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Language Deficits as a Preclinical Window into Parkinson’s Disease: Evidence from Asymptomatic Parkin and Dardarin Mutation Carriers

  • Adolfo M. García (a1) (a2) (a3), Lucas Sedeño (a1) (a2), Natalia Trujillo (a4) (a5) (a6), Yamile Bocanegra (a5) (a6), Diana Gomez (a4) (a6), David Pineda (a5) (a6), Andrés Villegas (a6), Edinson Muñoz (a7), William Arias (a8) and Agustín Ibáñez (a1) (a2) (a9) (a10) (a11)...


Objectives: The worldwide spread of Parkinson’s disease (PD) calls for sensitive and specific measures enabling its early (or, ideally, preclinical) detection. Here, we use language measures revealing deficits in PD to explore whether similar disturbances are present in asymptomatic individuals at risk for the disease. Methods: We administered executive, semantic, verb-production, and syntactic tasks to sporadic PD patients, genetic PD patients with PARK2 (parkin) or LRRK2 (dardarin) mutation, asymptomatic first-degree relatives of the latter with similar mutations, and socio-demographically matched controls. Moreover, to detect sui generis language disturbances, we ran analysis of covariance tests using executive functions as covariate. Results: The two clinical groups showed impairments in all measures, most of which survived covariation with executive functions. However, the key finding concerned asymptomatic mutation carriers. While these subjects showed intact executive, semantic, and action-verb production skills, they evinced deficits in a syntactic test with minimal working memory load. Conclusions: We propose that this sui generis disturbance may constitute a prodromal sign anticipating eventual development of PD. Moreover, our results suggest that mutations on specific genes (PARK2 and LRRK2) compromising basal ganglia functioning may be subtly related to language-processing mechanisms. (JINS, 2017, 23, 150–158)


Corresponding author

Correspondence and reprint requests to: Agustín Ibáñez, Institute of Cognitive and Translational Neuroscience & CONICET; Pacheco de Melo 1860, C1126AAB, Buenos Aires, Argentina. E-mail:


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Language Deficits as a Preclinical Window into Parkinson’s Disease: Evidence from Asymptomatic Parkin and Dardarin Mutation Carriers

  • Adolfo M. García (a1) (a2) (a3), Lucas Sedeño (a1) (a2), Natalia Trujillo (a4) (a5) (a6), Yamile Bocanegra (a5) (a6), Diana Gomez (a4) (a6), David Pineda (a5) (a6), Andrés Villegas (a6), Edinson Muñoz (a7), William Arias (a8) and Agustín Ibáñez (a1) (a2) (a9) (a10) (a11)...


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