Evidence map›Paper›PMID 32824762›Full record

ReviewInternational journal of molecular sciences2020

Matrix Metalloproteinases in Age-Related Macular Degeneration (AMD).

Luis García-Onrubia, Fco Javier Valentín-Bravo, Rosa M Coco-Martin, Rogelio González-Sarmiento, J Carlos Pastor, Ricardo Usategui-Martín, Salvador Pastor-Idoate

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.9field-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

32 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Matrix Metalloproteinase 14 in Corneal Neovascularization.International journal of molecular sciences · 2026
    Review
  6. Article
  7. Review
  8. Article
  9. Novel Therapeutic Effects ofPharmaceuticals (Basel, Switzerland) · 2024
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Risk of developing age-related macular degeneration in patients with osteoporosis: a population-based, longitudinal follow-up study.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2023
    Article
  17. Article
  18. Article
  19. Article
  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

7 authors at 2 institutions in 1 country.

Luis García-OnrubiaClinical University Hospital of Valladolid, Av. Ramón y Cajal, 3, 47003 Valladolid, Spain.ORCID 0000-0003-3563-2369
Fco Javier Valentín-BravoClinical University Hospital of Valladolid, Av. Ramón y Cajal, 3, 47003 Valladolid, Spain.ORCID 0000-0002-2062-3243
Rosa M Coco-MartinInstitute of Applied Ophthalmobiology (IOBA), University of Valladolid, 47011 Valladolid, Spain.ORCID 0000-0002-1811-1417
Rogelio González-SarmientoInstitute of Biomedical Research of Salamanca (IBSAL), 37007 Salamanca, Spain.ORCID 0000-0002-2726-6795
J Carlos PastorClinical University Hospital of Valladolid, Av. Ramón y Cajal, 3, 47003 Valladolid, Spain.ORCID 0000-0001-5934-7306
Ricardo Usategui-MartínInstitute of Applied Ophthalmobiology (IOBA), University of Valladolid, 47011 Valladolid, Spain.ORCID 0000-0001-7699-4388
Salvador Pastor-IdoateClinical University Hospital of Valladolid, Av. Ramón y Cajal, 3, 47003 Valladolid, Spain.ORCID 0000-0002-6463-4227
Universidad de Valladolid · ESUniversidad de Salamanca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is a complex, multifactorial and progressive retinal disease affecting millions of people worldwide. In developed countries, it is the leading cause of vision loss and legal blindness among the elderly. Although the pathogenesis of AMD is still barely understood, recent studies have reported that disorders in the regulation of the extracellular matrix (ECM) play an important role in its etiopathogenesis. The dynamic metabolism of the ECM is closely regulated by matrix metalloproteinases (MMPs) and the tissue inhibitors of metalloproteinases (TIMPs). The present review focuses on the crucial processes that occur at the level of the Bruch's membrane, with special emphasis on MMPs, TIMPs, and the polymorphisms associated with increased susceptibility to AMD development. A systematic literature search was performed, covering the years 1990-2020, using the following keywords: AMD, extracellular matrix, Bruch's membrane, MMPs, TIMPs, and MMPs polymorphisms in AMD. In both early and advanced AMD, the pathological dynamic changes of ECM structural components are caused by the dysfunction of specific regulators and by the influence of other regulatory systems connected with both genetic and environmental factors. Better insight into the pathological role of MMP/TIMP complexes may lead to the development of new strategies for AMD treatment and prevention.

Indexed as

AnimalsHumansMacular DegenerationMatrix Metalloproteinase InhibitorsMatrix MetalloproteinasesNeuroprotective AgentsPolymorphism, GeneticMatrix Metalloproteinase InhibitorsMatrix MetalloproteinasesNeuroprotective Agentsage-related macular degenerationBruch’s membraneextracellular matrixmatrix metalloproteinasesMMPs polymorphismstissue inhibitors of metalloproteinases

Identifiers

PMID32824762
PMCPMC7460693
OpenAlexW3064226249

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.