Evidence map›Paper›PMID 25972522›Full record

ArticleThe Journal of nutrition2015

Dietary Silicon Deficiency Does Not Exacerbate Diet-Induced Fatty Lesions in Female ApoE Knockout Mice.

Ravin Jugdaohsingh, Katharina Kessler, Barbara Messner, Martin Stoiber, Liliana D Pedro, Heinrich Schima, Günther Laufer, Jonathan J Powell, David Bernhard

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of nutrition, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.1field-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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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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

9 authors at 4 institutions in 3 countries.

Ravin JugdaohsinghMedical Research Council (MRC) Human Nutrition Research, Elsie Widdowson Laboratory, Cambridge, United Kingdom; ravin.jugdaohsingh@mrc-hnr.cam.ac.uk.
Katharina KesslerMedical Research Council (MRC) Human Nutrition Research, Elsie Widdowson Laboratory, Cambridge, United Kingdom; Cardiac Surgery Research Laboratories, Department of Surgery, and.
Barbara MessnerCardiac Surgery Research Laboratories, Department of Surgery, and.
Martin StoiberCenter for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria; Ludwig-Boltzmann-Cluster for Cardiovascular Research, Vienna, Austria; and.
Liliana D PedroMedical Research Council (MRC) Human Nutrition Research, Elsie Widdowson Laboratory, Cambridge, United Kingdom;
Heinrich SchimaCenter for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria; Ludwig-Boltzmann-Cluster for Cardiovascular Research, Vienna, Austria; and.
Günther LauferCardiac Surgery Research Laboratories, Department of Surgery, and.
Jonathan J PowellMedical Research Council (MRC) Human Nutrition Research, Elsie Widdowson Laboratory, Cambridge, United Kingdom;
David BernhardCardiac Surgery Research Laboratories, Department of Surgery, and Cardiac Surgery Research Laboratory Innsbruck, University Clinic for Cardiac Surgery, Medical University of Innsbruck, Innsbruck, Austria.
MRC Human Nutrition Research · GBLudwig Boltzmann Institute for Cardiovascular Research · ATSan Diego Cardiac Center · USInnsbruck Medical University · AT

Funding

Medical Research Council MC_U105960399Medical Research Council MC_US_A090_0008/Unit Program number U1059
6 · The paper itself

Abstract

backgroundDietary silicon has been positively linked with vascular health and protection against atherosclerotic plaque formation, but the mechanism of action is unclear.

objectivesWe investigated the effect of dietary silicon on 1) serum and aorta silicon concentrations, 2) the development of aortic lesions and serum lipid concentrations, and 3) the structural and biomechanic properties of the aorta.

methodsTwo studies, of the same design, were conducted to address the above objectives. Female mice, lacking the apolipoprotein E (apoE) gene, and therefore susceptible to atherosclerosis, were separated into 3 groups of 10-15 mice, each exposed to a high-fat diet (21% wt milk fat and 1.5% wt cholesterol) but with differing concentrations of dietary silicon, namely: silicon-deprived (-Si; <3-μg silicon/g feed), silicon-replete in feed (+Si-feed; 100-μg silicon/g feed), and silicon-replete in drinking water (+Si-water; 115-μg silicon/mL) for 15-19 wk. Silicon supplementation was in the form of sodium metasilicate (feed) or monomethylsilanetriol (drinking water).

resultsThe serum silicon concentration in the -Si group was significantly lower than in the +Si-feed (by up to 78%; P < 0.003) and the +Si-water (by up to 84%; P < 0.006) groups. The aorta silicon concentration was also lower in the -Si group than in the +Si-feed group (by 65%; P = 0.025), but not compared with the +Si-water group. There were no differences in serum and aorta silicon concentrations between the silicon-replete groups. Body weights, tissue wet weights at necropsy, and structural, biomechanic, and morphologic properties of the aorta were not affected by dietary silicon; nor were the development of fatty lesions and serum lipid concentrations.

conclusionsThese findings suggest that dietary silicon has no effect on atherosclerosis development and vascular health in the apoE mouse model of diet-induced atherosclerosis, contrary to the reported findings in the cholesterol-fed rabbit model.

Indexed as

DietAnimalsAortaApolipoproteins EAtherosclerosisBody WeightCholesterol, HDLCholesterol, LDLDietary SupplementsDiet, High-FatDisease Models, AnimalEndothelium, VascularFemaleMiceMice, Inbred C57BLMice, KnockoutApolipoproteins ECholesterol, HDLCholesterol, LDLSiliconTriglyceridesaorta silicon contentaortic lesionsapoE knockout micecollagen and elastin contentsdietary siliconelastic structure and morphologymonomethylsilanetriolnutritionserum lipidstensile strength and elasticity

Identifiers

PMID25972522
PMCPMC4478943
OpenAlexW2141065205

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Registered trials

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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.