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本文引用的文献

1
Safety and physiological effects of two different doses of elosulfase alfa in patients with morquio a syndrome: A randomized, double-blind, pilot study.两种不同剂量的艾洛硫酸酯酶α治疗黏多糖贮积症IVA型患者的安全性及生理效应:一项随机、双盲、试点研究。
Am J Med Genet A. 2015 Oct;167A(10):2272-81. doi: 10.1002/ajmg.a.37172. Epub 2015 Jun 10.
2
Role of the cardio-pulmonary exercise test and six-minute walking test in the evaluation of exercise performance in patients with late-onset Pompe disease.心肺运动试验和六分钟步行试验在晚发型庞贝病患者运动能力评估中的作用
Neuromuscul Disord. 2015 Jul;25(7):542-7. doi: 10.1016/j.nmd.2015.03.010. Epub 2015 Mar 23.
3
A systematic review of the prevalence of Morquio A syndrome: challenges for study reporting in rare diseases.莫尔基奥A综合征患病率的系统评价:罕见病研究报告面临的挑战
Orphanet J Rare Dis. 2014 Nov 18;9:173. doi: 10.1186/s13023-014-0173-x.
4
International guidelines for the management and treatment of Morquio A syndrome.莫尔基奥A综合征管理与治疗的国际指南。
Am J Med Genet A. 2015 Jan;167A(1):11-25. doi: 10.1002/ajmg.a.36833. Epub 2014 Oct 24.
5
Efficacy and safety of enzyme replacement therapy with BMN 110 (elosulfase alfa) for Morquio A syndrome (mucopolysaccharidosis IVA): a phase 3 randomised placebo-controlled study.BMN 110(艾洛硫酸酯酶α)酶替代疗法治疗莫氏综合征A(黏多糖贮积症IVA)的疗效和安全性:一项3期随机安慰剂对照研究。
J Inherit Metab Dis. 2014 Nov;37(6):979-90. doi: 10.1007/s10545-014-9715-6. Epub 2014 May 9.
6
Elosulfase alfa: first global approval.依洛硫酸酯酶 alfa:全球首次获批。
Drugs. 2014 Apr;74(6):713-8. doi: 10.1007/s40265-014-0210-z.
7
Pathogenesis of Morquio A syndrome: an autopsied case reveals systemic storage disorder.黏多糖贮积症 A 型的发病机制:尸检病例揭示全身性贮积紊乱。
Mol Genet Metab. 2013 Jul;109(3):301-11. doi: 10.1016/j.ymgme.2013.04.009. Epub 2013 Apr 16.
8
The Morquio A Clinical Assessment Program: baseline results illustrating progressive, multisystemic clinical impairments in Morquio A subjects.黏多糖贮积症 A 临床评估项目:基线结果表明黏多糖贮积症 A 患者存在进行性多系统临床损伤。
Mol Genet Metab. 2013 May;109(1):54-61. doi: 10.1016/j.ymgme.2013.01.021. Epub 2013 Feb 9.
9
Biomarkers and surrogate endpoints in clinical trials.生物标志物和临床试验中的替代终点。
Stat Med. 2012 Nov 10;31(25):2973-84. doi: 10.1002/sim.5403. Epub 2012 Jun 18.
10
Clinical overview and treatment options for non-skeletal manifestations of mucopolysaccharidosis type IVA.黏多糖贮积症 IVA 型非骨骼表现的临床概述和治疗选择。
J Inherit Metab Dis. 2013 Mar;36(2):309-22. doi: 10.1007/s10545-012-9459-0. Epub 2012 Feb 23.

心肺运动试验反映了莫尔基奥A综合征患者在接受治疗后运动能力的改善:一项针对两种不同剂量艾洛硫酸酯酶α的52周初步研究结果

Cardiopulmonary Exercise Testing Reflects Improved Exercise Capacity in Response to Treatment in Morquio A Patients: Results of a 52-Week Pilot Study of Two Different Doses of Elosulfase Alfa.

作者信息

Berger Kenneth I, Burton Barbara K, Lewis Gregory D, Tarnopolsky Mark, Harmatz Paul R, Mitchell John J, Muschol Nicole, Jones Simon A, Sutton V Reid, Pastores Gregory M, Lau Heather, Sparkes Rebecca, Shaywitz Adam J

机构信息

New York University School of Medicine, New York, NY, USA.

