Alfadhel Majid, Al Sannaa Nouriya, Sunbul Rawda, Al-Khawaja Huda, Askandarani Sumayah, Alanzi Talal, Elawad Mamoun, Fourtounas Konstantinos
Medical Genomics Research Department, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs (MNG-HA), Riyadh, Saudi Arabia.
King Saud Bin Abdulaziz University or Health Sciences (KSAU-HS), Ministry of National Guard Health Affairs (MNG-HA), Riyadh, Saudi Arabia.
Ther Clin Risk Manag. 2024 Sep 13;20:641-652. doi: 10.2147/TCRM.S475744. eCollection 2024.
Fabry disease (FD) is an X-linked lysosomal storage disorder caused by α-galactosidase A gene mutations. Its global incidence ranges from 1:40,000 to 1:170,000. This expert review evaluates the available guidelines, the status of diagnosed but untreated patients with FD, and the challenges in diagnosing and managing FD in the Kingdom of Saudi Arabia (KSA). An advisory board meeting (ABM) was conducted in two phases, with a survey that aimed to receive insights on the current unmet needs in the management of patients with FD in November 2022, and a second, offline meeting in February 2023. The goal of this ABM was to discuss current unmet needs in the management of Fabry patients in the Kingdom of Saudi Arabia. In the first ABM, experts opined on the best practices in the diagnosis, screening, and management of FD for healthcare professionals. These opinions on the management of FD relied on data from research and expert clinical judgments. In the second ABM, the same panel discussed different aspects of FD diagnosis, treatment, and management in the member countries of the Gulf Cooperation Council. The experts discussed the stigma associated with FD, patient awareness and knowledge, genetic screening, biomarkers, and home infusion therapy. They reviewed international guidelines and clinical criteria for enzyme replacement therapy (ERT). Furthermore, they also discussed the diagnosis of FD in men and women, the current guidelines followed for monitoring patients with FD, monitoring untreated patients with FD, Fabry Stabilization IndeX (FASTEX) as an assessment tool for the diagnosis of FD, FD management in KSA, challenges encountered while prescribing ERT in patients with FD, and the clinical criteria for starting ERT. The discussions led to the conclusion that currently, ERT is the only available therapy to manage FD and research should be focused on the early diagnosis and management of FD.
法布里病(FD)是一种由α-半乳糖苷酶A基因突变引起的X连锁溶酶体贮积症。其全球发病率在1:40000至1:170000之间。本专家综述评估了现有指南、已确诊但未治疗的FD患者的状况,以及沙特阿拉伯王国(KSA)在FD诊断和管理方面面临的挑战。咨询委员会会议(ABM)分两个阶段进行,2022年11月进行了一项调查,旨在了解FD患者管理方面当前未满足的需求,2023年2月举行了第二次线下会议。本次ABM的目标是讨论沙特阿拉伯王国法布里病患者管理方面当前未满足的需求。在第一次ABM中,专家们就医疗保健专业人员对FD的诊断、筛查和管理的最佳实践发表了意见。这些关于FD管理的意见依赖于研究数据和专家临床判断。在第二次ABM中,同一小组讨论了海湾合作委员会成员国FD诊断、治疗和管理的不同方面。专家们讨论了与FD相关的耻辱感、患者意识和知识、基因筛查、生物标志物和家庭输注治疗。他们回顾了酶替代疗法(ERT)的国际指南和临床标准。此外,他们还讨论了男性和女性FD的诊断、目前对FD患者进行监测所遵循的指南、对未治疗的FD患者的监测、法布里稳定指数(FASTEX)作为FD诊断的评估工具、沙特阿拉伯王国的FD管理、给FD患者开ERT时遇到的挑战以及开始ERT的临床标准。讨论得出的结论是,目前,ERT是治疗FD的唯一可用疗法,研究应侧重于FD的早期诊断和管理。