Evidence map›Paper›PMID 34062730›Full record

ArticleLife (Basel, Switzerland)2021

Association of SDF1 and MMP12 with Atherosclerosis and Inflammation: Clinical and Experimental Study.

María Marcos-Jubilar, Josune Orbe, Carmen Roncal, Florencio J D Machado, José Antonio Rodriguez, Alejandro Fernández-Montero, Inmaculada Colina, Raquel Rodil, Juan C Pastrana, José A Páramo

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

María Marcos-JubilarHaematology Service, Clínica Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0001-8038-972X
Josune OrbeLaboratory of Atherothrombosis, Program of Cardiovascular Diseases, Cima Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra, 31008 Pamplona, Spain.ORCID 0000-0001-6300-7670
Carmen RoncalLaboratory of Atherothrombosis, Program of Cardiovascular Diseases, Cima Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra, 31008 Pamplona, Spain.ORCID 0000-0003-0616-9600
Florencio J D MachadoLaboratory of Atherothrombosis, Program of Cardiovascular Diseases, Cima Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra, 31008 Pamplona, Spain.ORCID 0000-0002-2495-0786
José Antonio RodriguezLaboratory of Atherothrombosis, Program of Cardiovascular Diseases, Cima Universidad de Navarra, Instituto de Investigación Sanitaria de Navarra, 31008 Pamplona, Spain.
Alejandro Fernández-MonteroPreventive Medicine, Clínica Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0002-8741-7401
Inmaculada ColinaInternal Medicine Department, Clínica Universidad de Navarra, 31008 Pamplona, Spain.
Raquel RodilInternal Medicine Department, Complejo Hospitalario de Navarra, 31008 Pamplona, Spain.
Juan C PastranaInternal Medicine Department, Clínica Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0002-1066-4551
José A PáramoHaematology Service, Clínica Universidad de Navarra, 31008 Pamplona, Spain.ORCID 0000-0003-1497-6242
Clinica Universidad de Navarra · ESInstituto de Salud Carlos III · ESComplejo Hospitalario de Navarra · ESNavarre Institute of Health Research · ES

Funding

Centro de investigación biomédica en red - enfermedades cardiovasculares (CIBERCV), Institute of Health Carlos III, Madrid, Spain CB16/11/00371Sociedad Española de Arteriosclerosis, invstigación clínico-epidemiológica 2017VIRTO S.A.
6 · The paper itself

Abstract

backgroundAtherosclerosis is the main etiology of cardiovascular diseases (CVD), associated to systemic inflammation. Matrix metalloproteinases (MMPs) are related to atherosclerosis progression through the SDF1/CXCR4 axis promoting macrophages recruitment within the vascular wall. The goal was to assess new circulatory inflammatory markers in relation to atherosclerosis.

methodsMeasurement of SDF1, MMP12 and CRP in blood samples of 298 prospective patients with cardiovascular risk. To explore atherosclerosis progression, CXCR4/SDF1 axis and MMP12 expression were determined by RT-qPCR and by immunohistochemistry in the aorta of accelerated and delayed atherosclerosis mice models (Apoe-/- and Apoe-/-Mmp10-/-).

resultsSDF1, MMP12 and CRP were elevated in patients with clinical atherosclerosis, but after controlling by confounding factors, only SDF1 and CRP remained increased. Having high levels of both biomarkers showed 2.8-fold increased risk of presenting clinical atherosclerosis (

conclusionsThe combination of high circulating SDF1, MMP12 and CRP identified patients with particular inflammatory cardiovascular risk and increased mortality. SDF1/CXCR4 axis and MMP12 involvement in atherosclerosis development suggests that they could be possible atherosclerotic targets.

Indexed as

atherosclerosiscardiovascular riskinflammationMMP-12multimarker approachSDF1/CXCR4

Identifiers

PMID34062730
PMCPMC8147178
OpenAlexW3158727654

What OpenQuestion holds

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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.