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Table 1 Main characteristics of the studies on childhood-onset granulomatosis with polyangiitis and features of the patients at presentation

From: Childhood-onset granulomatosis with polyangiitis and microscopic polyangiitis: systematic review and meta-analysis

First author

Stegmayr [20]

Cabral [6]

Rottem [24]

Akikusa [5]

Tahghighi [22]

Gajic-Veljic [23]

Iudici [11]

Sacri [12]

Arulkumaran [7]

Wong [19]

Orlowski [18]

Bohm [9]

Kosalka [10]

Speciality

Paediatric Nephrology

Paediatric Rheumatology

Paediatrics

Paediatric Rheumatology

Paediatric Rheumatology

Paediatric Dermatology

Adult Internal Medicine

Paediatric Nephrology and Rheumatology

Adult Rheumatology

Paediatrics

Paediatrics

Paediatrics

Paediatrics

Country

Sweden, Germany

USA,

Canada

USA

Canada

Iran

Serbia

France

France

UK

UK

USA

International

Poland

Year of publication

2000

2009

1993

2007

2013

2013

2015

2015

2011

1998

1978

2014

2014

Years of enrolment

NA

since 2004

NA

1984–2005

2002–2011

1992–2011

1965–2014

1986–2011

1996–2010

1986–1991

1952–1976

2000–2010

1995–2013

Study design

Retrospective

Cross-sectional

2004–2007: retrospectively collected

March 2007-November 2008: prospectively collected

Prospective

Retrospective

Cross-sectional

Retrospective

Retrospective

Retrospective

Retrospective

Retrospective

Retrospective

Retrospective

Retrospective

Retrospective

Number of patients

7

65

23

25

11

3

25

28

7

12

6

56

9

Ethnicity (n)

Caucasian

41 Caucasian, 4 mixed, 3 East Indian, 3 African American, 2 Hispanic, 1 Asian, 1 Middle Eastern, 6 not available

NA

White 21/25

NA

NA

19 Caucasian

21 Caucasian

5 Caucasian, 2 Afro-Carribean

NA

6 Caucasians

46 Caucasian

NA

F (n)

3

43

16

20

5

3

18

21

5

8

3

38

6

Median age at onset (range), years

NA

NA

15.4 (9.3–19.4)

NA

NA

11 (6–16)

NA

NA

11.5 (9–15)

9 (0.5–14)

17 (13–20)

11.7 (1st and 3rd quartile 8.5–14.5)

12 (88–16)

Median age at diagnosis (range), years

14 (11–18)

14.2 (4–17)

 

14.5 (8.7–17.1)

11 (6–15)

 

14 (2–17)

12.8 (10.1–14.6)

     

Classification/diagnostic tool used

Presence of kidney biopsy, upper and lower respiratory tract disease, ANCA+

MD diagnosis

Clinical history compatible with GPA and histopathological evidence of vasculitis or granulomas, or both

ACR Criteria

EULAR/PRINTO/PRES

Clinical history compatible with GPA and histo-pathological evidence of vasculitis or granulomas, or both

EULAR/PRINTO/PRES and Revised Chapel-Hill

EULAR/PRINTO/PRES

EULAR/PRINTO/PRES

ACR Criteria

Histological examination in all patients

EULAR/PRINTO/PRES

EULAR/PRINTO/PRES or ACR criteria

cANCA positivity (ELISA), n (%)

6/7 (85.7)

43 (66.2)

NA

13/15 (86.7)

11 (100)

2 (66.6)

10/18 (55.5)

18/28 (64.2)

NA

4 (33.3)

NA

34/51 (66.6)

NA

pANCA positivity (ELISA), n (%)

1/7 (14.2)

8 (12.3)

NA

NA

2 (18)

1 (33.3)

4/18 (22.2)

6/28 (21.4)

NA

6 (50.0)

NA

13/50 (26.0)

NA

cANCA positivity (IFI), n (%)

NA

43 (66.2)

NA

13/15 (86.7)

11 (100)

2 (66.6)

12/20 (60.0)

NA

4/7 (57.1)

6 (50.0)

