Evidence map›Paper›PMID 29884190›Full record

ArticleJournal of translational medicine2018

Microfibrillar-associated protein 4 variation in symptomatic peripheral artery disease.

Line Ea Hemstra, Anders Schlosser, Jes Sanddal Lindholt, Grith L Sorensen

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  5. Review
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  8. Prediction of liver fibrosis severity in alcoholic liver disease by human microfibrillar-associated protein 4.Liver international : official journal of the International Association for the Study of the Liver · 2020
    Article
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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

4 authors at 2 institutions in 1 country.

Line Ea HemstraCancer and Inflammation Research, Department of Molecular Medicine, University of Southern Denmark, J.B. Winsløws Vej 25, 3rd Floor, Odense, Denmark.
Anders SchlosserCancer and Inflammation Research, Department of Molecular Medicine, University of Southern Denmark, J.B. Winsløws Vej 25, 3rd Floor, Odense, Denmark.
Jes Sanddal LindholtCardiovascular Research Unit, Viborg Hospital, Viborg, Denmark.
Grith L SorensenCancer and Inflammation Research, Department of Molecular Medicine, University of Southern Denmark, J.B. Winsløws Vej 25, 3rd Floor, Odense, Denmark. glsorensen@health.sdu.dk.ORCID 0000-0002-5273-1097
University of Southern Denmark · DKOdense University Hospital · DK

Funding

Lundbeckfonden (DK) j.nr R164-2013-15355Novo Nordisk NNF17OC0028222The Danish Research Council DFF - 7016-00038
6 · The paper itself

Abstract

backgroundSymptomatic peripheral artery disease (PAD) is an atherosclerotic occlusive disease affecting the lower extremities. The cause of symptomatic PAD is atherosclerosis, vascular dysfunctions, impaired angiogenesis and neointima formation. Microfibrillar-associated protein 4 (MFAP4) is an extracellular matrix protein, which is highly expressed in the heart and arteries and recently introduced as a potential mediator of pathological vascular remodeling and neointima formation. We aimed to investigate the relationship between serum MFAP4 (sMFAP4) and symptomatic PAD outcomes.

methodsA total of 286 PAD patients were analyzed if they had either intermittent claudication or critical lower-extremity ischemia (CLI) and followed for 7 years. The level of serum MFAP4 (sMFAP4) was measured by alphaLISA. Kaplan-Meier, Cox proportional hazard and logistic regression analysis were used to analyze the associations between upper tertile sMFAP4 and symptomatic PAD outcomes.

resultsPatients with upper tertile sMFAP4 had an odds ratio (OR) of 2.65 (p < 0.001) for having CLI diagnosis. Further analysis indicated that patients with upper tertile sMFAP4 had a hazard ratio (HR) of 1.97 (p = 0.04) for cardiovascular death during the 7-years follow-up. However, analysis of 2-year primary patency showed that patients with upper tertile sMFAP4 had decreased risk of vascular occlusion after reconstructive surgery with HR of 0.15 (p = 0.02).

conclusionssMFAP4 has potential as a prognostic marker for cardiovascular death, primary patency of reconstructed vessels and CLI diagnosis in symptomatic PAD patients. Confirmation of observations in larger cohorts is warranted.

Indexed as

Genetic VariationAgedCarrier ProteinsEndpoint DeterminationExtracellular Matrix ProteinsFemaleFollow-Up StudiesGenetic Predisposition to DiseaseGlycoproteinsHumansKaplan-Meier EstimateLogistic ModelsMaleMiddle AgedPeripheral Arterial DiseaseRisk FactorsCarrier ProteinsExtracellular Matrix ProteinsGlycoproteinsMFAP4 protein, humanLower-extremity ischemiaMFAP4MortalityPeripheral artery diseasePrimary patency

Identifiers

PMID29884190
PMCPMC5994031
OpenAlexW2807484119

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.