Skip to main content
. 2013 Dec;32(3):148–153.

Table 1.

Demographic and clinical data of patients. Values are given as median (range). (Normal values: CK women < 2.41 mmol / L*s, men <2.81 mmol / L*s, eosinophils <5%.) * Kruskal-Wallis One Way Analysis of Variance on Ranks, post hoc analysis using Dunn's method, n.a. not applicable

Disease Number (n) Gender (F/M) Age at biopsy (years) Disase duration (years) Creatine kinase (μmol/L*s) Increased eosinophil count in haemogram (n)
Hereditary myopathies
LGMD2A 12 4/8 30 (10-72) 7
(2-49)
8.3
(2.5-349)
1/7
LGMD2B 4 2/2 43
(34-52)
20
(6-22)
67
(38-123)
0/4
LGMD2L 3 1/2 49
(29-69)
6
(5-24)
37
(22-74)
0/3
FSHD 5 5/0 39
(21-71)
8(1-19) 2.2
(2-12)
1/3
DMD/BMD 8 0/8 11
(3-21)
3(1-13) 81
(18-293)
0/3
Idiopathic inflammatory myopathies
DM 11 5/6 54
(15-84)
0.5
(0.1-10)
8.6
(0.7-227)
1/6
PM 13 7/6 54
(32-77)
1.0
(0.3-6)
15
(0.9-112)
0/12
sIBM 10 5/5 70
(52-77)
3
(1-10)
9.4
(2-17)
1/7
Neurogenic control
ALS 11 6/5 47
(35-72)
1
(0.3-4)
8.2
(2-24)
1/7
Normal control# 24 13/11 5236
(24-75)
n.a. 1.98
(0.6-2.8)
0/8
p* <0.0001 <0.0002 0.0023
#

The normal controls were defined as having myalgia and exertion-induced complaints but no paresis or muscle atrophy, normal creatine kinase levels, normal EMG, and only mild unspecific changes or normal features in muscle biopsy. * Kruskal-Wallis One Way Analysis of Variance on Ranks, , post hoc analysis using Dunn's method, n.a. not applicable ALS amyotrophic lateral sclerosis, BMD muscular dystrophy Becker type, DM dermatomyositis, DMD muscular dystrophy Duchenne type, LGMD limb girdle muscular dystrophy, PM polymyositis, sIBM sporadic inclusion body myositis

*

post hoc analysis:

1

sIBM, DM, PM vs. DMD/BMD p<0.05, sIBM vs. LGMD2A, controls;

2

DM vs. LGMD2A, LGMD2B, LGMD2L,

3

controls vs. DMD/BMD, LGMD2A, LGMD2B, LGMD2L p<0.05.