Evidence map›Paper›PMID 40804403›Full record

Observational studyOrphanet journal of rare diseases2025

Epidemiology, disease burden and costs of Duchenne muscular dystrophy in Germany: an observational, retrospective health claims data analysis.

Joanna Diesing, Janbernd Kirschner, Astrid Pechmann, Jörg König, Leonie Kunk, Tarcyane Barata Garcia, Carolina Schwedhelm, Carsta Militzer-Horstmann, Ivonne Hänsel, Agnes Kisser

Abstract readObservational Study
In one paragraph

Observational study in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Myostatin inhibition with orally administeredFrontiers in neurology · 2025
    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

10 authors.

Joanna DiesingWIG2 GmbH, Scientific Institute for Health Economics and Health System Research, Markt 8, 04109, Leipzig, Germany.
Janbernd KirschnerDepartment of Neuropediatrics and Muscle Disorders, Faculty of Medicine, Medical Center - University of Freiburg, Breisacher Str. 62, 79106, Freiburg, Germany.
Astrid PechmannDepartment of Neuropediatrics and Muscle Disorders, Faculty of Medicine, Medical Center - University of Freiburg, Breisacher Str. 62, 79106, Freiburg, Germany.
Jörg KönigPfizer Pharma GmbH, Friedrichstraße 110, 10117, Berlin, Germany.
Leonie KunkPfizer Pharma GmbH, Friedrichstraße 110, 10117, Berlin, Germany.
Tarcyane Barata GarciaWIG2 GmbH, Scientific Institute for Health Economics and Health System Research, Markt 8, 04109, Leipzig, Germany.
Carolina SchwedhelmPfizer Pharma GmbH, Friedrichstraße 110, 10117, Berlin, Germany. carolina.schwedhelm@pfizer.com.ORCID http://orcid.org/0000-0001-7617-6641
Carsta Militzer-HorstmannWIG2 GmbH, Scientific Institute for Health Economics and Health System Research, Markt 8, 04109, Leipzig, Germany.
Ivonne HänselPfizer Pharma GmbH, Friedrichstraße 110, 10117, Berlin, Germany.
Agnes KisserPfizer Pharma GmbH, Friedrichstraße 110, 10117, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDuchenne muscular dystrophy (DMD) is a rare genetic disorder that primarily affects males. Beginning in childhood, patients experience ambulatory loss, heart failure and need ventilation. Disease management has improved, however, DMD remains debilitating, and has no cure. The rarity of the disease makes research difficult, and German prevalence data are lacking. Cost and resource utilization estimations are based on small sample sizes or self-reported data, limiting generalizability and adds the potential for recall bias. With a retrospective study on a healthcare claims database, we adapted algorithms to identify DMD patients and categorized them by disease stages 1-4 (early ambulatory, late ambulatory, early non-ambulatory, late non-ambulatory) with increasing disease progression. We analyzed annual prevalence, burden of disease, healthcare resource utilization and direct medical care costs, by time under observation (patient year).

resultsFrom 2016 to 2021, we identified 134 patients for which we could determine a disease stage and determined an extrapolated prevalence of DMD in Germany between 14.85 (95%CI 12.17, 17.95) and 18.91 (95%CI 15.70, 22.61) per 100,000 males under 40 years of age. Most patients we identified met DMD stage 4 group criteria (47.01%), followed by stage 3 (37.31%), stage 2 (33.58%) and only 4.48% in stage 1. The average age increased with progressing disease, from 4.27 years in stage 1, to 11.43, 18.86 and 23.21 in stage groups 2, 3 and 4, respectively. In the stage 2 group, diagnosis codes reflecting mobility support and orthopedic surgical interventions (15.56% of the group) were documented. In the stage 3 group, decubitus prevention was documented, increasing to around half of patients in the stage 4 group. Total direct mean healthcare costs per patient year increased substantially with disease severity group, from €2,180.73 (SD 16,258.90) in stage 1; €13,599.83 (SD 33,756.07) in stage 2; €14,472.08 (SD 27,245.78) in stage 3 and finally €41,888.70 (SD 117,718.13) in stage 4. Especially in stage groups 3 and 4, medical aids accounted for about half of total costs.

conclusionsWe present an algorithm on which further research can be based, and provide a current picture of epidemiology, burden of disease and healthcare utilization and direct costs of DMD in Germany.

Indexed as

Muscular Dystrophy, DuchenneAdolescentAdultChildChild, PreschoolCost of IllnessGermanyHealth Care CostsHumansMalePrevalenceRetrospective StudiesYoung AdultAlgorithmCostsDisease stagesDuchenne muscular dystrophyEpidemiologyGermanyHealthcare resource utilizationPrevalenceReal-world data

Identifiers

PMID40804403
PMCPMC12351880

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.