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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.
Abstract:
Huntington disease (HD) is an autosomal dominant genetic disorder characterized by movement disorders, cognitive impairment, and psychiatric symptoms. Relatives of HD patients experience a great burden as the latter suffer from altered social conduct and deterioration of interpersonal relationships. Theory of mind (ToM) is the ability to attribute mental states (to oneself and others). Deficits in ToM are thought to have a role in the changes in empathy and interpersonal difficulties that HD patients face. METHODS We conducted a cross sectional study to compare ToM task scores of patients with mild to moderate HD, their relatives (spouse or at-risk first-degree relative with a negative gene test) and controls.Individuals with dementia or depression were excluded. The ToM test battery included Spanish versions of the Reading Mind in the Eyes Test (RMET), Happé's Strange Stories (Social and Physical Stories subtests) and the Hinting Task. RESULTS The series comprised 12 HD patients, 12 relatives and 12 controls. The HD patients showed lower affective ToM scores than controls (RMET 19 [3.5] vs 23.9 [2.7], p = 0.016). Cognitive ToM tasks scores were lower in HD patients than controls as well (Happé's Social Stories 9 [2.6] vs 13 [1.9], p = 0.001; the Hinting Task 13.6 [3.4] vs 17.5 [4.0], p = 0.009). In the Hinting Task, HD relatives had lower scores in than controls (13 [3.2] vs 17.5 [4.0], p = 0.009) and similar scores to controls in the rest of the battery. CONCLUSION The HD patients with mild to moderate disease severity and their relatives show ToM deficits.
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