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Arquivos de Neuro-Psiquiatria

Print version ISSN 0004-282XOn-line version ISSN 1678-4227

Arq. Neuro-Psiquiatr. vol.77 no.8 São Paulo Aug. 2019  Epub Sep 05, 2019

https://doi.org/10.1590/0004-282x20190092 

Articles

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

Déficits en teoría de la mente en pacientes con enfermedad de Huntington y sus familiares

Leo Bayliss1 
http://orcid.org/0000-0003-3286-6741

Víctor Galvez2 

Adriana Ochoa-Morales3 

Mireya Chávez-Oliveros4 

Yaneth Rodríguez-Agudelo4 

Guillermo Delgado-García1 

Marie Catherine Boll5 

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

2Universidad Panamericana, Escuela de Psicologia, Laboratorio de Neurociencias Cognitivas y Desarrollo, Mexico City, Mexico

3Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Division of Genetics and Molecular Biology, Mexico City, Tlalpan, Mexico

4Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Department of Neuropsychology and Support Groups, Mexico City, Tlalpan, Mexico

5Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez, Clinical Research Laboratory, Mexico City, Tlalpan, Mexico


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.

Keywords: Huntington disease; neuropsychological test; dementia

RESUMEN

La enfermedad de Huntington (EH) es una enfermedad genética autosómica dominante caracterizada por trastornos del movimiento, deterioro cognitivo y síntomas psiquiátricos. Los familiares de las personas con EH experimentan gran carga dado que los pacientes sufren de conducta social alterada y deterioro de relaciones interpersonales. La Teoría de la mente (ToM) consiste en la habilidad para atribuir estados mentales (a uno mismo o a otros). Se piensa que déficits en ToM tienen un rol en los cambios en empatia y en las dificultades interpersonales que los pacientes con EH enfrentan.

Métodos:

Condujimos un estudio transversal para comparar el desempeño en puntajes de tareas de ToM en pacientes con EH leve a moderada, sus familiares (pareja o familiar en riesgo con prueba genética negativa) y controles sanos. Se excluyó a sujetos con demencia o depresión. La batería de pruebas de ToM incluyó versiones en español de la prueba de lectura de la mente en los ojos (RMET), Historias Extrañas de Happé (subpruebas Social y Física) y Hinting Task.

Resultados:

La serie consistió de 12 pacientes con EH, 12 familiares y 12 controles. Los pacientes con EH mostraron puntajes menores de tareas de ToM afectiva que los controles (RMET 19 [3.5] vs 23.9 [2.7], p = 0.016). Los puntajes de tareas de ToM cognitiva fueron inferiores a los controles en los pacientes con EH (Historias Sociales de Happé 9 [2.6] vs 13 [1.9], p = 0.001; Hinting task 13.6 [3.4] vs 175 [4.0], p = 0.009). En la Hinting task los familiares de pacientes con EH mostraron puntajes inferiores que los de los controles (13 [3.2] vs 175 [4.0], p = 0.009) y puntajes similares a aquellos de los controles en el resto de la batería.

Conclusión:

Los pacientes con EH con enfermedad leve a moderada y sus familiares muestran déficits en tareas de ToM.

Palabras-clave: Enfermedad de Huntington; pruebas neuropsicológicas; demencia

Huntington disease (HD) is an autosomal dominant genetic disorder characterized by movement disorders, cognitive dysfunction and psychiatric symptoms1.

Theory of mind (ToM) is the ability to attribute mental states (beliefs and feelings) to oneself and others, and to understand that others have beliefs and feelings different from one's own2. In clinical practice, ToM is evaluated using neuropsychological tasks, and these tasks are further classified as “affective ToM” (evaluates beliefs about feelings) and “cognitive ToM” (evaluates beliefs about beliefs). Affective ToM is thought to be mediated mainly by the ventromedial prefrontal cortex, whereas cognitive ToM appears to be mediated by the prefrontal cortex as a whole3. The ToM deficits have been shown to be present in HD in both cognitive and affective modalities4,5,6,7.

Relatives of HD patients experience a great burden as the patients suffer from social conduct and interpersonal relationship deterioration1. Deficits in ToM are thought to play a role in the changes in empathy and interpersonal difficulties that HD patients face8.

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 unrelated healthy controls.

