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Table 2 Quantification of kif21b expression in situ

From: Abundant kif21b is associated with accelerated progression in neurodegenerative diseases

Patient id

Age at death

Gender

Presenting symptom

Time to EDSS 6.0 (years)

Neuropathology assessment

Kif21b1

Kif21b genotype

Braak stage

Amyloid

Neu-rons

Glia cells

NDC2

49

F

NA

NA

0

ND

+

-

GA

NDC4

53

F

0

0

+/-

-

GA

NDC6

56

F

0

0

+/-

-

GG

NDC8

62

F

1

0

+/-

-

GA

NDC10

70

F

0

B

+

+

GA

NDC13

50

M

1

0

-

-

AA

NDC29

77

M

1

B

+/- / +

-

GG

NDC30

78

M

1

A

+/-

+/-

AA

NDC36

82

M

1

A

+/-

-

GG

MS4

50

F

Myelitis

7

ND

ND

-

-

GG

MS6

56

F

ND

4*

ND

ND

+

+

GG

MS8

63

F

Optic neuritis

17

0

0

+

-

GA

MS10

70

F

Cerebrum

30

1

0

-

-

GG

MS23

56

M

Myelitis

2

ND

ND

-

-

AA

MS25

57

M

Myelitis

6

ND

ND

+/-

-

GG

MS40

74

M

Myelitis

8

3

0

-

-

AA

AD2

57

F

NA

NA

6

C

+

+/-

GA

AD4

57

F

6

C

+

-

GG

AD6

59

F

5

C

+/++

+/++

GA

AD8

63

F

5

C

+/-

-

GG

AD10

70

F

5

C

+

-

GA

AD13

42

M

6

C

+/-

+/-

AA

AD15

54

M

6

C

+

+/-

AA

AD20

58

M

4

C

++

++

GG

AD42

76

M

5

C

+

+/-

GA

  1. In age-, gender- and genotyped matched MS and AD patients, kif21b protein expression was assessed. NA not applicable, ND not determined or documented.
  2. 1scored as: - no positive cells, +/-1-2 positive cells per field, + maximum of ~30% of the cells positive, ++ ~60% of the cells positive, +++ ~80% positive cells and +++ (virtually) all cells positive.
  3. *time to EDSS 9.0.
  4. Neuropathology assessment based on Braak criteria [12].