Frontotemporal lobar degeneration

There are 3 main histological subtypes found at post-mortem:

• FTLD-tau is characterised by tau positive inclusion bodies often referred to as Pick-bodies.[2] Examples of FTLD-tau include; Pick's disease, corticobasal degeneration, progressive supranuclear palsy.
• FTLD-TDP (or FTLD-U ) is characterised by ubiquitin and TDP-43 positive, tau negative, FUS negative inclusion bodies. The pathological histology of this subtype is so diverse it is subdivided into four subtypes based on the detailed histological findings:

• Type A presents with many small neurites and neuronal cytoplasmic inclusion bodies in the upper (superficial) cortical layers. Bar-like neuronal intranuclear inclusions can also be seen they are fewer in number.
• Type B presents with many neuronal and glial cytoplasmic inclusions in both the upper (superficial) and lower (deep) cortical layers, and lower motor neurons. However neuronal intranuclear inclusions are rare or absent. This is often associated with ALS and C9ORF72 mutations (see next section).
• Type C presents many long neuritic profiles found in the superficial cortical laminae, very few or no neuronal cytoplasmic inclusions, neuronal intranuclear inclusions or glial cytoplasmic inclusions. This is often associated with semantic dementia.
• Type D presents with many neuronal intranuclear inclusions and dystrophic neurites, and an unusual absence of inclusions in the granule cell layer of the hippocampus. Type D is associated with VCP mutations.
• Type E presents with neuronal granulofilamentous inclusions and abundant fine grains involving upper (superficial) and lower (deep) cortical layers. This has been associated with behavioral variant of frontotemporal dementia with a rapid clinical course.[3]

Two groups independently categorized the various forms of TDP-43 associated disorders. Both classifications were considered equally valid by the medical community, but the physicians and researchers in question have jointly proposed a compromise classification to avoid confusion.[4]

• FTLD-FUS; which is characterised by FUS positive cytoplasmic inclusions, intra nuclear inclusions, and neuritic threads. All of which are present in the cortex, medulla, hippocampus, and motor cells of the spinal cord and XIIth cranial nerve.

In December 2021 the structure of TDP-43 was resolved with cryo-EM[5][6] but shortly after it was argued that in the context of FTLD-TDP the protein involved could be TMEM106B (which has been also resolved with cryo-EM), rather than of TDP-43.[7][8]

There have been numerous advances in descriptions of genetic causes of FTLD, and the related disease amyotrophic lateral sclerosis.

• Mutations in the Tau gene (known as MAPT or Microtubule Associated Protein Tau) can cause a FTLD presenting with tau pathology (FTLD-tau).[9] There are over 40 known mutations at present.
• Mutations in the progranulin gene (PGRN) can cause a FTLD presenting with TDP-43 pathology (FTLD-TDP43). Patients with progranulin mutations have type 3 ubiquitin-positive, TDP-43 positive, tau-negative pathology at post-mortem. Progranulin is associated with tumorgenesis when overproduced, however the mutations seen in FTLD-TDP43 produce a haploinsufficiency, meaning that because one of the two alleles is damaged, only half as much progranulin is produced.[10]
• Mutations in the CHMP2B gene are associated with a rare behavioural syndrome akin to bvFTLD (mainly in a large Jutland cohort), presenting with a tau negative, TDP-43 negative, FUS negative, Ubiquitin positive pathology.
• Hypermorphic mutations in the VCP gene cause a TDP-43-positive FTLD which is associated with multisystem proteinopathy (MSP), also known as IBMPFD (inclusion body myopathy, Paget's disease and frontotemporal dementia)[11]
• A hypomorphic mutation in the VCP gene cause a unique type of FTLD-tau called vacuolar tauopathy with neurofibrillary tangles and neuronal vacuoles [12]
• Mutations in the TDP-43 gene (known as TARBP or TAR DNA-binding protein) are an exceptionally rare cause of FTLD, despite this protein being present in the pathological inclusions of many cases (FTLD-TDP43).[13] However, mutations in TARBP are a more common cause of ALS, which can present with frontotemporal dementia. Since these instances are not considered a pure FTLD they are not included here.

Mutations in all of the above genes cause a very small fraction of the FTLD spectrum. Most of the cases are sporadic (no known genetic cause).

