Evidence map›Paper›PMID 25664679›Full record

ArticleJournal of dietary supplements2016

Complementary Cholesterol-Lowering Response of a Phytosterol/α-Lipoic Acid Combination in Obese Zucker Rats.

Todd C Rideout, Bradley Carrier, Shin Wen, Amy Raslawsky, Richard W Browne, Scott V Harding

Open access · greenAbstract read
In one paragraph

Article in Journal of dietary supplements, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Chronic treatment of (R)-Pharmacology research & perspectives · 2017
    Article
  6. Review
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

6 authors at 2 institutions in 2 countries.

Todd C Rideouta 1 Department of Exercise and Nutrition Sciences, School of Public Health and Health Professions , University at Buffalo , Buffalo , NY , USA.
Bradley Carriera 1 Department of Exercise and Nutrition Sciences, School of Public Health and Health Professions , University at Buffalo , Buffalo , NY , USA.
Shin Wena 1 Department of Exercise and Nutrition Sciences, School of Public Health and Health Professions , University at Buffalo , Buffalo , NY , USA.
Amy Raslawskya 1 Department of Exercise and Nutrition Sciences, School of Public Health and Health Professions , University at Buffalo , Buffalo , NY , USA.
Richard W Browneb 2 Biotechnical and Clinical Laboratory Sciences, University at Buffalo , Buffalo, NY, USA.
Scott V Hardingc 3 Diabetes and Nutritional Sciences Division, Faculty of Life Sciences and Medicine, King's College London , London , United Kingdom.
University at Buffalo, State University of New York · USKing's College London · GB

Funding

Cardiovascular Protection by Phytosterols in Dyslipidemic Mothers and ProgenyK01AT007826 · NCCIH · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI RIDEOUT, TODD · 2013 to 2017
$724k
NCCIH NIH HHS K01 AT007826
6 · The paper itself

Abstract

To investigate the cholesterol-lowering effectiveness of a phytosterol/α-lipoic acid (PS/αLA) therapy, thirty-two male Zucker rats were randomly assigned to 1 of 4 diets for 30 days: (i) high fat diet (HF, 40% energy from fat); (ii) HF diet supplemented with 3% phytosterols; (iii) HF diet supplemented with 0.25% αLA; or (iv) HF diet supplemented with PS (3%) and αLA (0.25%, PS/αLA). Compared with the HF diet, combination PS/αLA proved more effective in reducing non-HDL cholesterol (-55%) than either the PS (-24%) or the αLA (-25%) therapies alone. PS supplementation did not affect LDL particle number, however, αLA supplementation reduced LDL particle number when supplemented alone (-47%) or in combination with PS (-54%). Compared with the HF-fed animals, evidence of increased HDL-particle number was evident in all treatment groups to a similar extent (21-22%). PS-mediated interruption of intestinal cholesterol absorption was evident by increased fecal cholesterol loss (+52%) and compensatory increase in HMG-CoA reductase mRNA (1.6 fold of HF), however, αLA supplementation did not affect fecal cholesterol loss. Hepatic mRNA and protein expression patterns suggested that αLA modulated multiple aspects of cholesterol homeostasis including reduced synthesis (HMG-CoA reductase mRNA, 0.7 fold of HF), reduced bile acid synthesis (CYP7a1 expression, 0.17 of HF), and increased cholesterol clearance (reduced PCSK9 mRNA, 0.5 fold of HF; increased LDLr protein, 2 fold of HF). Taken together, this data suggests that PS and αLA work through unique and complementary mechanisms to provide a superior and more comprehensive cholesterol lowering response than either therapy alone.

Indexed as

Diet, High-FatAcyl Coenzyme AAnimalsAnticholesteremic AgentsAntioxidantsBile Acids and SaltsCholesterolCholesterol, HDLCholesterol, LDLDietary FatsDietary SupplementsDrug SynergismHypercholesterolemiaIntestinal AbsorptionLiverMale3-hydroxy-3-methylglutaryl-coenzyme AAcyl Coenzyme AAnticholesteremic AgentsAntioxidantsBile Acids and SaltsCholesterolCholesterol, HDLCholesterol, LDLDietary FatsPCSK9 protein, ratPhytosterolsProprotein Convertase 9RNA, MessengerSerine EndopeptidasesThioctic AcidAlpha lipoic acidhigh fat dietlipidslipoproteinsphytosterols

Identifiers

PMID25664679
PMCPMC4530079
OpenAlexW2152700665

What OpenQuestion holds

Texttitle and abstract
LicenceTDM
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.