Evidence map›Paper›PMID 17917691›Full record

ArticleExpert review of ophthalmology2007

Genetic markers and biomarkers for age-related macular degeneration.

Robert J Ross, Varun Verma, Kevin I Rosenberg, Chi-Chao Chan, Jingsheng Tuo

Open access · greenAbstract read
In one paragraph

Article in Expert review of ophthalmology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
7.4field-weighted citation impact, top 3% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  5. Review
  6. Review
  7. Article
  8. Article
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  11. Review
  12. Risk factors and biomarkers of age-related macular degeneration.Progress in retinal and eye research · 2016
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. An association between environmental factors and the IVS4+44C>A polymorphism of the DMT1 gene in age-related macular degeneration.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2012
    Article
  18. Article
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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

5 authors at 2 institutions in 1 country.

Robert J RossNational Eye Institute Intramural Research Training Award Fellow, Laboratory of Immunology, National Eye Institute, National Institutes of Health, Bethesda, MD, USA, Tel.: +1 301 435 4563, , rossr@nei.nih.gov.
Varun Verma
Kevin I Rosenberg
Chi-Chao Chan
Jingsheng Tuo
National Eye Institute · USNational Institutes of Health · US

Funding

Genetic Variations and Age-Related Macular DegenerationZ01EY000418 · NEI · NATIONAL EYE INSTITUTE · PI CHAN, CHI-CHAO · 2004 to 2008
$3.4M
Intramural NIH HHS Z01 EY000418
6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is the leading cause of visual impairment and blindness in the USA. Although the treatment of AMD has evolved to include laser photocoagulation, photodynamic therapy, surgical macular translocation and antiangiogenesis agents, treatment options for advanced AMD are limited. Furthermore, the dry form of AMD, albeit less devastating than the wet form, has even fewer viable treatment options. This review summarizes the various biomarkers of AMD and analyzes whether or not they may one day be exploited to determine risks of disease onset, measure progression of disease or even assess the effects of treatment of AMD. Potential biomarkers are important to identify since some might be utilized to reflect the disease state of a particular patient and to individualize therapy. Although studies have yielded promising results for nutrient and inflammatory biomarkers, these results have been inconsistent. At present, the best available markers of AMD risk are single nucleotide polymorphisms (SNPs). SNPs in complement factor H (CFH) and PLEKHA1/ARMS2/HtrA1 capture a substantial fraction of AMD risk and permit the identification of individuals at high risk of developing AMD.

Identifiers

PMID17917691
PMCPMC2000850
OpenAlexW2119954358

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.