weighted models were used to examine the association of AAV (n = 1520) and CV events in a matched (1:4) control cohort (n = 5834). The main outcomes were major adverse CV events (MACE), defined as myocardial infarction (MI), stroke or CV death, its components, atrial fibrillation (AF) and congestive heart failure (CHF). Results Over a mean follow-up of 3.8 years, AAV (compared with non-AAV) was associated with a higher risk of stroke: cumulative incidence 7.0% versus 5.2%, sub-distribution hazard ratio (sHR) 1.49 [(95% confidence interval (95% CI) 1.10–2.02]; AF: cumulative incidence 16.4% versus 11.5%, sHR 1.51, 95% CI 1.30–1.75; and CHF: cumulative incidence 20.8% versus 13.3%, sHR 1.41, 95% CI 1.22–1.62; but not for MACE, MI or CV death. The risks for all CV events, except CV death, were significantly elevated in the early period after AAV diagnosis, in particular AF (365-day sHR 2.06, 95% CI 1.71–2.48; 90-day sHR 3.33, 95% CI 2.66–4.18) and CHF (365-day sHR 1.75, 95% CI 1.48–2.07; 90-day sHR 2.65, 95% CI 2.15–3.26). Conclusion AAV is associated with a high risk of certain types of CV events, particularly in the early period following diagnosis.

Funder

Paul Scherrer Institut

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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