Dehout F, Roland D, Treille de Granseigne S, Guillaume B, Van Maldergem L
Department of Nephrology, CHU, Intercommunale de Santé Publique du Pays de Charleroi, Charleroi, Belgium.
J Inherit Metab Dis. 2004;27(4):499-505. doi: 10.1023/B:BOLI.0000037342.59612.69.
Gastrointestinal symptoms, including diarrhoea and abdominal pain, are one of the earliest and most frequently reported signs of Fabry disease, a rare X-linked lipid storage disorder. As the disease progresses, renal, cardiac and cerebrovascular complications develop, resulting in more serious symptoms and early mortality. The present study evaluated the effects of enzyme replacement therapy (ERT) with agalsidase alfa on the gastrointestinal symptoms of Fabry disease. Following 6 months of treatment, both the severity ( p < 0.02) and frequency ( p < 0.02) of abdominal pain decreased. For those patients who had received agalsidase alfa for more than 6 months, the observed improvement was generally maintained. This is the first study indicating a significant beneficial effect of ERT on gastrointestinal symptoms in a group of patients treated for Fabry disease.
胃肠道症状,包括腹泻和腹痛,是法布里病(一种罕见的X连锁脂质贮积病)最早且最常报告的体征之一。随着疾病进展,会出现肾脏、心脏和脑血管并发症,导致更严重的症状和早期死亡。本研究评估了阿加糖酶α酶替代疗法(ERT)对法布里病胃肠道症状的影响。治疗6个月后,腹痛的严重程度(p<0.02)和频率(p<0.02)均有所降低。对于接受阿加糖酶α治疗超过6个月的患者,观察到的改善通常得以维持。这是第一项表明ERT对一组接受法布里病治疗患者的胃肠道症状有显著有益影响的研究。