Evidence map›Paper›PMID 23009893›Full record

ArticleOphthalmology2012

Genetic studies of age-related macular degeneration: lessons, challenges, and opportunities for disease management.

Rinki Ratna Priya, Emily Y Chew, Anand Swaroop

Abstract read
In one paragraph

Article in Ophthalmology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 2 pooled it
11.2field-weighted citation impact, top 1% 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

44 citing papers in PubMed, 2 syntheses or guidelines pooled it, 90 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
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  6. Article
  7. Review
  8. Observational
  9. Article
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  11. Review
  12. Treating patients with geographic atrophy: are we there yet?International journal of retina and vitreous · 2023
    Review
  13. Article
  14. Review
  15. The complement system in age-related macular degeneration.Cellular and molecular life sciences : CMLS · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

3 authors at 2 institutions in 1 country.

Rinki Ratna PriyaNational Eye Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Emily Y Chew
Anand Swaroop
National Institutes of Health · USNational Eye Institute · US

Funding

Interventional approaches for restoring visionZIAEY000474 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2019
$15.5M
Genetic susceptibility and common multi-factorial retinal/macular diseasesZIAEY000475 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2014
$6.9M
Intramural NIH HHS ZIA EY000474Intramural NIH HHS ZIA EY000475
6 · The paper itself

Abstract

backgroundAge-related macular degeneration (AMD) is a common cause of visual impairment in individuals >55 years of age worldwide. The varying clinical phenotypes of AMD result from contributions of genetic, epigenetic, and nongenetic (environmental) factors. Genetic studies of AMD have come of age as a direct result of tremendous gains from the human genome project, genome-wide association studies, and identification of numerous susceptibility loci. These findings have implicated immune response, high-density lipoprotein cholesterol metabolism, extracellular matrix, and angiogenesis signaling pathways in disease pathophysiology.

main outcome measuresHerein, we address how the wealth of genetic findings in AMD is expected to impact the practice of medicine, providing opportunities for improved risk assessment, molecular diagnosis, preventive, and therapeutic intervention.

conclusionsWe propose that the potential of using genetic variants for monitoring treatment response (pharmacogenetics) may usher in a new era of personalized medicine in the clinical management of AMD. FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosures may be found after the references.

Indexed as

Genetic VariationPharmacogeneticsPhotochemotherapyAngiogenesis InhibitorsDisease ProgressionEye ProteinsGene-Environment InteractionGenetic LinkageGenome-Wide Association StudyGenotypeHumansMacular DegenerationRisk AssessmentAngiogenesis InhibitorsEye Proteins

Identifiers

PMID23009893
PMCPMC3514599
OpenAlexW90671621

What OpenQuestion holds

Textmetadata
LicenceTDM
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.