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Table 1 Patient characteristics at erenumab initiation

From: Calcitonin gene related peptide monoclonal antibody treats headache in patients with active idiopathic intracranial hypertension

 

P1

P2

P3

P4

P5

P6

P7

Mean (SD)

Age (years)

42

34

46

24

36

25

25

33.1 (8.2)

Duration of IIH (years)

2

2

1

1

4

2

5

2.4 (1.5)

Headache exacerbation at IIH diagnosis

+++

+++

+++

+++

+++

+++

+++

 

Duration of headaches from resolution of papilloedema to initiation of erenumab (months)

12

3

3

3

24

6

3

7.7 (7.9)

Preventative drug class failure a

4

3

3

4

5

4

3

3.7 (0.8)

Preventative drug class trial b

3

2

1

0

4

1

1

1.7 (1.4)

Migraine family history

yes

no

missing

no

no

yes

no

 

Migraine prior to IIH

yes

yes

yes

no

no

yes

no

 

MmsHD 12 months prior

12

20

16

16

14

8

14

14.3 (3.5)

p = 0.778

MmsHD at erenumab initiation

13

17

15

20

14

11

12

14.6 (3.1)

MHD 12 months prior

30

30

30

30

28

30

20

28.3 (3.7)

p = 0.593

MHD at erenumab initiation

30

30

27

30

30

30

25

28.9 (2.0)

Headache severity (NRS) at erenumab initiation

5.7

5.2

7.2

7.3

5.2

4.5

7.1

6.0 (1.2)

Monthly analgesic days at erenumab initiation

2

6

6

20

7

4

12

8.1 (6.1)

HIT-6 score at erenumab initiation

68

65

70

75

66

68

63

67.9 (3.9)

Frisén grade at erenumab initiation (both eyes)

0

0

0

0

0

0

0

0

OCT global average RNFL thickness at Erenumab initiation worst eye (μm) c

118

93

123

113

107

118

103

110.7 (10.4)

BMI at erenumab initiation

31

46.2

35.2

37.3

42.1

29.4

28.8

35.7 (6.6)

IIH characteristics at erenumab initiation

B, T

B, T

B, T

B, D, T

B, D, T

D, T

B, T

 

Acetazolamide at erenumab initiation

no

no

no

no

no

500 mg

no

 
  1. Patient clinical characteristics at erenumab initiation. Monthly values refer to the 30-day pre-treatment period. *, p values indicate changes from the 30-day pre-treatment period prior to erenumab initiation
  2. aFailure defined as any of: inadequate efficacy with appropriate dosing and treatment duration; intolerable adverse effects; contraindications preventing use
  3. bTrial defined as any of: inadequate efficacy with appropriate dosing and treatment duration; intolerable adverse effects
  4. cHeidelberg Engineering SPECTRALIS, Heidelberg, Germany
  5. +++ severe
  6. Abbreviations: P Patient, IIH Idiopathic intracranial hypertension, MmsHD Monthly moderate/severe headache days, MHD Monthly headache days, NRS Numeric Rating Scale (0 = no pain to 10 = worst imaginable pain), HIT-6 Headache impact test-6, BMI Body mass index, B Blurred vision, D double vision, T Tinnitus, V Visual obscurations, OCT Optical coherence tomography, RNFL Retinal nerve fiber layer