Participants

Twelve consecutive HD patients from our outpatient clinic with a confirmed diagnosis by direct mutation analysis of the number of CAG repeats (four males, eight females) were included. The relatives accompanying the HD patients were invited to participate; 12 were included (nine gene-negative at-risk individuals and three spouses). Twelve unrelated individuals were paired by age and education with the HD patients. Clinical and epidemiological data were collected. We excluded individuals with dementia, depression (Center for Epidemiological Studies - depression scale score > 16)9, or those unable to read or unwilling to give their informed consent. The local research and ethics committees reviewed and approved the protocol. The research project complied with the requirements of the Declaration of Helsinki as revised in Fortaleza, Brazil, 2013. The participants’ confidentiality was preserved.

Instruments

Disease severity and motor dysfunction

The severity of HD was assessed using the Total Functional Capacity (TFC) scale, which evaluates the ability to work, handle finances, perform domestic chores, live independently and self-care tasks. The TFC categorizes a functionality deficit as mild (TFC = 10-13) or moderate (TFC = 7-9)10. Motor dysfunction was evaluated with the Unified Huntington's Disease Rating Scale (UHDRS)11.

Cognitive status and emotion recognition

Cognitive status was assessed with the Spanish version of the Montreal Cognitive Assessment (MoCA)12. Emotion recognition was evaluated with Pictures of Facial Affection (POFA), a portfolio of faces comprising 56 photographs of different individuals showing an emotion; the presentation of each face lasted 10 seconds on a computer screen13.

Affective ToM

Affective ToM was assessed with the Reading the Mind in the Eyes Test (RMET). This test comprises a portfolio of 36 pictures of a person's gaze associated with a feeling or thought. For each picture the participant chooses one feeling/thought option (out of four) that best fits. A score of 1 is given for correct choices and 0 for incorrect ones14. The Castilian Spanish version of the RMET for adults was from the Autism Research Centre website and adapted into Mexican Spanish14.

Cognitive ToM

The Spanish translations of the cognitive ToM tasks: Happé's Strange Stories15 and the Hinting Task16 were used. One researcher (VG) recorded and applied an audio version of cognitive ToM tasks in order to decrease the effect of reading comprehension skills on task performance. Evaluation required the patient to listen to the recorded test version, then answer verbally. Test scoring was performed thereafter by two neuropsychologists (MC, YR). Happé's Strange Stories consists of two subsets of tasks: social stories, related to mental states (ToM) and stories related to control of physical events. Answers are scored as zero points if wrong, one point if partially correct and two points if correct; each subtest can be scored from 0 to 16 points17. The Hinting Task test includes 10 short stories of situations with an underlying social event. The participant is asked to interpret the event; the item is rated: 0 if incorrect, 1 if additional information facilitates a correct answer and 2 if correct; test scores range from 0 to 20 points18.

Statistical analysis

Descriptive statistics are presented in medians and interquartile ranges, percentages and absolute numbers. Inferential statistics were performed in categorical variables with the chi square test and in quantitative variables with the Friedman test. To test for correlation, Spearman's method was used. Significant differences were considered at p < 0.05. Computing was performed in R package version 3.4. Charts were generated in R using the ggplot2 library.

RESULTS

This series comprised 36 participants allocated to three groups: 12 HD patients, 12 HD relatives and 12 healthy, unrelated controls. The series comprised young and middle age adults, predominantly women with a median 15.5 (IQR 5) years of education. There was no significant difference among the groups’ participant age, proportion of sexes or years of education (Table).

Table Descriptive characteristics of the study groups. 

Characteristic HD patients HD relatives Controls p-value
N 12 12 12
Sex: Female (%) 8 (67%) 7 (58%) 9 (75%) 0.694
Age in years, median (IQR) 42.7 (11.3) 44.7 (22.3) 371 (15.8) 0.264
Years of education 16.0 (5.0) 16 (6.2) 14.5 (7.5) 0.752
TFC Score 13.5 (1.2)
UHDRS motor score 12.5 (11.0)
Neuropsychological assessment
MoCA 24.5 (4.0) 270 (1.0) 28.5 (1.5) 0.079
POFA 43.5 (9.7) 47 (10.7) 45.5 (5.5) 0.192
Affective ToM
RMET 19 (3.5)* 24.5 (3.7) 24 (2.7) 0.016
Cognitive ToM
Happé's Strange Stories total 15.2 (6.9) 20.2 (5.5) 23.9 (7.2) 0.144
Happé's Social Stories 9(2.6) * 10.7(2.7) 12.5 (1.9) 0.001
Happé's Physical Stories 7.2 (4.9) 9.2 (4.6) 9.9 (4.3) 0.132
Hinting Task 13.6 (3.4) 13 (3.2) 17.5 (4.0)* 0.009

Absolute values and percentage (for sex distribution) or medians ± interquartile range (IQR; for all other variables) are shown. Chi square and Friedman test significance (p) values. ToM: Theory of Mind; TFC: Total functionality score; UHDRS: Unified Huntington's disease rating scale; MoCA: Montreal cognitive assessment; POFA: Pictures of facial affection; RMET: Reading the mind in the eyes test.

