Dysphagia in primary progressive aphasia: Clinical predictors and neuroanatomical basis

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 (nf...

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Published inEuropean journal of neurology Vol. 31; no. 9; pp. e16370 - n/a
Main Authors Mazzeo, Salvatore, Mulroy, Eoin, Jiang, Jessica, Lassi, Michael, Johnson, Jeremy C. S., Hardy, Chris J. D., Rohrer, Jonathan D., Warren, Jason D., Volkmer, Anna
Format Journal Article
LanguageEnglish
Published England John Wiley & Sons, Inc 01.09.2024
John Wiley and Sons Inc
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Summary: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.
Bibliography:Jason D. Warren and Anna Volkmer contributed equally to the work.
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ISSN:1351-5101
1468-1331
1468-1331
DOI:10.1111/ene.16370