Evidence map›Paper›PMID 24829491›Full record

ReviewThe American journal of clinical nutrition2014

Macular xanthophylls, lipoprotein-related genes, and age-related macular degeneration.

Euna Koo, Martha Neuringer, John Paul SanGiovanni

Open access · bronzeAbstract readReview
In one paragraph

Review in The American journal of clinical nutrition, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
3.1field-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.

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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Recent advances in carotenoid absorption, distribution, and elimination.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Influence of macular oedema on the measurement of macular pigment optical density.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2016
    Article
  12. Epigenetic Mechanisms of the Aging Human Retina.Journal of experimental neuroscience · 2015
    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 1 institution in 1 country.

Euna KooFrom the Department of Ophthalmology, University of California at San Francisco, San Francisco, CA (EK); the Oregon National Primate Research Center and Casey Eye Institute, Oregon Health Sciences University, Portland, OR (MN); and the National Eye Institute, National Institutes of Health, Bethesda, MD (JPS).
Martha NeuringerFrom the Department of Ophthalmology, University of California at San Francisco, San Francisco, CA (EK); the Oregon National Primate Research Center and Casey Eye Institute, Oregon Health Sciences University, Portland, OR (MN); and the National Eye Institute, National Institutes of Health, Bethesda, MD (JPS).
John Paul SanGiovanniFrom the Department of Ophthalmology, University of California at San Francisco, San Francisco, CA (EK); the Oregon National Primate Research Center and Casey Eye Institute, Oregon Health Sciences University, Portland, OR (MN); and the National Eye Institute, National Institutes of Health, Bethesda, MD (JPS).
National Eye Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant-based macular xanthophylls (MXs; lutein and zeaxanthin) and the lutein metabolite meso-zeaxanthin are the major constituents of macular pigment, a compound concentrated in retinal areas that are responsible for fine-feature visual sensation. There is an unmet need to examine the genetics of factors influencing regulatory mechanisms and metabolic fates of these 3 MXs because they are linked to processes implicated in the pathogenesis of age-related macular degeneration (AMD). In this work we provide an overview of evidence supporting a molecular basis for AMD-MX associations as they may relate to DNA sequence variation in AMD- and lipoprotein-related genes. We recognize a number of emerging research opportunities, barriers, knowledge gaps, and tools offering promise for meaningful investigation and inference in the field. Overviews on AMD- and high-density lipoprotein (HDL)-related genes encoding receptors, transporters, and enzymes affecting or affected by MXs are followed with information on localization of products from these genes to retinal cell types manifesting AMD-related pathophysiology. Evidence on the relation of each gene or gene product with retinal MX response to nutrient intake is discussed. This information is followed by a review of results from mechanistic studies testing gene-disease relations. We then present findings on relations of AMD with DNA sequence variants in MX-associated genes. Our conclusion is that AMD-associated DNA variants that influence the actions and metabolic fates of HDL system constituents should be examined further for concomitant influence on MX absorption, retinal tissue responses to MX intake, and the capacity to modify MX-associated factors and processes implicated in AMD pathogenesis.

Indexed as

DietGenetic VariationEpigenesis, GeneticHumansLipoproteins, HDLLuteinMacular DegenerationRetinaZeaxanthinsLipoproteins, HDLLuteinZeaxanthins

Identifiers

PMID24829491
PMCPMC4144106
OpenAlexW2164497634

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.