4.6 Article

Increasing incidence and improved survival in ANCA-associated vasculitis-a Danish nationwide study

期刊

NEPHROLOGY DIALYSIS TRANSPLANTATION
卷 37, 期 1, 页码 63-71

出版社

OXFORD UNIV PRESS
DOI: 10.1093/ndt/gfaa303

关键词

ANCA-associated vasculitis; ANCA testing; epidemiology; incidence; outcomes

资金

  1. Helen and Ejnar Bjornows Foundation
  2. Knud Hojgaards Foundation

向作者/读者索取更多资源

This study examined the temporal changes in incidence and mortality of ANCA-associated vasculitis (AAV) using nationwide healthcare registries in China. The results showed an increasing trend in ANCA testing and AAV diagnosis during the study period. Furthermore, the mortality and risk of end-stage renal disease (ESRD) decreased over time, which may be attributed to earlier diagnosis and changes in treatment practice.
Background. Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) carries a high risk of morbidity and mortality, with outcomes modified by treatment and an incidence that may be increasing. We examined temporal changes in incidence and mortality during 2000-15 using nationwide healthcare registries. Methods. Patients with incident AAV were identified using International Classification of Diseases Version 10 (ICD10) codes and grouped according to inclusion year (Period 1: 2000-04, Period 2: 2005-09, Period 3: 2010-15). Log link cumulative incidence regression adjusted for age, sex, renal function, cardiovascular disease, diabetes, hypertension and advanced disease severity were used to model survival. Results. We identified 1631 patients (52% male), corresponding to an incidence of 18.5 persons/million/year (Period 1: 15.1, Period 2: 18.5, Period 3: 21.4). The slope of incident serologic ANCA testing was steeper than that of AAV (P = 0.002). Mean [standard deviation (SD)] age was 60.2 (16.7) years and mean (SD) follow-up was 6.8 (4.7) years. A total of 571 (35%) patients died (5-year mortality of 22.1%), with an absolute risk ratio (ARR) for Periods 2 and 3 compared with Period 1 of 0.80 [confidence interval (CI) 0.65-0.98, P = 0.031] and 0.39 (CI 0.31-0.50, P < 0.001). About 274 patients developed end-stage renal disease (ESRD) [16.8% (Period 1: 23.3%, Period 2: 17.6%, Period 3: 12.5%)], with ARR decreasing over time: Period 2 0.61 (CI 0.42-0.87, P = 0.007) and Period 3 0.57 (CI 0.39-0.83, P = 0.003). The overall risk of death associated with ESRD or chronic kidney disease was 1.74 (CI 1.29-2.37, P < 0.001) and 1.58 (CI 1.21-2.07, P < 0.001). Conclusions. Incidence of ANCA testing and AAV diagnosis increased over the test period. Falls over time in mortality and ESRD risk may relate to earlier diagnosis and changes in treatment practice.

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