Evidence map›Paper›PMID 24858532›Full record

ArticleGenomics2014

Comparative genome-wide transcriptional analysis of human left and right internal mammary arteries.

Giovanni Ferrari, John Quackenbush, John Strobeck, Lan Hu, Christopher K Johnson, Andrew Mak, Richard E Shaw, Kathleen Sayles, Mariano E Brizzio, Alex Zapolanski and 1 more

Abstract read
In one paragraph

Article in Genomics, 2014. 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
–field-weighted citation impact
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. Review
  2. Perivascular Adipose Tissue Inflammation in Ischemic Heart Disease.Arteriosclerosis, thrombosis, and vascular biology · 2021
    Article
  3. Bilateral internal thoracic artery grafting:Annals of cardiothoracic surgery · 2018
    Article
  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

11 authors.

Giovanni FerrariThe Valley Columbia Heart Center, 223 North Van Dien Avenue Ridgewood, NJ 07450, USA; University of Pennsylvania, Department of Surgery, Glenolden, PA 19036, USA.
John QuackenbushCenter for Cancer Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
John StrobeckThe Valley Columbia Heart Center, 223 North Van Dien Avenue Ridgewood, NJ 07450, USA.
Lan HuCenter for Cancer Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Christopher K JohnsonThe Valley Columbia Heart Center, 223 North Van Dien Avenue Ridgewood, NJ 07450, USA.
Andrew MakThe Valley Columbia Heart Center, 223 North Van Dien Avenue Ridgewood, NJ 07450, USA.
Richard E ShawThe Valley Columbia Heart Center, 223 North Van Dien Avenue Ridgewood, NJ 07450, USA.
Kathleen SaylesThe Valley Columbia Heart Center, 223 North Van Dien Avenue Ridgewood, NJ 07450, USA.
Mariano E BrizzioThe Valley Columbia Heart Center, 223 North Van Dien Avenue Ridgewood, NJ 07450, USA; Columbia University College of Physicians and Surgeons, Department of Surgery, New York, NY 10032, USA.
Alex ZapolanskiThe Valley Columbia Heart Center, 223 North Van Dien Avenue Ridgewood, NJ 07450, USA; Columbia University College of Physicians and Surgeons, Department of Surgery, New York, NY 10032, USA.
Juan B GrauThe Valley Columbia Heart Center, 223 North Van Dien Avenue Ridgewood, NJ 07450, USA; Columbia University College of Physicians and Surgeons, Department of Surgery, New York, NY 10032, USA. Electronic address: jbg2136@cumc.columbia.edu.

Funding

MeV: Software for Next Generation Genomic Data AnalysisU01CA151118 · NCI · DANA-FARBER CANCER INST · PI QUACKENBUSH, JOHN · 2011 to 2015
$2.9M
NCI NIH HHS U01 CA151118
6 · The paper itself

Abstract

In coronary artery bypass grafting (CABG), the combined use of left and right internal mammary arteries (LIMA and RIMA) - collectively known as bilateral IMAs (BIMAs) provides a survival advantage over the use of LIMA alone. However, gene expression in RIMA has never been compared to that in LIMA. Here we report a genome-wide transcriptional analysis of BIMA to investigate the expression profiles of these conduits in patients undergoing CABG. As expected, in comparing the BIMAs to the aorta, we found differences in pathways and processes associated with atherosclerosis, inflammation, and cell signaling - pathways which provide biological support for the observation that BIMA grafts deliver long-term benefits to the patients and protect against continued atherosclerosis. These data support the widespread use of BIMAs as the preferred conduits in CABG.

Indexed as

TranscriptomeAgedAortaCoronary Artery BypassFemaleGene Expression ProfilingGenome, HumanHumansMaleMammary ArteriesMiddle AgedOrgan SpecificityCardiovascular diseaseCoronary artery bypass graftingGenomicsTranscriptome analysis

Identifiers

PMID24858532
PMCPMC4152843

What OpenQuestion holds

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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.