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Improvement of gastrointestinal symptoms in a significant proportion of male patients with classic Fabry disease treated with agalsidase beta: A Fabry Registry analysis stratified by phenotype

机译:用AgAlsidaseβ处理的经典法布里疾病的大量男性患者的胃肠道症状改善:通过表型分层的法布里登记分析

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摘要

Background: Fabry disease is an inherited disorder of glycolipid metabolism with progressive involvement of multiple organs, including the gastrointestinal tract, in classically affected male patients. Clinical presentations in males with later-onset Fabry phenotypes are more heterogeneous and largely dependent on the level of residual α-galactosidase A activity. Methods: We assessed agalsidase beta treatment outcomes of gastrointestinal symptoms in adult males with classic or later-onset Fabry disease. Self-reports of abdominal pain and diarrhea (‘present’/’not present’ since previous assessment) at last clinical visit (≥0.5 year of follow-up) were compared with treatment-baseline. Results: Classic male patients were considerably younger at first treatment than the fewer males with later-onset phenotypes (36 vs. ~47 years) and reported gastrointestinal symptoms more frequently at baseline (abdominal pain: 56% vs. 13%; diarrhea: 57% vs. 23%). As compared with baseline, significantly fewer classic patients reported abdominal pain after a median of 4.7 years of treatment (N = 171, 56% vs. 41%, P < 0.001). Moreover, significantly fewer patients reported diarrhea after 5.5 years of follow-up (N = 169, 57% vs. 47%, P < 0.05). Among the males with later-onset phenotypes, albeit statistically non-significant, abdominal pain reports reduced after a median of 4.2 years (N = 48, 13% vs. 4%) and diarrhea reports reduced after a median of 4.4 years of treatment (N = 47, 23% vs. 13%). Conclusions: Sustained treatment with agalsidase beta was associated with improvement in abdominal pain and diarrhea in a significant proportion of classic male Fabry patients. Males with later-onset phenotypes reported gastrointestinal symptoms much less frequently at baseline as compared with classic patients, and non-significant reductions were observed.
机译:背景:法布里病是糖脂代谢的多器官的逐步参与,包括胃肠道,在经典的影响男性患者的遗传性疾病。在与后发性法布里表型男性的临床表现是多种非均相和很大程度上依赖于残留α半乳糖苷酶A活性的水平。方法:我们评估的胃肠道症状阿加糖酶β治疗结果与经典或后发法布里病的成年男性。腹痛和腹泻自我报告(“存在” /”不存在”,因为之前的评估)在最后临床访视(≥0.5年的随访中)与治疗前相比。结果:经典的男性患者比与后发性的表型的男性少第一次治疗(36对〜47岁)相当年轻,在基线报告胃肠道症状更频繁(腹痛:56%对13%;腹泻:57 %对23%)。与基线相比,显著更少经典患者报告腹痛4.7年的治疗的中值后(N = 171,56%比41%,P <0.001)。此外,显著更少患者报告后5.5年随访(N = 169,57%对47%,P <0.05)的腹泻。间与后发性的表型,尽管4。2年(N = 48,13%对4%)中位数减少后统计学上无显著,腹痛报告的男性和4.4年的治疗的中值降低后的报告腹泻( N = 47,23%对13%)。结论:阿加糖酶β持续治疗与改善腹痛和腹泻经典的男性患者法布里的显著比例有关。与经典的患者相比,并观察非显著降低与后发性男性表型在基线报告胃肠道症状更频繁。

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