Evidence map›Paper›PMID 23857173›Full record

ReviewNutrients2013

Vitamin A derivatives as treatment options for retinal degenerative diseases.

Lindsay Perusek, Tadao Maeda

Open access · goldAbstract readReview
In one paragraph

Review in Nutrients, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 15% 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.

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

24 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Vitamin A and Its Related Diseases.Food science & nutrition · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. The Role of Vitamin A in Retinal Diseases.International journal of molecular sciences · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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 at 1 institution in 1 country.

Lindsay PerusekDepartment of Ophthalmology & Visual Sciences, School of Medicine, Case Western Reserve University, Cleveland, OH 44106-4965, USA. lxp106@case.edu
Tadao Maeda
Case Western Reserve University · US

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARK R CHANCE · 1987 to 2026
$142.3M
TISSUE CULTURE AND HYBRIDOMA MODULEP30EY011373 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI Irina A Pikuleva · 1997 to 2026
$17.7M
Reactive ocular aldehyde in degenerative retinal diseasesR01EY022658 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI MAEDA, AKIKO · 2012 to 2016
$1.9M
Retinal degeneration diseases and the visual retinoid cycleK08EY019031 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI MAEDA, AKIKO · 2008 to 2012
$430k
Genetics and Therapy of Age-related Retinal Dysfunction in A/J MiceK08EY019880 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI MAEDA, TADAO · 2010 to 2013
$324k
NCI NIH HHS P30 CA043703NEI NIH HHS K08 EY019031NEI NIH HHS K08 EY019880NEI NIH HHS K08EY019880NEI NIH HHS P30 EY011373NEI NIH HHS P30 EY11373NEI NIH HHS R01 EY022658
6 · The paper itself

Abstract

The visual cycle is a sequential enzymatic reaction for vitamin A, all-trans-retinol, occurring in the outer layer of the human retina and is essential for the maintenance of vision. The central source of retinol is derived from dietary intake of both retinol and pro-vitamin A carotenoids. A series of enzymatic reactions, located in both the photoreceptor outer segment and the retinal pigment epithelium, transform retinol into the visual chromophore 11-cis-retinal, regenerating visual pigments. Retina specific proteins carry out the majority of the visual cycle, and any significant interruption in this sequence of reactions is capable of causing varying degrees of blindness. Among these important proteins are Lecithin:retinol acyltransferase (LRAT) and retinal pigment epithelium-specific 65-kDa protein (RPE65) known to be responsible for esterification of retinol to all-trans-retinyl esters and isomerization of these esters to 11-cis-retinal, respectively. Deleterious mutations in these genes are identified in human retinal diseases that cause blindness, such as Leber congenital amaurosis (LCA) and retinitis pigmentosa (RP). Herein, we discuss the pathology of 11-cis-retinal deficiency caused by these mutations in both animal disease models and human patients. We also review novel therapeutic strategies employing artificial visual chromophore 9-cis-retinoids which have been employed in clinical trials involving LCA patients.

Indexed as

AcyltransferasesAnimalscis-trans-IsomerasesClinical Trials as TopicDisease Models, AnimalHumansRetinaRetinaldehydeRetinal DiseasesRetinal PigmentsRetinoid IsomerohydrolaseVision, OcularVitamin AAcyltransferasescis-trans-Isomeraseslecithin-retinol acyltransferaseRetinaldehydeRetinal PigmentsRetinoid IsomerohydrolaseVitamin A

Identifiers

PMID23857173
PMCPMC3738993
OpenAlexW2028934382

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.