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Table 2 Studies investigating changes in the human suprachiasmatic nucleus in aging and tauopathies

From: Neuronal and glial vulnerability of the suprachiasmatic nucleus in tauopathies: evidence from human studies and animal models

Tauopathy

Reference

Subjects

Tau inclusion(b)

Evidence of neuronal death(c)

Note

Sex

Age at death (years) (a)

Described diagnosis (Pathologically confirmed)

AD

Swaab et al. (1985) [9]

M:12

F:16

M: 16–85; mean [SEM]: 46[7] F: 10–93; mean [SEM]: 58[7]

Non-demented

Not tested

Control

Astrocytosis

M:1

F: 3

Pooled M/F; mean [SEM]: 79[5]

SDAT (Senile dementia of the Alzheimer’s type)

Not tested

* (AVP, number)

** (AVP, volume)

Swaab et al. (1992) [14]

M: 4

F: 3

M: 47–85; mean [SEM]: 72[9] F: 59–91; mean [SEM]: 79[10]

Non-demented

Absent

Control

M: 5

F: 7

M: 45–97; mean [SEM]: 71[9] F: 56–90; mean [SEM]: 75[5]

Alzheimer’s disease

Mild (only a very few/some)(b)

**

Zhou et al. (1995) [12]

M: 24

F: 22

M: 26–82; mean [SEM]: 53[3] F: 26–81; mean [SEM]: 53[3]

No primary neurological or psychiatric disease

Not tested

Control

M: 11

F: 10

M: 51–84; mean [SEM]: 68[4] F: 59–83; mean [SEM]: 71[3]

Alzheimer’s disease

Not tested

** (VIP, number)

** (VIP, volume)

Stopa et al. (1999) [10]

Pooled M/F: 10

Pooled M/F: mean [SEM]: 63[12]

Non-demented

Absent

Control

Pooled M/F: 19

Pooled M/F: mean [SEM]: 72[8] (d)

Alzheimer’s disease (Probable; NINCDS-ADRDA)

Rare

*** (AVP)

Wu et al. (2007) [13]

M: 11

F: 13

M: 19–83; mean [SEM]: 52[8] F: 21–85; mean [SEM]: 45[5]

Non-demented

Not tested

Control

M: 4

F: 7

M: 64–87; mean [SEM]: 71[5] F: 65–82; mean [SEM]: 73[2]

Alzheimer’s disease (Preclinical)

Not tested

NS (AVP/VIP number)

NS (AVP/VIP density)

M: 4

F: 7

M: 64–83; mean [SEM]: 72[5] F: 59–86; mean [SEM]: 72[4]

Alzheimer’s disease (Late clinical)

Not tested

* (AVP/VIP number)

* (AVP/VIP density)

Harper et al. (2008) [11]

M: 5

F: 4

Pooled M/F: mean [SEM]: 64[11]

Non-demented

Not tested

Control

M: 17–19 (e)

F: 0

Pooled M/F: mean [SEM]: 70[7]

Alzheimer’s disease (Pooled early (Braak III-IV) and late (Braak V-VI; including LBD)

Not tested

** (AVP)

*** (NT)

Increased Glia/Neuron ratio

Wang et al. (2015) [15]

Pooled M/F: 10

Pooled M/F: mean [SD]: 91[6]

Non-demented

Not tested

Pooled subjects and assessed a correlation coefficient between the number of VIP-SCN neurons and circadian actigraphy data (VIP only):

R = 0.83

P = 0.008

Delayed circadian activity rhythm phase

Pooled M/F: 7

Pooled M/F: mean [SD]: 90[5]

Alzheimer’s disease

Not tested

PiD

Harper et al. (2008) [11]

M: 5

F: 4

Pooled M/F: mean[SEM]: 64 11] 

Non-demented

Not tested

Control

 

M: 2 (PiD only; (f))

F: 0

Non-mentioned

Pick’s disease

Not tested

** (AVP)

Stopa et al. (1999) [10]

Pooled M/F: 13

Pooled M/F: mean[SEM]: 63[12] 

Non-demented

Not tested

Control

Pooled M/F: 3

Pooled M/F: mean[SEM]: 72[8]  (d)

Pick’s disease

Not tested

* (NT)

CBD

Harper et al. (2008) [11]

M: 5

F: 4

Pooled M/F: mean[SEM]: 64[11] 

Non-demented

Not tested

Control

M: 2/ F: 0

Non-mentioned

Corticobasal degeneration

Not tested

** (AVP)

PSP

De Pablo-Fernandes et al. (2018) [21]

Pooled M/F: 5

Pooled M/F: median (IQR): 84 (78–88) (g)

Non-demented

Absent

Control

Pooled M/F: 5

Pooled M/F: median (IQR): 74 (70–81) (g)

Progressive supranuclear palsy

2 subjects: Mild

3 subjects: Moderate

Not tested

  1. (a) Round to integer, (b) As described in the reference, (c) Statistical significance (As described in the reference), (d) Pooled all demented cases in the reference (AD and FTD, etc.), (e) Subjects- 19: total, 18: glia/neuron ratio, 17: AVP, NT data, (f) The number of cases is part of the pooled disease group (FTD; PiD and CBD), (g) Pooled subjects collected for another ROI investigation. Abbreviations: AD: Alzheimer’s disease, AVP: Arginine vasopressin, CBD: Corticobasal degeneration, FTD: Frontotemporal disorders, PiD: Pick’s disease, PSP: Progressive supranuclear palsy, N: the number of subjects (only patients), NT: Neurotensin