Tauopathies. A contemporary way to consider a set of neurodegenerative diseases based on their molecular signature. John Growdon, M.D. Neurofilament tangles are composed of paired helical filaments in AD, and straight filaments in conditions such as PSP.
A contemporary way to consider a set of neurodegenerative diseases based on their molecular signature
John Growdon, M.D.
Neurofilament tangles are composed of paired helical filaments in AD, and straight filaments in conditions such as PSP.
Electron microscopy of neurofilament fibers, labeled by polyclonal anti-tau.
Alzheimer’s disease filaments in AD, and straight filaments in conditions such as PSP.
Argyrophilic grain dementia
Nieman-Pick, type C
Autosomal recessive PDTauopathies: Clinical Diseases
History of LT born: 6/26/05 died: 11/16/87
1977: 72 y.o. woman with subtle onset of difficulty finding words in speaking.
1980:MGH examination. No focal neurologic signs. Speaking greatly impaired
with anomia & circumlocutions (pen=“something you write with”); intact
memory; no apraxia; preserved personality; independent ADLs. BDS = 2.
1982: worsening expressive language; sings better than she speaks. Recent onset
of apraxia. Stopped driving a car. Sweet personality. BDS = 12.
1983: expressive & receptive aphasia. Withdrawn personality with apathetic mood.
BDS = 16 .
1984: mute, but occasional non-verbal communication. No housework, but still
cares for personal hygiene.
2. Slow steady deterioration.
3. Two or more of the following:
a. Emotional blunting
b. Apathy or restlessness
c. Coarsening of social behavior
4. Relative preservation of memory & parietal-lobe functions.
Caregiver Report of Initial Symptoms in Pick Disease (PiD) and Alzheimer Disease (AD) Patients: Mean Prevalence (%)
Symptom PiD n=34 AD n=78
Memory 61.8 93.6 p<0.001
Speech 29.4 p<0.05 9.1
Use of objects 0.6 2.6
Socializing 2.9 2.6
Personality 53.3 p=0.07 14.1
Irritability/aggressiveness 11.8 3.9
Reasoning 5.9 6.5
Sense of direction 0.0 7.8
Vision 0.0 1.3
Mean Cognitive Test Scores (+/- SD) at Initial Examination for PiD, AD, and Normal Control Subject (NCS) Groups
Test PiD AD NCS
NYU Immediate Recall 3.1 (2.7) 2.5 (1.9) 8.4 (3.1)
NYU Delayed Recall 2.3 (3.1) 0.7 (1.3) 7.8 (3.2)
Geometric Figure Recall 4.0 (3.6) 2.2 (2.9) 7.2 (2.6)
Benton Visual Retention 9.2 (3.0) 8.3 (2.8) 11.9 (1.7)
Boston Naming 24.6 (9.7) 25.8 (9.1) 37.1 (5.0)
Stroop Color Naming 13.3 (10.1) 11.2 (7.6) 29.3 (10.9)
Luria Mental Rotation 8.1 (1.9) 6.0 (2.8) 8.3 (2.4)
Picture Arrangement 5.9 (4.3) 4.4 (3.1) 10.5 (5.1)
NCS scores were significantly superior to AD scores on all tests (p<0.05), and to PiD on all tests (p<0.05) on all tests except the Luria. PiD scores were significantly superior to AD scores on the NYU Delayed Recall and Luria tests (p<0.001).
Cognitive test scores over time: AD open circles; Pick black circles
As judged by global measures of dementia severity, PiD (black circles) progresses faster than AD (open circles).
Clinical Aspects: PcD vs. AD (black circles) progresses faster than AD (open circles).
Initial Symptoms: Personality change & language impairments are more commonly reported in PcD; memory loss reported in both, but was more common in AD.
Cognitive Tests: PcD superior to AD in explicit memory & visuospatial functions. Over time, dementia worsened in both. PcD dclined more rapidly than AD on language tests and measures of global dementia severity.
At the Massachusetts General Hospital between 1985 and 1996, 63% of the patients examined in the Memory Disorders Unit had a clinical diagnosis of AD. During the same period of time, only 2% of the patients had a clinical diagnosis of Pick’s disease.
Of autopsied cases (n=696), 52% had AD and 3% had Pick’s disease.
Six tau isoforms that are expressed in human brain: alternatively splicd exons 2,3 & 10 are shown in white; black bars indicate the microtubular-binding repeats.
Electrophoretic tau profiles distinguish AD from Pick’s disease (PiD).
Characteristic western immunoblots using phosphorylation-dependent monoclonal antibodies. In AD, all isoforms are phosphorylated; in PiD, only 3R isoforms.
MGH cases, courtesy of Andre Delacourte
History of Mr. GSC born: 3/17/26 died: 1/27/95
1979: Insidious onset of difficulty arising from a chair.
1985: Postural instability, with falling backward. Hip fracture.
1986: Difficulty focusing eyes and looking down when reading a page in a book.
1989:MGH Examination. Slow fractionated saccades; 3 mm vertical gaze. PD
stage 3 stigmata: akinesia, limb rigidity, en bloc turns. BDS = 2 (normal).
1991: Absent vertical saccades. Blepharospasms. Dsyphagia. Micrographia.
1992: Neck rigidity. Dysarthria. Requires assistance to stand; multiple falls with
fractured collarbone. Stage 4 PD.
1993: Eyes fixed…no volitional movement but intact oculocephalic reflex. Fell
with resultant skull fracture.
Memory is less affected in PSP than in classic dementing illnesses such as AD
Clinical Characteristics of PSP Patients and Separate Groups of Normal Control Subjects (NCS) Studied with Cognitive Tests & SPECT
Subjects Age, yrs. Duration, yrs. H&Y stage
PSP n=11 67.5 4.6 3.6
NCS- SPECT n=10 70.8 na na
NCS-Cognition n=16 66.5 na na
Cognitive Test PSP Control Subjects
Delayed Story Recall5.8 (3.0) 8.3 (2.5)
Boston Naming 33.5 (2.3)** 38.2 (3.9)
Verbal Fluency “S” 4.1 (2.2)*** 18.8 (7.0)
Stroop 39.9 (23.7)*** 106.3 (9.0)
Raven’s Matrices 23.6 (5.2)*** 32.5 (3.3)
Picture Arrangement 4.0 (2.8)** 11.4 (4.5)
** = p<.01***= p<0.001
Gel 8-15 %
AD2 at 1/10 000e
Quantification of pathological tau proteins
In PSP, aggregated filaments are largely hyperphosphorylated tau 4R isoforms encoded by exon 10
MGH case, courtesy of Andre Delacourte
1. Hyperphosphorylated 4R tau in tangles
2. The tau gene A0 allele (a dinucleotide repeat in the intron following exon 10) is over represented in PSP.
3. The tau H1 haplotype has high sensitivity (98%) but only modest specificy as a marker for PSP
4. There are rare families with atypical PSP apparently caused by mutations in the tau gene.
5. Mutations in the tau gene have not been found in most sporadic PSP cases.
6. Some tau smoke, but no fire…more to follow!