Do I misconstrue? Sarcasm detection, emotion recognition, and Theory of Mind in Huntington disease

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Standard

Do I misconstrue? Sarcasm detection, emotion recognition, and Theory of Mind in Huntington disease. / Larsen, Ida Unmack; Vinther-Jensen, Tua; Gade, Anders; Nielsen, Jørgen Erik; Vogel, Asmus Mejling.

I: Neuropsychology, Bind 30, Nr. 2, 2016, s. 181-189.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Larsen, IU, Vinther-Jensen, T, Gade, A, Nielsen, JE & Vogel, AM 2016, 'Do I misconstrue? Sarcasm detection, emotion recognition, and Theory of Mind in Huntington disease', Neuropsychology, bind 30, nr. 2, s. 181-189. https://doi.org/10.1037/neu0000224

APA

Larsen, I. U., Vinther-Jensen, T., Gade, A., Nielsen, J. E., & Vogel, A. M. (2016). Do I misconstrue? Sarcasm detection, emotion recognition, and Theory of Mind in Huntington disease. Neuropsychology, 30(2), 181-189. https://doi.org/10.1037/neu0000224

Vancouver

Larsen IU, Vinther-Jensen T, Gade A, Nielsen JE, Vogel AM. Do I misconstrue? Sarcasm detection, emotion recognition, and Theory of Mind in Huntington disease. Neuropsychology. 2016;30(2):181-189. https://doi.org/10.1037/neu0000224

Author

Larsen, Ida Unmack ; Vinther-Jensen, Tua ; Gade, Anders ; Nielsen, Jørgen Erik ; Vogel, Asmus Mejling. / Do I misconstrue? Sarcasm detection, emotion recognition, and Theory of Mind in Huntington disease. I: Neuropsychology. 2016 ; Bind 30, Nr. 2. s. 181-189.

Bibtex

@article{a10b3a12323340d68d24bf3c8630ee0e,
title = "Do I misconstrue?: Sarcasm detection, emotion recognition, and Theory of Mind in Huntington disease",
abstract = "OBJECTIVE: Emotion recognition has been widely studied in Huntington disease (HD), but only a few studies have investigated more complex social cognition and, when so, exclusively in manifest HD. The present study sought to investigate social-cognitive functions in a large, consecutive cohort of premanifest and manifest HD gene expansion carriers using tests assessing sarcasm detection, theory of mind (ToM), and emotion recognition. METHOD: Fifty manifest, 50 premanifest HD gene expansion carriers, and 39 at risk gene expansion negative healthy controls were included. All participants were tested with sarcasm detection, ToM, and emotion recognition tasks. Between-group comparisons of test performances and correlation analyses of test performances and disease burden scores were made. RESULTS: Group comparisons showed significant differences in performances on the social-cognitive tests between manifest HD gene expansion carriers and healthy controls, but differences in performances between premanifest HD gene expansion carriers and healthy controls were not statistically significant. Correlation analysis showed that the worse test performances were associated with higher disease burden scores in all HD gene expansion carriers. CONCLUSION: Our findings support a theory of impaired social-cognitive functions in the early stages of HD. Test performances decreased with increasing disease burden in all HD gene expansion carriers, suggesting that social-cognitive tests may be useful for tracking disease progression. Simple emotion recognition tasks are just as sensitive for measuring social-cognitive deficits as more complex measures, but knowledge of the quality of social-cognitive impairments in HD can be of great importance to both patients and caregivers.",
keywords = "Faculty of Social Sciences, Huntington Disease, social cognition",
author = "Larsen, {Ida Unmack} and Tua Vinther-Jensen and Anders Gade and Nielsen, {J{\o}rgen Erik} and Vogel, {Asmus Mejling}",
year = "2016",
doi = "10.1037/neu0000224",
language = "English",
volume = "30",
pages = "181--189",
journal = "Neuropsychology",
issn = "0894-4105",
publisher = "American Psychological Association",
number = "2",

}

RIS

TY - JOUR

T1 - Do I misconstrue?

T2 - Sarcasm detection, emotion recognition, and Theory of Mind in Huntington disease

AU - Larsen, Ida Unmack

AU - Vinther-Jensen, Tua

AU - Gade, Anders

AU - Nielsen, Jørgen Erik

AU - Vogel, Asmus Mejling

PY - 2016

Y1 - 2016

N2 - OBJECTIVE: Emotion recognition has been widely studied in Huntington disease (HD), but only a few studies have investigated more complex social cognition and, when so, exclusively in manifest HD. The present study sought to investigate social-cognitive functions in a large, consecutive cohort of premanifest and manifest HD gene expansion carriers using tests assessing sarcasm detection, theory of mind (ToM), and emotion recognition. METHOD: Fifty manifest, 50 premanifest HD gene expansion carriers, and 39 at risk gene expansion negative healthy controls were included. All participants were tested with sarcasm detection, ToM, and emotion recognition tasks. Between-group comparisons of test performances and correlation analyses of test performances and disease burden scores were made. RESULTS: Group comparisons showed significant differences in performances on the social-cognitive tests between manifest HD gene expansion carriers and healthy controls, but differences in performances between premanifest HD gene expansion carriers and healthy controls were not statistically significant. Correlation analysis showed that the worse test performances were associated with higher disease burden scores in all HD gene expansion carriers. CONCLUSION: Our findings support a theory of impaired social-cognitive functions in the early stages of HD. Test performances decreased with increasing disease burden in all HD gene expansion carriers, suggesting that social-cognitive tests may be useful for tracking disease progression. Simple emotion recognition tasks are just as sensitive for measuring social-cognitive deficits as more complex measures, but knowledge of the quality of social-cognitive impairments in HD can be of great importance to both patients and caregivers.

AB - OBJECTIVE: Emotion recognition has been widely studied in Huntington disease (HD), but only a few studies have investigated more complex social cognition and, when so, exclusively in manifest HD. The present study sought to investigate social-cognitive functions in a large, consecutive cohort of premanifest and manifest HD gene expansion carriers using tests assessing sarcasm detection, theory of mind (ToM), and emotion recognition. METHOD: Fifty manifest, 50 premanifest HD gene expansion carriers, and 39 at risk gene expansion negative healthy controls were included. All participants were tested with sarcasm detection, ToM, and emotion recognition tasks. Between-group comparisons of test performances and correlation analyses of test performances and disease burden scores were made. RESULTS: Group comparisons showed significant differences in performances on the social-cognitive tests between manifest HD gene expansion carriers and healthy controls, but differences in performances between premanifest HD gene expansion carriers and healthy controls were not statistically significant. Correlation analysis showed that the worse test performances were associated with higher disease burden scores in all HD gene expansion carriers. CONCLUSION: Our findings support a theory of impaired social-cognitive functions in the early stages of HD. Test performances decreased with increasing disease burden in all HD gene expansion carriers, suggesting that social-cognitive tests may be useful for tracking disease progression. Simple emotion recognition tasks are just as sensitive for measuring social-cognitive deficits as more complex measures, but knowledge of the quality of social-cognitive impairments in HD can be of great importance to both patients and caregivers.

KW - Faculty of Social Sciences

KW - Huntington Disease

KW - social cognition

U2 - 10.1037/neu0000224

DO - 10.1037/neu0000224

M3 - Journal article

C2 - 26301773

VL - 30

SP - 181

EP - 189

JO - Neuropsychology

JF - Neuropsychology

SN - 0894-4105

IS - 2

ER -

ID: 147098599