Department of Human Genetics, Emory University, 2165 North Decatur Road, Decatur, GA 30033, USA.
J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S73-81. doi: 10.1007/s10545-009-9025-6. Epub 2010 Jan 20.
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by the deficiency of alpha-galactosidase A. In addition to the debilitating physical symptoms of FD, there are also under-recognized and poorly characterized psychiatric features. As a first step toward characterizing psychiatric features of FD, we administered the Achenbach adult self report questionnaire to 30 FD patients and the Achenbach adult behavior checklist questionnaire to 28 partners/parents/friends of FD patients. Data from at least one of the questionnaires were available on 33 subjects. Analysis focused on social-adaptive functioning in various aspects of daily life and on criteria related to the Diagnostic and statistical manual of mental disorders IV (DSM-IV). Adaptive functioning scale values, which primarily measure social and relationship functioning and occupational success, showed that eight FD patients (six female and two male) had mean adaptive functioning deficits as compared to population norms. Greater rates of depression (P < 0.01), anxiety (P = 0.05), depression and anxiety (P = 0.03), antisocial personality (P < 0.001), attention-deficit/hyperactivity (AD/H; P < 0.01), hyperactivity-impulsivity (P < 0.01), and aggressive behavior (P = 0.03) were associated with poorer adaptive functioning. Decreased social-adaptive functioning in this study was not statistically significantly associated to disease severity, pain, or level of vitality. This study shows for the first time that FD patients, particularly women, are affected by decreased social-adaptive functioning. Comprehensive treatment plans for FD should consider assessments and interventions to evaluate and improve social, occupational, and psychological functioning. Attention to the behavioral aspects of FD could lead to improved treatment outcome and improved quality of life. Individuals affected by Fabry disease exhibited social-adaptive functioning deficits that were significantly correlated with anxiety, depression, antisocial behavior, and AD/H problems in a sampling of our male and female patients aged between 18 years and 59 years.
法布瑞氏病(FD)是一种 X 连锁溶酶体贮积病,由α-半乳糖苷酶 A 缺乏引起。除了 FD 的衰弱性身体症状外,还有一些未被认识到的、特征描述较差的精神特征。作为对 FD 精神特征进行特征描述的第一步,我们对 30 名 FD 患者进行了 Achenbach 成人自评问卷,对 28 名 FD 患者的伴侣/父母/朋友进行了 Achenbach 成人行为检查表问卷。至少有一份问卷的数据可用于 33 名受试者。分析集中在日常生活各个方面的社会适应功能,以及与精神障碍诊断与统计手册第四版(DSM-IV)相关的标准。适应性功能量表值主要衡量社会和人际关系功能以及职业成功,结果表明,8 名 FD 患者(6 名女性和 2 名男性)的平均适应性功能缺陷与人群正常值相比。更高的抑郁率(P < 0.01)、焦虑率(P = 0.05)、抑郁和焦虑率(P = 0.03)、反社会人格率(P < 0.001)、注意力缺陷/多动(AD/H;P < 0.01)、多动冲动率(P < 0.01)和攻击性行为率(P = 0.03)与较差的适应性功能相关。本研究中,社会适应功能下降与疾病严重程度、疼痛或活力水平无统计学显著相关性。这项研究首次表明,FD 患者,特别是女性,受到社会适应功能下降的影响。FD 的综合治疗计划应考虑评估和干预措施,以评估和改善社会、职业和心理功能。对 FD 的行为方面的关注可以改善治疗效果和提高生活质量。受 Fabry 病影响的个体表现出社会适应功能缺陷,这与我们的男性和女性患者样本中年龄在 18 岁至 59 岁之间的焦虑、抑郁、反社会行为和 AD/H 问题显著相关。