Evidence map›Paper›PMID 33255685›Full record

SynthesisInternational journal of molecular sciences2020

The Protective Effects of the Autophagic and Lysosomal Machinery in Vascular and Valvular Calcification: A Systematic Review.

Cédric H G Neutel, Jhana O Hendrickx, Wim Martinet, Guido R Y De Meyer, Pieter-Jan Guns

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Insights Into the Role of Mitochondria in Vascular Calcification.Frontiers in cardiovascular medicine · 2022
    Review
  8. Review
  9. 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

5 authors at 1 institution in 1 country.

Cédric H G NeutelLaboratory of Physiopharmacology, University of Antwerp, 2610 Antwerp, Belgium.ORCID 0000-0001-7074-226X
Jhana O HendrickxLaboratory of Physiopharmacology, University of Antwerp, 2610 Antwerp, Belgium.ORCID 0000-0001-7639-2926
Wim MartinetLaboratory of Physiopharmacology, University of Antwerp, 2610 Antwerp, Belgium.
Guido R Y De MeyerLaboratory of Physiopharmacology, University of Antwerp, 2610 Antwerp, Belgium.ORCID 0000-0003-3848-8702
Pieter-Jan GunsLaboratory of Physiopharmacology, University of Antwerp, 2610 Antwerp, Belgium.ORCID 0000-0002-8640-6620
University of Antwerp · BE

Funding

Fonds Wetenschappelijk Onderzoek 1S24720NFonds Wetenschappelijk Onderzoek G041216NUniversiteit Antwerpen BOF SEP 41477Universiteit Antwerpen BOF SEP 41478Universiteit Antwerpen DOCPRO 36663Universiteit Antwerpen GOA 33931
6 · The paper itself

Abstract

backgroundAutophagy is a highly conserved catabolic homeostatic process, crucial for cell survival. It has been shown that autophagy can modulate different cardiovascular pathologies, including vascular calcification (VCN).

objectiveTo assess how modulation of autophagy, either through induction or inhibition, affects vascular and valvular calcification and to determine the therapeutic applicability of inducing autophagy. DATA SOURCES: A systematic review of English language articles using MEDLINE/PubMed, Web of Science (WoS) and the Cochrane library. The search terms included autophagy, autolysosome, mitophagy, endoplasmic reticulum (ER)-phagy, lysosomal, calcification and calcinosis. Study characteristics: Thirty-seven articles were selected based on pre-defined eligibility criteria. Thirty-three studies (89%) studied vascular smooth muscle cell (VSMC) calcification of which 27 (82%) studies investigated autophagy and six (18%) studies lysosomal function in VCN. Four studies (11%) studied aortic valve calcification (AVCN). Thirty-four studies were published in the time period 2015-2020 (92%).

conclusionThere is compelling evidence that both autophagy and lysosomal function are critical regulators of VCN, which opens new perspectives for treatment strategies. However, there are still challenges to overcome, such as the development of more selective pharmacological agents and standardization of methods to measure autophagic flux.

Indexed as

Aortic ValveAortic Valve StenosisAutophagyCalcinosisCell SurvivalEndoplasmic ReticulumHumansLysosomesMuscle, Smooth, VascularMyocytes, Smooth MuscleVascular Calcificationaortic valve calcificationautophagylysosomesvalvular interstitial cell (VIC)vascular calcificationvascular smooth muscle cell (VSMC)

Identifiers

PMID33255685
PMCPMC7728070
OpenAlexW3106952727

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.