ALS and frontotemporal dementia belong to a common disease spectrum

Philippe Couratier (1, 2) , Philippe Corcia (3) , Géraldine Lautrette (2) , Marie Nicol (2, 1) , Benoît Marin (1, 4, 5)

1 EpiMaCT - Epidémiologie des Maladies Chroniques en zone tropicale
2 Service de Neurologie [CHU Limoges]
3 SLA CHRU Tours - Centre de compétence de la Sclérose Latérale Amyotrophique [CHRU Tours]
4 SIME - Service de l'Information Médicale et de l'Évaluation [CHU Limoges]
5 Laboratoire de Biostatistique et d'Informatique Médicale

ALS is now understood to be a complex multisystem neurodegenerative disease because areas other than the motor cortices of the brain undergo degeneration. Frontotemporal dementia (FTD) may be associated with motor neuron disease, and the transactive response DNA-binding protein 43 (TDP-43) is a major pathological substrate underlying both diseases. The recent discovery of a gene that can cause both FTD, ALS and FTD-ALS, C9ORF72, has modified the way for considering these two pathologies. These findings would allow the development of potential biomarkers and therapeutic targets for these devastating diseases. This review summarizes the key points leading up to our current understanding of the genetic, clinical and neuropathological overlap between FTD and ALS.

Mots clés: Amyotrophic lateral sclerosis; C9ORF72; Frontotemporal dementia; Motor neuron disease; TDP-43

Domaines: Santé publique et épidémiologie

Philippe Couratier, Philippe Corcia, Géraldine Lautrette, Marie Nicol, Benoît Marin. ALS and frontotemporal dementia belong to a common disease spectrum. Revue Neurologique, 2017, 173 (5), pp.273-279. ⟨10.1016/j.neurol.2017.04.001⟩. ⟨hal-03601424⟩