Evidence map›Paper›PMID 24244297›Full record

Trial reportPloS one2013

Subjects with low plasma HDL cholesterol levels are characterized by an inflammatory and oxidative phenotype.

Kirsten B Holven, Kjetil Retterstøl, Thor Ueland, Stine M Ulven, Marit S Nenseter, Marit Sandvik, Ingunn Narverud, Knut E Berge, Leiv Ose, Pål Aukrust and 1 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.7field-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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
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  6. The Effects of Social, Personal, and Behavioral Risk Factors and PMInternational journal of environmental research and public health · 2020
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  7. Systemic MCPIP1 deficiency in mice impairs lipid homeostasis.Current research in pharmacology and drug discovery · 2020
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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

11 authors at 3 institutions in 1 country.

Kirsten B HolvenDepartment of Nutrition, Institute for Basic Medical Sciences, University of Oslo, Oslo, Norway ; Faculty of Medicine, University of Oslo, Oslo, Norway.
Kjetil Retterstøl
Thor Ueland
Stine M Ulven
Marit S Nenseter
Marit Sandvik
Ingunn Narverud
Knut E Berge
Leiv Ose
Pål Aukrust
Bente Halvorsen
University of Oslo · NOOslo University Hospital · NOOsloMet – Oslo Metropolitan University · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpidemiological studies have shown that low plasma levels of high-density lipoprotein (HDL) cholesterol are associated with increased risk of cardiovascular disease, but the mechanisms for the possible atheroprotective effects of HDL cholesterol have still not been fully clarified, in particular in relation to clinical studies.

objectiveTo examine the inflammatory, anti-oxidative and metabolic phenotype of subjects with low plasma HDL cholesterol levels. METHODS AND

resultsFifteen subjects with low HDL cholesterol levels (eleven males and four females) and 19 subjects with high HDL (three males and 16 females) were recruited. Low HDL cholesterol was defined as ≤10th age/sex specific percentile and high HDL-C was defined as ≥90 age/sex specific percentile. Inflammatory markers in circulation and PBMC gene expression of cholesterol efflux mediators were measured. Our main findings were: (i) subjects with low plasma HDL cholesterol levels were characterized by increased plasma levels of CRP, MMP-9, neopterin, CXCL16 and ICAM-1 as well as low plasma levels of adiponectin, suggesting an inflammatory phenotype; (ii) these individuals also had reduced paraoxonase (PON)1 activity in plasma and PON2 gene expression in peripheral blood mononuclear cells (PBMC) accompanied by increased plasma levels of oxidized LDL suggesting decreased anti-oxidative capacity; and (iii) PBMC from low HDL subjects also had decreased mRNA levels of ABCA1 and ABCG1, suggesting impaired reverse cholesterol transport.

conclusionSubjects with low plasma HDL cholesterol levels are characterized by an inflammatory and oxidative phenotype that could contribute to the increased risk of atherosclerotic disorders in these subjects with low HDL levels.

Indexed as

PhenotypeAdultAgedAtherosclerosisATP Binding Cassette Transporter 1ATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 1Biological Transport, ActiveChemokine CXCL16Chemokines, CXCCholesterol, HDLC-Reactive ProteinFemaleHumansInflammationIntercellular Adhesion Molecule-1ABCA1 protein, humanABCG1 protein, humanATP Binding Cassette Transporter 1ATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily G, Member 1Chemokine CXCL16Chemokines, CXCCholesterol, HDLC-Reactive ProteinCXCL16 protein, humanIntercellular Adhesion Molecule-1Lipoproteins, LDLMatrix Metalloproteinase 9MMP9 protein, humanNeopterinoxidized low density lipoproteinReceptors, Scavenger

Identifiers

PMID24244297
PMCPMC3823918
OpenAlexW1980408806

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.