Evidence map›Paper›PMID 23633496›Full record

ArticleJournal of lipid research2013

Rare APOA5 promoter variants associated with paradoxical HDL cholesterol decrease in response to fenofibric acid therapy.

Ariel Brautbar, Maja Barbalic, Fengju Chen, John Belmont, Salim S Virani, Steve Scherer, Robert A Hegele, Christie M Ballantyne

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-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, 9 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
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

8 authors at 4 institutions in 2 countries.

Ariel BrautbarCenter for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI, USA. brautbar@bcm.edu
Maja Barbalic
Fengju Chen
John Belmont
Salim S Virani
Steve Scherer
Robert A Hegele
Christie M Ballantyne
Houston Methodist · USThe University of Texas Health Science Center at Houston · USHealth Services Research & Development · USRobarts Clinical Trials · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Individuals with mixed dyslipidemia, including high triglycerides (TGs) and low high density lipoprotein cholesterol (HDL-C), have increased risk for coronary events. We examined the effect of rare genetic variants in the APOA5 gene region on plasma HDL-C, apolipoprotein A-I (apoA-I), and TG response to fenofibric acid monotherapy and in combination with statins. The APOA5 gene region was sequenced in 1,612 individuals with mixed dyslipidemia in a randomized trial of fenofibric acid alone and in combination with statins. Student's t-test and rare variant burden tests were used to examine plasma HDL-C, apoA-I, and TG response. Rare APOA5 promoter region variants were associated with decreased HDL-C and apoA-I levels in response to fenofibric acid therapy; rare missense variants were associated with increased TG response to combination therapy. Further study is needed to examine the effect of these rare variants on coronary outcomes in this population in response to fenofibric acid monotherapy or combined with statins.

Indexed as

Amino AcidsApolipoprotein A-IApolipoprotein A-VApolipoproteins ACholesterol, HDLDyslipidemiasFemaleFenofibrateGenetic VariationHumansMalePromoter Regions, GeneticTriglyceridesAmino AcidsAPOA5 protein, humanApolipoprotein A-IApolipoprotein A-VApolipoproteins ACholesterol, HDLFenofibratefenofibric acidstatineTriglyceridesapolipoproteinscholesterol-lowering drugsfenofibric acidhigh density lipoproteinlipidsrare variants

Identifiers

PMID23633496
PMCPMC3679399
OpenAlexW2132069074

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.