Evidence map›Paper›PMID 37408197›Full record

ReviewCells2023

Genome Editing and Cardiac Arrhythmias.

Oliver M Moore, Kevin S Ho, Juwan S Copeland, Vaidya Parthasarathy, Xander H T Wehrens

Abstract readReview
In one paragraph

Review in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Impact of Sorbs2 dysfunction on cardiovascular diseases.Biochimica et biophysica acta. Molecular basis of disease · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. 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

5 authors.

Oliver M MooreCardiovascular Research Institute, Baylor College of Medicine, Houston, TX 77030, USA.
Kevin S HoCardiovascular Research Institute, Baylor College of Medicine, Houston, TX 77030, USA.ORCID 0000-0003-0015-5339
Juwan S CopelandDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Vaidya ParthasarathyCardiovascular Research Institute, Baylor College of Medicine, Houston, TX 77030, USA.
Xander H T WehrensCardiovascular Research Institute, Baylor College of Medicine, Houston, TX 77030, USA.ORCID 0000-0001-5044-672X

Funding

Medical Scientist Training ProgramT32GM136611 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI Katherine Yudeh King, James P Orengo · 2020 to 2026
$10.0M
Ryanodine receptor regulation in post-operative atrial fibrillationR01HL089598 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI WEHRENS, XANDER H.T. · 2007 to 2022
$6.5M
Junctophilin-2 cleavage in ischemic heart diseaseR01HL153350 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI WEHRENS, XANDER H.T. · 2021 to 2024
$2.3M
Role of Nucleoside-Diphosphate Kinase Signaling in Atrial FibrillationR01HL160992 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI Xander H.T. Wehrens · 2023 to 2026
$2.1M
Mechanisms underlying atrial fibrillation associated with chronic kidney diseaseR01HL147108 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI LI, NA, WEHRENS, XANDER H.T. · 2019 to 2022
$2.0M
Genome Editing Treatment for Catecholaminergic Polymorphic Ventricular TachycardiaF30HL156669 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MOORE, OLIVER · 2021 to 2024
$172k
NHLBI NIH HHS F30 HL156669NHLBI NIH HHS R01 HL089598NHLBI NIH HHS R01 HL147108NHLBI NIH HHS R01 HL153350NHLBI NIH HHS R01 HL160992NIGMS NIH HHS T32 GM136611NIH HHS GM136611NIH HHS HL089598NIH HHS HL147108NIH HHS Hl153350NIH HHS HL156669NIH HHS HL160992
6 · The paper itself

Abstract

This article reviews progress in the field of cardiac genome editing, in particular, its potential utility in treating cardiac arrhythmias. First, we discuss genome editing methods by which DNA can be disrupted, inserted, deleted, or corrected in cardiomyocytes. Second, we provide an overview of in vivo genome editing in preclinical models of heritable and acquired arrhythmias. Third, we discuss recent advancements in cardiac gene transfer, including delivery methods, gene expression optimization, and potential adverse effects associated with therapeutic somatic genome editing. While genome editing for cardiac arrhythmias is still in its infancy, this approach holds great promise, especially for inherited arrhythmia syndromes with a defined genetic defect.

Indexed as

Gene EditingTachycardia, VentricularArrhythmias, CardiacHumansMyocytes, Cardiacarrhythmiascatecholaminergic polymorphic ventricular tachycardiaCRISPR/Cas9genome editinglong QT syndromeryanodine receptorRyR2

Identifiers

PMID37408197
PMCPMC10216508

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.