Retraining speech production and fluency in non-fluent/agrammatic primary progressive aphasia

Maya L. Henry, H. Isabel Hubbard, Stephanie M. Grasso, Maria Luisa Mandelli, Stephen M. Wilson, Mithra T. Sathishkumar, Julius Fridriksson, Wylin Daigle, Adam L. Boxer, Bruce L. Miller, Maria Luisa Gorno-Tempini

Producción científica: Articlerevisión exhaustiva

102 Citas (Scopus)

Resumen

The non-fluent/agrammatic variant of primary progressive aphasia (nfvPPA) presents with a gradual decline in grammar and motor speech resulting from selective degeneration of speech-language regions in the brain. There has been considerable progress in identifying treatment approaches to remediate language deficits in other primary progressive aphasia variants; however, interventions for the core deficits in nfvPPA have yet to be systematically investigated. Further, the neural mechanisms that support behavioural restitution in the context of neurodegeneration are not well understood. We examined the immediate and long-term benefits of video implemented script training for aphasia (VISTA) in 10 individuals with nfvPPA. The treatment approach involved repeated rehearsal of individualized scripts via structured treatment with a clinician as well as intensive home practice with an audiovisual model using 'speech entrainment'. We evaluated accuracy of script production as well as overall intelligibility and grammaticality for trained and untrained scripts. These measures and standardized test scores were collected at post-treatment and 3-, 6-, and 12-month follow-up visits. Treatment resulted in significant improvement in production of correct, intelligible scripted words for trained topics, a reduction in grammatical errors for trained topics, and an overall increase in intelligibility for trained as well as untrained topics at post-treatment. Follow-up testing revealed maintenance of gains for trained scripts up to 1 year post-treatment on the primary outcome measure. Performance on untrained scripts and standardized tests remained relatively stable during the follow-up period, indicating that treatment helped to stabilize speech and language despite disease progression. To identify neural predictors of responsiveness to intervention, we examined treatment effect sizes relative to grey matter volumes in regions of interest derived from a previously identified speech production network. Regions of significant atrophy within this network included bilateral inferior frontal cortices and supplementary motor area as well as left striatum. Volumes in a left middle/inferior temporal region of interest were significantly correlated with the magnitude of treatment effects. This region, which was relatively spared anatomically in nfvPPA patients, has been implicated in syntactic production as well as visuo-motor facilitation of speech. This is the first group study to document the benefits of behavioural intervention that targets both linguistic and motoric deficits in nfvPPA. Findings indicate that behavioural intervention may result in lasting and generalized improvement of communicative function in individuals with neurodegenerative disease and that the integrity of spared regions within the speech-language network may be an important predictor of treatment response.

Idioma originalEnglish
Páginas (desde-hasta)1799-1814
Número de páginas16
PublicaciónBrain
Volumen141
N.º6
DOI
EstadoPublished - jun 1 2018

Nota bibliográfica

Publisher Copyright:
© The Author(s) (2018). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For permissions, please email: [email protected].

Financiación

This work was funded by grants from the National Institutes of Health (M.H., NIDCD R01 DC016291), (M.H., NIDCD R03 DC013403), (M.GT., NINDS R01 NS050915), (M.GT., NIDCD K24 DC015544), (S.W., NIDCD R01 DC013270), (S.W., NIDCD R21 DC016080), (B.M., NIA P01 AG019724), (B.M., NIA P50 AG023501), (A.B., NINDS U54 NS092089), (A.B., NIA R01 AG038791) (J.F., NIDCD P50 DC014664) and the Darrell K Royal Research Fund for Alzheimer’s Disease (M.H.).

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)
National Institute on AgingR01 AG038791, P50 DC014664, P50 AG023501, P01 AG019724, U54 NS092089
National Institute on Deafness and Other Communication DisordersR01DC016291, R03 DC013403
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilR01 NS050915, R21 DC016080, K24 DC015544, R01 DC013270

    ASJC Scopus subject areas

    • Clinical Neurology

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