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对于长期每两周给药一次的法布里病患者,每周进行酶替代疗法可能会减缓肾功能下降。

Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing.

作者信息

Schiffmann Raphael, Askari Hasan, Timmons Margaret, Robinson Chevalia, Benko William, Brady Roscoe O, Ries Markus

机构信息

Developmental and Metabolic Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Building 10, Room 3D03, 9000 Rockville Pike, Bethesda, MD 20892-1260, USA.

出版信息

J Am Soc Nephrol. 2007 May;18(5):1576-83. doi: 10.1681/ASN.2006111263. Epub 2007 Apr 4.

DOI:10.1681/ASN.2006111263
PMID:17409308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1978101/
Abstract

This study was performed to determine whether adult male patients with Fabry disease who demonstrate a continuing decline in renal function despite 2 to 4 yr of conventionally dosed agalsidase alfa therapy (0.2 mg/kg every other week [EOW]) show an improved slope of decline with weekly administration using the same dosage. Eleven (27%) of 41 adult male patients with Fabry disease who participated in long-term agalsidase alfa clinical trials and who had demonstrated a slope of decline in estimated GFR (eGFR) of > or =5 ml/min per 1.73 m(2)/yr while receiving long-term treatment with agalsidase alfa at the currently recommended dosage of 0.2 mg/kg, infused EOW, were enrolled in this open-label, prospective study. Patients were switched from EOW to weekly infusions and followed for an additional 24 mo. Before switching to weekly dosing, eGFR was 53.7 +/- 6.3 ml/min per 1.73 m(2) (mean +/- SEM), and mean rate of change in eGFR was -8.0 +/- 0.8 ml/min per 1.73 m(2)/yr. During the 24-mo follow-up period after switching to weekly dosing, the mean rate of change in eGFR was observed to slow to -3.3 +/- 1.4 ml/min/1.73 m(2)/yr (P = 0.01 versus EOW). After switching to weekly dosing, three patients demonstrated an improvement in eGFR and six patients demonstrated a slowing in the rate of eGFR decline; only two patients failed to improve their eGFR slope. A multiple regression model confirmed that the weekly infusion regimen was the strongest explanatory variable for the change in eGFR (P = 0.0008), with a weaker contribution from the concomitant use of angiotensin converting enzyme inhibitors/angiotensin receptor blockers (P = 0.02). These results suggest that weekly infusions of agalsidase alfa at a dosage of 0.2 mg/kg may be beneficial in the subgroup of patients who have Fabry disease and whose kidney function continues to decline after 2 to 4 yr or more of standard EOW dosing.

摘要

本研究旨在确定,对于接受常规剂量阿加糖酶α治疗(每两周一次[EOW],0.2mg/kg)2至4年但肾功能仍持续下降的成年男性法布里病患者,使用相同剂量改为每周给药后肾功能下降斜率是否会改善。41名参与阿加糖酶α长期临床试验的成年男性法布里病患者中,有11名(27%)在接受目前推荐剂量0.2mg/kg阿加糖酶α长期治疗(EOW输注)时,估计肾小球滤过率(eGFR)下降斜率≥5ml/min/1.73m²/年,这些患者被纳入这项开放标签的前瞻性研究。患者从EOW给药改为每周输注,并随访额外24个月。在改为每周给药前,eGFR为53.7±6.3ml/min/1.73m²(均值±标准误),eGFR平均变化率为-8.0±0.8ml/min/1.73m²/年。在改为每周给药后的24个月随访期内,观察到eGFR平均变化率减缓至-3.3±1.4ml/min/1.73m²/年(与EOW给药相比,P=0.01)。改为每周给药后,3名患者的eGFR有所改善,6名患者的eGFR下降速率减缓;只有2名患者的eGFR斜率未改善。多元回归模型证实,每周输注方案是eGFR变化的最强解释变量(P=0.0008),同时使用血管紧张素转换酶抑制剂/血管紧张素受体阻滞剂的影响较弱(P=0.02)。这些结果表明,对于患有法布里病且在标准EOW给药2至4年或更长时间后肾功能仍持续下降的患者亚组,每周输注0.2mg/kg阿加糖酶α可能有益。

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本文引用的文献

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The Dutch Fabry cohort: diversity of clinical manifestations and Gb3 levels.荷兰法布里病队列研究:临床表现及Gb3水平的多样性
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Agalsidase-beta therapy for advanced Fabry disease: a randomized trial.阿加糖酶β治疗晚期法布里病:一项随机试验。
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