Evidence map›Paper›PMID 25744334›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2015

Multimodal assessment of choroideremia patients defines pre-treatment characteristics.

Immanuel P Seitz, Ahmad Zhour, Susanne Kohl, Pablo Llavona, Tobias Peter, Barbara Wilhelm, Eberhart Zrenner, Marius Ueffing, Karl Ulrich Bartz-Schmidt, M Dominik Fischer

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01461213 (An Open Label Dose Escalation Phase 1 Clinical Trial of Retinal Gene Therapy for Choroideraemia Using an Adeno-associated Viral Vector), which is not on this map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
2.9field-weighted citation impact, top 9% of its field
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.

NCT01461213 phase1 / phase2completednot on this map

An Open Label Dose Escalation Phase 1 Clinical Trial of Retinal Gene Therapy for Choroideraemia Using an Adeno-associated Viral Vector (AAV2) Encoding Rab-escort Protein 1 (REP1)

TypeinterventionalSponsorUniversity of OxfordRan2011 to 2017Enrolled14ConditionsChoroideremiaArmsrAAV2.REP1
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 3 syntheses or guidelines pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Choroideremia: The Endpoint Endgame.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Colour discrimination ellipses in choroideremia.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2018
    Article
  14. Article
  15. Review
  16. Gene and cell-based therapies for inherited retinal disorders: An update.American journal of medical genetics. Part C, Seminars in medical genetics · 2016
    Review
  17. Clinical applications of fundus autofluorescence in retinal disease.International journal of retina and vitreous · 2016
    Review
  18. Intravitreal, Subretinal, and Suprachoroidal Injections: Evolution of Microneedles for Drug Delivery.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics
    Review
  19. 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

10 authors at 3 institutions in 2 countries.

Immanuel P SeitzUniversity Eye Hospital, University of Tübingen, Tübingen, Germany.
Ahmad ZhourUniversity Eye Hospital, University of Tübingen, Tübingen, Germany.
Susanne KohlInstitute for Ophthalmic Research, University of Tübingen, Tübingen, Germany.
Pablo LlavonaInstitute for Ophthalmic Research, University of Tübingen, Tübingen, Germany.
Tobias PeterSTZ Eyetrial, Centre for Ophthalmology, University of Tübingen, Tübingen, Germany.
Barbara WilhelmSTZ Eyetrial, Centre for Ophthalmology, University of Tübingen, Tübingen, Germany.
Eberhart ZrennerUniversity Eye Hospital, University of Tübingen, Tübingen, Germany.
Marius UeffingInstitute for Ophthalmic Research, University of Tübingen, Tübingen, Germany.
Karl Ulrich Bartz-SchmidtUniversity Eye Hospital, University of Tübingen, Tübingen, Germany.
M Dominik FischerUniversity Eye Hospital, University of Tübingen, Tübingen, Germany. dominik.fischer@ndcn.ox.ac.uk.
STZ eyetrial · DEUniversity of Tübingen · DEUniversity of Oxford · GB

Funding

Medical Research Council MR/K003690/1
6 · The paper itself

Abstract

purposeChoroideremia (CHM) is a X-chromosomal disorder leading to blindness by progressive degeneration of choroid, retinal pigment epithelium (RPE), and retinal neurons. A current clinical gene therapy trial (NCT01461213) showed promising safety and efficacy data in a carefully selected patient population. The present study was performed to shed light on pre-treatment characteristics of a larger cohort of CHM patients using a high resolution multi-modal approach.

methodsIn a retrospective cross-sectional study, data from 58 eyes of 29 patients with clinically confirmed CHM were analysed including best-corrected visual acuity (BCVA), refractive error, spectral-domain optical coherence tomography (SD-OCT), fundus autofluorescence (FAF), perimetry, and tonometry. Residual retinal volume, area of residual RPE, and foveal thickness were quantified to further define natural disease progression and assess symmetry.

resultsWe evaluated 98 data points of BCVA [0.34 ± 0.06 (logMAR); mean ± 95 % confidence interval], 80 of IOP (14.6 ± 0.6 mmHg), and 98 of refraction (-2.16 ± 1.08 spherical equivalent). Visual fields (n  = 76) demonstrated variable degrees of concentric constriction (54 % <10°, 25 % 10-30°, 21 % >30°). Mean residual RPE area on FAF (n  = 64) measured 8.47 ± 1.91 mm(2) (range 0.30-38.5 mm(2)), while mean neuroretinal volume (n  = 42) was found to be 1.76 ± 0.12 mm(3). Age at examination was exponentially associated with BCVA, while logarithmic functions best described progressive loss of retinal area and volume. A high degree of left to right symmetry was found in all modalities with structural markers showing the best correlation (r (2) area = 0.83; r (2) volume = 0.75).

conclusionAnalysis of these widely available clinical data defines the natural disease characteristics of a relevant patient population eligible for gene therapeutic intervention. In the wake of preliminary reports on safety and efficacy of CHM gene therapy (NCT01461213), this multi-modal assessment of a cohort of CHM patients provides important evidence of the natural rate of disease progression and degree of symmetry between eyes.

Indexed as

Genetic TherapyMultimodal ImagingAdaptor Proteins, Signal TransducingAdolescentAdultChildChild, PreschoolChoroideremiaCross-Sectional StudiesFemaleFluorescein AngiographyHumansMaleMiddle AgedMutationPolymerase Chain ReactionAdaptor Proteins, Signal TransducingCHM protein, humanAutofluorescenceChoroideremiaGene therapySymmetry

Identifiers

PMID25744334
OpenAlexW2020676423

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.