Table 1 Demographic data and percentage of resPrPD T2 detected in the brain of sCJDVV1, sCJDVV2 and sCJDVV1-2.

From: Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics

sCJD subtype

Case #

Disease onseta

Disease durationa

% resPrPD T2b

Cerebral cortexa,c

Subcortical regionsa,d

Cerebelluma

Whole braina,e

VV2

1-8

68 ± 8f

6 ± 2f

100

100

100

100

VV1-2

1

55

4

97

100

100

98

2

70

3

100

100

76

98

3

70

17

94

97

100

96

4

66

4

93

99

100

95

5

74

5

90

99

100

93

6

73

7

100

62

100

93

7

44

7

88

99

99

92

8

45

5

87

100

100

91

9

57

8

69

93

100

77

10

60

5

63

87

100

72

11

79

8

48

91

100

63

12

84

4

45

73

100

55

13

60

5

38

78

64

48

14

68

4

26

45

100

37

15

69

26

2

28

0

9

16

71

18

6

10

10

8

17

66

3

9

1

ND

7

18

52

7

4

5

ND

4

 

65 ± 11f

8 ± 6f

59 ± 37f

70 ± 36f

84 ± 33f

65 ± 41f

VV1

1-5

32 ± 5f

11 ± 2f

0

0

0

0

  1. aExpressed as individual numerical values or means ± SD. bAll T2% values determined by densitometry on long gels WB probed with Ab 3F4 and 1E4. cAverage of frontal (superior and middle gyrus), temporal, parietal, occipital (visual and non-visual), entorhinal and hippocampal cortices. dAverage of putamen, thalamus and substantia nigra. eAverage of previous three brain regions. fExpressed as mean ± standard deviation. ND: Neither T1 nor T2 were detected.