Long-Term Outcome of Infantile Onset Pompe Disease Patients Treated with Enzyme Replacement Therapy - Data from a German-Austrian Cohort.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Charlotte Pfrimmer, Martin Smitka, Nicole Muschol, Ralf A Husain, Martina Huemer, Julia B Hennermann, Rahel Schuler, Andreas Hahn
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Abstract

Background: Enzyme replacement therapy (ERT) with recombinant human alglucosidase alfa (rhGAA) was approved in Europe in 2006. Nevertheless, data on the long-term outcome of infantile onset Pompe disease (IOPD) patients at school age is still limited.

Objective: We analyzed in detail cardiac, respiratory, motor, and cognitive function of 15 German-speaking patients aged 7 and older who started ERT at a median age of 5 months.

Results: Starting dose was 20 mg/kg biweekly in 12 patients, 20 mg/kg weekly in 2, and 40 mg/kg weekly in one patient. CRIM-status was positive in 13 patients (86.7%) and negative or unknown in one patient each (6.7%). Three patients (20%) received immunomodulation. Median age at last assessment was 9.1 (7.0-19.5) years. At last follow-up 1 patient (6.7%) had mild cardiac hypertrophy, 6 (42.9%) had cardiac arrhythmias, and 7 (46.7%) required assisted ventilation. Seven patients (46.7%) achieved the ability to walk independently and 5 (33.3%) were still ambulatory at last follow-up. Six patients (40%) were able to sit without support, while the remaining 4 (26.7%) were tetraplegic. Eleven patients underwent cognitive testing (Culture Fair Intelligence Test), while 4 were unable to meet the requirements for cognitive testing. Intelligence quotients (IQs) ranged from normal (IQ 117, 102, 96, 94) in 4 patients (36.4%) to mild developmental delay (IQ 81) in one patient (9.1%) to intellectual disability (IQ 69, 63, 61, 3x <55) in 6 patients (54.5%). White matter abnormalities were present in 10 out of 12 cerebral MRIs from 7 patients.

Conclusion: Substantial motor, cardiac, respiratory, and cognitive deficits are frequent in IOPD long-term survivors who started ERT before 2016. The findings of this study can be valuable as comparative data when evaluating the impact of newer treatment strategies including higher enzyme dosage, immunomodulation, modified enzymes, or early start of treatment following newborn screening.

用酶替代疗法治疗婴儿起病庞贝病患者的长期预后——来自德国-奥地利队列的数据
背景:重组人α糖苷酶(rhGAA)酶替代疗法(ERT)于2006年在欧洲获得批准。然而,关于学龄期婴儿起病庞贝病(IOPD)患者长期预后的数据仍然有限。目的:我们详细分析了15名年龄在7岁及以上的德语患者的心脏、呼吸、运动和认知功能,这些患者的中位年龄为5个月。结果:起始剂量为20mg /kg, 12例患者双周,2例患者每周20mg /kg, 1例患者每周40mg /kg。13例患者(86.7%)的crim状态为阳性,1例患者(6.7%)为阴性或未知。3例患者(20%)接受免疫调节。最后一次评估的中位年龄为9.1(7.0-19.5)岁。最后随访时,1例(6.7%)患者出现轻度心肌肥厚,6例(42.9%)患者出现心律失常,7例(46.7%)患者需要辅助通气。7例患者(46.7%)达到独立行走能力,5例患者(33.3%)在最后随访时仍能行走。6名患者(40%)能够在没有支持的情况下坐着,而其余4名患者(26.7%)四肢瘫痪。11例患者接受认知测试(文化公平智力测验),4例患者不符合认知测试要求。智商(IQ)从4例(36.4%)的正常(IQ 117、102、96、94)到1例(9.1%)的轻度发育迟缓(IQ 81)到智力残疾(IQ 69、63、61、3x)。结论:在2016年之前开始ERT治疗的IOPD长期存活患者中,存在大量的运动、心脏、呼吸和认知缺陷。这项研究的结果可以作为评估新治疗策略的影响的有价值的比较数据,包括更高的酶剂量,免疫调节,改良酶,或新生儿筛查后早期开始治疗。
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
CiteScore
7.20
自引率
4.30%
发文量
567
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