• A proportion of FTLD-TDP43 [with ALS] cases had shown genetic linkage to a region on chromosome 9 (FTLD-TDP43/Ch9). This linkage has recently been pinned down to the C9ORF72 gene. Two groups published identical findings back-to-back in the journal Neuron in mid-2011, showing that a hexanucleotide repeat expansion of the GGGGCC genetic sequence within an intron of this gene was responsible. This expansion was found to be present in a large proportion of familial and sporadic cases, particularly in the Finnish population[14]

For diagnostic purposes, magnetic resonance imaging (MRI) and ([18F]fluorodeoxyglucose) positron emission tomography (FDG-PET) are applied. They measure either atrophy or reductions in glucose utilization. The three clinical subtypes of frontotemporal lobar degeneration, frontotemporal dementia, semantic dementia and progressive nonfluent aphasia, are characterized by impairments in specific neural networks.[15] The first subtype with behavioral deficits, frontotemporal dementia, mainly affects a frontomedian network discussed in the context of social cognition. Semantic dementia is mainly related to the inferior temporal poles and amygdalae; brain regions that have been discussed in the context of conceptual knowledge, semantic information processing, and social cognition, whereas progressive nonfluent aphasia affects the whole left frontotemporal network for phonological and syntactical processing.

United States Senator Pete Domenici (R-NM) was a known sufferer of FTLD, and the illness was the main reason behind his October 4, 2007, announcement of retirement at the end of his term. American film director, producer, and screenwriter Curtis Hanson died as a result of FTLD on September 20, 2016. British journalist Ian Black died from the disease on January 22, 2023.[16]

• Frontotemporal dementia and parkinsonism linked to chromosome 17

• Cairns, Nigel J.; Bigio, Eileen H.; MacKenzie, Ian R. A.; Neumann, Manuela; Lee, Virginia M.-Y.; Hatanpaa, Kimmo J.; White, Charles L.; Schneider, Julie A.; Grinberg, Lea Tenenholz; Halliday, Glenda; Duyckaerts, Charles; Lowe, James S.; Holm, Ida E.; Tolnay, Markus; Okamoto, Koichi; Yokoo, Hideaki; Murayama, Shigeo; Woulfe, John; Munoz, David G.; Dickson, Dennis W.; Ince, Paul G.; Trojanowski, John Q.; Mann, David M. A.; Consortium for Frontotemporal Lobar Degeneration (2007). "Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: Consensus of the Consortium for Frontotemporal Lobar Degeneration". Acta Neuropathologica. 114 (1): 5–22. doi:10.1007/s00401-007-0237-2. PMC 2827877. PMID 17579875.
• Cairns, N. J.; Grossman, M.; Arnold, S. E.; Burn, D. J.; Jaros, E.; Perry, R. H.; Duyckaerts, C.; Stankoff, B.; Pillon, B.; Skullerud, K.; Cruz-Sanchez, F. F.; Bigio, E. H.; MacKenzie, I. R.A.; Gearing, M.; Juncos, J. L.; Glass, J. D.; Yokoo, H.; Nakazato, Y.; Mosaheb, S.; Thorpe, J. R.; Uryu, K.; Lee, V. M.-Y.; Trojanowski, JQ. (2004). "Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease". Neurology. 63 (8): 1376–1384. doi:10.1212/01.wnl.0000139809.16817.dd. PMC 3516854. PMID 15505152.
• Mackenzie IR, Baborie A, Pickering-Brown S, et al. (November 2006). "Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype". Acta Neuropathologica. 112 (5): 539–49. doi:10.1007/s00401-006-0138-9. PMC 2668618. PMID 17021754.
• MacKenzie, Ian R. A.; Munoz, David G.; Kusaka, Hirofumi; Yokota, Osamu; Ishihara, Kenji; Roeber, Sigrun; Kretzschmar, Hans A.; Cairns, Nigel J.; Neumann, Manuela (2011). "Distinct pathological subtypes of FTLD-FUS". Acta Neuropathologica. 121 (2): 207–218. doi:10.1007/s00401-010-0764-0. PMID 21052700. S2CID 21435429.
• Davidson Y, Kelley T, Mackenzie IR, et al. (May 2007). "Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43". Acta Neuropathologica. 113 (5): 521–33. doi:10.1007/s00401-006-0189-y. PMID 17219193. S2CID 22524747.
• Neary D, Snowden JS, Gustafson L, et al. (December 1, 1998). "Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria". Neurology. 51 (6): 1546–54. doi:10.1212/wnl.51.6.1546. PMID 9855500. S2CID 37238391. Retrieved 2009-06-20.
• Pickering-Brown SM (July 2007). "The complex aetiology of frontotemporal lobar degeneration". Experimental Neurology. 206 (1): 1–10. doi:10.1016/j.expneurol.2007.03.017. PMID 17509568. S2CID 1280814.

• Hodges, John R. The Frontotemporal Dementia Syndromes. Cambridge University Press. 2007 ISBN 978-0-521-85477-1
• OMIM entries on FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS as well as C9ORF72
• GeneReviews/NCBI/NIH/UW entry on Amyotrophic Lateral Sclerosis Overview