Evidence map›Paper›PMID 24369445›Full record

ReviewMediators of inflammation2013

Mechanism of inflammation in age-related macular degeneration: an up-to-date on genetic landmarks.

Francesco Parmeggiani, Francesco S Sorrentino, Mario R Romano, Ciro Costagliola, Francesco Semeraro, Carlo Incorvaia, Sergio D'Angelo, Paolo Perri, Katia De Nadai, Elia Bonomo Roversi and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Mediators of inflammation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 60 citations in OpenAlex.

  1. The roles of glycerophospholipids in the aging retina and age-related macular degeneration.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. Association of genetic variants rs641153 (Experimental biology and medicine (Maywood, N.J.) · 2021
    Article
  6. Article
  7. Review
  8. Associations ofClinical ophthalmology (Auckland, N.Z.) · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Evaluation of serum interferons in patients with age-related macular degeneration.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2019
    Article
  13. International journal of ophthalmology · 2019
    Article
  14. Inhibition of integrin α5β1 ameliorates VEGF-induced retinal neovascularization and leakage by suppressing NLRP3 inflammasome signaling in a mouse model.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2018
    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

13 authors at 3 institutions in 1 country.

Francesco ParmeggianiDepartment of Biomedical and Specialty Surgical Sciences, Ophthalmology Unit, University of Ferrara, Corso Giovecca 203, 44121 Ferrara, Italy.
Francesco S SorrentinoDepartment of Biomedical and Specialty Surgical Sciences, Ophthalmology Unit, University of Ferrara, Corso Giovecca 203, 44121 Ferrara, Italy.
Mario R RomanoDepartment of Ophthalmology, Istituto Clinico Humanitas, Milan, Italy ; Department of Health Sciences, University of Molise, Campobasso, Italy.
Ciro CostagliolaDepartment of Health Sciences, University of Molise, Campobasso, Italy.
Francesco SemeraroDepartment of Ophthalmology, University of Brescia, Brescia, Italy.
Carlo IncorvaiaDepartment of Biomedical and Specialty Surgical Sciences, Ophthalmology Unit, University of Ferrara, Corso Giovecca 203, 44121 Ferrara, Italy.
Sergio D'AngeloDepartment of Biomedical and Specialty Surgical Sciences, Ophthalmology Unit, University of Ferrara, Corso Giovecca 203, 44121 Ferrara, Italy.
Paolo PerriDepartment of Biomedical and Specialty Surgical Sciences, Ophthalmology Unit, University of Ferrara, Corso Giovecca 203, 44121 Ferrara, Italy.
Katia De NadaiDepartment of Biomedical and Specialty Surgical Sciences, Ophthalmology Unit, University of Ferrara, Corso Giovecca 203, 44121 Ferrara, Italy ; Center for Retinitis Pigmentosa of Veneto Region, ULSS 15 Alta Padovana, Camposampiero, Italy.
Elia Bonomo RoversiDepartment of Biomedical and Specialty Surgical Sciences, Medical Genetic Unit, University of Ferrara, Ferrara, Italy.
Paola FranceschelliDepartment of Biomedical and Specialty Surgical Sciences, Medical Genetic Unit, University of Ferrara, Ferrara, Italy.
Adolfo SebastianiDepartment of Biomedical and Specialty Surgical Sciences, Ophthalmology Unit, University of Ferrara, Corso Giovecca 203, 44121 Ferrara, Italy.
Michele RubiniDepartment of Biomedical and Specialty Surgical Sciences, Medical Genetic Unit, University of Ferrara, Ferrara, Italy.
University of Ferrara · ITUniversity of Molise · ITUniversity of Brescia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is the most common cause of irreversible visual impairment among people over 50 years of age, accounting for up to 50% of all cases of legal blindness in Western countries. Although the aging represents the main determinant of AMD, it must be considered a multifaceted disease caused by interactions among environmental risk factors and genetic backgrounds. Mounting evidence and/or arguments document the crucial role of inflammation and immune-mediated processes in the pathogenesis of AMD. Proinflammatory effects secondary to chronic inflammation (e.g., alternative complement activation) and heterogeneous types of oxidative stress (e.g., impaired cholesterol homeostasis) can result in degenerative damages at the level of crucial macular structures, that is photoreceptors, retinal pigment epithelium, and Bruch's membrane. In the most recent years, the association of AMD with genes, directly or indirectly, involved in immunoinflammatory pathways is increasingly becoming an essential core for AMD knowledge. Starting from the key basic-research notions detectable at the root of AMD pathogenesis, the present up-to-date paper reviews the best-known and/or the most attractive genetic findings linked to the mechanisms of inflammation of this complex disease.

Indexed as

AgingCholesterolChromosome MappingComplement System ProteinsGenetic VariationHomeostasisHumansInflammationLipaseMacular DegenerationOxidative StressRisk FactorsTissue Inhibitor of Metalloproteinase-3CholesterolComplement System ProteinsLipaseTIMP3 protein, humanTissue Inhibitor of Metalloproteinase-3

Identifiers

PMID24369445
PMCPMC3863457
OpenAlexW2079397885

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.