Evidence map›Paper›PMID 19947886›Full record

ReviewHuman gene therapy2010

Cardiac gene therapy: optimization of gene delivery techniques in vivo.

Michael G Katz, JaBaris D Swain, Jennifer D White, David Low, Hansell Stedman, Charles R Bridges

Open access · greenAbstract readReview
In one paragraph

Review in Human gene therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Recent advances in gene therapy for atrial fibrillation.Journal of cardiovascular electrophysiology · 2021
    Review
  4. Review
  5. Gene Therapy for the Treatment of Cardiac Arrhythmias: Current and Emerging Applications.The Journal of innovations in cardiac rhythm management · 2018
    Review
  6. Article
  7. Review
  8. Advanced techniques in biology & medicine · 2017
    Article
  9. Modified mRNA as a therapeutic tool to induce cardiac regeneration in ischemic heart disease.Wiley interdisciplinary reviews. Systems biology and medicine · 2017
    Review
  10. Somatic Cell Reprogramming into Cardiovascular Lineages.Journal of cardiovascular pharmacology and therapeutics · 2014
    Article
  11. Gene therapy to treat cardiovascular disease.Journal of the American Heart Association · 2013
    Review
  12. Article
  13. Article
  14. AAV-microdystrophin therapy improves cardiac performance in aged female mdx mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2011
    Article
  15. Methods in cardiomyocyte isolation, culture, and gene transfer.Journal of molecular and cellular cardiology · 2011
    Review
  16. Article
  17. Review
  18. Review
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

6 authors at 1 institution in 1 country.

Michael G KatzDivision of Cardiovascular Surgery, Department of Surgery, University of Pennsylvania Medical Center, Philadelphia, PA 19104, USA.
JaBaris D Swain
Jennifer D White
David Low
Hansell Stedman
Charles R Bridges
University of Pennsylvania · US

Funding

Translational Studies in Heart Failure Gene TherapyR01HL083078 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BRIDGES, CHARLES R · 2007 to 2018
$9.2M
NHLBI NIH HHS 1-R01-HL083078-01A2
6 · The paper itself

Abstract

Vector-mediated cardiac gene therapy holds tremendous promise as a translatable platform technology for treating many cardiovascular diseases. The ideal technique is one that is efficient and practical, allowing for global cardiac gene expression, while minimizing collateral expression in other organs. Here we survey the available in vivo vector-mediated cardiac gene delivery methods--including transcutaneous, intravascular, intramuscular, and cardiopulmonary bypass techniques--with consideration of the relative merits and deficiencies of each. Review of available techniques suggests that an optimal method for vector-mediated gene delivery to the large animal myocardium would ideally employ retrograde and/or anterograde transcoronary gene delivery,extended vector residence time in the coronary circulation, an increased myocardial transcapillary gradient using physical methods, increased endothelial permeability with pharmacological agents, minimal collateral gene expression by isolation of the cardiac circulation from the systemic, and have low immunogenicity.

Indexed as

Gene Transfer TechniquesAnimalsCricetinaeDisease Models, AnimalDogsGenetic TherapyGenetic VectorsHeart FailureHumansMyocytes, Cardiac

Identifiers

PMID19947886
PMCPMC2865214
OpenAlexW2022563863

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.