Evidence map›Paper›PMID 24416716›Full record

ArticleJACC. Heart failure2013

Gene Expression Profiles of Peripheral Blood Mononuclear Cells Reveal Transcriptional Signatures as Novel Biomarkers for Cardiac Remodeling in Rats with Aldosteronism and Hypertensive Heart Disease.

Ivan C Gerling, Robert A Ahokas, German Kamalov, Wenyuan Zhao, Syamal K Bhattacharya, Yao Sun, Karl T Weber

Open access · greenAbstract read
In one paragraph

Article in JACC. Heart failure, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 1 institution in 1 country.

Ivan C GerlingDivision of Endocrinology, University of Tennessee Health Science Center, Memphis, TN, USA.
Robert A AhokasDepartment of Obstetrics and Gynecology, University of Tennessee Health Science Center, Memphis, TN, USA.
German KamalovDivision of Cardiovascular Diseases, University of Tennessee Health Science Center, Memphis, TN, USA.
Wenyuan ZhaoDivision of Cardiovascular Diseases, University of Tennessee Health Science Center, Memphis, TN, USA.
Syamal K BhattacharyaDivision of Cardiovascular Diseases, University of Tennessee Health Science Center, Memphis, TN, USA.
Yao SunDivision of Cardiovascular Diseases, University of Tennessee Health Science Center, Memphis, TN, USA.
Karl T WeberDivision of Cardiovascular Diseases, University of Tennessee Health Science Center, Memphis, TN, USA.
University of Tennessee Health Science Center · US

Funding

Molecular Phenotyping of NOD MiceR01DK062103 · NIDDK · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI GERLING, IVAN C · 2002 to 2010
$2.1M
Aldosteronism: An Immunostimulatory StateR01HL073043 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI WEBER, KARL T · 2004 to 2008
$1.8M
Recovery from Cachexia in Heart and Skeletal MuscleR01HL090867 · NHLBI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI WEBER, KARL T · 2008 to 2011
$1.5M
NHLBI NIH HHS R01 HL073043NHLBI NIH HHS R01 HL090867NIDDK NIH HHS R01 DK062103
6 · The paper itself

Abstract

objectivesIn searching for a noninvasive surrogate tissue having mimicry with the prooxidant/-proinflammatory hypertensive heart disease (HHD) phenotype, we turned to peripheral blood mononuclear cells (PBMC). We tested whether iterations in [Ca

backgroundInappropriate neurohormonal activation contributes to pathologic remodeling of myocardium in HHD associated with aldosteronism. In rats receiving chronic ALDOST, evidence of reparative fibrosis replacing necrotic cardiomyocytes and coronary vasculopathy appears at wk 4 associated with the induction of oxidative stress by mitochondria that overwhelms endogenous, largely Zn

methodsIn PBMC and cardiomyocytes, quantitation of cytoplasmic free Ca

resultsCompared to controls, at wk 1 and 4 ALDOST, we found comparable: increments in [Ca

conclusionsSignificant overlapping demonstrated in the molecular mimicry of PBMC and cardiomyocytes during preclinical and pathologic stages of ALDOST implicates that transcriptional signatures of PBMC may serve as early noninvasive and novel sentinels predictive of impending pathologic remodeling in HHD.

Indexed as

aldosteronismcalciumcardiomyocytesgene chip arrayoxidative stressperipheral blood mononuclear cellszinc

Identifiers

PMID24416716
PMCPMC3885325
OpenAlexW1963952492

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.