UCL Discovery Stage
UCL home » Library Services » Electronic resources » UCL Discovery Stage

Dysphagia in primary progressive aphasia: Clinical predictors and neuroanatomical basis

Mazzeo, Salvatore; Mulroy, Eoin; Jiang, Jessica; Lassi, Michael; Johnson, Jeremy CS; Hardy, Chris JD; Rohrer, Jonathan D; ... Volkmer, Anna; + view all (2024) Dysphagia in primary progressive aphasia: Clinical predictors and neuroanatomical basis. European Journal of Neurology 10.1111/ene.16370. (In press). Green open access

[thumbnail of Euro J of Neurology - 2024 - Mazzeo - Dysphagia in primary progressive aphasia  Clinical predictors and neuroanatomical.pdf]
Preview
PDF
Euro J of Neurology - 2024 - Mazzeo - Dysphagia in primary progressive aphasia Clinical predictors and neuroanatomical.pdf - Published Version

Download (1MB) | Preview

Abstract

Background and purpose: Dysphagia is an important feature of neurodegenerative diseases and potentially life-threatening in primary progressive aphasia (PPA) but remains poorly characterized in these syndromes. We hypothesized that dysphagia would be more prevalent in nonfluent/agrammatic variant (nfv)PPA than other PPA syndromes, predicted by accompanying motor features, and associated with atrophy affecting regions implicated in swallowing control. Methods: In a retrospective case–control study at our tertiary referral centre, we recruited 56 patients with PPA (21 nfvPPA, 22 semantic variant [sv]PPA, 13 logopenic variant [lv]PPA). Using a pro forma based on caregiver surveys and clinical records, we documented dysphagia (present/absent) and associated, potentially predictive clinical, cognitive, and behavioural features. These were used to train a machine learning model. Patients' brain magnetic resonance imaging scans were assessed using voxel-based morphometry and region-of-interest analyses comparing differential atrophy profiles associated with dysphagia presence/absence. Results: Dysphagia was significantly more prevalent in nfvPPA (43% vs. 5% svPPA and no lvPPA). The machine learning model revealed a hierarchy of features predicting dysphagia in the nfvPPA group, with excellent classification accuracy (90.5%, 95% confidence interval = 77.9–100); the strongest predictor was orofacial apraxia, followed by older age, parkinsonism, more severe behavioural disturbance, and more severe cognitive impairment. Significant grey matter atrophy correlates of dysphagia in nfvPPA were identified in left middle frontal, right superior frontal, and right supramarginal gyri and right caudate. Conclusions: Dysphagia is a common feature of nfvPPA, linked to underlying corticosubcortical network dysfunction. Clinicians should anticipate this symptom particularly in the context of other motor features and more severe disease.

Type: Article
Title: Dysphagia in primary progressive aphasia: Clinical predictors and neuroanatomical basis
Open access status: An open access version is available from UCL Discovery
DOI: 10.1111/ene.16370
Publisher version: http://dx.doi.org/10.1111/ene.16370
Language: English
Additional information: This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third-party material in this article are included in the Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences, Neurosciences & Neurology, Alzheimer dementia, dysphagia, primary progressive aphasia, semantic dementia, swallowing, SUPRANUCLEAR PALSY, DIAGNOSIS, PATHOLOGY, APRAXIA, STROKE, TIME
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Div of Psychology and Lang Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Div of Psychology and Lang Sciences > Language and Cognition
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases
URI: https://discovery-pp.ucl.ac.uk/id/eprint/10194665
Downloads since deposit
456Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item