André Cournand Pulmonary Physiology Laboratory, Bellevue Hospital, New York, NY, USA.

出版信息

JIMD Rep. 2018;42:9-17. doi: 10.1007/8904_2017_70. Epub 2017 Nov 21.

DOI:10.1007/8904_2017_70
PMID:29159458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6226396/
Abstract

OBJECTIVE

To assess impact of a 52-week elosulfase alfa enzyme replacement therapy (ERT) on exercise capacity in Morquio A patients and analyze cardiorespiratory and metabolic function during exercise to uncover exercise limitations beyond skeletal abnormalities.

METHODS

Morquio A patients aged ≥7 years, able to walk >200 m in the 6-minute walk test (6MWT), received elosulfase alfa 2.0 mg/kg/week (N = 15) or 4.0 mg/kg/week (N = 10) for 52 weeks in the randomized, double-blind MOR-008 study ( ClinicalTrials.gov NCT01609062) and its extension. Exercise capacity was assessed by 6MWT, 3-minute stair climb test (3MSCT), and cardiopulmonary exercise test (CPET; N = 15 dosage groups combined).

RESULTS

Changes over 52 weeks in 6MWT and 3MSCT were minimal. Baseline CPET results showed impaired weight-adjusted peak oxygen uptake (VO), partly attributable to inability to increase tidal volume during exercise. CPET measures of exercise function showed significant improvement at 25 and/or 52 weeks in exercise duration, peak workload, O pulse, and peak tidal volume (% increases in duration, 16.9 (P = 0.0045) and 9.4 (P = 0.0807); peak workload, 26.5 (P = 0.0026) and 21.2 (P = 0.0132); O pulse, 10.7 (P = 0.0187) and 2.3 (P = 0.643); peak tidal volume, 11.7 (P = 0.1117) and 29.1 (P = 0.0142)). In addition, decreased VO/work ratio was noted (% decrease -7.6 [-11.9, 1.3] and -9.2 [-25.7, 5.1]), indicating performance of work at reduced oxygen cost.

CONCLUSIONS

CPET uncovers limitation in exercise capacity in Morquio A related to reduced lung function. ERT improves exercise capacity and efficiency of oxygen utilization, not attributable to changes in cardiac or pulmonary function. Further study of the long-term impact of ERT on exercise capacity and the clinical relevance of the observed changes is warranted.

摘要

目的

评估52周的艾洛硫酸酯酶α酶替代疗法(ERT)对黏多糖贮积症IVA型(Morquio A)患者运动能力的影响,并分析运动期间的心肺和代谢功能,以发现骨骼异常之外的运动限制因素。

方法

在随机、双盲的MOR-008研究(ClinicalTrials.gov标识符:NCT01609062)及其扩展研究中,年龄≥7岁、在6分钟步行试验(6MWT)中能够行走超过200米的Morquio A患者,接受52周的2.0毫克/千克/周(N = 15)或4.0毫克/千克/周(N = 10)的艾洛硫酸酯酶α治疗。通过6MWT、3分钟爬楼梯试验(3MSCT)和心肺运动试验(CPET;将15个剂量组合并)评估运动能力。

结果

6MWT和3MSCT在52周内的变化极小。基线CPET结果显示,体重调整后的峰值摄氧量(VO)受损,部分原因是运动期间无法增加潮气量。CPET运动功能指标显示,在25周和/或52周时,运动持续时间、峰值工作量、氧脉搏和峰值潮气量有显著改善(持续时间增加百分比分别为16.9(P = 0.0045)和9.4(P = 0.0807);峰值工作量分别为26.5(P = 0.0026)和21.2(P = 0.0132);氧脉搏分别为10.7(P = 0.0187)和2.3(P = 0.643);峰值潮气量分别为11.7(P = 0.1117)和29.1(P = 0.0142))。此外,VO/工作量比值降低(降低百分比为-7.6 [-11.9, 1.3]和-9.2 [-25.7, 5.1]),表明以更低的氧消耗进行工作。

结论

CPET揭示了Morquio A患者运动能力受限与肺功能降低有关。ERT可提高运动能力和氧利用效率,这并非归因于心肺功能的变化。有必要进一步研究ERT对运动能力的长期影响以及所观察到的变化的临床相关性。