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Table 2 Summary of cases form the University of Florida Neuromedicine Human Brain and Tissue Bank used in this study

From: Disease-, region- and cell type specific diversity of α-synuclein carboxy terminal truncations in synucleinopathies

Case

Clinical diagnosis

Primary pathological diagnosis

Secondary pathological diagnosis

Amyloid score (Thal)

Braak

CERAD

Gender

Age

PMI (hrs)

Control 1

Normal

AD low

 

1

II

none

M

88

4

Control 2

Normal

PART

 

0

II

none

F

72

4

Control 3

Normal

No significant pathological findings

 

0

0

none

F

55

12

Control 4

Progressive Myoclonic Epilepsy (Unverricht-Lundborg variant: EPM1)*

No significant pathological findings

 

0

0

0

M

51

31

FTLD-1

FTLD

FTLD-TDP43

 

1

0

none

F

67

30

MSA-1

MSA-C

MSA

 

0

0

none

F

67

4

MSA-2

MSA-P

MSA

AD low

1

I

none

F

60

6

MSA-3

MSA-P

MSA

PART

0

II

none

M

77

18

MSA-4

MSA-C

MSA

AD low; CAA

2

I

sparse

M

71

4

MSA-5

MSA-C

MSA

AD intermediate

2

III

sparse

M

59

4

MSA-6

MSA-P/C

MSA

PART, CAA

0

I

none

F

66

22

MSA-7

MSA-P

MSA

 

0

0

none

F

66

14

LBD-1

DLB

LBD diffuse neocortical

AD intermediate; CAA

3

IV

moderate

M

67

13

LBD-2

DLB

LBD diffuse neocortical

AD intermediate; CAA; ARTAG

3

III

sparse

F

67

4

LBD-3

AD

LBD diffuse neocortical

AD intermediate; CAA

3

IV

frequent

F

81

15

LBD-4

AD

LBD diffuse neocortical

AD high; CAA

3

V

frequent

F

74

8

LBD-5

AD

LBD diffuse neocortical

AD high; CAA

3

VI

frequent

M

80

21

AD/ALB-1

AD

LBD limbic-transitional

AD intermediate; CAA

2

V

moderate

F

83

9

AD/ALB-2

AD

LBD amygdala

AD high; CAA

3

VI

frequent

M

64

3

AD/ALB-3

AD

LBD amygdala

AD high; CAA

3

VI

frequent

F

67

8

  1. Listed are the clinical and pathological diagnoses, the sex, age at death, amyloid score (Thal), Braak stage and CERAD ratings. AD Alzheimer’s disease, AD/ALB AD with amygdala restricted Lewy bodies, ARTAG aging related tau astrogliopathy, CAA cerebral amyloid angiopathy, DLB dementia with Lewy body, FTLD frontotemporal lobar degeneration, LATE limbic-predominant age related TDP-43 encephalopathy, LBD Lewy body dementia, MSA-C multiple system atrophy with predominant cerebellar ataxia, MSA-P multiple system atrophy with predominant Parkinsonism, PART primary age-related tauopathy, PMI postmortem interval. * CTSB mutation