Primary progressive aphasias associated with C9orf72 expansions: Another side of the story. (December 2021)
- Record Type:
- Journal Article
- Title:
- Primary progressive aphasias associated with C9orf72 expansions: Another side of the story. (December 2021)
- Main Title:
- Primary progressive aphasias associated with C9orf72 expansions: Another side of the story
- Authors:
- Saracino, Dario
Géraudie, Amandine
Remes, Anne M.
Ferrieux, Sophie
Noguès-Lassiaille, Marie
Bottani, Simona
Cipriano, Lorenzo
Houot, Marion
Funkiewiez, Aurélie
Camuzat, Agnès
Rinaldi, Daisy
Teichmann, Marc
Pariente, Jérémie
Couratier, Philippe
Boutoleau-Bretonnière, Claire
Auriacombe, Sophie
Etcharry-Bouyx, Frédérique
Levy, Richard
Migliaccio, Raffaella
Solje, Eino
Le Ber, Isabelle
Auriacombe, Sophie
Belliard, Serge
Blanc, Frédéric
Benchetrit, Eve
Bertin, Hugo
Boutoleau-Bretonnière, Claire
Bertrand, Anne
Bissery, Anne
Bombois, Stéphanie
Boncoeur, Marie-Paule
Brice, Alexis
Ceccaldi, Mathieu
Chastan, Mathieu
Chen, Yaohua
Chupin, Marie
Colliot, Olivier
Couratier, Philippe
Delbeuck, Xavier
Delmaire, Christine
Deramecourt, Vincent
Didic, Mira
Duyckaerts, Charles
Etcharry-Bouyx, Frédérique
Formaglio, Maïté
Gerardin, Emmanuel
Golfier, Véronique
Habert, Marie-Odile
idier Hannequin,
Lacomblez, Lucette
Lagarde, Julien
Lautrette, Géraldine
Le Ber, Isabelle
Le Toullec, Benjamin
Mackowiak, Marie-Anne
Martinaud, Olivier
Michel, Bernard-François
Monteil, Jacques
Oya, Assi-Hervé
Pariente, Jérémie
Pasquier, Florence
Petyt, Grégory
Rinaldi, Daisy
Rollin-Sillaire, Adeline
Roué-Jagot, Carole
Sayah, Sabrina
Sarazin, Marie
Thauvin-Robinet, Christel
Thomas-Anterion, Catherine
Sellal, François
Vercelletto, Martine
Wallon, David
… (more) - Abstract:
- Abstract: C9orf72 repeat expansions are rarely associated with primary progressive aphasias (PPA). In-depth characterization of the linguistic deficits, and the underlying patterns of grey-matter atrophy in PPA associated with the C9orf72 expansions (PPA- C9orf72 ) are currently lacking. In this study, we comprehensively analyzed a unique series of 16 patients affected by PPA- C9orf72 . Eleven patients were issued from two independent French and Finnish cohorts, and five were identified by means of literature review. Voxel-based morphometry (VBM) studies were performed on three of them. This study depicts the spectrum of C9orf72 –related aphasic phenotypes, and illustrates their linguistic presentation. The non-fluent/agrammatic variant was the most frequent phenotype in our series (9/16 patients, 56%), with apraxia of speech being the main defining feature. Left frontal lobe atrophy was present in these subjects, peaking in inferior frontal gyrus. Three patients (19%) showed the semantic variant, with progression of atrophy in temporo-polar regions, later involving orbitofrontal cortex. Anterior temporal lobe dysfunction was also particularly relevant in two patients (12.5%) with mixed forms of PPA. Lastly, two patients (12.5%) had unclassifiable PPA with predominating word-finding difficulties. No PPA- C9orf72 patients in our series fulfilled the criteria of the logopenic variant. Importantly, this study underlines the role of C9orf72 mutation in the disruption of the mostAbstract: C9orf72 repeat expansions are rarely associated with primary progressive aphasias (PPA). In-depth characterization of the linguistic deficits, and the underlying patterns of grey-matter atrophy in PPA associated with the C9orf72 expansions (PPA- C9orf72 ) are currently lacking. In this study, we comprehensively analyzed a unique series of 16 patients affected by PPA- C9orf72 . Eleven patients were issued from two independent French and Finnish cohorts, and five were identified by means of literature review. Voxel-based morphometry (VBM) studies were performed on three of them. This study depicts the spectrum of C9orf72 –related aphasic phenotypes, and illustrates their linguistic presentation. The non-fluent/agrammatic variant was the most frequent phenotype in our series (9/16 patients, 56%), with apraxia of speech being the main defining feature. Left frontal lobe atrophy was present in these subjects, peaking in inferior frontal gyrus. Three patients (19%) showed the semantic variant, with progression of atrophy in temporo-polar regions, later involving orbitofrontal cortex. Anterior temporal lobe dysfunction was also particularly relevant in two patients (12.5%) with mixed forms of PPA. Lastly, two patients (12.5%) had unclassifiable PPA with predominating word-finding difficulties. No PPA- C9orf72 patients in our series fulfilled the criteria of the logopenic variant. Importantly, this study underlines the role of C9orf72 mutation in the disruption of the most anterior parts of the language network, including prefrontal and temporo-polar areas. It provides guidelines for C9orf72 testing in PPA patients, with important clinical impact as gene-specific therapies are upcoming. … (more)
- Is Part Of:
- Cortex. Volume 145(2021)
- Journal:
- Cortex
- Issue:
- Volume 145(2021)
- Issue Display:
- Volume 145, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 145
- Issue:
- 2021
- Issue Sort Value:
- 2021-0145-2021-0000
- Page Start:
- 145
- Page End:
- 159
- Publication Date:
- 2021-12
- Subjects:
- Primary progressive aphasia -- Frontotemporal dementia -- Frontotemporal lobar degeneration -- C9orf72 -- Progranulin (GRN)
Neuropsychology -- Periodicals
Nervous system -- Periodicals
Neurology -- Periodicals
Psychophysiology -- Periodicals
Behavior -- Periodicals
Neurology -- Periodicals
612.825 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00109452 ↗
http://www.sciencedirect.com/science/journal/00109452 ↗
http://www.cortex-online.org ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cortex.2021.09.005 ↗
- Languages:
- English
- ISSNs:
- 0010-9452
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3477.150000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20074.xml