Evidence map›Paper›PMID 24504737›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2014

Tissue-specific RNA-Seq in human evoked inflammation identifies blood and adipose LincRNA signatures of cardiometabolic diseases.

Yichuan Liu, Jane F Ferguson, Chenyi Xue, Rachel L Ballantyne, Ian M Silverman, Sager J Gosai, Jacquelyn Serfecz, Michael P Morley, Brian D Gregory, Mingyao Li and 1 more

Abstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
–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

46 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Review
  6. Article
  7. Frontiers in immunology · 2022
    Article
  8. Article
  9. Review
  10. Role of the long non-coding RNA HOTAIR/miR-126 axis in anExperimental and therapeutic medicine · 2021
    Article
  11. Article
  12. Article
  13. NcRNAs in Vascular and Valvular Intercellular Communication.Frontiers in molecular biosciences · 2021
    Review
  14. Article
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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.

Yichuan LiuFrom the Departments of Biostatistics and Epidemiology and Biology, Cardiovascular Institute, Perelman School of Medicine and School of Arts and Science at the University of Pennsylvania, Philadelphia.
Jane F Ferguson
Chenyi Xue
Rachel L Ballantyne
Ian M Silverman
Sager J Gosai
Jacquelyn Serfecz
Michael P Morley
Brian D Gregory
Mingyao Li
Muredach P Reilly

Funding

The Nicotinic Acid Receptor HM74A in Vascular InjuryP50HL083799 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2006 to 2010
$15.8M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM008216 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI EPSTEIN, DOUGLAS J · 1987 to 2023
$8.3M
Elucidation of Tissue-Specific Transcriptomic Profiles in Cardiometabolic DiseaseR01HL113147 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI LI, MINGYAO, REILLY, MUREDACH P · 2012 to 2022
$6.8M
Genetics of atherosclerosis in renal diseaseR01DK071224 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI REILLY, MUREDACH P · 2006 to 2010
$2.9M
Fractalkine in Adipose Inflammation and Insulin ResistanceR01DK090505 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI REILLY, MUREDACH P · 2011 to 2015
$2.8M
Glycomics of Heart and Lung Disease in the Genomic EraU01HL108636 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI REILLY, MUREDACH P · 2011 to 2014
$2.4M
Developing Statistical Methods for Disease Gene DiscoveryR01HG004517 · NHGRI · VANDERBILT UNIVERSITY · PI LI, CHUN, LI, MINGYAO · 2008 to 2012
$1.9M
Mentored Patient Oriented Research in Cardiometabolic DiseaseK24HL107643 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI REILLY, MUREDACH P · 2011 to 2020
$1.4M
Statistical Methods for Gene Mapping Studies in Admixed PopulationsR01HG005854 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI LI, MINGYAO · 2010 to 2012
$978k
NHGRI NIH HHS R01 HG004517NHGRI NIH HHS R01HG004517NHGRI NIH HHS R01 HG005854NHGRI NIH HHS R01HG005854NHLBI NIH HHS K24 HL107643NHLBI NIH HHS K24-HL107643NHLBI NIH HHS P50 HL083799NHLBI NIH HHS R01 HL113147NHLBI NIH HHS U01 HL108636NHLBI NIH HHS U01-HL108636NIDDK NIH HHS R01 DK071224NIDDK NIH HHS R01-DK071224NIDDK NIH HHS R01 DK090505NIDDK NIH HHS R01-DK-090505NIGMS NIH HHS T32 GM008216
6 · The paper itself

Abstract

objectiveInappropriate transcriptional activation of innate immunity is a pathological feature of several cardiometabolic disorders, but little is known about inflammatory modulation of long intergenic noncoding RNAs (lincRNAs) in disease-relevant human tissues. APPROACH AND

resultsWe applied deep RNA sequencing (>500 million filtered reads per sample) to blood and adipose during low-dose experimental endotoxemia (lipopolysaccharide) in a healthy human, with targeted replication in separate individuals undergoing endotoxemia (n=6), to identify inflammatory lincRNAs. A subset of these lincRNAs was examined for expression in adipocytes and monocytes, modulation in adipose of obese humans, and overlap with genome-wide association study signals for inflammatory and cardiometabolic traits. Of a stringent set of 4284 lincRNAs, ≈11% to 22% were expressed with 201 and 56 lincRNAs modulated by lipopolysaccharide in blood or adipose, respectively. Tissue-specific expression of a subset of 6 lipopolysaccharide-lincRNAs was replicated with lipopolysaccharide modulation confirmed for all 3 expressed in blood and 2 of 4 expressed in adipose. The broader generalizability of findings in blood of subject A was confirmed by RNA sequencing in 7 additional subjects. We confirmed adipocytes and monocytes as potential cell-sources of selective lipopolysaccharide-regulated lincRNAs, and 2 of these, linc-DMRT2 (P=0.002) and linc-TP53I13 (P=0.01), were suppressed in adipose of obese humans. Finally, we provide examples of lipopolysaccharide-modulated lincRNAs that overlap single nucleotide polymorphisms that are associated with cardiometabolic traits.

conclusionsOur findings provide novel insights into tissue-level, inflammatory transcriptome regulation in cardiometabolic diseases. These are complementary to more usual approaches limited to interrogation of DNA variations.

Indexed as

High-Throughput Nucleotide SequencingAdipocytesAdultBinding SitesCase-Control StudiesCells, CulturedEndotoxemiaFemaleGene Expression ProfilingGene Expression RegulationGenetic MarkersGenome-Wide Association StudyHumansInflammationInflammation MediatorsLipopolysaccharidesGenetic MarkersInflammation MediatorsLipopolysaccharidesRNA, Long NoncodingTranscription FactorsgenomicslincRNARNA sequence

Identifiers

PMID24504737
PMCPMC3966947

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Registered trials

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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.