NA

NA

NA

pANCA positivity (IFI), n (%)

NA

14 (21.5)

NA

2/15 (13.3)

NA

1 (33.3)

4/20 (20.0)

NA

1/7 (14.2)

1 (14.2)

NA

NA

NA

Clinical manifestations

Systemic, n (%)

7 (100)

58 (89.2)

5 (71.4)

24 (96.0)

9 (81.8)

3 (100)

17 (68.0)

23 (82.1)

3 (42.8)

0

5 (83.3)

50 (89.2)

8 (88.8)

Mucocutaneous, n (%)

2 (28.5)

23 (35.4)

2 (8.6)

8 (32.0)

3 (27.2)

3 (100)

6 (24.0)

15 (53.5)

4 (57.1)

10 (83.3)

3 (50.0)

36 (64.2)

4 (44.4)

Musculoskeletal, n (%)

4 (57.1)

37 (56.9)

7 (30.4)

24 (96.0)

3 (27.2)

2 (66.6)

9 (36.0)

16 (57.1)

5 (71.4)

9 (75.0)

2 (33.3)

33 (58.9)

3 (33.3)

Ocular, n (%)

0

24 (36.9)

3 (13.0)

13 (52.0)

2 (18.8)

2 (66.6)

7 (28.0)

6 (21.4)

3 (42.8)

0

1 (16.6)

19 (33.9)

1 (11.1)

Ear, nose, and throat, n (%)

7 (100)

52 (80.0)

20 (87)

21 (84.0)

8 (72.7)

2 (33.3)

21 (84.0)

21 (75.0)

4 (57.1)

11 (91.6)

6 (100)

51 (91.0)

5 (55.5)

Respiratory, n (%)

6 (85.7)

52 (80.0)

5 (21.7)

20 (80.0)

2 (18.1)

0

17 (68.0)

19 (67.8)

3 (42.8)

7 (58.3)

5 (83.3)

44 (78.5)

7 (77.7)

Cardiovascular, n (%)

0

0

2 (8.7)

5 (20.0)

1 (9.0)

0

0

0

0

0

0

0

0

Gastrointestinal, n (%)

0

27 (41.5)

0

3 (12.0)

3 (27.2)

0

5 (20.0)

5 (17.8)

1 (14.2)

6 (50.0)

0

9 (16.0)

5 (55.5)

Neurological, n (%)

0

16 (24.6)

1 (4.3)

2 (8.0)

1 (9.0)

0

1 (4.0)

1 (3.5)

1 (14.2)

2 (16.6)

1 (16.6)

8 (14.2)

1 (11.1)

Renal, n (%)

7 (100)

49 (75.4)

2 (8.6)

22 (88.0)

4 (36.3)

3 (100)

9 (36.0)

22 (78.5)

4 (57.1)

4 (33.3)

5 (83.3)

38 (67.8)

8 (88.8)

Treatment

Oral GCs ± IS, n (%)

7 (100)

60 (92.3)

23 (100)

25 (100)

NA

3 (100)

21 (84.0)

28 (100)

NA

NA

5 (83.3)

NA

9 (100)

GCs ± CYC, n (%)

6 (85.7)

54 (83.0)

18 (78.2)

15 (60.0)

NA

3 (100)

18 (72.0)

NA

NA

NA

3 (50.0)

NA

9 (100)

GCs ± MTX, n (%)

0

7 (10.7)

1 (4.3)

5 (20.0)

NA

0

2 (8.0)

NA

NA

NA

0

NA

0

GCs ± AZA, n (%)

0

0

2 (8.6)

0

NA

0

2 (8.0)

NA

NA

NA

0

NA

0

Plasmapheresis, n (%)

4 (57.1)

9 (13.8)

0

0

NA

1 (33.3)

1 (4.0)

NA

NA

NA

0

NA

0

  1. NA not available, ELISA enzyme-linked immunosorbent assay, IFI indirect immunofluorence, GCs glucocorticoids, IS immunosoppressors, CYC cyclophosphamide, MTX methotrexate, AZA azathioprine, GPA granulomatosis with polyangiitis