Evidence map›Paper›PMID 31197405›Full record

ReviewCellular and molecular life sciences : CMLS2019

Metalloproteinases and their tissue inhibitors in Alzheimer's disease and other neurodegenerative disorders.

Santiago Rivera, Laura García-González, Michel Khrestchatisky, Kévin Baranger

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 5% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 105 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Matrix Metalloproteinase 14 in Corneal Neovascularization.International journal of molecular sciences · 2026
    Review
  6. Article
  7. Review
  8. Review
  9. Implications of Mucin-TypeMolecules (Basel, Switzerland) · 2025
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. The TIMP protein family: diverse roles in pathophysiology.American journal of physiology. Cell physiology · 2024
    Review
  19. Selected Cytokines and Metalloproteinases in Inflammatory Bowel Disease.International journal of molecular sciences · 2023
    Review
  20. Article
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

4 authors at 1 institution in 1 country.

Santiago RiveraAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, Marseille, France. santiago.rivera@univ-amu.fr.ORCID http://orcid.org/0000-0001-6649-2712
Laura García-GonzálezAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, Marseille, France.
Michel KhrestchatiskyAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, Marseille, France.
Kévin BarangerAix-Marseille Univ, CNRS, INP, Inst Neurophysiopathol, Marseille, France.
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As life expectancy increases worldwide, age-related neurodegenerative diseases will increase in parallel. The lack of effective treatment strategies may soon lead to an unprecedented health, social and economic crisis. Any attempt to halt the progression of these diseases requires a thorough knowledge of the pathophysiological mechanisms involved to facilitate the identification of new targets and the application of innovative therapeutic strategies. The metzincin superfamily of metalloproteinases includes matrix metalloproteinases (MMP), a disintegrin and metalloproteinase (ADAM) and ADAM with thrombospondin motifs (ADAMTS). These multigenic and multifunctional proteinase families regulate the functions of an increasing number of signalling and scaffolding molecules involved in neuroinflammation, blood-brain barrier disruption, protein misfolding, synaptic dysfunction or neuronal death. Metalloproteinases and their physiological inhibitors, the tissue inhibitors of metalloproteinases (TIMPs), are therefore, at the crossroads of molecular and cellular mechanisms that support neurodegenerative processes, and emerge as potential new therapeutic targets. We provide an overview of current knowledge on the role and regulation of metalloproteinases and TIMPs in four major neurodegenerative diseases: Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis and Huntington's disease.

Indexed as

ADAM ProteinsAlzheimer DiseaseAmyloid beta-PeptidesAmyloid beta-Protein PrecursorHumansHuntington DiseaseMatrix MetalloproteinasesNeurodegenerative DiseasesParkinson DiseaseTissue Inhibitor of MetalloproteinasesADAM ProteinsAmyloid beta-PeptidesAmyloid beta-Protein PrecursorMatrix MetalloproteinasesTissue Inhibitor of MetalloproteinasesADAMAmyotrophic lateral sclerosisHuntington’s diseaseNeurodegenerative brain diseaseParkinson’s diseaseTIMP

Identifiers

PMID31197405
PMCPMC11105182
OpenAlexW2953342712

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.