Evidence map›Paper›PMID 22215018›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2012

Concomitant intravenous nitroglycerin with intracoronary delivery of AAV1.SERCA2a enhances gene transfer in porcine hearts.

Ioannis Karakikes, Lahouaria Hadri, Kleopatra Rapti, Dennis Ladage, Kiyotake Ishikawa, Lisa Tilemann, Geng-Hua Yi, Charlotte Morel, Judith K Gwathmey, Krisztina Zsebo and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2012. 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
2.7field-weighted citation impact, top 9% 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, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Gene Therapy Approaches to Biological Pacemakers.Journal of cardiovascular development and disease · 2018
    Review
  7. Article
  8. Review
  9. Article
  10. Biological Therapies for Atrial Fibrillation: Ready for Prime Time?Journal of cardiovascular pharmacology · 2016
    Review
  11. Review
  12. Cardiac I-1c overexpression with reengineered AAV improves cardiac function in swine ischemic heart failure.Molecular therapy : the journal of the American Society of Gene Therapy · 2014
    Article
  13. Review
  14. Cardiovascular gene therapy for myocardial infarction.Expert opinion on biological therapy · 2014
    Review
  15. Review
  16. Review
  17. Article
  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

13 authors at 3 institutions in 1 country.

Ioannis KarakikesThe Cardiovascular Research Center, Mount Sinai School of Medicine, New York, New York 10029, USA.
Lahouaria Hadri
Kleopatra Rapti
Dennis Ladage
Kiyotake Ishikawa
Lisa Tilemann
Geng-Hua Yi
Charlotte Morel
Judith K Gwathmey
Krisztina Zsebo
Thomas Weber
Yoshiaki Kawase
Roger J Hajjar
Icahn School of Medicine at Mount Sinai · USCardiovascular Research Foundation · USCelladon Corporation (United States) · US

Funding

TRIP: Targeted Gene Therapy for the Treatment of Heart FailureP50HL112324 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ASCHEIM, DEBORAH DAVIS, HAJJAR, ROGER J. · 2012 to 2014
$6.4M
PICOT and Cardiac HypertrophyR01HL080498 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI HAJJAR, ROGER J. · 2006 to 2010
$2.2M
Targeting Calcium Cycling in Pre-Clinical Model CardiacR01HL083156 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI HAJJAR, ROGER J. · 2006 to 2010
$1.7M
Genetic Editing of Ca Cycling in Diabetic CardiomyopathyR01HL078731 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAJJAR, ROGER J. · 2007 to 2010
$1.7M
C-TRIP: Targeted Gene Therapy for the Treatment of Heart Failure (P20)P20HL100396 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAJJAR, ROGER J. · 2010 to 2011
$1.7M
Gene Therapy with Cardiotropic Vectors for the Treatment of Heart FailureR01HL088434 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAJJAR, ROGER J. · 2010 to 2013
$1.7M
K and Ca Channels in Cardiac Hypertrophy and FailureR01HL071763 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI HAJJAR, ROGER J. · 2003 to 2006
$1.6M
Regression of cardiac hypertrophyR01HL093183 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAJJAR, ROGER J. · 2009 to 2010
$1.1M
Protein Phosphatase Inhibitor-1 and vascular smooth muscle cell functionK01HL103176 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HADRI, LAHOUARIA · 2010 to 2014
$674k
NHLBI NIH HHS HL071763NHLBI NIH HHS HL080498NHLBI NIH HHS HL083156NHLBI NIH HHS HL088434NHLBI NIH HHS K01 HL103176NHLBI NIH HHS P20 HL100396NHLBI NIH HHS P20HL100396NHLBI NIH HHS P50 HL112324NHLBI NIH HHS R01 HL071763NHLBI NIH HHS R01 HL078731NHLBI NIH HHS R01 HL080498NHLBI NIH HHS R01 HL083156NHLBI NIH HHS R01 HL088434NHLBI NIH HHS R01 HL093183
6 · The paper itself

Abstract

SERCA2a gene therapy improves contractile and energetic function of failing hearts and has been shown to be associated with benefits in clinical outcomes, symptoms, functional status, biomarkers, and cardiac structure in a phase 2 clinical trial. In an effort to enhance the efficiency and homogeneity of gene uptake in cardiac tissue, we examined the effects of nitroglycerin (NTG) in a porcine model following AAV1.SERCA2a gene delivery. Three groups of Göttingen minipigs were assessed: (i) group A: control intracoronary (IC) AAV1.SERCA2a (n = 6); (ii) group B: a single bolus IC injection of NTG (50 µg) immediately before administration of intravenous (IV) AAV1.SERCA2a (n = 6); and (iii) group C: continuous IV NTG (1 µg/kg/minute) during the 10 minutes of AAV1.SERCA2a infusion (n = 6). We found that simultaneous IV infusion of NTG and AAV1.SERCA2a resulted in increased viral transduction efficiency, both in terms of messenger RNA (mRNA) as well as SERCA2a protein levels in the whole left ventricle (LV) compared to control animals. On the other hand, IC NTG pretreatment did not result in enhanced gene transfer efficiency, mRNA or protein levels when compared to control animals. Importantly, the transgene expression was restricted to the heart tissue. In conclusion, we have demonstrated that IV infusion of NTG significantly improves cardiac gene transfer efficiency in porcine hearts.

Indexed as

Gene Transfer TechniquesAnimalsCells, CulturedCoronary CirculationDependovirusGene ExpressionGenetic VectorsHemodynamicsInfusions, Intra-ArterialInfusions, IntravenousMaleMyocardiumMyocytes, CardiacNitroglycerinRatsRats, Sprague-DawleyNitroglycerinRNA, MessengerSarcoplasmic Reticulum Calcium-Transporting ATPases

Identifiers

PMID22215018
PMCPMC3293603
OpenAlexW2082748796

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.