Evidence map›Paper›PMID 41462273›Full record

ArticleInternational breastfeeding journal2025

Enzyme replacement therapy during pregnancy and breastfeeding in late-onset Pompe disease.

Magdalena Bachmann, David Kasper, Sabine Scholl-Bürgi, Julian Margreitter, Alexander Höller, Wolfgang Löscher, Daniela Karall, Thomas Zöggeler

Abstract readCase Reports
In one paragraph

Article in International breastfeeding journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Magdalena BachmannDepartment of Pediatrics I, Medical University of Innsbruck, Anichstrasse 35, Innsbruck, 6020, Austria.
David KasperARCHIMEDlife Laboratories, Vienna, 1010, Austria.
Sabine Scholl-BürgiDepartment of Pediatrics I, Medical University of Innsbruck, Anichstrasse 35, Innsbruck, 6020, Austria.
Julian MargreitterDepartment of Pediatrics I, Medical University of Innsbruck, Anichstrasse 35, Innsbruck, 6020, Austria.
Alexander HöllerDivision of Nutrition and Dietetics, University Hospital Innsbruck, Innsbruck, 6020, Austria.
Wolfgang LöscherDepartment of Neurology, Medical University of Innsbruck, Innsbruck, 6020, Austria.
Daniela Karall *Department of Pediatrics I, Medical University of Innsbruck, Anichstrasse 35, Innsbruck, 6020, Austria. daniela.karall@i-med.ac.at.
Thomas Zöggeler *Department of Pediatrics I, Medical University of Innsbruck, Anichstrasse 35, Innsbruck, 6020, Austria. thomas.zoeggeler@i-med.ac.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPompe disease is an autosomal recessively inherited lysosomal storage disorder, caused by enzyme deficiency of acid alpha-glucosidase (GAA). This deficiency leads to the accumulation of glycogen in lysosomes and subsequent muscle dysfunction, thus affecting heart and skeletal muscle. Since 2006, enzyme replacement therapy (ERT) is available. The use of ERT during pregnancy and lactation remains a topic of concern due to limited data on the safety of ERT during these periods. Despite this, some previous case reports suggest that ERT is safe during pregnancy and lactation. CASE PRESENTATION: In this case series, we collected the data on five pregnancies in three women with late-onset Pompe disease who were on ERT and continued it during pregnancy and lactation. In two of the children, during the lactation period activity levels of alglucosidase alfa were measured in breastmilk on dried blood spots.

conclusionThese case reports add to the literature experience by presenting the information on five so far not reported pregnancies in three women with late-onset Pompe disease, where ERT was continued during pregnancy and lactation. The results showed that acid alpha-glucosidase activity in milk from a woman with Pompe disease in two different breastfeeding periods was in the same range as acid alpha glucosidase activity in milk from five healthy women. As for the outcome in the five children, all have age-appropriated growth and development, confirming that ERT in this cohort was feasible and safe. These findings reinforce the safety of continuing ERT during pregnancy and breastfeeding in Pompe disease. Breastfeeding not only is the age adequate nutrition but also supports the well-being and development of the child as well as benefits maternal health. The value of breastfeeding being the recommended form of nutrition for infants cannot be emphasized enough. Thus, breastfeeding has to be especially supported in situations where there is a chronic disease/condition or medication. Further reports and appropriate guidelines are needed to soundly provide good advice to women with Pompe disease (or Morbus Pompe) during pregnancy and breastfeeding.

Indexed as

alpha-GlucosidasesBreast FeedingEnzyme Replacement TherapyGlycogen Storage Disease Type IIMilk, HumanPregnancy ComplicationsAdultFemaleHumansInfant, NewbornLactationPregnancyalpha-GlucosidasesGAA protein, humanAlglucosidase alfaBreastfeedingEnzyme replacement therapyGlycogen storage disease type IILactationPompe diseasePregnancy

Identifiers

PMID41462273
PMCPMC12751353

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.