Evidence map›Paper›PMID 27040450›Full record

ArticleJournal of lipid research2016

WAT apoC-I secretion: role in delayed chylomicron clearance in vivo and ex vivo in WAT in obese subjects.

Yannick Cyr, Hanny Wassef, Simon Bissonnette, Valerie Lamantia, Jean Davignon, May Faraj

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Diabetes and dyslipidemia: characterizing lipoprotein metabolism.Diabetes, metabolic syndrome and obesity : targets and therapy · 2017
    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 1 institution in 1 country.

Yannick CyrInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, Québec, Canada Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada Montreal Diabetes Research Center (MDRC), Montréal, Québec, Canada.
Hanny WassefInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, Québec, Canada Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada Montreal Diabetes Research Center (MDRC), Montréal, Québec, Canada.
Simon BissonnetteInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, Québec, Canada Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada Montreal Diabetes Research Center (MDRC), Montréal, Québec, Canada.
Valerie LamantiaInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, Québec, Canada Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada Montreal Diabetes Research Center (MDRC), Montréal, Québec, Canada.
Jean DavignonInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, Québec, Canada Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada Faculty of Medicine, McGill University, Montréal, Québec, Canada.
May FarajInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, Québec, Canada Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada Montreal Diabetes Research Center (MDRC), Montréal, Québec, Canada may.faraj@umontreal.ca.
Montreal Clinical Research Institute · CA

Funding

CIHR 93581
6 · The paper itself

Abstract

Reduced white adipose tissue (WAT) LPL activity delays plasma clearance of TG-rich lipoproteins (TRLs). We reported the secretion of apoC-I, an LPL inhibitor, from WAT ex vivo in women. Therefore we hypothesized that WAT-secreted apoC-I associates with reduced WAT LPL activity and TRL clearance. WAT apoC-I secretion averaged 86.9 ± 31.4 pmol/g/4 h and 74.1 ± 36.6 pmol/g/4 h in 28 women and 11 men with BMI ≥27 kg/m(2), respectively, with no sex differences. Following the ingestion of a (13)C-triolein-labeled high-fat meal, subjects with high WAT apoC-I secretion (above median) had delayed postprandial plasma clearance of dietary TRLs, assessed from plasma (13)C-triolein-labeled TGs and apoB48. They also had reduced hydrolysis and storage of synthetic (3)H-triolein-labeled ((3)H)-TRLs in WAT ex vivo (i.e., in situ LPL activity). Adjusting for WAT in situ LPL activity eliminated group differences in chylomicron clearance; while adjusting for plasma apoC-I, (3)H-NEFA uptake by WAT, or body composition did not. apoC-I inhibited in situ LPL activity in adipocytes in both a concentration- and time-dependent manner. There was no change in postprandial WAT apoC-I secretion. WAT apoC-I secretion may inhibit WAT LPL activity and promote delayed chylomicron clearance in overweight and obese subjects. We propose that reducing WAT apoC-I secretion ameliorates postprandial TRL clearance in humans.

Indexed as

Adipose Tissue, WhiteAgedAnimalsApolipoprotein B-48Apolipoprotein C-IApolipoproteins EBody Mass IndexCarbon IsotopesChylomicronsDiet, High-FatFemaleHumansLipoprotein LipaseLipoproteins, HDLMaleMiceApolipoprotein B-48Apolipoprotein C-IApolipoproteins ECarbon IsotopesChylomicronsHDL-triglycerideLipoprotein LipaseLipoproteins, HDLTriglyceridesTrioleinadipocytesapolipoprotein C-Icardiometabolic riskfat storagelipase/lipoproteinlipolysis and fatty acid metabolismobesitytriglyceride-rich lipoproteintriglycerideswhite adipose tissue

Identifiers

PMID27040450
PMCPMC4878191
OpenAlexW2419115749

What OpenQuestion holds

Textmetadata
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.