Evidence map›Paper›PMID 42850292›Full record

ReviewDie Ophthalmologie2026

[Genetic therapies for Stargardt disease].

Georg Ansari, Lucas Janeschitz-Kriegl, Pietro De Angeli, Martin Gliem, Mantian Wang, Kristina Pfau, Stylianos Michalakis, Susanne Kohl, Bence György, Maximilian Pfau

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review in Die Ophthalmologie, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Georg AnsariAugenklinik, Universitätsspital Basel, Mittlere Str. 91, 4031, Basel, Schweiz.ORCID http://orcid.org/0009-0008-4693-2061
Lucas Janeschitz-KrieglAugenklinik, Universitätsspital Basel, Mittlere Str. 91, 4031, Basel, Schweiz.
Pietro De AngeliForschungsinstitut für Augenheilkunde, Universitätsklinikum Tübingen, Elfriede-Aulhorn-Str. 7, 72076, Tübingen, Deutschland.
Martin GliemBoehringer Ingelheim, Binger Str. 173, 55216, Ingelheim am Rhein, Rheinland-Pfalz, Deutschland.
Mantian WangF. Hoffmann-La Roche Ltd, Grenzacherstr. 124, 4070, Basel, Schweiz.
Kristina PfauAugenklinik, Universitätsspital Basel, Mittlere Str. 91, 4031, Basel, Schweiz.
Stylianos MichalakisAugenklinik und Poliklinik, Klinikum der Ludwig-Maximilians-Universität München, Mathildenstr. 8, 80336, München, Deutschland.
Susanne KohlForschungsinstitut für Augenheilkunde, Universitätsklinikum Tübingen, Elfriede-Aulhorn-Str. 7, 72076, Tübingen, Deutschland.
Bence GyörgyAugenklinik, Universitätsspital Basel, Mittlere Str. 91, 4031, Basel, Schweiz.
Maximilian PfauAugenklinik, Universitätsspital Basel, Mittlere Str. 91, 4031, Basel, Schweiz. Maximilian.Pfau@ukbonn.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stargardt disease is caused by biallelic variants in the ABCA4 gene and is the most frequent autosomal recessive macular degeneration in childhood and adolescence. No approved disease-modifying treatment has yet been approved. The size of the ABCA4 gene represents a challenge for conventional gene therapy based on adeno-associated viruses (AAV) and was the stimulus for the development of innovative strategies. Gene supplementation therapies use lentiviral or dual AAV vectors to introduce complete copies of the healthy ABCA4 gene into the target cells, whereas gene editing procedures, such as RNA exon editing or base editing, enable direct correction of the mutations causing the diseases. Intravitreal injection of antisense oligonucleotides selectively addresses splicing defects and provides a less invasive intravitreal approach but requires repeated applications. Indirect therapies modulate the visual cycle or neuroprotective signalling pathways and can be applied independent of variants. Finally, disease-agnostic approaches, such as optogenetics, enable restoration of vision in cases of advanced degeneration by the use of preserved inner retinal layers. The diversity of these approaches takes account of the broad spectrum of diseases that ranges from a disease limited to the macula to a generalized rod-cone dystrophy and perspectively opens up individualized treatment strategies depending on the genotype and phenotype.

Indexed as

ABCA4 geneAntisense oligonucleotidesAutosomal recessive macular degenerationGene supplementation therapyOptogenetics

Identifiers

PMID42850292

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.