Evidence map›Paper›PMID 33006292›Full record

ArticleJournal of the American Heart Association2020

Unmasking Arrhythmogenic Hubs of Reentry Driving Persistent Atrial Fibrillation for Patient-Specific Treatment.

Brian J Hansen, Jichao Zhao, Katelynn M Helfrich, Ning Li, Alexander Iancau, Alexander M Zolotarev, Stanislav O Zakharkin, Anuradha Kalyanasundaram, Megan Subr, Nawshin Dastagir and 13 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Journal of the American Heart Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

  1. Phase 2 Re-Entry Without IJACC. Clinical electrophysiology · 2023
    Trial
  2. Article
  3. Article
  4. Review
  5. Are drivers recurring or ephemeral? observations from serial mapping of persistent atrial fibrillation.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Future Directions for Mapping Atrial Fibrillation.Arrhythmia & electrophysiology review · 2022
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. 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

23 authors at 3 institutions in 3 countries.

Brian J HansenDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Jichao ZhaoUniversity of Auckland Auckland New Zealand.
Katelynn M HelfrichDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Ning LiDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Alexander IancauDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Alexander M ZolotarevDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Stanislav O ZakharkinDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Anuradha KalyanasundaramDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Megan SubrDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Nawshin DastagirUniversity of Auckland Auckland New Zealand.
Roshan SharmaUniversity of Auckland Auckland New Zealand.
Esthela J ArtigaDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Nicholas SalgiaDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Mustafa M HoumsseDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Omar KahalyDavis Heart & Lung Research InstituteThe Ohio State University Wexner Medical Center Columbus OH.
Paul M L JanssenDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Peter J MohlerDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
Nahush A MokadamDavis Heart & Lung Research InstituteThe Ohio State University Wexner Medical Center Columbus OH.
Bryan A WhitsonDavis Heart & Lung Research InstituteThe Ohio State University Wexner Medical Center Columbus OH.
Muhammad R AfzalDavis Heart & Lung Research InstituteThe Ohio State University Wexner Medical Center Columbus OH.
Orlando P SimonettiDavis Heart & Lung Research InstituteThe Ohio State University Wexner Medical Center Columbus OH.
John D HummelDavis Heart & Lung Research InstituteThe Ohio State University Wexner Medical Center Columbus OH.
Vadim V FedorovDepartment of Physiology & Cell Biology and Frick Center for Heart Failure and Arrhythmia The Ohio State University Wexner Medical Center Columbus OH.
The Ohio State University Wexner Medical Center · USUniversity of Auckland · NZSkolkovo Institute of Science and Technology · RU

Funding

Targeting the Arrhythmogenic Sources of Human Atrial FibrillationR01HL135109 · NHLBI · OHIO STATE UNIVERSITY · PI Vadim V Fedorov · 2017 to 2026
$6.0M
Frequency-dependent modulation of cardiac myofilament function in health/diseaseR01HL113084 · NHLBI · OHIO STATE UNIVERSITY · PI JANSSEN, PAULUS ML · 2012 to 2023
$4.6M
Integration of structure and signaling in cardiac pacemaker functionR01HL115580 · NHLBI · OHIO STATE UNIVERSITY · PI FEDOROV, VADIM V · 2013 to 2021
$4.2M
Training To Provide the Knowledge, Skills, and Culture To the Next Generation of Cardiovascular ScientistsT32HL134616 · NHLBI · OHIO STATE UNIVERSITY · PI Brandon J Biesiadecki, Jill A Rafael-Fortney · 2017 to 2026
$2.6M
Integrated functional and structural mapping for targeting substrates of reentrant atrial fibrillation drivers in the human heartF30HL142179 · NHLBI · OHIO STATE UNIVERSITY · PI HANSEN, BRIAN J. · 2018 to 2021
$139k
NHLBI NIH HHS F30 HL142179NHLBI NIH HHS R01 HL113084NHLBI NIH HHS R01 HL115580NHLBI NIH HHS R01 HL135109NHLBI NIH HHS T32 HL134616
6 · The paper itself

Abstract

Background Atrial fibrillation (AF) driver mechanisms are obscured to clinical multielectrode mapping approaches that provide partial, surface-only visualization of unstable 3-dimensional atrial conduction. We hypothesized that transient modulation of refractoriness by pharmacologic challenge during multielectrode mapping improves visualization of hidden paths of reentrant AF drivers for targeted ablation. Methods and Results Pharmacologic challenge with adenosine was tested in ex vivo human hearts with a history of AF and cardiac diseases by multielectrode and high-resolution subsurface near-infrared optical mapping, integrated with 3-dimensional structural imaging and heart-specific computational simulations. Adenosine challenge was also studied on acutely terminated AF drivers in 10 patients with persistent AF. Ex vivo, adenosine stabilized reentrant driver paths within arrhythmogenic fibrotic hubs and improved visualization of reentrant paths, previously seen as focal or unstable breakthrough activation pattern, for targeted AF ablation. Computational simulations suggested that shortening of atrial refractoriness by adenosine may (1) improve driver stability by annihilating spatially unstable functional blocks and tightening reentrant circuits around fibrotic substrates, thus unmasking the common reentrant path; and (2) destabilize already stable reentrant drivers along fibrotic substrates by accelerating competing fibrillatory wavelets or secondary drivers. In patients with persistent AF, adenosine challenge unmasked hidden common reentry paths (9/15 AF drivers, 41±26% to 68±25% visualization), but worsened visualization of previously visible reentry paths (6/15, 74±14% to 34±12%). AF driver ablation led to acute termination of AF. Conclusions Our ex vivo to in vivo human translational study suggests that transiently altering atrial refractoriness can stabilize reentrant paths and unmask arrhythmogenic hubs to guide targeted AF driver ablation treatment.

Indexed as

AdenosineAdultAtrial FibrillationFemaleHeartHeart AtriaHumansImaging, Three-DimensionalMaleMicroelectrodesMiddle AgedMyocardiumVoltage-Sensitive Dye ImagingAdenosineatrial fibrillationfibrosismagnetic resonance imagingmultielectrode mappingnear‐infrared optical mapping

Identifiers

PMID33006292
PMCPMC7792422
OpenAlexW3091714175

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.