Evidence map›Paper›PMID 23735785›Full record

ArticleJournal of molecular and cellular cardiology2013

miRNA-548c: a specific signature in circulating PBMCs from dilated cardiomyopathy patients.

Manveen K Gupta, Carmel Halley, Zhong-Hui Duan, Jason Lappe, Jamie Viterna, Subhra Jana, Katarzyna Augoff, Maradumane L Mohan, Neelakantan T Vasudevan, Jie Na and 5 more

Abstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 3 pooled it
1.6field-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

28 citing papers in PubMed, 3 syntheses or guidelines pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Role of miRNAs in hypoxia-related disorders.Journal of biosciences · 2018
    Review
  20. 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

15 authors at 3 institutions in 1 country.

Manveen K GuptaDepartment of Molecular Cardiology, Lerner Research Institute, Cleveland Clinic, USA.
Carmel Halley
Zhong-Hui Duan
Jason Lappe
Jamie Viterna
Subhra Jana
Katarzyna Augoff
Maradumane L Mohan
Neelakantan T Vasudevan
Jie Na
Khalid Sossey-Alaoui
Xiuping Liu
Chang-Gong Liu
W H Wilson Tang
Sathyamangla V Naga Prasad
Cleveland Clinic Lerner College of Medicine · USThe University of Texas Health Science Center at Houston · USUniversity of Akron · US

Funding

Nitrative stress in heart failureR01HL103931 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI TANG, WAI HONG WILSON · 2010 to 2014
$3.8M
Novel Regulation of Beta Andregenic Receptor FunctionR01HL089473 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI PRASAD, SATHYAMANGLA V · 2008 to 2017
$3.7M
NHLBI NIH HHS R01 HL089473NHLBI NIH HHS R01 HL103931NHLBI NIH HHS R01HL103931
6 · The paper itself

Abstract

High fidelity genome-wide expression analysis has strengthened the idea that microRNA (miRNA) signatures in peripheral blood mononuclear cells (PBMCs) can be potentially used to predict the pathology when anatomical samples are inaccessible like the heart. PBMCs from 48 non-failing controls and 44 patients with relatively stable chronic heart failure (ejection fraction of ≤ 40%) associated with dilated cardiomyopathy (DCM) were used for miRNA analysis. Genome-wide miRNA-microarray on PBMCs from chronic heart failure patients identified miRNA signature uniquely characterized by the downregulation of miRNA-548 family members. We have also independently validated downregulation of miRNA-548 family members (miRNA-548c & 548i) using real time-PCR in a large cohort of independent patient samples. Independent in silico Ingenuity Pathway Analysis (IPA) of miRNA-548 targets shows unique enrichment of signaling molecules and pathways associated with cardiovascular disease and hypertrophy. Consistent with specificity of miRNA changes with pathology, PBMCs from breast cancer patients showed no alterations in miRNA-548c expression compared to healthy controls. These studies suggest that miRNA-548 family signature in PBMCs can therefore be used to detect early heart failure. Our studies show that cognate networking of predicted miRNA-548 targets in heart failure can be used as a powerful ancillary tool to predict the ongoing pathology.

Indexed as

Breast NeoplasmsCardiomyopathy, DilatedCells, CulturedFemaleGene Expression ProfilingHeart FailureHumansLeukocytes, MononuclearMaleMicroRNAsMiddle AgedMicroRNAsBiomarkerCanonical signaling networksDilated cardiomyopathymicroRNA-548Peripheral blood mononuclear cells (PBMC)

Identifiers

PMID23735785
PMCPMC3735826
OpenAlexW1986368978

What OpenQuestion holds

Textmetadata
LicenceTDM
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.