Characterization of neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, Colombia

Introduction Huntington’s disease (HD) is a rare (1-9/100 000), inherited disease characterized by an elongated CAG repeat on chromosome 4p, leading to a degeneration of neurons. Also, psychiatric symptoms are very common in the early stage and may appear before motor symptoms. Objectives To chara...

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Main Authors: D. Vasquez, M. Agudelo, C. Gomez, D. Aguillon, J. Quintero, S. Rassi, M. Zuluaga, D. Pineda, O. Buritica, F. Lopera
Format: Article
Language:English
Published: Cambridge University Press 2022-06-01
Series:European Psychiatry
Subjects:
Online Access:https://www.cambridge.org/core/product/identifier/S0924933822011488/type/journal_article
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author D. Vasquez
M. Agudelo
C. Gomez
D. Aguillon
J. Quintero
S. Rassi
M. Zuluaga
D. Pineda
O. Buritica
F. Lopera
author_facet D. Vasquez
M. Agudelo
C. Gomez
D. Aguillon
J. Quintero
S. Rassi
M. Zuluaga
D. Pineda
O. Buritica
F. Lopera
author_sort D. Vasquez
collection DOAJ
description Introduction Huntington’s disease (HD) is a rare (1-9/100 000), inherited disease characterized by an elongated CAG repeat on chromosome 4p, leading to a degeneration of neurons. Also, psychiatric symptoms are very common in the early stage and may appear before motor symptoms. Objectives To characterize neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, Colombia. Methods Data obtained from clinical records of individuals with HD (motor-manifest or pre-motor with triplets count) evaluated for ENROLL-HD project in the Group of Neuroscience of Antioquia. We explored variables related to substances abuse, neuropsychiatric symptoms, the respective age of onset, sex, and triplet count when available. Results Twenty-six (53%) were women, 8% had a familiar history of psychotic illness in a first-degree relative and 88% presented motor symptoms. Also, 59% had a history of depression, 53% irritability, 57% aggressiveness, 34% apathy, 29% perseverative/obsessive behavior, 14% psychosis, and 30% mild cognitive impairment. Ten individuals (20%) had motor without neuropsychiatric symptoms. Also, thirty-seven individuals (76%) presented motor and neuropsychiatric symptoms; of these, 41% had neuropsychiatric symptoms before motor symptoms. No psychiatric symptoms were associated with the use of alcohol, cigarettes, or drugs of abuse. Conclusions Neuropsychiatric symptoms are highly prevalent among individuals with HD and studies oriented to create relevant knowledge for the development of advice oriented to people with this disease are necessary. Disclosure No significant relationships.
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spelling doaj.art-1d378493de334e84a3abf7e9fd520db72023-11-17T05:07:39ZengCambridge University PressEuropean Psychiatry0924-93381778-35852022-06-0165S453S45310.1192/j.eurpsy.2022.1148Characterization of neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, ColombiaD. Vasquez0M. Agudelo1C. Gomez2D. Aguillon3J. Quintero4S. Rassi5M. Zuluaga6D. Pineda7O. Buritica8F. Lopera9Universidad de Antioquia, Grupo De Neurociencias De Antioquia, Medellin, ColombiaUniversidad de Antioquia, Neurología, Medellin, ColombiaUniversidad de Antioquia, Psiquiatría, Medellin, ColombiaUniversidad de Antioquia, Grupo De Neurociencias De Antioquia, Medellin, ColombiaUniversidad de Antioquia, Grupo De Neurociencias De Antioquia, Medellin, ColombiaUniversidad de Antioquia, Grupo De Neurociencias De Antioquia, Medellin, ColombiaUniversidad de Antioquia, Grupo De Neurociencias De Antioquia, Medellin, ColombiaUniversidad de Antioquia, Grupo De Neurociencias De Antioquia, Medellin, ColombiaUniversidad de Antioquia, Grupo De Neurociencias De Antioquia, Medellin, ColombiaUniversidad de Antioquia, Grupo De Neurociencias De Antioquia, Medellin, Colombia Introduction Huntington’s disease (HD) is a rare (1-9/100 000), inherited disease characterized by an elongated CAG repeat on chromosome 4p, leading to a degeneration of neurons. Also, psychiatric symptoms are very common in the early stage and may appear before motor symptoms. Objectives To characterize neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, Colombia. Methods Data obtained from clinical records of individuals with HD (motor-manifest or pre-motor with triplets count) evaluated for ENROLL-HD project in the Group of Neuroscience of Antioquia. We explored variables related to substances abuse, neuropsychiatric symptoms, the respective age of onset, sex, and triplet count when available. Results Twenty-six (53%) were women, 8% had a familiar history of psychotic illness in a first-degree relative and 88% presented motor symptoms. Also, 59% had a history of depression, 53% irritability, 57% aggressiveness, 34% apathy, 29% perseverative/obsessive behavior, 14% psychosis, and 30% mild cognitive impairment. Ten individuals (20%) had motor without neuropsychiatric symptoms. Also, thirty-seven individuals (76%) presented motor and neuropsychiatric symptoms; of these, 41% had neuropsychiatric symptoms before motor symptoms. No psychiatric symptoms were associated with the use of alcohol, cigarettes, or drugs of abuse. Conclusions Neuropsychiatric symptoms are highly prevalent among individuals with HD and studies oriented to create relevant knowledge for the development of advice oriented to people with this disease are necessary. Disclosure No significant relationships. https://www.cambridge.org/core/product/identifier/S0924933822011488/type/journal_articleHuntington’s diseaseMotor symptomsNeuropsychiatric symptomsChorea
spellingShingle D. Vasquez
M. Agudelo
C. Gomez
D. Aguillon
J. Quintero
S. Rassi
M. Zuluaga
D. Pineda
O. Buritica
F. Lopera
Characterization of neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, Colombia
European Psychiatry
Huntington’s disease
Motor symptoms
Neuropsychiatric symptoms
Chorea
title Characterization of neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, Colombia
title_full Characterization of neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, Colombia
title_fullStr Characterization of neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, Colombia
title_full_unstemmed Characterization of neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, Colombia
title_short Characterization of neuropsychiatric symptoms in a group of individuals with manifest or pre-motor Huntington’s disease in Medellín, Colombia
title_sort characterization of neuropsychiatric symptoms in a group of individuals with manifest or pre motor huntington s disease in medellin colombia
topic Huntington’s disease
Motor symptoms
Neuropsychiatric symptoms
Chorea
url https://www.cambridge.org/core/product/identifier/S0924933822011488/type/journal_article
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