Table 2 Characteristics of enrolled patients.

From: Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases

Disease

Number of cases (n)

Female (n)

Age (years)

Proteinuria (g/g Cr)

Serum alb (g/dL)

eGFR (ml/min/1.73 m2)

IgA nephropathy

17

9

12 (7–15)

1.1 (0.0–4.9)

3.8 (3.1–4.9)

107 (79–130)

IgA vasculitis with nephritis

6

2

5 (5–15)

3.8 (0.2–15.9)

3.0 (1.7–4.4)

115 (103–139)

Lupus nephritis

9

7

13 (8–18)

0.7 (0.1–5.5)

3.3 (2.7–4.5)

108 (63–198)

MPGN

5

2

13 (5–16)

1.5 (0.2–2.8)

3.6 (1.1–4.6)

122 (37–201)

Membranous nephropathy

2

0

5 (3–7)

1.9 (1.8–2.1)

3.4 (3.2–3.5)

119 (110–128)

Idiopathic nephrotic syndrome

11

6

7 (2–16)

0.1 (0.0–29.1)

4.1 (1.7–4.6)

109 (87–142)

Oligomeganephronia

3

1

15 (12–16)

0.7 (0.3–1.2)

4.2 (4.1–4.5)

62 (58–66)

Alport syndrome

2

2

3.5 (3–4)

0.3 (0.2–0.4)

4.4 (4.2–4.5)

134 (126–142)

Dense deposit disease

1

0

10

1.4

3.6

78

Crescentic glomerulonephritis

1

1

17

3.3

4.0

102

C3 glomerulonephritis

1

0

12

0.1

4.6

94

PSAGN

1

1

8

10.8

1.9

42

Hemolytic uremic syndrome

1

1

4

1.1

4.9

55

  1. Data were obtained at the time of renal biopsy and are presented as median (range).
  2. alb albumin, eGFR estimated glomerular filtration rate, MPGN membranoproliferative glomerulonephritis, PSAGN poststreptococcal acute glomerulonephritis.