Evidence map›Paper›PMID 21224289›Full record

Trial reportJournal of lipid research2011

Reconstituted high-density lipoprotein infusion modulates fatty acid metabolism in patients with type 2 diabetes mellitus.

Brian G Drew, Andrew L Carey, Alaina K Natoli, Melissa F Formosa, Donna Vizi, Medini Reddy-Luthmoodoo, Jacquelyn M Weir, Christopher K Barlow, Gerrit van Hall, Peter J Meikle and 2 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of lipid research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00395148 (A Novel Mechanism Mediating Anti-atherosclerotic and Metabolic Actions of HDL Cholesterol), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 8% 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.

NCT00395148 nacompletednot on this map

A Novel Mechanism Mediating Anti-atherosclerotic and Metabolic Actions of HDL Cholesterol

TypeinterventionalSponsorBayside HealthRan2006 to 2008Enrolled13ConditionsHeart Disease, DiabetesArmsrHDL
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 42 citations in OpenAlex.

  1. Trial
  2. HDL and Therapy.Advances in experimental medicine and biology · 2022
    Article
  3. Review
  4. Article
  5. Apolipoprotein A-I Supports MSCs Survival under Stress Conditions.International journal of molecular sciences · 2020
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Lipidomics to Assess Omega 3 Bioactivity.Journal of clinical medicine · 2015
    Review
  12. Article
  13. Article
  14. Review
  15. Role of HDL in those with diabetes.Current cardiology reports · 2014
    Review
  16. HDL-targeted therapies: progress, failures and future.Nature reviews. Drug discovery · 2014
    Review
  17. Review
  18. Article
  19. Article
  20. 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

12 authors at 2 institutions in 3 countries.

Brian G DrewBaker IDI Heart and Diabetes Institute, Melbourne, Victoria, Australia. bdrew@mednet.ucla.edu
Andrew L Carey
Alaina K Natoli
Melissa F Formosa
Donna Vizi
Medini Reddy-Luthmoodoo
Jacquelyn M Weir
Christopher K Barlow
Gerrit van Hall
Peter J Meikle
Stephen J Duffy
Bronwyn A Kingwell
Baker Heart and Diabetes Institute · AUUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We recently demonstrated that reconstituted high-density lipoprotein (rHDL) modulates glucose metabolism in humans via both AMP-activated protein kinase (AMPK) in muscle and by increasing plasma insulin. Given the key roles of both AMPK and insulin in fatty acid metabolism, the current study investigated the effect of rHDL infusion on fatty acid oxidation and lipolysis. Thirteen patients with type 2 diabetes received separate infusions of rHDL and placebo in a randomized, cross-over study. Fatty acid metabolism was assessed using steady-state tracer methodology, and plasma lipids were measured by mass spectrometry (lipidomics). In vitro studies were undertaken in 3T3-L1 adipocytes. rHDL infusion inhibited fasting-induced lipolysis (P = 0.03), fatty acid oxidation (P < 0.01), and circulating glycerol (P = 0.04). In vitro, HDL inhibited adipocyte lipolysis in part via activation of AMPK, providing a possible mechanistic link for the apparent reductions in lipolysis observed in vivo. In contrast, circulating NEFA increased after rHDL infusion (P < 0.01). Lipidomic analyses implicated phospholipase hydrolysis of rHDL-associated phosphatidylcholine as the cause, rather than lipolysis of endogenous fat stores. rHDL infusion inhibits fasting-induced lipolysis and oxidation in patients with type 2 diabetes, potentially through both AMPK activation in adipose tissue and elevation of plasma insulin. The phospholipid component of rHDL also has the potentially undesirable effect of increasing circulating NEFA.

Indexed as

3T3-L1 CellsAdenylate KinaseAdipocytesAnimalsDiabetes Mellitus, Type 2Fatty AcidsHumansInsulin ResistanceLipolysisLipoproteins, HDLMiceOxidation-ReductionSignal TransductionAdenylate KinaseFatty AcidsLipoproteins, HDL

Identifiers

PMID21224289
PMCPMC3035694
OpenAlexW2104792407

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.