Polistena Barbara, Rigante Donato, Sicignano Ludovico Luca, Verrecchia Elena, Manna Raffaele, d'Angela Daniela, Spandonaro Federico
Department of Economic and Finance, University of Rome Tor Vergata, C.R.E.A. Sanità, via Columbia n. 2, 00133 Rome, Italy.
Department of Life Sciences and Global Health, Fondazione Policlinico A. Gemelli IRCCS, 00168 Rome, Italy.
Diseases. 2021 Oct 15;9(4):72. doi: 10.3390/diseases9040072.
Fabry disease (FD) is a genetic disease included in the group of lysosomal storage disorders, caused by X-linked deficiency of the enzyme alpha-galactosidase A. The aim of this study was to evaluate different aspects related to the quality of life (QoL) of a multicentre cohort of Italian patients with FD. An observational survey was conducted to measure health-related quality of life (HR-QoL) in FD patients using the CAPI (Computer-Assisted Personal Interview) method: 106 patients (mostly women) responded to the questionnaire. Geographically, 53.7% of patients lived in northern Italy, 18.9% in central Italy and 27.4% in southern Italy or the Islands. All data were collected through a five-dimensional EuroQoL questionnaire referring to functional aspects (mobility, personal care, routine activities) and perception of physical/mental well-being (pain or discomfort, anxiety or depression). A descriptive analysis of responses was performed; FD patients were compared in terms of QoL with subjects suffering from other chronic diseases, such as Crohn's disease, chronic hepatitis, cirrhosis and multiple sclerosis. Difficulty in normal daily activities was reported by 47.2% of FD patients. About one third of subjects also had mobility difficulties. Feelings of loneliness and isolation were reported by 33.3% of those being 60-69 years old. Anxiety was equally reported in both oldest and youngest patients (66.7%), while depression, relational problems, fear of other people's judgement increased along with age, reaching 66.7% in the over-70-years group. Male patients were largely troubled about the risk of physical disability, particularly those aged 60 years or over. Furthermore, FD patients had a poorer QoL than people suffering from other chronic inflammatory disorders. Our study upholds that FD patients have a poor QoL, as already known, negatively impacting psychic well-being and social activities. Our survey has also found a worse QoL in FD patients compared with other severe chronic disorders.
法布里病(FD)是一种溶酶体贮积症,由X连锁的α-半乳糖苷酶A缺乏引起。本研究的目的是评估意大利多中心队列FD患者生活质量(QoL)的不同方面。采用计算机辅助个人访谈(CAPI)方法进行观察性调查,以测量FD患者的健康相关生活质量(HR-QoL):106名患者(大多数为女性)回答了问卷。从地理位置来看,53.7%的患者居住在意大利北部,18.9%在意大利中部,27.4%在意大利南部或岛屿。所有数据均通过一份涉及功能方面(活动能力、个人护理、日常活动)以及身体/心理健康感知(疼痛或不适、焦虑或抑郁)的五维欧洲生活质量问卷收集。对回答进行了描述性分析;将FD患者的生活质量与患有其他慢性疾病(如克罗恩病、慢性肝炎、肝硬化和多发性硬化症)的受试者进行了比较。47.2%的FD患者报告日常活动有困难。约三分之一的受试者也有活动能力困难。60 - 69岁的受试者中有33.3%报告有孤独和孤立感。最年长和最年轻的患者中焦虑报告率均为66.7%,而抑郁、人际关系问题、对他人评判的恐惧随年龄增长而增加,在70岁以上组达到66.7%。男性患者大多担心身体残疾的风险,尤其是60岁及以上的男性。此外,FD患者的生活质量比患有其他慢性炎症性疾病的人更差。我们的研究支持FD患者生活质量较差这一已知情况,这对心理健康和社会活动有负面影响。我们的调查还发现,与其他严重慢性疾病相比,FD患者的生活质量更差。