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. 2013 Aug 21;26(6):925–934. doi: 10.1007/s10534-013-9668-5

Table 1.

Clinical characteristics of study participants

WND patients
(n = 108)
Controls
(n = 90)
p value
treatment naive
N = 38
treated
N = 70
all
Age, years; median (IQR) 28.5 (16.0) 30.5 (15.0) 30.0 (15.0) 41.5 (29.5)

a < 0.0001

b < 0.0001

c < 0.000004

d < 0.3

Women/men; n (%)

19/19

(50/50)

36/34

(51/49)

55/53

(51/49)

60/30

(67/33)

a < 0.07

b < 0.5

c < 0.02

d < 0.9

Serum copper, μg/dL; median [IQR] 45.5 [37.0] 23.5 [46.0] 33.5 [51.0] 111.0 [33.0]

a < 0.000000

b < 0.000000

c < 0.000000

d < 0.003

Serum ceruloplasmin, mg/dl; median [IQR] 9.2[13.6] 5.4[10.9] 5.7 [11.4] 34.3[10.8]

a < 0.000000

b < 0.000000

c < 0.000000

d < 0.04

Reference range values: ceruloplasmin: 25–45 mg/dl; copper: 70–140 μg/dl. p values were determined with χ2 test or the Mann–Whitney U test as appropriate, p value in the last column is given for the following comparisons: a—treatment naive WND and controls, b—WND patients on treatment and controls, c—all WND patients and controls, d—WND patients treatment naive and WND patients on treatment

WND Wilson’s disease, IQR interquartile range