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Erschienen in: Acta Neuropathologica 1/2011

01.07.2011 | Consensus Letter

A harmonized classification system for FTLD-TDP pathology

verfasst von: Ian R. A. Mackenzie, Manuela Neumann, Atik Baborie, Deepak M. Sampathu, Daniel Du Plessis, Evelyn Jaros, Robert H. Perry, John Q. Trojanowski, David M. A. Mann, Virginia M. Y. Lee

Erschienen in: Acta Neuropathologica | Ausgabe 1/2011

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Excerpt

In 2006, two papers were published, each describing pathological heterogeneity in cases of frontotemporal lobar degeneration (FTLD) with ubiquitin-positive, tau-negative inclusions (FTLD-U) [7, 11]. In both studies, large series of cases were evaluated and the investigators felt that they could recognize three distinct histological patterns, based on the morphology and anatomical distribution of ubiquitin immunoreactive neuronal inclusions. The findings of Sampathu et al. were further supported by differential labelling of the pathology, using a panel of novel monoclonal antibodies; whereas, Mackenzie et al. found relatively specific clinicopathological correlations. Most importantly, the pathological features that defined the subtypes in these two studies were almost identical, providing powerful validation of the results. However, because the studies were conducted simultaneously and independently, the numbering of the subtypes, used in the respective papers, did not match (Table 1).
Table 1
Proposed new classification system for FTLD-TDP pathology, compared with existing systems
New system
Mackenzie et al. [7]
Sampathu et al. [11]
Cortical pathology
Common phenotype
Associated genetic defects
Type A
Type 1
Type 3
Many NCI
bvFTD
GRN mutations
Many short DN
PNFA
Predominantly layer 2
Type B
Type 3
Type 2
Moderate NCI
bvFTD
Linkage to chromosome 9p
MND with FTD
Few DN
All layers
Type C
Type 2
Type 1
Many long DN
SD
 
bvFTD
Few NCI
Predominantly layer 2
Type D
Type 4a
Type 4a
Many short DN
Familial IBMPFD
VCP mutations
Many lentiform NII
Few NCI
All layers
bvFTD behavioural variant frontotemporal dementia, DN dystrophic neurites, GRN progranulin gene, IBMPFD inclusion body myopathy with Paget’s disease of bone and frontotemporal dementia, MND motor neuron disease, NCI neuronal cytoplasmic inclusions, NII neuronal intranuclear inclusions, PNFA progressive non-fluent aphasia, SD semantic dementia, VCP valosin-containing protein gene
aDescribed subsequently by Forman et al. [4]
Literatur
1.
Zurück zum Zitat Cairns NJ, Neumann M, Bigio EH et al (2007) TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. Am J Pathol 171:227–240PubMedCrossRef Cairns NJ, Neumann M, Bigio EH et al (2007) TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions. Am J Pathol 171:227–240PubMedCrossRef
2.
Zurück zum Zitat Davidson Y, Kelley T, Mackenzie IRA et al (2007) Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43. Acta Neuropathol 113:521–533PubMedCrossRef Davidson Y, Kelley T, Mackenzie IRA et al (2007) Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43. Acta Neuropathol 113:521–533PubMedCrossRef
3.
Zurück zum Zitat Dickson DW (2008) TDP-43 immunoreactivity in neurodegenerative disorders: disease versus mechanism specificity. Acta Neuropathol 115:147–149PubMedCrossRef Dickson DW (2008) TDP-43 immunoreactivity in neurodegenerative disorders: disease versus mechanism specificity. Acta Neuropathol 115:147–149PubMedCrossRef
4.
Zurück zum Zitat Forman MS, Mackenzie IR, Cairns NJ et al (2006) Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations. J Neuropathol Exp Neurol 65:571–581PubMedCrossRef Forman MS, Mackenzie IR, Cairns NJ et al (2006) Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations. J Neuropathol Exp Neurol 65:571–581PubMedCrossRef
5.
Zurück zum Zitat Geser F, Martinez-Lage M, Robinson J et al (2009) Clinical and pathological continuum of multisystem TDP-43 proteinopathies. Arch Neurol 66:180–189PubMedCrossRef Geser F, Martinez-Lage M, Robinson J et al (2009) Clinical and pathological continuum of multisystem TDP-43 proteinopathies. Arch Neurol 66:180–189PubMedCrossRef
6.
Zurück zum Zitat Josephs KA, Stroh A, Dugger B, Dickson DW (2009) Evaluation of subcortical pathology and clinical correlations in FTLD-U. Acta Neuropathol 118:349–358PubMedCrossRef Josephs KA, Stroh A, Dugger B, Dickson DW (2009) Evaluation of subcortical pathology and clinical correlations in FTLD-U. Acta Neuropathol 118:349–358PubMedCrossRef
7.
Zurück zum Zitat Mackenzie IRA, Baborie A, Pickering-Brown S et al (2006) Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype. Acta Neuropathol 112:539–549PubMedCrossRef Mackenzie IRA, Baborie A, Pickering-Brown S et al (2006) Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype. Acta Neuropathol 112:539–549PubMedCrossRef
8.
Zurück zum Zitat Mackenzie IR, Neumann M, Bigio EH et al (2009) Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations. Acta Neuropathol 117:15–18PubMedCrossRef Mackenzie IR, Neumann M, Bigio EH et al (2009) Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations. Acta Neuropathol 117:15–18PubMedCrossRef
9.
Zurück zum Zitat Neumann M, Mackenzie IR, Cairns NJ et al (2007) TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations. J Neuropathol Exp Neurol 66:152–157PubMedCrossRef Neumann M, Mackenzie IR, Cairns NJ et al (2007) TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations. J Neuropathol Exp Neurol 66:152–157PubMedCrossRef
10.
Zurück zum Zitat Neumann M, Sampathu DM, Kwong LK et al (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314:130–133PubMedCrossRef Neumann M, Sampathu DM, Kwong LK et al (2006) Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 314:130–133PubMedCrossRef
11.
Zurück zum Zitat Sampathu DM, Neumann M, Kwong LK et al (2006) Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies. Am J Pathol 169:1343–1352PubMedCrossRef Sampathu DM, Neumann M, Kwong LK et al (2006) Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies. Am J Pathol 169:1343–1352PubMedCrossRef
Metadaten
Titel
A harmonized classification system for FTLD-TDP pathology
verfasst von
Ian R. A. Mackenzie
Manuela Neumann
Atik Baborie
Deepak M. Sampathu
Daniel Du Plessis
Evelyn Jaros
Robert H. Perry
John Q. Trojanowski
David M. A. Mann
Virginia M. Y. Lee
Publikationsdatum
01.07.2011
Verlag
Springer-Verlag
Erschienen in
Acta Neuropathologica / Ausgabe 1/2011
Print ISSN: 0001-6322
Elektronische ISSN: 1432-0533
DOI
https://doi.org/10.1007/s00401-011-0845-8

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