Evidence map›Paper›PMID 39773286›Full record

ReviewOrphanet journal of rare diseases2025

Clinical management of female patients with Fabry disease based on expert consensus.

Eva Brand, Aleš Linhart, Patrick Deegan, Ruxandra Jurcut, Antonio Pisani, Roser Torra, Ulla Feldt-Rasmussen

Abstract readReview
In one paragraph

Review 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Progress and Challenges in the Treatment of Fabry Disease.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  10. 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

7 authors.

Eva Brand *Department of Nephrology, Hypertension and Rheumatology, and Interdisciplinary Fabry Centre Münster (IFAZ), University Hospital Münster, Münster, Germany. Eva.Brand@ukmuenster.de.ORCID http://orcid.org/0009-0004-3243-5508
Aleš Linhart *2nd Department of Internal Cardiovascular Medicine, General University Hospital, Prague, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Patrick DeeganLysosomal Disorders Unit, Addenbrooke's Hospital, Cambridge, UK.
Ruxandra JurcutExpert Center for Rare Genetic Cardiovascular Diseases, Institute of Emergency for Cardiovascular Diseases "Prof. Dr. C.C. Iliescu", University of Medicine and Pharmacy "Carol Davila", Bucharest, Romania.
Antonio PisaniDepartment of Public Health, University Federico II of Napoli, Napoli, Italy.
Roser TorraInherited Kidney Diseases, Nephrology Department, Fundació Puigvert, Institut Recerca Sant Pau (IR-SANT PAU), Universitat Autònoma de Barcelona, Barcelona, Spain.
Ulla Feldt-RasmussenDepartment of Nephrology and Endocrinology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Funding

Sanofi Sanofi
6 · The paper itself

Abstract

Fabry disease is an X-linked lysosomal storage disorder that causes accumulation of glycosphingolipids in body tissues and fluids, leading to progressive organ damage and life-threatening complications. It can affect both males and females and can be classified into classic or later-onset phenotypes. The disease severity in females ranges from asymptomatic to the more severe, classic phenotype. Most females are hemizygous and the X-linked inheritance is associated with variable X-activation pattern and residual enzymatic activity. The heterogeneity of clinical presentation in females requires different approaches to diagnosis and management than males. A European group of 7 physicians, experienced in the management of Fabry disease, convened to discuss patient perspectives and published guidelines. The experts discussed the need to focus on psychological treatment in relation to individual coping styles when monitoring targets, and the lack of data supporting the use of plasma globotriaosylsphingosine over enzyme activity in the diagnosis of these patients. It was suggested that the high phenotypic variability in female patients may be related to the dynamic nature of the X-chromosome inactivation process and further understanding of this process could help predict the progression of Fabry disease in females and facilitate timely intervention. Due to the range of disease severity they exhibit, female patients with Fabry disease may require a more individualized treatment approach than males. Despite current recommendations, the experts agreed that early disease-specific treatment initiation in high-risk females could improve clinical outcome.

Indexed as

Fabry DiseaseConsensus Statements as TopicFemaleHumansMaleEarly diagnosisEnzyme replacement therapyFabry diseaseFemalePatient-reported outcome measures

Identifiers

PMID39773286
PMCPMC11707893

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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.