Evidence map›Paper›PMID 41244789›Full record

ReviewFrontiers in medicine2025

Therapeutic landscape of Fabry disease: advances and challenges from classical strategies to emerging therapies.

Miao Zhang, Chendan Wang

Abstract readReview
In one paragraph

Review in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

2 authors.

Miao ZhangThe Fifth Clinical Medical College of Shanxi Medical University, Taiyuan, China.
Chendan WangThe Fifth Clinical Medical College of Shanxi Medical University, Taiyuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fabry disease (FD), as an X-linked lysosomal storage disorder (LSD), has seen significantly improved in patient prognosis since enzyme replacement therapy (ERT) was applied clinically in 2001. However, ERT has drawbacks such as immunogenicity, individual efficacy variability, and long-term treatment burdens. With deeper insights into the multidimensional pathological mechanisms of FD and breakthroughs in new delivery systems (such as mRNA therapy, engineered adeno-associated virus vectors), various emerging therapies have gradually developed. Nevertheless, each therapeutic strategy still faces areas needing improvement due to high disease heterogeneity, cytotoxicity, insufficient targeted tissue delivery efficiency, and a lack of long-term safety data. This article systematically reviews the development of different treatment strategies for FD, outlines the evolution from ERT clinical application to emerging technologies like novel vector delivery, analyzes the technical breakthroughs and clinical limitations of therapies at each stage, reveals the intrinsic connection between deepened understanding of pathological mechanisms and innovative treatments, and explores potential optimization directions for future treatment strategies based on global accessibility data.

Indexed as

AAV-mediated gene therapyenzyme replacement therapyFabry diseasemRNA therapypharmacological chaperone therapysubstrate reduction therapy

Identifiers

PMID41244789
PMCPMC12616745

What OpenQuestion holds

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Registered trials

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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.