Evidence map›Paper›PMID 41148004›Full record

ArticleJournal of neuromuscular diseases2026

A retrospective cohort study describing the disease burden in patients with Pompe disease treated with enzyme replacement therapy in the United States.

Nishitha R Pillai, Faryn Solomon, Robert D Steiner, Bin Xie, Tmirah Haselkorn, Christopher Young, Nigel Rozario, Mark Walzer, Benedikt Schoser

Abstract read
In one paragraph

Article in Journal of neuromuscular diseases, 2026. 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. Review
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

9 authors.

Nishitha R PillaiDivision of Genetics & Metabolism, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Faryn SolomonAstellas Pharma Global Development, Inc., Northbrook, IL, USA.
Robert D SteinerDepartment of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.ORCID 0000-0003-4177-4590
Bin XieAstellas Pharma Global Development, Inc., Northbrook, IL, USA.
Tmirah HaselkornAstellas Pharma Global Development, Inc., Northbrook, IL, USA.
Christopher YoungAstellas Pharma Global Development, Inc., Northbrook, IL, USA.
Nigel RozarioAstellas Pharma Global Development, Inc., Northbrook, IL, USA.
Mark WalzerAstellas Pharma Global Development, Inc., Northbrook, IL, USA.
Benedikt SchoserFriedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University, Munich, Germany.ORCID 0000-0002-2757-8131

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectiveTo describe the disease burden in patients with Pompe disease treated with enzyme replacement therapy (ERT) in the US as defined by comorbid conditions, supportive services, and treatment patterns.MethodsA retrospective cohort study (01/01/2012-09/30/2022) was conducted using the Merative™ MarketScan Research Databases. Inclusion criteria were: ≥ 2 outpatient or ≥1 inpatient claims of Pompe disease, ≥ 1 claim of ERT, and continuous enrollment in medical/prescription coverage for ≥90 days before diagnosis date for patients ≥2 years and ≥1-month post-index date. Patients were stratified into infantile-onset Pompe disease (IOPD) or late-onset Pompe disease (LOPD) cohorts based on age at diagnosis and clinical presentation. Key comorbidities, supportive services, and treatment modifications were presented as cumulative incidence.ResultsA total of 105 patients were included (IOPD: n = 50; LOPD: n = 55). For IOPD and LOPD groups, the 12-month cumulative incidence was 84.5% and 79.4% for respiratory, 57.4% and 54.3% for ambulatory, 67.8% and 33.4% for gastrointestinal, and 16.9% and 28.7% for cardiovascular comorbidities, respectively; 12-month cumulative incidence was 66.9% and 31.8% for physical therapy, 59.5% and 3.9% for speech therapy, 48.6% and 1.8% for immune tolerance induction or intravenous immunoglobulin, 47.3% and 11.2% for nutritional therapy, 15.1% and 17.0% for respiratory support, 27.8% and 3.7% for occupational therapy, and 8.3% and 11.1% for ambulatory support, respectively. Fourteen (IOPD: n = 2; LOPD: n = 12) patients switched ERT therapy, and 21 (IOPD: n = 14; LOPD: n = 7) had ≥1 dose modification.ConclusionsPatients with Pompe disease demonstrate substantial comorbidity burden and utilization of supportive services despite ERT treatment.

Indexed as

Cost of IllnessEnzyme Replacement TherapyGlycogen Storage Disease Type IIAdolescentAdultChildChild, PreschoolComorbidityFemaleHumansInfantMaleMiddle AgedRetrospective StudiesUnited StatesYoung Adultcomorbiditiesdisease burdenenzyme replacement therapyPompe diseasereal-worldsupportive services

Identifiers

PMID41148004
PMCPMC13438606

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.