Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Meta-Analysis
. 2022 Feb;269(2):733-741.
doi: 10.1007/s00415-021-10526-5. Epub 2021 Apr 13.

Clinical efficacy of the enzyme replacement therapy in patients with late-onset Pompe disease: a systematic review and a meta-analysis

Affiliations
Meta-Analysis

Clinical efficacy of the enzyme replacement therapy in patients with late-onset Pompe disease: a systematic review and a meta-analysis

Berli Sarah et al. J Neurol. 2022 Feb.

Abstract

In patients with late-onset Pompe disease (LOPD), the efficacy of the enzyme replacement therapy (ERT) with recombinant human alpha-glucosidase (rhGAA) is difficult to evaluate, due to the clinical heterogeneity and the small sample sizes in published studies. Therefore, we conduct a systematic literature review and meta-analysis of the literature to evaluate the efficacy of ERT in LOPD patients considering the walking distance, respiratory function and muscle strength. Particularly, six-minute walk test (6MWT), forced vital capacity (FVC), medical research council (MRC) grading, quantitative muscle testing (QMT), and quick motor function test (QMFT) were outcomes of interest. Overall, 619 studies were identified in PubMed, EMBASE and by manual search on July 18th, 2020. After an initial assessment, 16 studies were included in the meta-analysis, containing clinical data from 589 patients with LOPD. For the 6MWT, 419 patients were analyzed. Walking distance improved on average, 32.2 m greater during the observed period (p = 0.0003), compared to the distance at the baseline. The meta-analysis did not show any improvement in FVC and only a tendency towards better muscle strength after treatment with ERT, but the difference was not statistically significant. In conclusion, the available data showed that ERT has a significant beneficial efficacy in the improvement of walking distance in LOPD patients and a non-significant improvement of muscle strength. No improvement in respiratory capacity was found. More prospective and controlled trials are needed to demonstrate a clear clinical benefit of ERT.

Keywords: Enzyme replacement therapy; Gycogen storage disease type II; Late-onset Pompe disease; Meta-analyse; Pompe disease; Recombinant human alpha-glucosidase; Systematic review.

PubMed Disclaimer

Conflict of interest statement

The authors declare that there is no conflict of interest regarding the publication of this paper.

Figures

Fig. 1
Fig. 1
Study selection Flow diagram
Fig. 2
Fig. 2
Forest plot of effect of enzyme replacement therapy on motor performance, as assessed by 6-min-walk test
Fig. 3
Fig. 3
Funnel plot of comparison of 6-min-walk test
Fig. 4
Fig. 4
Forest plot of effect of enzyme replacement therapy on respiratory function, as assessed by forced vital capacity
Fig. 5
Fig. 5
Funnel plot of comparison of forced vital capacity
Fig. 6
Fig. 6
Forest plot of effect of enzyme replacement therapy on muscle strength, as assessed by medical research council grading scale, quantitative muscles testing and quick motor function test
Fig. 7
Fig. 7
Funnel plot of comparison of medical research council grading scale, quantitative muscles testing and quick motor function test

References

    1. van der Ploeg AT, Clemens PR, Corzo D, Escolar DM, Florence J, Groeneveld GJ, et al. A randomized study of alglucosidase alfa in late-onset Pompe’s disease. N Engl J Med. 2010;362(15):1396–1406. doi: 10.1056/NEJMoa0909859. - DOI - PubMed
    1. Dasouki M, Jawdat O, Almadhoun O, Pasnoor M, McVey AL, Abuzinadah A, et al. Pompe disease: literature review and case series. Neurol Clin. 2014;32(3):751–776. doi: 10.1016/j.ncl.2014.04.010. - DOI - PMC - PubMed
    1. Bembi B, Cerini E, Danesino C, Donati MA, Gasperini S, Morandi L, et al. Management and treatment of glycogenosis type II. Neurology. 2008;71(23 Suppl 2):S12–36. doi: 10.1212/WNL.0b013e31818da93f. - DOI - PubMed
    1. Pascual SIP. Phenotype variations in early onset Pompe disease: diagnosis and treatment results with Myozyme. Adv Exp Med Biol. 2009;652:39–46. doi: 10.1007/978-90-481-2813-6_4. - DOI - PubMed
    1. Patel TT, Banugaria SG, Case LE, Wenninger S, Schoser B, Kishnani PS. The impact of antibodies in late-onset Pompe disease: a case series and literature review. Mol Genet Metab. 2012;106(3):301–309. doi: 10.1016/j.ymgme.2012.04.027. - DOI - PubMed

MeSH terms

Substances

LinkOut - more resources