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F46 Relationship between distinct motor symptoms and apathy in huntington’s disease: clues to mechanism

Authors :
Robb B. Rutledge
Sarah J. Tabrizi
Akshay Nair
N. Ahmad Aziz
Geraint Rees
Source :
Journal of neurology, neurosurgery, and psychiatry 89(Supplement 1), A56 (2018). doi:10.1136/jnnp-2018-EHDN.150, EHDN 2018 Plenary Meeting, Vienna, Austria, 2018-09-14-2018-09-16
Publication Year :
2018
Publisher :
BMJ Publishing Group Ltd, 2018.

Abstract

Introduction Disrupted gating of motor control through striatal pathways is thought to drive the development of motor symptoms in Huntington’s disease (HD). The range of motor symptoms, from chorea to bradykinesia, is thought to be driven by disruption in different striatal pathways. Aside from motor control, striatal pathways are also thought to play a key role in the expression of motivated behaviour. On this basis we asked whether the association between apathy and specific motor symptoms is in keeping with the hypothesis that apathy in HD is another manifestation of dysfunctional striatal gating. Methods Clinical data on 2608 patients with manifest HD disease was retrieved from the ENROLL-HD database. A linear mixed model was built to assess the relationship between motor symptoms and apathy (measured using the PBA and square root transformed) controlling for cognitive impairment, depression, medication use, disease duration, CAG repeat size and age. In a separate analysis the bradykinesia item was replaced by voluntary finger tapping performance. Results Although both bradykinesia and chorea were significantly associated with apathy, their effects were in opposite directions. Bradykinesia was associated with greater apathy (β=0.14, p Conclusion This analysis suggests that the processes driving distinct motor symptoms in HD may also underlie hard-to-treat psychiatric symptoms such as apathy. A common substrate and likely target for this shared mechanism is the disruption of specific striatal pathways that gate actions, decisions and motivated behaviour.

Details

Database :
OpenAIRE
Journal :
Clinical studies
Accession number :
edsair.doi.dedup.....4460097f3716418566d6803a2ef562ed
Full Text :
https://doi.org/10.1136/jnnp-2018-ehdn.150