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Table 1 Demographic and clinical characteristics of the study population and healthy controls

From: Hepatitis E virus as a trigger for Guillain-Barré syndrome

 

GBS

(n = 163)

Healthy controls

(n = 263)

Median age in years (SD; range)

59 (17;18–87)

28 (15;18–89)

Sex:

 Male

95 (58.3)

119 (45.2)

 Female

68 (41.7)

144 (54.8)

GBS Variants:

 Classical GBS

140 (85.9)

n.a.

  sensorimotor

93 (57.1)

  pure motor

22 (13.5)

  pure sensory

5 (3.1)

  paraparetic

10 (6.1)

  Pharyngeal-cervical-brachial

2 (1.2)

  Bilateral facial palsy with paraesthesias

8 (4.9)

Miller-Fisher syndrome (MFS)

22 (13.5)

MFS-GBS overlap

1 (0.6)

GBS disability score at nadir:

Mean (SD)

3.2 ± 1.2

n.a.

Median

3.0

  0 - Healthy

  1 - Minor signs or symptoms of neuropathy, capable of manual work

12 (7.4)

  2 - Able to walk without support of a stick but incapable of manual work

39 (23.9)

  3 - Able to walk with a stick, appliance or support

42 (25.8)

  4 - Confined to bed or wheelchair-bound

49 (30.1)

  5 - Requiring assisted ventilation

21 (12.9)

  6 - Dead

CSF analysis (n = 161):

 Albuminocytological dissociation

113 (70.2)

 

 Slightly increased cell count (5–50/μl) and increased protein level

26 (16.2)

 Increased cell count (50–100/μl) and increased protein level

2 (1.2)

 Normal

20 (12.4)

Electrophysiological testing:

  

 Pathological

144 (88.3)

  AIDP

31 (19.0)

  Axonal-demyelinating subtype

55 (33.7)

  Predominantly demyelinating subtype

22 (13.5)

  Predominantly axonal subtype

11 (6.8)

  AMAN

7 (4.3)

  AMSAN

9 (5.5)

  Not classifiable

9 (5.5)

  Normal

19 (11.7)

  1. Data are listed as numbers (%) unless indicated otherwise
  2. AIDP acute inflammatory demyelinating polyradiculoneuropathy, AMAN acute motor axonal neuropathy, AMSAN acute motor sensory axonal neuropathy CSF cerebrospinal fluid, GBS Guillain-Barré Syndrome, n.a. not applicable, n number, SD standard deviation