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Impaired Interoceptive Accuracy in Semantic Variant Primary Progressive Aphasia

Marshall, CR; Hardy, CJD; Russell, LL; Clark, CN; Dick, KM; Brotherhood, EV; Bond, RL; Mummery, CJ; Schott, JM; Rohrer, JD; et al. Marshall, CR; Hardy, CJD; Russell, LL; Clark, CN; Dick, KM; Brotherhood, EV; Bond, RL; Mummery, CJ; Schott, JM; Rohrer, JD; Kilner, JM; Warren, JD (2017) Impaired Interoceptive Accuracy in Semantic Variant Primary Progressive Aphasia. Frontiers in Neurology, 8. p. 610. ISSN 1664-2295 https://doi.org/10.3389/fneur.2017.00610
SGUL Authors: Clark, Camilla Neegaard

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Abstract

Background: Interoception (the perception of internal bodily sensations) is strongly linked to emotional experience and sensitivity to the emotions of others in healthy subjects. Interoceptive impairment may contribute to the profound socioemotional symptoms that characterize frontotemporal dementia (FTD) syndromes, but remains poorly defined. Methods: Patients representing all major FTD syndromes and healthy age-matched controls performed a heartbeat counting task as a measure of interoceptive accuracy. In addition, patients had volumetric MRI for voxel-based morphometric analysis, and their caregivers completed a questionnaire assessing patients’ daily-life sensitivity to the emotions of others. Results: Interoceptive accuracy was impaired in patients with semantic variant primary progressive aphasia relative to healthy age-matched individuals, but not in behavioral variant frontotemporal dementia and nonfluent variant primary progressive aphasia. Impaired interoceptive accuracy correlated with reduced daily-life emotional sensitivity across the patient cohort, and with atrophy of right insula, cingulate, and amygdala on voxel-based morphometry in the impaired semantic variant group, delineating a network previously shown to support interoceptive processing in the healthy brain. Conclusion: Interoception is a promising novel paradigm for defining mechanisms of reduced emotional reactivity, empathy, and self-awareness in neurodegenerative syndromes and may yield objective measures for these complex symptoms.

Item Type: Article
Additional Information: Copyright: © 2017 Marshall, Hardy, Russell, Clark, Dick, Brotherhood, Bond, Mummery, Schott, Rohrer, Kilner and Warren. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Keywords: 1109 Neurosciences, 1103 Clinical Sciences, 1701 Psychology
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Frontiers in Neurology
ISSN: 1664-2295
Dates:
DateEvent
16 November 2017Published
2 November 2017Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
MR/M008525/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
091673/Z/10/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
URI: https://openaccess.sgul.ac.uk/id/eprint/112255
Publisher's version: https://doi.org/10.3389/fneur.2017.00610

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