Malestar psicológico en portadores y no portadores de la mutación causante de enfermedad de Huntington y su relación con la carga de la enfermedad

IF 3.1 4区 医学 Q2 CLINICAL NEUROLOGY
Y. Rodríguez-Agudelo , M. Chávez-Oliveros , A. Ochoa-Morales , L. Martínez-Ruano , A. Camacho-Molina , F. Paz-Rodríguez
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引用次数: 0

Abstract

Introduction

Huntington's disease (HD) is a neurodegenerative and hereditary disorder, due to the predictive diagnosis, incipient clinical characteristics have been described in the prodromal phase. Several studies have reported an increase in psychiatric symptoms in carriers of the HD gene without motor symptoms.

Objective

To identify psychological distress in carriers of the mutation that causes HD, without motor symptoms, utilizing the Symptom Checklist 90 (SCL-90), and to correlate with the burden and proximity of the disease.

Method

A sample of 175 participants in a HD Predictive Diagnostic Program (PDP-HD) was divided into HEP carriers (39.4%) and NPEH non-carriers (61.6%) of the HD-causing mutation. By means of mathematical formulas, the disease burden and proximity to the manifest stage in the PEH group were obtained and it was correlated with the results of the SCL-90-R.

Results

Comparing the results obtained in the SCL-90-R of the PEH and NPEH, the difference is observed in the positive somatic male index, where the PEH obtains higher average scores. The correlations between disease burden and psychological distress occur in the domains; obsessions and compulsions, interpersonal sensitivity, hostility, global severity index and positive somatic distress index. A low correlation is observed between the burden of disease and the scores obtained in psychological discomfort.

Conclusions

In general, we found that the PEH group obtained a higher score in the dimensions evaluated with the SCL-90-R, showing a relationship with the burden and differences due to the proximity of the disease. Higher scores on the SCL-90-R dimensions in carriers of the HD gene may suggest an early finding of psychological symptoms in the disease.
亨廷顿氏症突变携带者和非携带者的心理不适及其与疾病负担的关系
亨廷顿舞蹈病(HD)是一种神经退行性和遗传性疾病,由于其预测性诊断,早期临床特征在前驱期被描述。几项研究报告了无运动症状的HD基因携带者的精神症状增加。目的利用症状自评量表(SCL-90),分析HD基因突变携带者无运动症状时的心理困扰,并探讨其与疾病负担和临近性的关系。方法将175名HD预测诊断项目(PDP-HD)参与者分为HD致病突变的HEP携带者(39.4%)和NPEH非携带者(61.6%)。通过数学公式计算PEH组的疾病负担和与表现期的接近程度,并与SCL-90-R结果相关。结果比较PEH和NPEH的SCL-90-R结果,在阳性体细胞男性指数上存在差异,其中PEH获得更高的平均分。疾病负担与心理困扰之间存在相关性;强迫与强迫、人际敏感性、敌意、整体严重程度指数和积极躯体痛苦指数。疾病负担与心理不适得分之间的相关性较低。结论总的来说,我们发现PEH组在SCL-90-R评估的维度上得分更高,这与负担和疾病邻近性的差异有关。HD基因携带者在SCL-90-R维度上得分较高,可能表明该疾病的早期心理症状。
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来源期刊
Neurologia
Neurologia 医学-临床神经学
CiteScore
5.90
自引率
2.60%
发文量
135
审稿时长
48 days
期刊介绍: Neurología es la revista oficial de la Sociedad Española de Neurología y publica, desde 1986 contribuciones científicas en el campo de la neurología clínica y experimental. Los contenidos de Neurología abarcan desde la neuroepidemiología, la clínica neurológica, la gestión y asistencia neurológica y la terapéutica, a la investigación básica en neurociencias aplicada a la neurología. Las áreas temáticas de la revistas incluyen la neurologia infantil, la neuropsicología, la neurorehabilitación y la neurogeriatría. Los artículos publicados en Neurología siguen un proceso de revisión por doble ciego a fin de que los trabajos sean seleccionados atendiendo a su calidad, originalidad e interés y así estén sometidos a un proceso de mejora. El formato de artículos incluye Editoriales, Originales, Revisiones y Cartas al Editor, Neurología es el vehículo de información científica de reconocida calidad en profesionales interesados en la neurología que utilizan el español, como demuestra su inclusión en los más prestigiosos y selectivos índices bibliográficos del mundo.
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