Psychiatric Diagnoses and Medications in Wolfram Syndrome.

IF 1.4 Q3 PSYCHIATRY
Angela M Reiersen, Jacob S Noel, Tasha Doty, Richa A Sinkre, Anagha Narayanan, Tamara Hershey
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Abstract

Background: Wolfram Syndrome is a rare genetic disorder usually resulting from pathogenic variation in the WFS1 gene, which leads to an exaggerated endoplasmic reticulum (ER) stress response. The disorder is typically characterized by diabetes insipidus, diabetes mellitus, optic nerve atrophy, hearing loss, and neurodegenerative features. Existing literature suggests it may also have psychiatric manifestations.

Objective: To examine lifetime psychiatric diagnoses and medication history in Wolfram Syndrome.

Method: Child, adolescent, and young adult Wolfram Syndrome participants (n=39) were assessed by a child & adolescent psychiatrist to determine best estimate DSM-5 lifetime psychiatric diagnoses as well as psychoactive medication history. In addition, the Child & Adolescent Symptom Inventory-5 (CASI-5) Parent Checklist was used to determine likely psychiatric diagnoses based on symptom counts in Wolfram Syndrome patients (n=33), type 1 diabetes (n=15), and healthy comparison (n=18) groups.

Results: Study participants with Wolfram Syndrome had high lifetime rates of anxiety disorders (77%). Also, 31% had an obsessive-compulsive spectrum disorder, 33% had a mood disorder, 31% had a neurodevelopmental or disruptive behavior disorder, and 31% had a sleep-wake disorder. More than half of Wolfram Syndrome participants had taken at least one psychoactive medication, and one third had taken at least one selective serotonin reuptake inhibitor (SSRI). Some individuals reported poor response to sertraline but better response after switching to another SSRI (fluoxetine or citalopram). In general, people with Wolfram Syndrome often reported benefit from psychotherapy and/or commonly used psychoactive medications appropriate for their psychiatric diagnoses.

Conclusions: Wolfram Syndrome may be associated with elevated risk for anxiety and obsessive-compulsive spectrum disorders, which seem generally responsive to usual treatments for these disorders.

Abstract Image

Wolfram综合征的精神病学诊断和药物治疗。
背景:Wolfram综合征是一种罕见的遗传性疾病,通常由WFS1基因的致病性变异导致内质网(ER)应激反应过度引起。这种疾病的典型特征是尿崩症、糖尿病、视神经萎缩、听力丧失和神经退行性特征。现有文献表明,它也可能有精神病学的表现。目的:探讨Wolfram综合征患者的终生精神病学诊断和用药史。方法:儿童、青少年和年轻成人Wolfram综合征参与者(n=39)由儿童和青少年精神病学家评估,以确定DSM-5终身精神病学诊断的最佳估计以及精神活性药物史。此外,儿童和青少年症状量表-5 (CASI-5)父母检查表用于根据Wolfram综合征患者(n=33)、1型糖尿病患者(n=15)和健康对照组(n=18)的症状计数确定可能的精神病学诊断。结果:患有Wolfram综合征的研究参与者一生中焦虑症的发生率很高(77%)。此外,31%的人患有强迫症,33%的人患有情绪障碍,31%的人患有神经发育或破坏性行为障碍,31%的人患有睡眠障碍。超过一半的Wolfram综合征参与者至少服用了一种精神活性药物,三分之一的人至少服用了一种选择性血清素再摄取抑制剂(SSRI)。有些人报告舍曲林反应差,但改用另一种SSRI(氟西汀或西酞普兰)后反应更好。一般来说,患有沃尔夫勒姆综合症的人经常报告从心理治疗和/或常用的精神活性药物中受益,这些药物适合他们的精神诊断。结论:Wolfram综合征可能与焦虑和强迫谱系障碍的风险升高有关,这些障碍似乎通常对这些障碍的常规治疗有反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
5.30%
发文量
12
审稿时长
8 weeks
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