Evidence map›Paper›PMID 39066479›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2024

CITED4 gene therapy protects against maladaptive cardiac remodeling after ischemia/reperfusion injury in mice.

Carolin Lerchenmüller, Margaret H Hastings, Charles P Rabolli, Fynn Betge, Mani Roshan, Laura X Liu, Xiaojun Liu, Chiara Heß, Jason D Roh, Colin Platt and 6 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. TargetingJournal of the American Heart Association · 2025
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. CITED4 gene therapy: Can it be cited for preventing maladaptive post-ischemic cardiac remodeling?Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Carolin LerchenmüllerDepartment of Cardiology, University Hospital Heidelberg, 69120 Heidelberg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Heidelberg/Mannheim, 69120 Heidelberg, Germany; Chair of Gender Medicine, University of Zurich, 8006 Zurich, Switzerland; Department of Cardiology, University Hospital Zurich, 8091 Zurich, Switzerland.
Margaret H HastingsStanley and Judith Frankel Institute for Heart and Brain Health, University of Michigan Medical Center, Ann Arbor, MI 48109, USA.
Charles P RabolliDepartment of Cardiology, University Hospital Heidelberg, 69120 Heidelberg, Germany; Cardiology Division and Corrigan Minehan Heart Center, Massachusetts General Hospital, Boston, MA 02114, USA.
Fynn BetgeDepartment of Cardiology, University Hospital Heidelberg, 69120 Heidelberg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Heidelberg/Mannheim, 69120 Heidelberg, Germany.
Mani RoshanDepartment of Cardiology, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Laura X LiuCardiology Division and Corrigan Minehan Heart Center, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Medical School, Boston, MA 02115, USA.
Xiaojun LiuCardiology Division and Corrigan Minehan Heart Center, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Medical School, Boston, MA 02115, USA.
Chiara HeßDepartment of Cardiology, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Jason D RohCardiology Division and Corrigan Minehan Heart Center, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Medical School, Boston, MA 02115, USA.
Colin PlattCardiology Division and Corrigan Minehan Heart Center, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Medical School, Boston, MA 02115, USA.
Vassilios BezzeridesHarvard Medical School, Boston, MA 02115, USA; Cardiology Department, Boston Children's Hospital, Boston, MA 02115, USA.
Martin BuschDepartment of Cardiology, University Hospital Heidelberg, 69120 Heidelberg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Heidelberg/Mannheim, 69120 Heidelberg, Germany.
Hugo A KatusDepartment of Cardiology, University Hospital Heidelberg, 69120 Heidelberg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Heidelberg/Mannheim, 69120 Heidelberg, Germany.
Norbert FreyDepartment of Cardiology, University Hospital Heidelberg, 69120 Heidelberg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Heidelberg/Mannheim, 69120 Heidelberg, Germany.
Patrick MostDepartment of Cardiology, University Hospital Heidelberg, 69120 Heidelberg, Germany; German Center for Cardiovascular Research (DZHK), Partner Site Heidelberg/Mannheim, 69120 Heidelberg, Germany.
Anthony RosenzweigStanley and Judith Frankel Institute for Heart and Brain Health, University of Michigan Medical Center, Ann Arbor, MI 48109, USA. Electronic address: anthros@med.umich.edu.

Funding

Understanding the Cardiac Benefits of Exercise at the Cellular and Molecular LevelR35HL155318 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANTHONY ROSENZWEIG · 2021 to 2026
$5.4M
Role of Activin Type II receptor signaling in age-related heart failureR01AG061034 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ROSENZWEIG, ANTHONY · 2019 to 2023
$3.0M
The role of C/EBPbeta and CITED4 in the heartR01HL110733 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ROSENZWEIG, ANTHONY · 2011 to 2015
$2.1M
Placental Senescence in Peripartum CardiomyopathyR01HL170058 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI JASON DAVID ROH · 2023 to 2026
$1.9M
NHLBI NIH HHS R01 HL110733NHLBI NIH HHS R01 HL170058NHLBI NIH HHS R35 HL155318NIA NIH HHS R01 AG061034
6 · The paper itself

Abstract

Cardiac signaling pathways functionally important in the heart's response to exercise often protect the heart against pathological stress, potentially providing novel therapeutic targets. However, it is important to determine which of these pathways can be feasibly targeted in vivo. Transgenic overexpression of exercise-induced CITED4 has been shown to protect against adverse remodeling after ischemia/reperfusion injury (IRI). Here we investigated whether somatic gene transfer of CITED4 in a clinically relevant time frame could promote recovery after IRI. Cardiac CITED4 gene delivery via intravenous AAV9 injections in wild type mice led to an approximately 3-fold increase in cardiac CITED4 expression. After 4 weeks, CITED4-treated animals developed physiological cardiac hypertrophy without adverse remodeling. In IRI, delivery of AAV9-CITED4 after reperfusion resulted in a 6-fold increase in CITED4 expression 1 week after surgery, as well as decreased apoptosis, fibrosis, and inflammatory markers, culminating in a smaller scar and improved cardiac function 8 weeks after IRI, compared with control mice receiving AAV9-GFP. Somatic gene transfer of CITED4 induced a phenotype suggestive of physiological cardiac growth and mitigated adverse remodeling after ischemic injury. These studies support the feasibility of CITED4 gene therapy delivered in a clinically relevant time frame to mitigate adverse ventricular remodeling after ischemic injury.

Indexed as

Genetic TherapyVentricular RemodelingAnimalsApoptosisDependovirusDisease Models, AnimalGenetic VectorsMaleMiceMyocardial Reperfusion InjuryMyocardiumReperfusion Injurycardiac remodelingcardioprotectionexercisegene therapy

Identifiers

PMID39066479
PMCPMC11489533

What Socratic 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 Socratic graph.