Evidence map›Paper›PMID 31254285›Full record

ReviewBritish journal of pharmacology2019

The role of smooth muscle cells in plaque stability: Therapeutic targeting potential.

Jennifer L Harman, Helle F Jørgensen

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 4% 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

81 citing papers in PubMed, 1 synthesis or guideline pooled it, 149 citations in OpenAlex.

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  20. Vascular Extracellular Matrix in Atherosclerosis.International journal of molecular sciences · 2024
    Review

21 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Jennifer L HarmanDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0001-7678-177X
Helle F JørgensenDivision of Cardiovascular Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0002-7909-2977
University of Cambridge · GB

Funding

British Heart Foundation CH/ 20000003British Heart Foundation FS/15/38/31516British Heart Foundation FS/15/62/32032British Heart Foundation PG/12/86/29930British Heart Foundation RE/13/6/30180British Heart Foundation RM/13/3/30159
6 · The paper itself

Abstract

Events responsible for cardiovascular mortality and morbidity are predominantly caused by rupture of "vulnerable" atherosclerotic lesions. Vascular smooth muscle cells (VSMCs) play a key role in atherogenesis and have historically been considered beneficial for plaque stability. VSMCs constitute the main cellular component of the protective fibrous cap within lesions and are responsible for synthesising strength-giving extracellular matrix components. However, lineage-tracing experiments in mouse models of atherosclerosis have shown that, in addition to the fibrous cap, VSMCs also give rise to many of the cell types found within the plaque core. In particular, VSMCs generate a substantial fraction of lipid-laden foam cells, and VSMC-derived cells expressing markers of macrophages, osteochondrocyte, and mesenchymal stem cells have been observed within lesions. Here, we review recent studies that have changed our perspective on VSMC function in atherosclerosis and discuss how VSMCs could be targeted to increase plaque stability.

Indexed as

AnimalsHumansMuscle, Smooth, VascularMyocytes, Smooth MusclePlaque, Atherosclerotic

Identifiers

PMID31254285
PMCPMC6780045
OpenAlexW2955387872

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.