*statistically significant difference.

The HD group functionality, according to the TFC scores, was preserved in seven patients, mildly affected in three and moderately in two. Nine patients had involuntary movements with a median evolution of 6.8 (IQR 6.1) years. Four patients were taking antidepressants and one was also taking olanzapine. The TFC scores correlated positively with the MoCA scores (Spearman's rho =0.636, p < 0.05) and negatively with the UHDRS (Spearman's rho = -.789, p < 0.01), (Table).

Neuropsychological assessment

Montreal cognitive assessment

The MoCA scores were not significantly different among groups (Table), although 7/12 HD patients presented with mild cognitive impairment (MoCa score < 26 points). The MoCA scores did not correlate with education across groups (Spearman's rho = 0.08, p = 0.65).

Pictures of facial affection

The POFA scores among groups showed no differences (Table). No selective emotion recognition deficit was found in HD patients. Whole-series POFA scores showed a positive correlation with scores of the RMET (Spearman's rho =.472, p = 0.003).

Theory of mind tasks

Affective ToM

The RMET scores were lower in HD patients than those of HD relatives and controls (19 [3.5] vs 24.5 [3.7] vs 23.9 [7.2], p = 0.016) (Table and Figure).

Figure Box plot comparing Theory of Mind (ToM) tasks scores by groups. Statistically significant differences are marked by an asterisk (*). Groups labels: (C) control participant, (R) relative, (H) Huntington's disease. 

Cognitive ToM

The HD patients had lower scores than controls in the Happé's Social Stories subtest (9 [2.6] vs 12.5 [1.9], p = 0.001), while Happé's Physical Stories scores showed no significant difference among the groups. Happé's Social Stories subtest scores negatively correlated with the UHDRS scores (Spearman's rho = 0.753, p = 0.005). The Hinting Task scores were significantly lower in HD patients and HD relatives than in controls (13.6 [3.4] vs 13 [3.2] vs 17.5 [4.0], p = 0.009).

Across groups, cognitive ToM tasks and MoCA scores were positively correlated with Happé's Social Stories (Spearman's rho = 0.336, p = 0.04), Happé's Physical Stories (Spearman's rho = 0.328, p = 0.04), as well as the Hinting Task (Spearman's rho = 0.516, p = 0.001).

DISCUSSION

HD patients with mild to moderate disease severity showed impaired performance in affective ToM tasks (RMET) and cognitive ToM tasks (Happé's Social Stories and Hinting Task). This finding has previously been reported in HD patients performing related tasks4,5,6,7. Because our HD patients had a mild-to-moderate disease and no statistically significant lower MoCA or POFA scores, ToM tasks score may represent an early marker of dysfunction in HD4,6. A previously-reported correlation between RMET and MoCA scores in HD patients7 was not replicated in this study. This may be explained by an even lower severity of disease in terms of functionality and motor impairment in our series. These findings need to be confirmed in a larger series, as ToM tasks may have a relevant role in tracking HD progression and correlate with frontal lobe dysfunction3.

The HD relatives showed dysfunction in cognitive but not in affective ToM and had a similar performance to controls in the rest of the tests. Similarly, ToM deficits in first degree relatives of schizophrenia patients have been reported4,19. The ToM dysfunction may be related either to a genetic trait or an effect of family interaction with HD patients, and requires validation. Limitations of this study are the small sample size and type 1 error, and that the test versions used were not validated translations. Further study in this area may help clarify the particular social difficulties HD families face and may be relevant in genetic counseling20.

To our knowledge, this is the first study assessing ToM performance in Latin American HD patients and their relatives. These findings suggest a role of ToM testing in the early cognitive profile and social and family interaction of HD patients and these may parallel those found in schizophrenia and their relatives.

Acknowledge

The authors would like to thank to all the patients and their families for the cooperation provided.

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Received: February 25, 2019; Revised: April 25, 2019; Accepted: May 08, 2019

Correspondence: Leo Bayliss; Instituto Nacional de Neurología y Neurocirugía Manuel Velasco Suárez - Neurology; Insurgentes Sur 3877 La Fama Mexico City Mexico City Mexico City 14269, Mexico; E-mail: leobayliss@gmail.com

Conflict of interest: There is no conflict of interest to declare.

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