Clinical outcomes in elderly patients receiving agalsidase alfa treatment in the Fabry Outcome Survey

IF 3.7 2区 生物学 Q2 ENDOCRINOLOGY & METABOLISM
Albina Nowak , Jaco Botha , Christina Anagnostopoulou , Derralynn A. Hughes
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Abstract

Background and objectives

Treatment with agalsidase alfa in patients with Fabry disease is most effective when initiated early in the disease course; however, the clinical benefits in elderly patients are less well established. This analysis assesses outcomes in patients aged 65 years or older from the Fabry Outcome Survey (FOS) who were treated with agalsidase alfa.

Methods

FOS data were extracted for adult patients aged 65 years or older who received agalsidase alfa, had baseline data and at least 3 years of post-baseline data, and had undergone no renal transplantation and/or dialysis before treatment. The data of patients who had undergone renal transplantation and/or dialysis during follow-up were excluded from estimated glomerular filtration rate (eGFR) analysis after the date of the renal transplantation and/or dialysis. Adult patients were stratified into two groups: those who started treatment before 65 years of age and who were still being treated when aged 65 years or older (group A), and those who started treatment when aged 65 years or older (group B). Mean annual changes in left ventricular mass index (LVMI), eGFR and proteinuria were assessed in group A (before and after the age of 65 years to understand if there was an age-related effect once patients turned 65 years of age) and in group B.

Results

Estimated mean (standard error [SE]) annual changes in LVMI were 0.46 (0.26) g/m2.7 and 0.21 (0.42) g/m2.7 in patients in group A when they were younger than 65 years and when they were aged 65 years or older, respectively, and 0.12 (0.65) g/m2.7 in patients in group B. For eGFR, mean (SE) annual changes were 0.83 (2.12) mL/min/1.73 m2 and 2.64 (2.18) mL/min/1.73 m2 in patients in group A when they were younger than 65 years and when they were aged 65 years or older, respectively, and 2.31 (1.44) mL/min/1.73 m2 in patients in group B. Proteinuria remained relatively stable in both subgroups of group A (before and after the age of 65 years) and group B.

Conclusions

Continuation and initiation of agalsidase alfa treatment in patients aged 65 years or older with Fabry disease were associated with stabilization of proteinuria and minimal increases in cardiac (LVMI) and renal (eGFR) outcomes.

法布里结果调查中接受阿加西酶α治疗的老年患者的临床结果
背景和目标法布里病患者在病程早期开始使用阿加西酶α治疗效果最佳;但是,老年患者的临床获益还没有得到很好的证实。本分析评估了法布里结果调查(FOS)中接受阿加苷酶α治疗的 65 岁及以上患者的疗效。方法提取了接受阿加苷酶α治疗的 65 岁及以上成年患者的 FOS 数据,这些患者拥有基线数据和至少 3 年的基线后数据,并且在治疗前未接受过肾移植和/或透析。在随访期间接受过肾移植和/或透析的患者的数据不包括在肾移植和/或透析日期之后的估计肾小球滤过率(eGFR)分析中。成年患者被分为两组:65 岁前开始治疗且 65 岁或以上仍在接受治疗的患者(A 组)和 65 岁或以上开始治疗的患者(B 组)。评估了 A 组(65 岁之前和之后,以了解患者年满 65 岁后是否存在与年龄相关的影响)和 B 组的左心室质量指数 (LVMI)、eGFR 和蛋白尿的年均变化。结果A组患者在65岁以下和65岁或以上时的LVMI估计年平均变化(标准误差[SE])分别为0.46(0.26)g/m2.7和0.21(0.42)g/m2.7,B组患者为0.12(0.65)g/m2.7。就 eGFR 而言,A 组患者在 65 岁以下和 65 岁或以上时的平均(SE)年变化分别为 0.83 (2.12) mL/min/1.73 m2 和 2.64 (2.18) mL/min/1.73 m2,B 组患者为 2.31 (1.44) mL/min/1.73 m2。结论对 65 岁或以上的法布里病患者继续和开始阿加西酶α治疗与蛋白尿的稳定以及心脏(LVMI)和肾脏(eGFR)预后的最小增长有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular genetics and metabolism
Molecular genetics and metabolism 生物-生化与分子生物学
CiteScore
5.90
自引率
7.90%
发文量
621
审稿时长
34 days
期刊介绍: Molecular Genetics and Metabolism contributes to the understanding of the metabolic and molecular basis of disease. This peer reviewed journal publishes articles describing investigations that use the tools of biochemical genetics and molecular genetics for studies of normal and disease states in humans and animal models.
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