Theory of mind impairment in Huntington's disease patients and their relatives

Leo Bayliss1, Víctor Galvez2, Adriana Ochoa-Morales3

  • 1Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Division of Neurology, Mexico City, Tlalpan, Mexico.

Insights

Huntington disease (HD) patients and their relatives exhibit deficits in theory of mind (ToM), impacting social cognition. These findings highlight the pervasive effects of HD on interpersonal relationships and empathy.

Area of Science:

  • Neuroscience
  • Genetics
  • Psychology

Background:

  • Huntington disease (HD) is an autosomal dominant disorder causing movement, cognitive, and psychiatric issues.
  • HD significantly burdens families, affecting social conduct and relationships.
  • Theory of Mind (ToM) deficits are implicated in HD-related empathy and interpersonal difficulties.

Purpose of the Study:

  • To compare ToM task performance in mild-to-moderate HD patients, their relatives, and controls.
  • To investigate the role of ToM deficits in the social and interpersonal challenges faced by HD patients and their families.

Main Methods:

  • Cross-sectional study comparing ToM scores in 12 HD patients, 12 relatives, and 12 controls.
  • Excluded individuals with dementia or depression.
  • Utilized Spanish versions of the Reading Mind in the Eyes Test (RMET), Happé's Strange Stories, and the Hinting Task.

Main Results:

  • HD patients scored significantly lower on affective ToM (RMET) and cognitive ToM (Happé's Social Stories, Hinting Task) compared to controls.
  • HD relatives showed lower scores than controls on the Hinting Task, but similar scores on other ToM measures.
  • These results indicate ToM deficits in both HD patients and their relatives.

Conclusions:

  • Mild-to-moderate Huntington disease patients demonstrate significant deficits in both affective and cognitive Theory of Mind.
  • Relatives of HD patients also exhibit impaired Theory of Mind, particularly in cognitive aspects measured by the Hinting Task.
  • These findings underscore the broad impact of Huntington disease on social cognition within affected families.

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