The frontotemporal dementia-motor neuron disease continuum

James R. Burrell, Glenda M. Halliday, Jillian J. Kril, Lars M. Ittner, Jürgen Götz, Matthew C. Kiernan, John R. Hodges*

*Corresponding author for this work

Research output: Contribution to journalReview article

113 Citations (Scopus)

Abstract

Early reports of cognitive and behavioural deficits in motor neuron disease might have been overlooked initially, but the concept of a frontotemporal dementia-motor neuron disease continuum has emerged during the past decade. Frontotemporal dementia-motor neuron disease is now recognised as an important dementia syndrome, which presents substantial challenges for diagnosis and management. Frontotemporal dementia, motor neuron disease, and frontotemporal dementia-motor neuron disease are characterised by overlapping patterns of TAR DNA binding protein (TDP-43) pathology, while the chromosome 9 open reading frame 72 (C9orf72) repeat expansion is common across the disease spectrum. Indeed, the C9orf72 repeat expansion provides important clues to disease pathogenesis and suggests potential therapeutic targets. Variable diagnostic criteria identify motor, cognitive, and behavioural deficits, but further refinement is needed to define the clinical syndromes encountered in frontotemporal dementia-motor neuron disease.

Original languageEnglish
Pages (from-to)919-931
Number of pages13
JournalThe Lancet
Volume388
Issue number10047
DOIs
Publication statusPublished - 27 Aug 2016
Externally publishedYes

Fingerprint Dive into the research topics of 'The frontotemporal dementia-motor neuron disease continuum'. Together they form a unique fingerprint.

  • Cite this

    Burrell, J. R., Halliday, G. M., Kril, J. J., Ittner, L. M., Götz, J., Kiernan, M. C., & Hodges, J. R. (2016). The frontotemporal dementia-motor neuron disease continuum. The Lancet, 388(10047), 919-931. https://doi.org/10.1016/S0140-6736(16)00737-6