4.2 Article

Comparison of severity classification in Japanese patients with antineutrophil cytoplasmic antibody-associated vasculitis in a nationwide, prospective, inception cohort study

Journal

MODERN RHEUMATOLOGY
Volume 26, Issue 5, Pages 730-737

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.3109/14397595.2016.1140274

Keywords

Antineutrophil cytoplasmic antibody-associated vasculitis; Eosinophilic granulomatosis with polyangiitis; Granulomatosis with polyangiitis; Inception cohort; Microscopic polyangiitis

Categories

Funding

  1. Teijin Pharma, Ltd.
  2. Abbott Japan Co., Ltd.
  3. Astellas Pharma Inc.
  4. Bristol-Myers Squibb K.K.
  5. Chugai Pharmaceutical Co., Ltd.
  6. Eisai Co., Ltd.
  7. Janssen Pharmaceutical K.K.
  8. Mitsubishi Tanabe Pharma Co.
  9. Santen Pharmaceutical Co., Ltd.
  10. Takeda Pharmaceutical Co., Ltd.
  11. Pfizer Japan Inc.
  12. Pfizer Inc.
  13. AbbVie Inc.
  14. Daiichi Sankyo Co. Ltd.
  15. Otsuka Pharmaceutical Co., Ltd.
  16. Astellas
  17. Boehringer-Ingelheim
  18. Daiichi Sankyo
  19. Dainippon Sumitomo
  20. Kyowa Hakko Kirin
  21. Mochida
  22. MSD
  23. Novartis
  24. Novo Nordisk
  25. Pfizer
  26. Takeda
  27. Tanabe Mitsubishi
  28. Research Committee of Intractable Vasculitis Syndrome of the Ministry of Health, Labour, and Welfare of Japan
  29. Research Committee of Intractable Renal Disease of the Ministry of Health, Labour, and Welfare of Japan
  30. study group for strategic exploration of drug seeds for ANCA-associated vasculitis and construction of clinical evidence from Japan Agency for Medical Research and development, AMED

Ask authors/readers for more resources

Objective: To compare disease severity classification systems for six-month outcome prediction in patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). Methods: Patients with newly diagnosed AAV from 53 tertiary institutions were enrolled. Six-month remission, overall survival, and end-stage renal disease (ESRD)-free survival were evaluated. Results: According to the European Vasculitis Study Group (EUVAS)-defined disease severity, the 321 enrolled patients were classified as follows: 14, localized; 71, early systemic; 170, generalized; and 66, severe disease. According to the rapidly progressive glomerulonephritis (RPGN) clinical grading system, the patients were divided as follows: 60, grade I; 178, grade II; 66, grade III; and 12, grade IV. According to the Five-Factor Score (FFS) 2009, 103, 109, and 109 patients had <= 1, 2, and >= 3 points, respectively. No significant difference in remission rates was found in any severity classification. The overall and ESRD-free survival rates significantly differed between grades I/II, III, and IV, regardless of renal involvement. Severe disease was a good predictor of six-month overall and ESRD-free survival. The FFS 2009 was useful to predict six-month ESRD-free survival but not overall survival. Conclusions: The RPGN grading system was more useful to predict six-month overall and ESRD-free survival than the EUVAS-defined severity or FFS 2009.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available