Evidence map›Paper›PMID 28942094›Full record

Trial reportJournal of clinical lipidology

Effects of n-3 fatty acid treatment on monocyte phenotypes in humans with hypertriglyceridemia.

Xiao-Yuan Dai Perrard, Zeqin Lian, George Bobotas, Mary R Dicklin, Kevin C Maki, Huaizhu Wu

Open access · greenAbstract readClinical Trial, Phase IClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical lipidology. 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
0.8field-weighted citation impact, top 28% 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, 15 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Established and Emerging Lipid-Lowering Drugs for Primary and Secondary Cardiovascular Prevention.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2023
    Review
  6. Article
  7. Article
  8. Nature versus Number: Monocytes in Cardiovascular Disease.International journal of molecular sciences · 2021
    Review
  9. Dietary and Pharmacological Fatty Acids and Cardiovascular Health.The Journal of clinical endocrinology and metabolism · 2020
    Review
  10. Article
  11. 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 1 country.

Xiao-Yuan Dai PerrardDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA.
Zeqin LianDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA.
George BobotasMatinas BioPharma, Inc, Bedminster, NJ, USA.
Mary R DicklinMidwest Biomedical Research/Center for Metabolic and Cardiovascular Health, Glen Ellyn, IL, USA.
Kevin C MakiMidwest Biomedical Research/Center for Metabolic and Cardiovascular Health, Glen Ellyn, IL, USA.
Huaizhu WuDepartment of Medicine, Baylor College of Medicine, Houston, TX, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA. Electronic address: hwu@bcm.edu.
Baylor College of Medicine · USMB Clinical Research and Consulting (United States) · US

Funding

Monocyte Activation and the Role of CD11c in obesity-linked metabolic syndromeR01HL098839 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI WU, HUAIZHU · 2010 to 2019
$3.2M
American Heart Association-American Stroke Association 16GRNT30410012NHLBI NIH HHS R01 HL098839
6 · The paper itself

Abstract

backgroundHypertriglyceridemia increases risk for atherosclerotic cardiovascular disease and may contribute to atherosclerosis by changing circulating monocyte phenotypes. High-dose n-3 polyunsaturated fatty acids reduce blood triglyceride levels. Effects of triglyceride-lowering therapy on monocyte phenotypes are not well known.

objectiveWe examined effects of n-3 polyunsaturated fatty acid treatments (eicosapentaenoic acid [EPA] plus docosapentaenoic acid [MAT9001] vs EPA ethyl esters [EPA-EE]) on monocyte phenotypes in individuals with hypertriglyceridemia.

methodsIndividuals with triglycerides 200 to 400 mg/dL were recruited. Subjects received 2 treatments in randomized order for 14 days each: MAT9001 and EPA-EE, at 4 g/d. At 2 days before the start of, and on the last day of, each treatment, nile red staining for lipids and phenotypes of each monocyte subset were examined by flow cytometry after an overnight fast and postprandially after a high-fat meal.

resultsTreatment with MAT9001 or EPA-EE reduced fasting triglyceride levels and decreased proportions of intermediate monocytes. Only MAT9001 decreased postprandial blood triglyceride levels, lowered fasting nile red levels, indicating less lipid in classical and intermediate monocytes, and reduced postprandial CD11c levels on nonclassical monocytes. MAT9001 and EPA-EE each reduced fasting and postprandial CD11c and CD36 levels on classical and intermediate monocytes and postprandial CCR5 levels on intermediate and nonclassical monocytes, with no significant differences between the 2 treatments.

conclusionsTreatment with MAT9001 in individuals with hypertriglyceridemia reduced fasting nile red staining for lipids in classical and intermediate monocytes. MAT9001 and EPA-EE each improved fasting and postprandial monocyte phenotypes, which could potentially help to protect against atherosclerosis.

Indexed as

AdolescentAdultAgedAtherosclerosisCD11c AntigenCD36 AntigensDrug CombinationsEicosapentaenoic AcidFatty Acids, Omega-3Fatty Acids, UnsaturatedFemaleFlow CytometryHumansHypertriglyceridemiaMaleMiddle AgedCD11c AntigenCD36 Antigensdocosapentaenoic acidDrug CombinationsEicosapentaenoic AcidFatty Acids, Omega-3Fatty Acids, UnsaturatedTriglyceridesAtherosclerosisDocosapentaenoic acidEicosapentaenoic acidHypertriglyceridemiaMonocytesn-3 polyunsaturated fatty acids

Identifiers

PMID28942094
PMCPMC5698114
OpenAlexW2747257164

What OpenQuestion holds

Textmetadata
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.