Tuan Sheng-Hui, Chiu Pao-Chin, Liou I-Hsiu, Lu Wen-Hsien, Huang Hung-Ya, Wu Shin-Yi, Chen Guan-Bo, Lin Ko-Long
Department of Rehabilitation Medicine, Cishan Hospital, Ministry of Health and Welfare, Kaohsiung, Taiwan.
Department of Physical Therapy, Shu-Zen Junior College of Medicine and Management, Kaohsiung, Taiwan.
J Rehabil Med Clin Commun. 2020 Feb 27;3:1000028. doi: 10.2340/20030711-1000028. eCollection 2020.
Fabry disease, a rare X-linked disorder, can lead to exercise intolerance. In Taiwan, the cardiac variant of Fabry disease has a significantly higher prevalence than the classic variant. The cardiac variant of Fabry disease primarily involves the heart. Enzyme replacement therapy has been used to treat both variants. We aimed to study the impact of enzyme replacement therapy on exercise and cardiac structures between the classic (CL-FD) and cardiac variant (CV-FD) Fabry disease.
Retrospective analysis of 2 groups of patients with Fabry disease (5 patients with the classic variant and 5 with the cardiac variant), who were undergoing enzyme replacement therapy. Patients were assessed annually for 3 years using symptom-limited cycle ergometry and echocardiography.
Subjects were 5 women, mean age 53 (standard deviation (SD) 14.05) years with CL-FD Fabry disease, and 5 men, mean age 65 (SD 2.35) years with CV-FD. The percentage of peak oxygen consumption to predicted value for all included patients was significantly lower (78.78% (SD 12.72)) than 100%. Annual serial measurement showed that peak metabolic equivalent and percentage of peak oxygen consumptiondecreased significantly over a period of 3 years in patients with CV-FD ( = 0.002, and =0.004, respectively), but not in those with CL-FD. There were no significant changes in annual serial measurements of left ventricular mass or interventricular septal thickness in patients with either variant of Fabry disease over a period of 3 years.
Peak exercise capacity of the patients with Fabry disease was lower than that of normal peers. Peak exercise capacity decreased over time.
法布里病是一种罕见的X连锁疾病,可导致运动不耐受。在台湾,法布里病的心脏变异型患病率显著高于经典型。法布里病的心脏变异型主要累及心脏。酶替代疗法已用于治疗这两种变异型。我们旨在研究酶替代疗法对经典型(CL-FD)和心脏变异型(CV-FD)法布里病患者运动和心脏结构的影响。
对两组接受酶替代疗法的法布里病患者(5例经典型和5例心脏变异型)进行回顾性分析。使用症状限制式踏车运动试验和超声心动图对患者进行为期3年的年度评估。
受试者中,5例为患有CL-FD法布里病的女性,平均年龄53岁(标准差(SD)14.05);5例为患有CV-FD的男性,平均年龄65岁(SD 2.35)。所有纳入患者的峰值耗氧量占预测值的百分比显著低于100%(78.78%(SD 12.72))。年度系列测量显示,CV-FD患者在3年期间峰值代谢当量和峰值耗氧量百分比显著下降(分别为P = 0.002和P = 0.004),而CL-FD患者则无此现象。在3年期间,两种变异型法布里病患者的左心室质量或室间隔厚度的年度系列测量均无显著变化。
法布里病患者的峰值运动能力低于正常同龄人。峰值运动能力随时间下降。